ZMP
macf1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate microtubule-actin crosslinking factor 1 (MACF1) [Source:UniProtK
Human Orthologue:
MACF1
Human Description:
microtubule-actin crosslinking factor 1 [Source:HGNC Symbol;Acc:13664]
Mouse Orthologue:
Macf1
Mouse Description:
microtubule-actin crosslinking factor 1 Gene [Source:MGI Symbol;Acc:MGI:108559]
Alleles
There are 27 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12481 | Nonsense | Available for shipment | Available now |
sa36881 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12708 | Nonsense | Available for shipment | Available now |
sa39255 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36880 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43318 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36879 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45679 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15741 | Nonsense | Available for shipment | Available now |
sa11432 | Nonsense | Available for shipment | Available now |
sa13865 | Nonsense | Available for shipment | Available now |
sa23566 | Nonsense | Available for shipment | Available now |
sa36878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32250 | Nonsense | Available for shipment | Available now |
sa17558 | Nonsense | Available for shipment | Available now |
sa25094 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36877 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23565 | Nonsense | Available for shipment | Available now |
sa43317 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12481
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 34 | 7964 | 2 | 97 |
ENSDART00000140075 | Nonsense | 77 | 1586 | 2 | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36770295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35634815 |
GRCz11 | 19 | 35221935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTCTTGTTTTCTGCTGTTTCCTCCTCTCTMTCTCTCTCTTCTCAGATGAA[C/T]GAGACCGGGTGCAAAAGAAAACTTTCACAAAATGGGTCAACAAACAWCTC
Long Flanking Sequence:
TTATTTATTTAAATGTAATTAAATTTAACTTTTATTTTTGAATTTAAGTTAATTTTAATTTAATTTTATTTTTAGTTAAAAAATTATTTTAGCTTTTAATTTAAGTTCTTTTTAATTGTAGTTAATTTAAATGATTTTTTATTTGTTTGTTTATTTTAATTTAATTTAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTTTATTCTATTTATTTAATTTAACTTTTATTTTATTTTATTGCCTTACTATAAATATCATGGCTTTCTTTTAAATGTTTTTGATCATCAATACACTATTAGGAATTTTCTACTTTTAAATTCAGACTGTTTGAATCATGACTGGAGGGATGCTTGAACCACAGAGCCATATGATTGTGCTGTAGTCTTCCTCCTGCGTTACATAATTAACTCAATCTCTCTTCCTCCCCCGTCTTGTCTCTTCCTCTTGTTTTCTGCTGTTTCCTCCTCTCTATCTCTCTCTTCTCAGATGAA[C/T]GAGACCGGGTGCAAAAGAAAACTTTCACAAAATGGGTCAACAAACATCTCATAAAGGTACAGTCCAACACGCTGGTTATTTTTGTCCTTTCTGCTGCCCTGCATGATGATAAGGCCTGCTGGCTACTTGGCCCCAGTCCCACTAAAGACACAGTGTGTGTGTCACACACACACACACACATCTATACGAACAGCCATTTTTACGGGGGCTTCCCATAGCTGTAAGGATTTTTGTACTGTACATATTGTATATTCTATCCACCTACCCCAACCCTACATCTAAACCCAACCCTCACAGGAAACAATCTGCAATTCTACATTTTCAAAATACTTAATTCTGTGTGATCTATGAGGCGTTTGCTCTTATGGGGACCAAAATATAGCCCCACAAGGTCAAAATTCCTTTAGTGTCATAAGGAATACAAGGTCTCTCTCTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36881
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 164 | 7964 | 6 | 97 |
ENSDART00000140075 | Nonsense | 207 | 1586 | 6 | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36742440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35606960 |
GRCz11 | 19 | 35194080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGTCAGGTGACCTCACGGCGAAAGAGAAGCTGCTAATATGGAGTCAA[C/T]AGGCCACTGAGGGCTACCCCGGTCTACGCTGTACCAATTTCTCCTCCAGC
Long Flanking Sequence:
ATCTGTAATTTTCTCACACGTTTGTCTGTGCTCTCAGAATTGTCTGCATTCATGCCAGGATTTAAAGAATTCCTTGCTAGCGCTGCATGAAAAAAAGCAGGCAGGGATGTGAATAGGGGCATATGAGAGGAATGACAAAGGAATACAGATTAGAGCCTGGCACAGACTGATACTGCAGTTACTGACTCTCTTTGTTTTAGAGGAAGAGGGAGTGAAAGTCGAGGAAAATGATAAGTGAAAGGTTCATGACCTTGCTATGGTTTCATTTGGTACTTGGGGTCAAAGAAACATGGAATAACCCTAAAAATTTACATTTGCAAGGAAGTAATGCTCAACCTTTTTGGTGCACGGATCCGGTCACTTTCCTTATATTCAGTTAAGTCATTTGATGACATTCAGATACAATAACAGCCTTTTCTTTTTCCCAGATCTCTGAGATCTATGTGAGCGGTGAGTCAGGTGACCTCACGGCGAAAGAGAAGCTGCTAATATGGAGTCAA[C/T]AGGCCACTGAGGGCTACCCCGGTCTACGCTGTACCAATTTCTCCTCCAGCTGGAGCGATGGACGCTTGTTCAACGCTCTTCTGCACAGATACAGGTTCACACACGTTTAAGTATATTGACCAGTTTAAAAGAAAATATGTATATTAGGGGGTAACACTCTATTTTGATGGTCCACTTGAGTATGAGTAGACTATCTGCTTAACGTCTGTTGATATTGCTTCTTCAACTGACTATAAGAAACATCGCAAGTCTACTTGACAGTCTACTTATAATCTAATAAAAATTAGTTGGCATGTAGATGCAATGTAACTTAAATTCACCCAACAGACCTTCAAAATAAAGTTTGACCTATTAGGGCATTGACACTCATGATCTTATGTCATTTTTAGGCCGGACCTAATTGACATGCAAGTGGTTGCGCAACAGAGTAACCGTGAGAACCTTGAACAGGCCTTTGAGATTGCCGAGTCATTAGGGGTGACTCGACTCCTGGATGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12708
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 553 | 7964 | 14 | 97 |
ENSDART00000140075 | Nonsense | 596 | 1586 | 14 | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36732705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35597225 |
GRCz11 | 19 | 35184345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGTAGCCATGTCCTCCTCTGAGGATGAAGGCAGTCTGCGCTTTATTTA[T/A]GAGCTGCTGGGATGGGTWGAAGAAAMGCAAGATCTGCTGGAGCGAGCTGA
Long Flanking Sequence:
GGGCAGCCGGTGCGGTGTGAGAATGAATTGGGGATGTATCTGCAGGATTGCGAGGCTCTGGTCAGACAGCTTCACCTTGACCTGCAGGTCCTCCGAGATGAGAAGTACTACCAAGTTGAGCAGCTGGCTTTCAGGTAAGAGAAAAGTGCAGCCAGTTTGAATCATCCTTGCTGAACAAAATGTGCACATTTATATTTCCATCCAGCAGTTCTAATCCTCATGTTATTTTCCTCTTGTAGGGTGTCATGTCTGCAGGAGGAGCTGGTCTCTTTGCGCCTGCAGTGTGCCAGCGTGTACAGGAAGGGTCATTTCTCTACGGGTGGTTTGCTGGGGGAGCATGTGGGTCAGAGGGGATCTTCAGGGGGTCTGGCTACACTGGGAGCACAGACTCTTTTGGGAGCAGTGGCTGCTGCTGCATCCCTTCTCAGACGGCCCATGTCTCGTGCAGATCTGGTAGCCATGTCCTCCTCTGAGGATGAAGGCAGTCTGCGCTTTATTTA[T/A]GAGCTGCTGGGATGGGTAGAAGAAACGCAAGATCTGCTGGAGCGAGCTGAGTGGGGTTCTGATCTGCCGTCTGTAGAACAGCATTTGCAGGACCACCATATCATTCACACTGCGGTGGAGGATCTTTTGAATAGCCTCAAAGAGGCTCGAACATATGAGGTAAATTAATTGTTGAATGAAGTCTTTGTATCAAAGGGCCTTTCACACCAATTCTGATGTAGTGCGAGATTCAGGAGATGTGCACACAGAAGTACAACATTGTTGATTTACATTTGAACAGCTCATGATGCATTTATATATTAGTGTCTTGAAATGGATTGGGTTGCAATAAATTCTGCTCCATTCAACATGATGTCAAACATATATAAAAGAACATTGTTTGTAAAGAAATCTATAGTTCCCCTATGAATAATTATTTATAGCCAAGTTAATTTAAATATTAGTTGTTGATCACTGTTGTAAAATAAAATTATCATTATTATTATTATTATTATTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39255
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Essential Splice Site | 1228 | 7964 | 27 | 97 |
ENSDART00000140075 | Essential Splice Site | 1271 | 1586 | 27 | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36708007)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35572527 |
GRCz11 | 19 | 35159647 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGCTTACAGACAGGTGGAGTGGAGTCCGCAGGCAGATGGAGACACG[G/A]TGAGTCCTTCACAAGACTATTATCATGTGGGTTGTTGACATGGTTTTGCA
Long Flanking Sequence:
TATATTAAATATTTAAATAAATAATAATAGTAAATCCATTCCAAATAGATTATTATTTTGGATACAGTTATTCATAACAATTCATTTGATGTAAATATTGCCCAAAAATATGTGCAAAAATACTATTAATATTTCACCTCATGCAGATAGTCTTCATTTTAGTCAAGTTTCCCAAATCATATATGTTCTGTACATTTCTACATGTGTAAGTTTAGGCTTTTGTTTGTGTGAGGTATTGAAAAGGTGACCCTACATTGTTTAATTCAATTATTTTTTATTATATTTTACACTCTGTATGTCACTCAGCAATGGCACTCGGAGCTGCAGGAGCAGGATCACATATTTCAGAGTTTGAGTTTAGAGGTCCAGCAGGCTAGAGAGGTGGGCAACCAGCTCAGCCAGCTTCACCCGGACCGCAGCCCTGAATTGGACCGCTATCAGGAGAAAGCACACCAGCTTACAGACAGGTGGAGTGGAGTCCGCAGGCAGATGGAGACACG[G/A]TGAGTCCTTCACAAGACTATTATCATGTGGGTTGTTGACATGGTTTTGCATTTTCACTGTCACACAGGACATTATTTGATTATAATTCCTATTGTCATCATTTAAATTGCAGTGAATGGTTAAACATTTCAGCATTTTCCATGGACCTTTTTTAATAAAAACTGCTTTTTTAGCAAATGGCAATCATTTTTTTTCATCTATATATTTTAAAAACATATTGTGACACCTCTTGTCAAATAGCACCATGTCCTCTGGTGTGACAATAGATGCTAATTTTCAGTGTTGGGGAAAGTTATTTTTGAAAGTAATGCATTACAATATTGAGTTACTCCCACAAAAAAGTAACTAATTAAGTTACGTAGTTCCTTTTTTATTGCAAGTAAAGCGTTACATTACTTTTGAGTTTCTTTTGTGTTACTTTTTATTACTTGTTTGAGGCTTGATCTCTTAAAGAACTTGCTTTTTTTTCTTTTTCTTTTTAAATAGAGGAGCTCTGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36880
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 2696 | 7964 | 35 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36694671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35559191 |
GRCz11 | 19 | 35146311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTACATAATGTGAACTTACAAGAGAAAGTTTTGCCATCAGAAAAGTA[T/G]AAAGAATCCAGGATTAAGGAAGACGAGACTGCAAGCAAGAAGACCAACAT
Long Flanking Sequence:
ATTAGAAAAGGCAAAATTGCCTTGACTAACACAAATGTAGGCAATACAATAGAAAGAGCAGAGGAAGATCATGCGCTCTTGACAGGCACAGTCAGATCTCTTACAGAGCCTTTACATAAAGAGAATGAGCAAGAAGTTCTGTCATCAGGCCAATATAATAAACTCAAGATTAAAAAGGGGGAAACTACCAGCGATAAGACTAAATTGGGTGAGACACTAGAAAGACAAAAGGAAGTTGTTGCAGCTTTGACTGGCTCTGAAGAAGCCTTAATAGAGCCAATACTTCAAGTTGTTTTGCAAGAGGAAGTTCTTCCTTCAAAAGAATATGACGAGCCCATGATGATACAAGGTGAAGATACCCGGATGAACATAGGTGTAGGTGAGACAATAGAAAGAGCCGAAGAAGAAACAACAGAAGATTGTGCACTTTTGACAGGTACAACTATAGAGCCTTTACATAATGTGAACTTACAAGAGAAAGTTTTGCCATCAGAAAAGTA[T/G]AAAGAATCCAGGATTAAGGAAGACGAGACTGCAAGCAAGAAGACCAACATTGGTGAGATGCCAGAAAGACAAAAGGATGATGTTGCAGCGTTGACTGGCAGAGAATTAGAGTCAATGGATGAGTTTGTTCAGCAAGAGAAAGTGTTGTCATCAGATGAATGTGAAAATTCCATGATTATAATGGGTAAAATGGCCTGGGTGAACACTGCTGTGGGTGAGACAGTTGAAAGAACCGAGGAAGATCTTGCCCCCATAGCAGATACAGCCAGAGCATTGACAGAGCCTTTACAGGAAGTGAACTTACAAGAAAAAGTTCTATCAACAGGAAAATATAAAGAACTCAAGATTAAAGAAAATGAAGCTGCCAGTAAGATACTGCCACCAAGATCAGAGGAAGATCTTTCCCGCTTATCAGGCACAAAAGAAACGTATATGGTGACTTCACATAAGCTCTGGGAAGAGCAAGTTCTGTCATCAGGAGAATGCAATGATGATGCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43318
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 2882 | 7964 | 35 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36694115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35558635 |
GRCz11 | 19 | 35145755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGATAAAACAGACAGGAAGAAACTTGATATGAGTAGGAGTTGTGAA[C/T]AAGCTAAGGAAAGACTTTCCTCATTGACAGGCACAAAAAGCCCATTTATA
Long Flanking Sequence:
AGATGCCAGAAAGACAAAAGGATGATGTTGCAGCGTTGACTGGCAGAGAATTAGAGTCAATGGATGAGTTTGTTCAGCAAGAGAAAGTGTTGTCATCAGATGAATGTGAAAATTCCATGATTATAATGGGTAAAATGGCCTGGGTGAACACTGCTGTGGGTGAGACAGTTGAAAGAACCGAGGAAGATCTTGCCCCCATAGCAGATACAGCCAGAGCATTGACAGAGCCTTTACAGGAAGTGAACTTACAAGAAAAAGTTCTATCAACAGGAAAATATAAAGAACTCAAGATTAAAGAAAATGAAGCTGCCAGTAAGATACTGCCACCAAGATCAGAGGAAGATCTTTCCCGCTTATCAGGCACAAAAGAAACGTATATGGTGACTTCACATAAGCTCTGGGAAGAGCAAGTTCTGTCATCAGGAGAATGCAATGATGATGCTAAGACTAAAAAAGATAAAACAGACAGGAAGAAACTTGATATGAGTAGGAGTTGTGAA[C/T]AAGCTAAGGAAAGACTTTCCTCATTGACAGGCACAAAAAGCCCATTTATAGAGCCACTGCAAGAAGAGTGCTGGCAAAAGAAAGAGAAAAAGGTATCTGAGGCATCAGAACAATATGAAAAATCCAGTATTAAAACACAAAAAATTGCCAGCAAATTGACTGATTTGGGTAAGACTATTGAAAGGACAACAGAGCATCTTACACCTTCAGCAGAGATGGGACAAACCTCAATAGTGGCTTCAAATACAAGCTCAACTTTACCAAAGACTATATCAGATAACAAGATGCTCTCTGAACATCATATTGCAGATTCAACTGTAAATCAATCTGAAAATAAGCAAATTCCAAAGGTGGAACAAGCAGAGACCAGTGTGGTGGAGATAACTGAACAAAAACAGATTGATGTGGATGAAGGCAGTAGACTAACTTCGCAAGATACTGTAAAAATTGTACAATATGATCCGCTAAATAGCAAACTAAAAGAAGCTAGGACTTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36879
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 3108 | 7964 | 35 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36693437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35557957 |
GRCz11 | 19 | 35145077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAATTTGAGAATATGCCTATGGAACGACAGCAGGGTGATCTTGAAATT[A/T]AAGGTGCCGGCCATATGAGAAAAGATGGGCTTGAAACAGAGATCTTTCCT
Long Flanking Sequence:
TTGAAAGGACAACAGAGCATCTTACACCTTCAGCAGAGATGGGACAAACCTCAATAGTGGCTTCAAATACAAGCTCAACTTTACCAAAGACTATATCAGATAACAAGATGCTCTCTGAACATCATATTGCAGATTCAACTGTAAATCAATCTGAAAATAAGCAAATTCCAAAGGTGGAACAAGCAGAGACCAGTGTGGTGGAGATAACTGAACAAAAACAGATTGATGTGGATGAAGGCAGTAGACTAACTTCGCAAGATACTGTAAAAATTGTACAATATGATCCGCTAAATAGCAAACTAAAAGAAGCTAGGACTTTAAAACAGTCTGTGGAACTGGACATTTTTGAACATGATGCAAACAGAGACTGTTTTGACAAACCTGATAAAGAAAAGAAAGAAGATCCTTTGGAATTTAAGACTTTGTCTGTGGAACTAAGTGCTGATGATGTAAAATTTGAGAATATGCCTATGGAACGACAGCAGGGTGATCTTGAAATT[A/T]AAGGTGCCGGCCATATGAGAAAAGATGGGCTTGAAACAGAGATCTTTCCTGATTCAGAAAGCAAGAAACAGCTGGTTGATACAGTGATTCAGGAGAGCAATGACACATCATTGGAGGTCCTGACTGAATTTACCTTGAAAGCAGAAAAAAGACTTCAGCAGGCCATTAAAGACATAAGGCCTTCAAAAGGCAAATATGTCAAATCAGAGCAAACTCGAAGTACTAATCAACCTCAAGAGACTTCTGAGATCAGATGGCAAGAGGTTGAAGTTGGGAATTCAACAACATTACCCGACTGCACCACAGAGACAAATATCCTAAGGCAGACAGACACTAAATCTGCAATTTCTACTGCCAGTTTCTCAGAAAACAATGGTGACAGCAAGGAACAAGTCCTATCTACTAAGGAAACAAAAGCAAAGACTAGGGTCAAGTGCCAAACAGTAAGTGAGCCTGCAGTCTCTAATGTTATTTCTTCAGATATTGATGAAGACTTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45679
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 3291 | 7964 | 35 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36692888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35557408 |
GRCz11 | 19 | 35144528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACAAGGAACACATGCTAAAAGAAAAAAAAACGGGAGGTCATGGTTTT[G/T]AGGCAGAAGCTGAGGAAATGAAGGACAGCAAGACAGATGGATTTGATGTG
Long Flanking Sequence:
CTGATTCAGAAAGCAAGAAACAGCTGGTTGATACAGTGATTCAGGAGAGCAATGACACATCATTGGAGGTCCTGACTGAATTTACCTTGAAAGCAGAAAAAAGACTTCAGCAGGCCATTAAAGACATAAGGCCTTCAAAAGGCAAATATGTCAAATCAGAGCAAACTCGAAGTACTAATCAACCTCAAGAGACTTCTGAGATCAGATGGCAAGAGGTTGAAGTTGGGAATTCAACAACATTACCCGACTGCACCACAGAGACAAATATCCTAAGGCAGACAGACACTAAATCTGCAATTTCTACTGCCAGTTTCTCAGAAAACAATGGTGACAGCAAGGAACAAGTCCTATCTACTAAGGAAACAAAAGCAAAGACTAGGGTCAAGTGCCAAACAGTAAGTGAGCCTGCAGTCTCTAATGTTATTTCTTCAGATATTGATGAAGACTTGCAAAACAAGGAACACATGCTAAAAGAAAAAAAAACGGGAGGTCATGGTTTT[G/T]AGGCAGAAGCTGAGGAAATGAAGGACAGCAAGACAGATGGATTTGATGTGGTTTCTACAACCACAATGGAAGTAAAGGTACCAGGAAAGAAGAAAGGTAGAGGGAAAAACAGCAAGAAAGCTAAAATGGAAAAGGATGAGAGGCCACTTGTTTCAGACACCTCAGTCAGAATATTTCCTTCAGAAAAAGCAGAGCTTGATGAACAAGGTGGCTTTACAACCAGTCAAGAACCTTTCATAAAAGATGGCAATGAGACAGTACAGCAGTCAGAGATGACCCAAGGAAGTGGAACTGTGTCAGGGAGTGGAGAGAATGTTCAAGGCCAAGATATGGAAACTGGGATAGATAGAACTGCTAATGAAATGAAAGCCCCCAAATGGGAGTCTGATCGTGAAAACAATACAAGCCAGAAAGAGAAGACTTTAACACCACACAGTCCAACAATTTACAAAGGCAAAACAGACCAGAATCAGGAAGTTACTGAGGTCTCTAAAGACCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15741
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 3806 | 7964 | 35 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36691341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35555861 |
GRCz11 | 19 | 35142981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGRTTATGCCAGAGTCTGATAACACGCAAAAGGAAGTGGTGGAAGAATA[T/A]CCAATGGGTTCAGTGGAGAGACAACCTGAAGTTCTTCAAGTTAATATTGA
Long Flanking Sequence:
GACAAGAAAACTAAATCAGGATTAAGTGAGGATGATATGAATCAGGACATTTCATCCTTGAAGTCCTCTGATGACATTGTGGACATTAAGCAGAAATATATTGTTAAAATACCAAATTTTATTGGGGAAACCAAAGAAAGAAAGGCAGAAGAACAAAACATTGAGCCATTATATTCAGAAGATGAAAAGTTAATTGAATCTGTAATTGAATTGACATCACCATCAAGCAGTCACGAAGTTGCCAAATCGTTACCAGTCGAACATGTTACTGACATTCCTGCAATAAAAGACTCTAAAGAGCTTCTGTCAAGTGAGGCGTGTACTCCGATGGTCAAGATAGAACCAAAAAAGGTGAAATCAAGTGAAATTTATTCGAAAAGAAATGAGGAGACCCTTTTCAAAGATGAACCTTTTAACCAAGAAAATAACATTTCTGGGCTACCCTTTAAGGAGGTTATGCCAGAGTCTGATAACACGCAAAAGGAAGTGGTGGAAGAATA[T/A]CCAATGGGTTCAGTGGAGAGACAACCTGAAGTTCTTCAAGTTAATATTGAAGAAATGGGTAGGGATGCTACAAAAGTCAGCAAGGTAAAGAGTCATTCTATAGTTTATATTTATATACAGTTTACTATAAATTGGATCTTTTAAATAATTTTCCTTCTCTTTCAGTCCTCACTTGCCCGGCAAGAGTGCTTGGAGCACGACCAACAGATTGTGGCCCTGCTTTCCATGGTGAGACACATTGAGGTTCGCCTTAAGCAGCAGCAGCAACAGTCCGTTGGTCGAAGTCTCTCCACACTTGATGACATAATCAGGCAGACAGAGGTATTTGCTATGTGTTACAATTAAAGTTTAGCATGCATAGTAGTTCATTTTTACAAGTTAAGATAACAAGGGGTATATTTTATTTTAATTCTCTTTTCAGGCCCTTGTTCTAGAAATTGGGGATCTGGAACCAGAAGTGCACACTGAGATTGAATCAGCTACACAGCTACTGGAGTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11432
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 4082 | 7964 | 39 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | Nonsense | 248 | 248 | 4 | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36689153)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35553673 |
GRCz11 | 19 | 35140793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGCCAGAGCAGAGGCACTATTAGCCCARCAGATGAGAGAGCATGAA[C/T]GACTGAAGAAAGAACAGAAAGWGAAAGAAGAGAAAATGGAAAAAGAGAGW
Long Flanking Sequence:
GCTCCTTGAGCCGGAAGTTCCATGTTATAGCTCTCCACGACCAGCAGCCAATCAGAACCTGGACCACATTAACATGGTAGCGTATGGGAAAATAAAAACAAAACAAGAAAGTGGGACAAAGAAAAAAACTAAATAAATAAACTTTAGTCATTACAGAAACCCATACCAAAATCAGTTCAGTAAATCTAGAGAATCTGCGAATTTTGAAGTACATTTACATTTGAATACAGCATATTTTTCACAGTTATATATTTTTATTTTTATTTTTTCCTTCACTGCAGCAGTTACAGAACTCTCTCACTGCCCGATCCAATGAAGTCGGCAACGTGGCGTTCAATATTCAGGTGTTCATCTCTGAGCATGCTCAAGACCTGCTGCCTGATCAGAGCAGACACCTTCTTGGACAGCTGGAGCAGCTGCAGAGGGTCTTTCACCAGGCCGTTGGTCTCAATGATGCCAGAGCAGAGGCACTATTAGCCCAGCAGATGAGAGAGCATGAA[C/T]GACTGAAGAAAGAACAGAAAGTGAAAGAAGAGAAAATGGAAAAAGAGAGACAAGCTACAAGGGATAGAGAGGTTTGCAAACAAACGAATAACCGCTTGAGCTGGCAGATGAATAATAAGAATATTAATTTTTCTTTTCAATGGAGACTAAGGAGAACTTGTAATGCATAAGAGCAAAACATTTGTGGTAACACTAATGATGCATGCAATACTCGTTAGCATGAATGCTGAATTTGAAAATGAAAGTAATATTCACATGCATGAGATTATAAGTATATTCTACTTGTGTGTTTAGCACCAGTATTGCTCATAATGCTAATATTTTTTTTCTCAATAATGCTTATGCAGGACTCAACAATGACGACTTTTGTCTACCGTCTACTCAAACAAGTCATTTAGAATTTTTGTTATATATTTAAATGTGGATGTGTATTTCTTTTGGCTATACAAAAACATTTAAATCTAAAAACAAGTACATTTTATGGCTAAAATGATTGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13865
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Nonsense | 196 | 2818 | 2 | 41 |
ENSDART00000054274 | Nonsense | 5227 | 7964 | 56 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Nonsense | 276 | 2898 | 4 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36669821)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35534341 |
GRCz11 | 19 | 35121461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACTGGGGAGATCCGCTCGGAACTGGAACAAAGACGGGGACAATTGTCC[C/T]ARGCTGAACAGCTGTGTACGGAGCTCAGCGCAATTGTGGCTGAACCATAT
Long Flanking Sequence:
ACCTACTATATAAAAATATATACTTGTAGTGTGTGTAATTGTGTGTATTGTAATTATAAAGTAAATATTTTAGTCATATTTAATTTCTGCTATATTTTCTTTATGACCGTCAGTTCATGCTGCGTGAGTTTGAGACACGCCAACCCCAGTTTGACCAACTGACCCGGGCTGCAGAGGGAATCCTCTCTCTGACTGGAGATGAGAGATCGAGAGATGAACAAGACCTAGAGGAGGTGAGACGGGAGCTGGCAGACATTTCAGCGCAGTGGGACGACCTCACCTCTCGCCTCAGCGGCCGCTCACAGCAGATCGACCAGGCACAAGGAACAAGCCAACACTACCTGACCCTTCTCAGAGAGCTGTCCCAGAGCGTGGCGGATCTAGGCGAAAGGCTTGATGCGCAGGCCTCTCTAAGTGCTCAGCCCGAAGCACTGCGTCGCAGGCTTCAGGAAACTGGGGAGATCCGCTCGGAACTGGAACAAAGACGGGGACAATTGTCC[C/T]AAGCTGAACAGCTGTGTACGGAGCTCAGCGCAATTGTGGCTGAACCATATCTCAGAGACGAGTTGCACAAGAGACTGGAAAGCGTGAGCGGCCCCCTCAAGAACCTAGAAGAACGGGCTGGTGAGTAACATTTACTGATATGCAAGGTCAGATATGAAGTTGAAAGATAGGGTTGGCGATTTTAGAGAGGCTATCAGTTTCTAAAGATAAAGATCCTGCCAGTGCTGGATGATCAGTGAGTATGTTTACATGGACACCAATTCTTTAATAAGATTAATACATTACTCTGATTAAGAGTTTTTCATGTAAACACCATTTTATCATGACCTCAACCCAACTAACGTCATAATCGAACTAAAGAGAAATCGAATTAATGCATGTGGAGTATTCCTATTTTAGTGGCATTATTGATATGCAGTACAGACATGTAAACACCGCAATCAAACTATTAACGTTTTGTGGTACTTTTAGCTACGACACACACACAGGGCAGTTGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23566
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Nonsense | 214 | 2818 | 2 | 41 |
ENSDART00000054274 | Nonsense | 5245 | 7964 | 56 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Nonsense | 294 | 2898 | 4 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36669767)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35534287 |
GRCz11 | 19 | 35121407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAACAGCTGTGTACGGAGCTCAGCGCAATTGTGGCTGAACCATATCTC[A/T]GAGACGAGTTGCACAAGAGACTGGAAAGCGTGAGCGGCCCCCTCAAGAAC
Long Flanking Sequence:
TATAAAGTAAATATTTTAGTCATATTTAATTTCTGCTATATTTTCTTTATGACCGTCAGTTCATGCTGCGTGAGTTTGAGACACGCCAACCCCAGTTTGACCAACTGACCCGGGCTGCAGAGGGAATCCTCTCTCTGACTGGAGATGAGAGATCGAGAGATGAACAAGACCTAGAGGAGGTGAGACGGGAGCTGGCAGACATTTCAGCGCAGTGGGACGACCTCACCTCTCGCCTCAGCGGCCGCTCACAGCAGATCGACCAGGCACAAGGAACAAGCCAACACTACCTGACCCTTCTCAGAGAGCTGTCCCAGAGCGTGGCGGATCTAGGCGAAAGGCTTGATGCGCAGGCCTCTCTAAGTGCTCAGCCCGAAGCACTGCGTCGCAGGCTTCAGGAAACTGGGGAGATCCGCTCGGAACTGGAACAAAGACGGGGACAATTGTCCCAAGCTGAACAGCTGTGTACGGAGCTCAGCGCAATTGTGGCTGAACCATATCTC[A/T]GAGACGAGTTGCACAAGAGACTGGAAAGCGTGAGCGGCCCCCTCAAGAACCTAGAAGAACGGGCTGGTGAGTAACATTTACTGATATGCAAGGTCAGATATGAAGTTGAAAGATAGGGTTGGCGATTTTAGAGAGGCTATCAGTTTCTAAAGATAAAGATCCTGCCAGTGCTGGATGATCAGTGAGTATGTTTACATGGACACCAATTCTTTAATAAGATTAATACATTACTCTGATTAAGAGTTTTTCATGTAAACACCATTTTATCATGACCTCAACCCAACTAACGTCATAATCGAACTAAAGAGAAATCGAATTAATGCATGTGGAGTATTCCTATTTTAGTGGCATTATTGATATGCAGTACAGACATGTAAACACCGCAATCAAACTATTAACGTTTTGTGGTACTTTTAGCTACGACACACACACAGGGCAGTTGTCAGGCATTTGACGACAAACAAATGAGAATGGGTTCAAGCAAAAGATCACTATTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36878
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Nonsense | 330 | 2818 | 3 | 41 |
ENSDART00000054274 | Nonsense | 5361 | 7964 | 57 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Nonsense | 410 | 2898 | 5 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36667807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35532327 |
GRCz11 | 19 | 35119447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCATCTCTCCTGGCATCCCTTCCTGCGGGAGATGAGCGGTTAGCCTTA[C/T]AGACTCGCTTGAACAACTTACGGCAAGACTGGGAGGTCTTAAACCAACAT
Long Flanking Sequence:
CAGCAAAATTGTCCACAAATTTCTGGGAATAACCGCCACAAAATAATTTTTCGCAAAAAATCACAAAACAAATCGTGAAAAACTAGAAGGTCTGATAAGTGTAGACCACTTAACATAATTGCTATTCAGTCATACTCTTTATTTGTTAACAGCCATAATGTTTTGTGCATGCATTATTGTTCATAATAGTAATTGTCAATCTTTTCTGTCTTCTTCCAGCTGATGGCTTGTCTCAGCTTCAGGCCGCTCTGTCCAGCACTCAACAGTTCCAGCAGATGTTTGATGAGCTTCGTAGCTGGTTGGACGGAAACACTGGGAATCAAACAACTGGGATGTCCGAAACCCTCCCTTGCCAACCTGACGCTCTGAAGACCCTTCTCACCCAACAAGAGGATTTCCAGCGAGCCATAGCACAACAACGCGGATCCTACGAGCTTATCCAGGCTGAGGGAGCATCTCTCCTGGCATCCCTTCCTGCGGGAGATGAGCGGTTAGCCTTA[C/T]AGACTCGCTTGAACAACTTACGGCAAGACTGGGAGGTCTTAAACCAACATGCGTCAGAGAAACATTGCCGGATAAAAGAGACACTGACCCGTGCTGAGCTGTACCAACAACATCGCAATGAGCTTGTGCCGTGGATTGCGGAATGTGAGGTAAAGGAGGCAGAAATCAACCCATCGCTGGATGCTGCTGTCTTAGACGACTCTTTGCAGAAGGCTAGACAGTTGAGTCTTGATCTGGATCGCCGACGACCACTTTTAGAGTCTCTGAACACAGCAGCCGATCAGTTGCTGGAGCAGAGCTGCACTGGCGAAGAGGAAGTGAGAGATGAAAAGGCACAGCTCAATCGTAGAGTAGATGGGCTCTCAGAGCGACTGCAGGGACGCACGGCTCAGCTTGAGGAGTTAGGAAGCAGATTGAAAGAGTTTGAGGATGGCAGACAGGCTGTGGAAAGAAGACTAGAAGCTGCCAGGCATCAGATCGAGGTTCAAGAGGCGCTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32250
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Nonsense | 503 | 2818 | 3 | 41 |
ENSDART00000054274 | Nonsense | 5534 | 7964 | 57 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Nonsense | 583 | 2898 | 5 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36667288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35531808 |
GRCz11 | 19 | 35118928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATCAGATCGAGGTTCAAGAGGCGCTTGGACCACAAGCTTGTAGCAAC[A/T]AAAGCCTGGAGCGTCTGCGAAGCCAACAGGAGCTGTTAAACTCTGTACAG
Long Flanking Sequence:
TACGGCAAGACTGGGAGGTCTTAAACCAACATGCGTCAGAGAAACATTGCCGGATAAAAGAGACACTGACCCGTGCTGAGCTGTACCAACAACATCGCAATGAGCTTGTGCCGTGGATTGCGGAATGTGAGGTAAAGGAGGCAGAAATCAACCCATCGCTGGATGCTGCTGTCTTAGACGACTCTTTGCAGAAGGCTAGACAGTTGAGTCTTGATCTGGATCGCCGACGACCACTTTTAGAGTCTCTGAACACAGCAGCCGATCAGTTGCTGGAGCAGAGCTGCACTGGCGAAGAGGAAGTGAGAGATGAAAAGGCACAGCTCAATCGTAGAGTAGATGGGCTCTCAGAGCGACTGCAGGGACGCACGGCTCAGCTTGAGGAGTTAGGAAGCAGATTGAAAGAGTTTGAGGATGGCAGACAGGCTGTGGAAAGAAGACTAGAAGCTGCCAGGCATCAGATCGAGGTTCAAGAGGCGCTTGGACCACAAGCTTGTAGCAAC[A/T]AAAGCCTGGAGCGTCTGCGAAGCCAACAGGAGCTGTTAAACTCTGTACAGCCACAGGTGGTGTACCTCCGAAATCTGGCTCAGGGACTGCTGCAGGACGCACCCCAGATATCTGCAGCCGGCCAAGATGGAGGCCAGAAGCTGCTGCAGCAAGCTTGCGATACGGAAAAAGAGTTTGAAGAAGTTACTGAGAAGGTGAGAGAATTTGCACATGATCAGGAGCCCCTGGAATGTGTCAGAAGGTTATATATAAAACCCGATCTGTAGTTGTGTCTGCGTTCATGTCGTGTCTGCTGAAATAAGACAGTCTTTTTCTGGCTTGCTCCAGATTTGTCTGGTCTTGTCATTTTCATATCTTGTAATCTTTTAATTTATTGTAGTACTACTACTACTACTTTTATTTTTAATGCTAATAATACAAAGACTAATGGTAGTAATAACAGTAGAAACAGTAGCAGTAGTAGTAGTAATAGTAGCGGTAATACTGTAGTAGAAGCGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17558
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | None | None | 2818 | None | 41 |
ENSDART00000054274 | Nonsense | 6081 | 7964 | 63 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | None | None | 2898 | None | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36630534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35495054 |
GRCz11 | 19 | 35082174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCTAGCTGAGGTGGCCCAGAGACTGGCTGAGGTCTCAGTSCAGAGTTA[T/A]CAGCCGGAGCWCCTAGAGCAGCAGCACAAACACACACTGGTATGATTCTG
Long Flanking Sequence:
CGTGATCCTGCCCACATACATCTCCATTTCATTATGGTTTCATTTTTTATGATTGTGTTTCATTTCATTTTGTTTTGATCCATGTATTTTTTTGTTAATTATGATTTGTCGTTATTCTGCATTGTCATATATGTTTATGTTTGCCTTGTCTTTTTTTTTCCTTCTTCTTATCATCCAATCGCATCTTTTCTTTACTCTGGGCTACTATCCCAGGCTCTCCAAGAGGAAGTCTCCTCTCGAGAGAATAATGTAGACCGTCTTGAGAGTCTCAGCCAATCGCTCCATCCGCTCAGCTGCGCAGCCGATCAGGATTGGCTGGGCGAGCGTGTGGGTGCAGTGCGCAGCGGGCACACAGAGCTGCGTGATTGGTGCGTTCGGAGAGAGGCCATGCTGGAGCAGGCGCTGGCCAATGCACAGCTGTTTGGAGAGGAAGAGGTGGAGGTCCTGAACTGGCTAGCTGAGGTGGCCCAGAGACTGGCTGAGGTCTCAGTGCAGAGTTA[T/A]CAGCCGGAGCACCTAGAGCAGCAGCACAAACACACACTGGTATGATTCTGCAGGTTTTAGCAGCACAGGGTTAAAATATTTTCTGAGTCCTTTTGGAGATGATGAATACTGAGGGGGGAAAAGCAGAATAAAGAATAATACTAGGGCTGCCAGTGAGGTGACCACCGGGTTACTGTTTTTTTGCGGGTCAGAAGATGTTATTTTGCCGTACAATGGAGGGAGAGATACGTTTGACCACATAAACGCTAATATACACTACCTGACAAAAGTCTCGTCGCCTATCCAAGTTTTAGGAACAACAAATAATAACTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTAATGTGAAAGGCAAAGGCTTCTAGATTAGGCTTATTTTACCTAAATTAAAATATGATCATGTCTTGATTTTTAATTCTTTATTAGGACAGTAAGGTCTGACTTTGCTAAGACAAAAGTCTTAAGTCACTTAACAGAAATAATGTGCAGTATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25094
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Nonsense | 1113 | 2818 | 11 | 41 |
ENSDART00000054274 | Nonsense | 6253 | 7964 | 66 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Nonsense | 1193 | 2898 | 13 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36626874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35491394 |
GRCz11 | 19 | 35078514 |
KASP Assay ID:
554-7690.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTGCTGATGCCAATCAGCGATACCGCCAAGCAGACGAGACCATCACA[C/T]AGAGAGTGCAGTTAGTGCAGGCTGCCATCCAAAGGTCACAGCAGGTACTG
Long Flanking Sequence:
AATTGGCATTTCTGTGTGGAGTTTGCATGTTCTTCCTGTGTTCGCATGGATTTCCTCAGGGTGTTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAAATGTCTAAACGTAGTTTATATGTGTGTGGGTGAATGCGAGAGTGTTTCCCAGTGCTGGGTTGCGGCTGAAAGGGCATCTGCCTAGTAAAACATGTGCTGGAATAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTGATAAATAAGGAACTAAGCTGAAAGAAAATTAATGAATTAATGAATGAATGAATAACTCAAATTAATGTCATTACTGAATGTGCATGTCTGGCTCAGGAGCTGAAGTGTGTTTCTGCTGAGAAGAGGTTAGTTCTGGACACAGTGAATGAGGTGGGCAGTGCTTTACTGGATCTGGTACCCTGGCGTGCACGGGAAGGACTGGACCGCCTGGTTGCTGATGCCAATCAGCGATACCGCCAAGCAGACGAGACCATCACA[C/T]AGAGAGTGCAGTTAGTGCAGGCTGCCATCCAAAGGTCACAGCAGGTACTGCAATAAATACTGCACAGATGCATTTTTTTTTCAAAATATAATTCTGTAACTTGCAATATTTGAGAGCTTACAATACTATTTAAAGAGGAGAAAAAAAGTAATAATATATATAATGCTTTCCATTTATTCCGTAGCCCCTTTCTGTTTTTTTAGTTTTAAAGAGAAAGTAAGGATTTCCATCTTCCAGGTTTCTATAACAATTACTTTCCAATCTTCTAAAATAGGAGGGGTTGAAGGAAGCCATTTACGTGTAATAGCCTTCTTAGCTGCAACCAGAAGTATTCTCCATTAATATGTGTCTCTAGCCTCATGCAAATCAATAATTCCTAAGTATAACACTGAAAAATGAAACTGGATTTCGATCTTCAATCCACAGATGCATTTTAAATAATACATTTTGCAACAAACCCTATTGTTCAAAAACATATTGTATACCGCTATATACAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36877
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Essential Splice Site | 1345 | 2818 | 15 | 41 |
ENSDART00000054274 | Essential Splice Site | 6485 | 7964 | 70 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Essential Splice Site | 1425 | 2898 | 17 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36621414)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35485934 |
GRCz11 | 19 | 35073054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTAGTGTGCTGTATGTGCTCTGACCATCGTCATCTCTCTATCATTTCA[G/T]TTTCATGATAAGATGGACCCTCTGTTGGAGACTCTGGAAGGCGCAGTCCA
Long Flanking Sequence:
ATTCTGTAGCACCTAGTTATTTGTTTAATATCTCAGTTTATGTAATGATTATAATAAGTACATAGTTTGCACATGTAAAACAGGACTGTGAAATAAGGTGCATCCCCAGCTGACTTATAGACAGTATCTTGTTAGTAATAAACATGTATAAGATAAGCTCAGTCAGGAACATGCTGCCTTCATGTATGACACAAGCAACGTAAAAGTTCCAATATGTATTGAGTATTTTTAAGGCTAATATACTCTCCAAACCTGTATATGTCTGTTCAATATACAGCAATACTGTGAAACACTGTTACAATGTAGAATAACCTGTTGTCATTTATCATCATGAAGGTGTCATTATTCTAATGCGTTTTCTGTATTAATAGTAGTAGTAAGTATTCCTTCTATAACACCATCTTCTACCCTTTAGCATGTGTCTGAGATACATCTCTCCTGCACCACTTACTTTAGTGTGCTGTATGTGCTCTGACCATCGTCATCTCTCTATCATTTCA[G/T]TTTCATGATAAGATGGACCCTCTGTTGGAGACTCTGGAAGGCGCAGTCCAGCGCTTGCGGCAGCCTCCTCCAGTGGCCGCTGAGGTGGAGAAGATCCGGGAACAGCTGGCGGAGCACCGGGCCACAGGTCTAGAGCTGGACAAACTCCTGCCATCGTTCAGCGCTCTATGTGCCCGAGGGGAAGAGCTCATCAGTCGCGCTCCACATGATGATCCTGCCGCCCAGGGTAAAAATCTTTCATCTCAAGTGACAGACACGTATGAAATAAGGCCTGTGTTCTGATCAATGTGTATTTTGTTCTTGTCCTCAGCGGTGCGTTCACGACTCTTGCGGCTGCGCTCCCTGTGGGATGAGATCAGACAGAGAGCAGAGGAGAGAGAGGGAAAGCTTCAGGATGTACTAGATCTTGCTGGAAAGTTTTGGGCCGACATGGCTGCTCTTCTGAGCACGCTCAGAGACTCTCAGGACATCGTCAAAGATCTGGAAGACCCGGGCGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23565
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Nonsense | 1512 | 2818 | 17 | 41 |
ENSDART00000054274 | Nonsense | 6652 | 7964 | 72 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Nonsense | 1592 | 2898 | 19 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36618359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35482879 |
GRCz11 | 19 | 35069999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCATTAAAGCAGAGACAGATGGGCTGAGGGAGGAACTGGAGATCGTA[C/T]GAACACTCGGAGCTGACCTCATCTTTGCCTGCGGAGAGACTGAAAAACCA
Long Flanking Sequence:
TTTTATTAAGGCGTATCCATGTAAATGGCCCACCCTGTATATAGCATCATCTGCTGTGTAAAACATATGTCGGAATAGTTGGCAGTTCATTCCACTGTGGCACCATCTGATAAATAAGAAACAAAGCCAAAGGAAAATGAATGAAATCTACAAATATGTAAATGAGTAAAATCTAAACTCTATATGCGTACTGGAATGTATTTATGCTACTGTATCCTAATATAACAATAGTCAATAAGTTCATAAACTGATATAAAATTAAATGAAATAAAGAAAATATTTAAATATTCCATAAGACTAAGGAACAATATAAATGGATGACTAGTGTAGCCTGTGTGTTCAGTTTAATAAAAGGCTTTATGATGGATAATTAGACTAGACTTAACTCTATAATGTTGTGTCAGGACAAATATTACCAGAGTGAGGTCATGATGTTTTCCTTTCTCACTCAGGCCATTAAAGCAGAGACAGATGGGCTGAGGGAGGAACTGGAGATCGTA[C/T]GAACACTCGGAGCTGACCTCATCTTTGCCTGCGGAGAGACTGAAAAACCAGAGGTCAAGAAGACAATCGATGAGGTAAGAGGCTTGAAGAGTGATTAGCCAATGGGAAATGGTCAAATTGATCACGTTCAATAAAATATCTCTGTTTTATCTTTACATTACAGATGAATGGCGCCTGGGAAGGTTTGAACCGCACATGGAGAGAGAGAATGGAAAGACTGGATGAGGCCATGACTGCCTCTGTGCAGTACCAGGATGCTCTTCAGGTGTCTATTACTCTGATGCAATCACAAAAACTACTCTGATTGCTCATGCAAACTGTTCTCAATCATCAATTTATGTCTCCTCAGGGCATGTTTGACTACTTGGACAATGCTGTCATCAAACTGTGTGACATGCCAGCCGTCGGGACAGATCTCAGCACTGTCAAACAACAGATTGAAGAGCTCAAGGTTGGAATCAGATCTTATCTCCAATTCTCTCTCAACAGAACACCATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43317
Status:
Mutation detected in F1 DNA
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007535 | None | None | 134 | None | 3 |
ENSDART00000039136 | Essential Splice Site | 2220 | 2818 | 30 | 41 |
ENSDART00000054274 | Essential Splice Site | 7360 | 7964 | 85 | 97 |
ENSDART00000140075 | None | None | 1586 | None | 34 |
ENSDART00000144798 | None | None | 248 | None | 4 |
ENSDART00000146394 | Essential Splice Site | 2300 | 2898 | 32 | 43 |
ENSDART00000147054 | None | None | 180 | None | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 36609092)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 35473612 |
GRCz11 | 19 | 35060732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCCTGTCCGTTTCAAAGCAGACGCGCCTCCAGCAGGCTCTTAAACAGG[T/C]ACGGCTGACCCTTATTTACACTTCTATTGTAATGCTTTTGAAAGACGTCT
Long Flanking Sequence:
TAAATGGTTACCTAAAAAGTGCATGAAATGAATTAAGATGAGACCTATTTTGGTGTATGCATCAAATCACTTTAAAAAAGTGATTTTATACACATAAAAAGCACATTAAATGACACGTTAAAATATGGCTCAAATAATGTTCTATTATCATTCACCCTCTTTCAGCATTAATTCTAAATGCAGCTTAAAATATGTGAAAGTGCTGGAATTTTCCGCTGCATTATTAATGCAGTGAGTACATTTGTCCTAAAGGACATTTCTGAGTGGGAAAGATCCCAACACTGCTGTTTTTATTGCTCTGCAGGTCTTCCAGAAAGAGCTGGGGAAACGGACCAGCAGTGTACAGGCTTTGAAACGCTCTGCTCGAGAGCTGATGGAGACCGGCCGAGATGACACCGCCTGGGTGAAAGTTCAACTGCAGGAGCTGAGCAACCGCTGGGACACCGTCTGCGCCCTGTCCGTTTCAAAGCAGACGCGCCTCCAGCAGGCTCTTAAACAGG[T/C]ACGGCTGACCCTTATTTACACTTCTATTGTAATGCTTTTGAAAGACGTCTGTACTGCTCAGCAAGCTGATAAAAGAAACAATAAATATAAATAAATATATGCAATCAAAACAACATTATATATTACATCAGTTTAAGTTAAATGCAATTGATTCCTGGAGGGGCGTAACGGACATTTTAAATGTGGGGGGAGGGCAGCTGAATGAGATCCAAAAGTTTACTTCCATATAATTATTATTAATCACCTTTCTAAATCCTCTGACTCTAAAAGTGAGGGGGATATATTCTCCAGTCTCTGAGCATTAGTGCAGTGTTAATCTTTTATTCTGACTCTGTGTTTTCCTGCAGGCAGAGGAGTTCCGCACAGCTGTTCAGATGCTGCTGGAGTGGCTGTCAGAGGCCGAGCAAACATTGCGTTTTCGGGGCGTCCTGCCAGAAGAAGCAGAGACTCTGCAAGCTCTATTGCACACGCATCGAGATTTCATGCAGACAGTGGAGGAG
Associated Phenotype:
Not determined