ZMP
SHANK1 (1 of 3)
Ensembl ID:
Description:
SH3 and multiple ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:15474]
Human Orthologue:
SHANK1
Human Description:
SH3 and multiple ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:15474]
Mouse Orthologue:
Shank1
Mouse Description:
SH3/ankyrin domain gene 1 Gene [Source:MGI Symbol;Acc:MGI:3613677]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20034 | Nonsense | Available for shipment | Available now |
sa33198 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40086 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33197 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40085 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45142 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20033 | Nonsense | Available for shipment | Available now |
sa40084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33196 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12603 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20034
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 |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 36 | 1695 | 1 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30921246)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30639285 |
GRCz11 | 3 | 30770127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCAGTCTGACTGAGTCTCTGAGGGATGTTTTAAACTATGGTCTTTTT[C/T]AACCTGCCACTGACGGGCACGATGCCAAGTTCCTGGAGGAGGAGAGGCCG
Long Flanking Sequence:
TGCAACTATAAAATTACCCAAACAAATTAATACAATTACTATAAAAAAAGTATTTACATAATTTACTATAGTATTTTTCATGGTGGAATAGTGTAAAATACTATTTGCCCTAGGAAATGTTAAATTAATAAAAATAAGAACTTAAAATACATTTTTTACTGAATGTTGTCTGCAAGTTCTCCATTGTAAAAGTGGGTTTTTACTGTGTGTGTCTCATTAATATTCCCACCACTAGCCTTGTACTTTTCTGCCTATATTTTTCACTAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATTGTATGATATAAACTCAGCAGCTAAATCTGTTTGTCTGACAGACATTGTTTTTTCTTTCTGTCTCCATAGAAATGTCTGAGGTTCAACCCTGATGCAACCGTATGGAAGGCGAAGCAGCAGGTGATGTGCAGTCTGACTGAGTCTCTGAGGGATGTTTTAAACTATGGTCTTTTT[C/T]AACCTGCCACTGACGGGCACGATGCCAAGTTCCTGGAGGAGGAGAGGCCGCTCCGCGAGTACCCACAATCCTTTGAGAAAGGAGTACCTTACCTGGAGGTAGCTTTCCTTTTGTTTCCGTTTTGTGTTTTACTTTTTTTTTAATGTTTTTTTTACTCTTGCTCTATAATTGAATGTGAACATTGGTGCTAGGAAACTGCTGCTTCAAATTGTTTGTTGCCTTGGTGATAATTCTTTTAGCAGCTTCTCTGGTAACTATGAATCTTAATAACCCTTACATGGAAATTTGTCATGTAATAAGAACTATTACAATTATTATTATTTATTATATTTTGAGCAAGTACTATTATACAACAATAGTCAGCTTAGAGTCCAATTCCTAGAAGCCTGTTTTATCTAATGTTGATCATAATAATACTGATAGTGACACCTCTTTGTTAAAGGAACTCAAATGCTACTGTTTTCCCATTTATGAAGAGTTACAGCTCACGATTAACAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33198
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 183 | 1695 | 5 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30909760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30627799 |
GRCz11 | 3 | 30758641 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGTTCAAATTAAAATGTAATCCCGTGTCTTCTACTGTTCAGACGCTGT[T/A]GTCTTTGGGGGCGTCTTCTGATTATAAGGACAGCCGTGGGCTGACACCAC
Long Flanking Sequence:
GCCAACTGGAAGATCCATATACGTATACACGCAAAGCATAATGGGCAATTTTTAATTCTATGGAAAAGGTCTATAGGAAAAAAGTCTCCCTCCCATATGCCTGCATGCAACTTTCTTTGAAGCAAAACACATGAGCATCTGAGGTAATACGTCAGAGGCGCAACTAAATGTGACACATGAATGTGTACACTATACTGACAACTAACCCTAACATGAGTACTCAAACTCTGTCTGTGTGTGTGAAACAGAGACTCCACTCACTCTGGCCGTACAGACGGAGCCGGGCGGAAGTGAGATCATCAGGGTGCTGGTGATGGGTGGAGCCCACATTGACTTTAGGGCGAGAGATGGCTTGACCCCTCTGCACAAGGCTGTCAGAGCACATGCACACACTGCCCTACTGGTAACACAAACACAAAGGCAACTTTACATCCTGATTAGGATTTAAAACAGGTTCAAATTAAAATGTAATCCCGTGTCTTCTACTGTTCAGACGCTGT[T/A]GTCTTTGGGGGCGTCTTCTGATTATAAGGACAGCCGTGGGCTGACACCACTGTACCACACTGTGCTGATAGGGGGCGACACCTCCTGCTGCGAGACCCTGCTATACCACAGAGCCAGGCTGGGGCTCCGCGATGAGAACGGCTGGGATGAGACACATCAGGTATGAAAAAAAAAATTGCTGACAATAAGTGGATGACAGATACTGGAAATGTGTGGAAGTGACAATTTTTAAGACCAGGGGTTTAAGCTTTGCATAAAACATTTCACTAGTAATTAAACTGTGATGATAATATTATTAATTATATTAATACTACTAATAATAATAATAGTGTGTCACTTGAGCACCAAAGCAGCATTATAGAATAATTTTTGAAGGACAATGTGCTGAAGACATTAGAAATTCAGCTTTGCCACCACAGAATGTTTTATTAGTATTTTTTTAAATGTGCAAAATTTCTCATATTCAATAATATATTTCGCCTAGTTAAGTAGTAACCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40086
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 |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 274 | 1695 | 6 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30908100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30626139 |
GRCz11 | 3 | 30756981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCCCAGAATGCCTCAGGAAACACTGCCCTGCACATATGTGCTTTATA[T/G]AACAAGGTATAACCACTGCACCTTACACACAAAAACAAAGCAAATATTGT
Long Flanking Sequence:
TAAAAATAAAAGAATATACATATATAATAAAAAACCAGTACACAGACTAAATAGCAGTAGTAGTAGTAAAAAAGATATATACATATAATTAATGAACAAAAATAGAAATAAAATATCATATTATCCAATATATCATATATTATTCAATATATCGTATCATTCATATATATCATTTTATTCATTTATATCAATAAAAATAATAATAGATCAGAATGCACTGTGAATCTAAAAATCAACATTTTAGGATAAAACAGAAATAAAAGAACAATAATAATCAGTATTTTTGCAATGAATGAATTAGAATCACCTAGATGTGTGTGTGTGTGTATGTGTATGTGTGTGTGTGTATCAGCATCACTGATATTTTCATTGGTCTGTCTCTTTCTCCAGGCGTGTCAAAATGGGAACTCTCAACATTTAGAGCACCTGCTTTTTTATGGTGCAGACTCCTCATCCCAGAATGCCTCAGGAAACACTGCCCTGCACATATGTGCTTTATA[T/G]AACAAGGTATAACCACTGCACCTTACACACAAAAACAAAGCAAATATTGTATATACTCACCAACTTACTTTATAGGTACACCTTACTACTAGAAGGTTGGATCCCTTTTTGACTTCACTGCCTATCTGCCACAATGATGTGTGGTGTTTAATGATTCAATTCATCTTAATGTCTATAGTGATTTTACAATGTGGATTGTGTCAAAGCAGCTTAACATAGAAGTTCTAGTAAACTGAAATTGTGTCAGTCCAGTTTTCAGAGTTGAAGTTTAGTTGAGTGTGGTTTAATTTTCACTGCTGAAAGTCCAAACACTGAAGAGCAAGCTCATCGATGAGCAGCTCCATAAGTTTCAAAACCAAGCAAGCCAGCAGCGACGGTGGCAAGGAACAAACTTCACTAATTGACGAAAGTGAGGGAAAAAAAACTAGAGAGAAACATAGGCTCAGTTGGGCATGACCATTTCTCCTTTGGCCAGACTTCTTGTGCAGAGCTGCAGCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33197
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 460 | 1695 | 12 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30900622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30618661 |
GRCz11 | 3 | 30749503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTACAGCGCCGTTCCTGGCCGAGTTTTTGTTGCCACTCGCTCACACT[C/A]GGCCCAGGGTGACCGCGAAATCAGCTTCAACAAGGGAGACAAAGTCAAAG
Long Flanking Sequence:
TGCAGTCATTCTAATGAATTGTTTTCTAATTGAATTGTGGCATTTTTGTAGGGATTCCTGCTTATGCTAACCAAGTCAATGCTTTTTCGATTAAAATGTACTTAATTCTACCAGGCTTATCTGTAATGATTAGAAAACATTTTAATATTACTAGTAAATTAACTCTTTCATTTATTACATCAAGTAAATGTGTAAATATTAAAAATTTTACTTGGCAATTCTTGACATTTAATATTAAAATTTTAAAATGATGACGGGAAATTTCTTAGAATTTATTACACCAAAAAGCTATTTAACTTCCAGTATAGTCACTCACATCCGATGAAGACAGACACTTGAATGAATAAAGCCAATAATAAATGAATGATAACCCTGTTGTCTGATACCTGTGCCATTGTGTAGAGCGGGATCCATCAGTAGTCAGGGCACAGCCAGCGGGCAGCGGCGGCGTCTCTACAGCGCCGTTCCTGGCCGAGTTTTTGTTGCCACTCGCTCACACT[C/A]GGCCCAGGGTGACCGCGAAATCAGCTTCAACAAGGGAGACAAAGTCAAAGGTGAATGTGTGTGTGTGTGAGTTTGTCTCTCTTTGTAAGCAGGAGCAATGATGTGCGCTGTGCGTGTCTGTAAATTGGTCCCATTAAATGTGTGTTTGTTTCTGTATGTTTTCCACAGGTGTGGATAAACGTTGTCTGTGTATGTATTCTGGTGATATGTGTTGGTATGTCAGTATATGTCTGTTTGTGAGCAATGTCAGCGTGCATGCATGTGCATACAACTCTACAGCCATCATGTCTTTGCATGTGTTTTGTGATTCAATGTGTGTGTGTGTGTGTGTGTTTGTGTATCAGGAGCGTCATGCAGTGATTATTTTTAATGGGTAAAGGGTCCTGTTTACAACAGGTATTAACTGATCTGATCTTTTGATTTATTAGCATGCATAGCATACTGATGAGATCACTTGTGTTTTGATTTTTTAAAGACATATACATTTTTTGCAGACATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40085
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 |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 522 | 1695 | 14 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30897158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30615197 |
GRCz11 | 3 | 30746039 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGATGCGGTTGTGTTTGCATCTTTCAGAGAGCCGCAGTGAGAGAGCC[A/T]AGAGACTCTTCCGGCATTATACTGTTGGATCCTACGACAGCTTCGATGCG
Long Flanking Sequence:
GCTATTGGGAAGGGACGGTTCGAGGACGCACAGGCTGGTTCCCCTCAGACTGCGTGGAGGAAGTTGCTCTCCGTAGCCTGGAATCTCGTTCAGGTGAGACTCCTTTCTCACACAAAAACACATTAAAAGTATCAAAGACATCTGCGCCACACTTAGAGCTGTCATTTCCATAGTCCCAGATGTGTTTGCAGGACAGTCGGATTGCCACAGCTTCTCTGTGATGTTGTGATGCCAGACTCTGTGAGGGAGAGCAGCTATGATGACTATTAATAGTTTACAGCACTACTGGAGTGTGAGAGGGAGCGATTGTGCCATTTCACGCTGGCTAAACTCACCGTGGTTTGGGCCAGTGCGCTCTGTCAGAGCGGGAAACTTCGAGTCGGACATGTGTTGTGTTATCATGCTGTAGTTGCAGCCTCTACTGATATAAGAGATATCAACTTGTGACAATGTGGATGCGGTTGTGTTTGCATCTTTCAGAGAGCCGCAGTGAGAGAGCC[A/T]AGAGACTCTTCCGGCATTATACTGTTGGATCCTACGACAGCTTCGATGCGCCCAGGTAAGATCACTTTTACTGTTGACCATTTTCAGGTGTGGTGCTGATATTTGGATGCTGATATGTCAAAATGAAGAGCTTTTTGCTGTGAGCGGTTCTCAAGGGTCATGGAATATCTGGAATATCATTTTAAAAGGTCTGTTCCAGACATTAAAAGTCAGGGAAATTTGTATTTTTTTGACAAAGTCGTAGAATATCAGAGAGTTTATTTTAATTTAATTTTAGTTTTTGTTTATCAAAAATGTATTGTGCCTGACAAGTCTTGTTGTCGATCCCAGTTGTAAGAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTGGAGAAGTGGCAGATCTTCTTCAGTATCATCACAAATACTGAAGAAGACCTATTGGAACCCTCATGGACCCAAGATTCTCACAAAAATCAGTAAAGTTTGGTGAAGAAAAAAATCATGGTTTGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45142
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 768 | 1695 | 20 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30857323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30575362 |
GRCz11 | 3 | 30706204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCCCGCACGGTATGCTGCGACAGAAGTCTATCGGTGAGGCTGTCTGTT[T/A]GTCCATCTGTCTGTCTGCCCACCTGTGTGTCTGTTTAACCATACTGGTGT
Long Flanking Sequence:
GTAGCAAAACTTACGCATTTTAAAACTAAAACGTATTCGCGTAAATGGGGCCTAATTAAAGCTAAGAATGTAAAGTTGTACTGTAAGTGAATGAACGAAATCATTCTTTTTTTTCATGTTTCTTTTTCTCTGTCAGATAAACTGGATGAGATTTTAGCAGCAGCACAGCAGACCATTAATACAAATGAGGCTCCAGGGCCCCGGGTTCAGGGGGTAAAAAGAGAACGGGGCAGAGGCTTTTATAATGAGGTTTGTGTGTGAGCTCGTACAGTAGTTACTAGAGATTTCTAAATTGCATTCTTTTAAATCTTGGTATAATTTAATGTATATTATTATTTTTAACATTTATTATGTCTTTTGCCAGCCAAATTTCGACCAAACTGGAATGGGGATGACATCATCTGGGGCAGGGTTAGGCTACGACCGTGGTCAATTTGTGTCTGGCCATGGCCCCCCGCACGGTATGCTGCGACAGAAGTCTATCGGTGAGGCTGTCTGTT[T/A]GTCCATCTGTCTGTCTGCCCACCTGTGTGTCTGTTTAACCATACTGGTGTACGTCTATGGTACGTGCGTTGAGAGCACTCCAAAGAGTGCAGCTGTGGGTTTGCTTTAATGCTTATCATTTGTATTGCTTTATTGCTCCAGATTAGTGACTGTACAATTCAAACACTTCATAGGAATCTTGTCAGGGGTTTGACTGGGATCTAGGACAAACCAATTATTAAAACAAATTTGAATGTTATTATTATTATTTTTGAATCTTTTACTTTTGGTGTTCAGCATCAGTGTTCCTTTTTGGTTGAACTATAAAATTGACAGCCCATTTATAACCCTCAAGATAATAATAATAATAATAATAATAATAATAAGAGCACACTGACTGTACAGGGAAAATGCTTGCTATCCCATGGCATGAAGGCAAAAAACATTCATGTGATGTTAAATATGTAAATTCTTACTTTCTTAGTTTACAAAATTGGAACCTTTATGTGCACTAGAGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20033
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 |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 846 | 1695 | 21 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30856123)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30574162 |
GRCz11 | 3 | 30705004 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTATGTCTCAGTCTACTTCCTCTGCTGCACATTATCAACTCTACTCA[C/T]AGTCAGTACATGTTACTCACGGACCAAGGGACAGGTCCCCTGGACCACCT
Long Flanking Sequence:
TCAGTCATGGTAATAAACAGACAAGCTGACAGACAGACAGACAGACTACAAGATGGTCTCTTTTCTGTATCCTGTTTTGTTTGTCCTTTGCTCAGTATTAGAAAATAAATATATCTTTTCCTTTTTTGGTTATTTTCTCACTTCCAAATGTTGTACATTTATCTTGTCTCCCAAAAATATTTTTCTTTCGTCTTTGTTGTTTAGAAACATTTTATTTTAATTCTCCCTTTATACATTTTCTTGAAAATGTATTTCATCTTTTTTTTTCTGCAGGGGTTCCTGAGGAGGAGAAGCAGTTTCTTCATCCTCCAGCCATGAAGTTTGCCCGTAGTCTTTCAGTACCTGGCCCAGATGAAATCCCTCCTCCACCTACTACAGCACCCCCTGAGCCCCCTTTTTCCTCAGCTCCTCCGCTTGGCTTTAGGGGCAAGACATCTCAACAGCCGTCTGTTTCTATGTCTCAGTCTACTTCCTCTGCTGCACATTATCAACTCTACTCA[C/T]AGTCAGTACATGTTACTCACGGACCAAGGGACAGGTCCCCTGGACCACCTACTGGGTCTGGAACTGGGGACCTTGCTTATTCCCATGCCCAAGCCCACCCCTCTGTACCAAGTAGGACTGCCTCCAGGAAGGTGATTGGGTACACAGGAGATCTTGCAGGGGCTGGAGGAGTGGCTGGGGCCAAAGCTGCAGCATTGAGAAGGGGTTACAGCAATGCAGTCCCACCCACCAGTGTCGCTACTGTGATTCCACAACAGCAGCAGACTACTCAGAACCAACCTTCCAGAATGGACCGGAGTGGAATGGGGGTAGGGGCTGGTGGTGTACCAAAAGGCGGTGCTCGTAGAGGAAAGGGGCCCTTGGTGAAACAGTCAAAGGTGGAAGACCTGCGTCAAGGTCAAGACACTCTAGAAGCAAAGGTGTCAGTGGAGAAGAGCTCTATTCCAATCCCAACTATCATTGTTAAAGCCCCTTCCACCAGCAGTAGTGGACGCAGTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40084
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 |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 1022 | 1695 | 25 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30855262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30573301 |
GRCz11 | 3 | 30704143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTCAGACTTCTCAACAGCAGCTGAGTTCCCAGCCTTCACCACGCCTG[C/T]GACCATCCAAATCTATAGATGAAGGCATGTTCTCAGGTGATACTTTTATC
Long Flanking Sequence:
TGGTGAAACAGTCAAAGGTGGAAGACCTGCGTCAAGGTCAAGACACTCTAGAAGCAAAGGTGTCAGTGGAGAAGAGCTCTATTCCAATCCCAACTATCATTGTTAAAGCCCCTTCCACCAGCAGTAGTGGACGCAGTAGCCAAGGCAGCAGTGTGGAGGCTGAACCACCGCCCCCAGGAGAAAGTGACAGTTCTAAACCAGAACCTGTTGTTCCCCCACCTGCACCAACCGTGCCACCACCAGCCCCTCCATCTATACCTGCTCCTCCACCCCCATCACTGCCATCACTTCGTACTCAAGAGAGTCTGGACTTCACCAGCCAGTTTGGTGCTGCCATTGTAGGGGCAGCTCGCAGGGACAGAGAACGATTTCATGAAGCACGACGCAAGAGTGCCTCCTTTTTTCTTTCTGCTGAGGAAGAGTTGAGTGGAGCTGGAGGAGCAGGAGGGCGGACTCAGACTTCTCAACAGCAGCTGAGTTCCCAGCCTTCACCACGCCTG[C/T]GACCATCCAAATCTATAGATGAAGGCATGTTCTCAGGTGATACTTTTATCCATCACACACGCAGTATGCCTCCTGCATTTGGCTTGCCTGAGTACTCCTCACCTGCTCCTCAAGGGGATTACCAGCCTAAGTCTGTACCTGCTGACTTCTATGGGGCAGGATCCAGACAACAGCAGCAGCAGCAGCAGCAGCAAGCCCCCACCACAACTTTTATTCACCCACTAACTGGAAAAGTACTGGACCCTTCATCCCCTCTAGGCTTGGCTTTGGCTGCACGGGAACGTGCCTTGAAGGATGATGGACGTATACGTAGGGAAAGGACCACTGAACATCATTTTACCCGTCAGTTGTCAAGCATTGGGGCCTTTTCCTCATCCACTTCACAGCCAACATCACACATTTCCTACCCAATGGCCTCGTCTTCCTCTGCAACCTCCTCTGCTGCTCAATCCACAAACACCTCTTCATATCTTGTTACCTCCTCATCATTAGCTGCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33196
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 |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 1388 | 1695 | 29 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30853216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30571255 |
GRCz11 | 3 | 30702097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGCACAATGCCAAAGCCGCTAGCACTGCATCCACCTACCCAAAAACA[C/T]AGAGGTACAGAGAAGGCACCCGGGCTGGAGATCTTCGACGCCAGACCAGC
Long Flanking Sequence:
CCACCCCTGCAACTTCTGTATCAATCAGAGGTGCCTCAACTGTGACCGCAAGCTGTTCCACAACTGCTTCTACAACTGTCACCTCTCCTAGTACTACTGCTGCTGCCACACCACACACACGCATAGCAACTGTCTCCACAGTAGCTACAGGGGGTAGTAGGCGTCCCAGTGCAGAGCATCATCCACCACCTAGTGCAACCAAGAGTGGTGAGTCCCAGGAGACAGTGGTAGATTCTGGGATTGAGGAGCTGGACAGCCGAAGCAGCAGTGATCATCACTTAGACAGCATTCTTGCACTCAGTGGTAGTGGGGTCAGAGAGAGGTTGGAACGAGCAGGGATGAGTAGCATAGGTGGAATTGGAGGGAGAGATGGTGCAACTGAGGTTGACAGGACAAGTGGGGCAGACTTTTTAGAGTCTTACATGAGCTACCTTGATGGGCAGACTTTTGAAATGCACAATGCCAAAGCCGCTAGCACTGCATCCACCTACCCAAAAACA[C/T]AGAGGTACAGAGAAGGCACCCGGGCTGGAGATCTTCGACGCCAGACCAGCACAGCACCTCCTGCATACCACCGTCGTAGAGAGGAGGAAGAGGAAGAGGATGAGGCCGAGGAGGTAGAGGAGGAGGATTTGAGTGCCCGTGATGGCTATGGGATGAGGGAAGGGCCAGGGATTGCTCGCTCCTCTGTAATGTACTTTGACCGGCCCCGCACTCCAGAGATAAAACCACTGTGGGGAGATGGGTCGACTGGAGCATCACAGACCATGGGGGAGGGAGGGGGCCAGATAGTGGGAACATATGTGGAGCCACGTAAACTACATCCTCCCATGACTGGTATGAAAGCAAACATCATTAATGAACTAAGCACCAAATTACAGCAGAGAAGTAAAGGAACAGAGAACTGGGGGGCCCAGAGATCATTGAGCAGACATAGGTAATTGTGTTACCAATAGTATAGGTACATGTGCATGGATATATGTTTGTGTCTGCATGGTGGCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12603
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085327 | Nonsense | 1640 | 1695 | 33 | 33 |
Genomic Location (Zv9):
Chromosome 3 (position 30851563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30569602 |
GRCz11 | 3 | 30700444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGCCTCAAAACCTCTCCCATACTGGACCAAGTATGATGTTGCAGATT[G/A]GCTGGGCTACCTGAACCTGGGTGAACAMAGGGAGCGATTCTTAGACAATG
Long Flanking Sequence:
CAAACACCGGCCTGTTTATCGCACCAAAGCTCTGGAGTTCCAATTTATTCCCAGTCGAGAGTCACGAAAGTCAGAGTCGCATCATGCCCAGCGCAGACGAGCACCCAGCCCTTTAATTTCTCCATCTGACCGTCCCAAGCTTGGCCCTCCCCGCCCCTCTTCCCTTCCTATTCTCCCCACTACACCCCTCTATAGCAGCCTGTATGACCTTCGTGGTTCTATTACTCCACCCTCACCTGCCAATCCCCTTGGGGACCCCTACTTTTCCCCCTCCCCCCCTCTATTTGCCCCCTCGGGTGCTCCCCCTCCTCCAAATTCCTCTCTGGTGGTCTCACGGTCCCTGTCACCCACTCACTTCCTGTCAGGGACTTCATCCCCACCTCTCCACCCCATTCCTCCACCCACTTGCCTGAGTTACCCCCATCTTCCACCCCCCTCACCCACAAAGCCCTTTGCCTCAAAACCTCTCCCATACTGGACCAAGTATGATGTTGCAGATT[G/A]GCTGGGCTACCTGAACCTGGGTGAACACAGGGAGCGATTCTTAGACAATGAAATTGATGGCACGCACCTGCCCTCTCTTACCAAGGATGACTACCTGGACCTGGGTGTGACCCGAGTTGGCCATCGCATGAACATAGAGAGGGCGCTCAGGAGAGTTATGGACAGGTGAGAGGAGAGAAAAGGGGGAAGCAGAGAGATGCAAGGGATGTCTGCAATGGAGAGGGATTAGGGTGAGGGGTAGTGCATGAGCAAAAAAGCTATTATACTTAAGGTAACTCTTGATATGCTATTGATTGCTAACTTCAGAGAACACTTGGAGTGGGCCACTGCATGAGGTCCAGGATGGCATGGGGAAAGAAATGGAGAACTGAAAGAGGGGGATGTGGGAGAGCAAGAGAAAAATACTTCCTTATAAAGACTTTCCACCTTCCCCCCCCTATCATCAGGCTGTCTTCTAGCACTTTCCCCATTTCTGCTCTCTCTCCTCGAAATGGACGGAC
Associated Phenotype:
Not determined