ZMP
si:rp71-86k19.1
Ensembl ID:
ZFIN IDs:
Description:
Zgc:171522 protein [Source:UniProtKB/TrEMBL;Acc:A9JR85]
Human Orthologue:
SDK1
Human Description:
sidekick homolog 1, cell adhesion molecule (chicken) [Source:HGNC Symbol;Acc:19307]
Mouse Orthologue:
Sdk1
Mouse Description:
sidekick homolog 1 (chicken) Gene [Source:MGI Symbol;Acc:MGI:2444413]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39561 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11498 | Essential Splice Site, Missense | Available for shipment | Available now |
sa9553 | Essential Splice Site, Missense | Available for shipment | Available now |
sa19443 | Essential Splice Site | Available for shipment | Available now |
sa9945 | Nonsense | Available for shipment | Available now |
sa5935 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24835 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11705 | Nonsense | Available for shipment | Available now |
sa38249 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39560 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17607 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39561
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091205 | Essential Splice Site | 89 | 2120 | 2 | 46 |
ENSDART00000141238 | Essential Splice Site | 90 | 2095 | 2 | 44 |
ENSDART00000144164 | Essential Splice Site | 89 | 199 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10549841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10682179 |
GRCz11 | 1 | 11366290 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGGATGGGAGCGCTGATCCAGACGAGAGCCGATGTTCGTGTGGCTTG[T/C]AAGTACACGTGTATGATGTTAGAAAGGGAGTTCGGGAGGCTGAAGCACAA
Long Flanking Sequence:
ACCAATGTGGCGGCACTATTGACGCATGCTCAGGGTCCCTATGCGATATCTAGTGTATATATCTATGATTACTTCCTAATGTTATAACAGCTGTGTAATGTTGAAGCAATGTGCTAATAAAAGTTTCATATGAGTACACAGTGGATTCACGTTTATTATTATTATTTCAACCCCCCGGTCCGCAGTAAAATTGTCAAGCGTTGACCGGTCCACAGTTAGAAAAAGGTTGGGGACCACTGTTTTAGACAACAATGCCGTACACCACAGTCTAAAACATGTATCATTGCATAATGTGCTCATACTGAAAAGATGATGGAGTACAGTGTTTATCTACAGTCCATTACTCGAGTGAGCCCTATGTAAATCCGAGCTCCGTCTGCTTTGTTTTCCAGGTACACGATCGTGTCTTTAAAGCGTGAGGATGCGGGTGTGTATCAGTGCGCGGTGAGGAACAGGATGGGAGCGCTGATCCAGACGAGAGCCGATGTTCGTGTGGCTTG[T/C]AAGTACACGTGTATGATGTTAGAAAGGGAGTTCGGGAGGCTGAAGCACAAATGGGTTTCACACATCAGCACACACACCTACGACACACACATATGCATGTACTGTAGCGCAGGGTCCCATTAGAGATGAACTGGAAGTGACATTCAGGAAACACTTCAGTGATTTCTAAATATGCTGTCAGTTCAGTACACTTTATTTTTTGTCGTGCGTTTGGGACACTTGTGCAAATATGCAGCCAAAACTATAGTTGGAGTCAGAGTTATTAGCCTTCCTGTTCAATTCTAATTCTTGCATATTTTTTCTCAATTTCTGTTTAACGGAAAGAAGATTTTTTTCCTACTCATTTCTGAACATACAGTGCATGCAGAAAGTATTCATTGTGTAAATGCTACAGCCTTATTCCAAAATAGATTAAATTCATTTATTCCTCAGAATTCTACACACATTACCCCATAATGACAATGTGAAAAAGATTTTTTAAAATTGCTGCAAATTTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11498
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:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091205 | Essential Splice Site | 183 | 2120 | None | 46 |
ENSDART00000141238 | Essential Splice Site | 184 | 2095 | None | 44 |
ENSDART00000144164 | Missense | 183 | 199 | 4 | 4 |
ENSDART00000091205 | Essential Splice Site | 183 | 2120 | None | 46 |
ENSDART00000141238 | Essential Splice Site | 184 | 2095 | None | 44 |
ENSDART00000144164 | Missense | 183 | 199 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10523972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10656310 |
GRCz11 | 1 | 11340421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTAATGGGGAAAACAAAACCAGTCCTTCCATTTACCTGAGCATAGCAAG[T/A]AAGTTGTTTTGTCATTYATACTGTTTTGCTGTATTATTTAAATATATGTA
Long Flanking Sequence:
TTTTGTTGTGTTTTTCTTCAGCGAGTTATTTTTTGTAATCCTGTCCTCGAGAGATATAAAAATATCGGTCGGGAAAGTGACAAAAGCCTCGGTTAATGTAAGTGGATGTGCGCGCGTGTTTGTGCATGTTCATTTTCCACGTATTGATTTGCGCACGTGTGCTGAATGAGTAATTATCACATTGCCCTCCCGATGATGAGAAACCAGCCAGAACTAAAACAATACAACGCTCTTGTGCTTTACTTCTGGCTCAGTTTTACAAGTGAACAGATTCAGTACAGTTCACCCTTAGATTATGAAGGAAATGACAACACAAATGGATGATCTTGCACATCATTTTTACATGTGTTTTTTTCTAATTTCAGAGCTATAACGTTGGACAATCAGCTGGTGGTGTTGAGTACGGCAGCGGCAGATGCAGGGCGCTATTATGTACAGGCTGTTAATGAACGTAATGGGGAAAACAAAACCAGTCCTTCCATTTACCTGAGCATAGCAAG[T/A]AAGTTGTTTTGTCATTCATACTGTTTTGCTGTATTATTTAAATATATGTAAATGTGCGCGTGTGTGTGTGTGTGTGTGTGTCTGTACATGTGGCTAAGTTAGTGAAATGTCTTGTAGGCCTACATTTTAAAGTAGTTATACATGTTTCAGGCAAATTAGTCATTTTTTGTGATAGTGTGGTGTACAGTTTTTGGACACATTGGACTGATTGTGTTTTGTCTGTTGTGTATTTCACTTTACATTTGCTATTAAGGTGGTATGTTACAAATACAGAATGAGTGTATGTGTTACAAATGCAGTTGTGTACATAAATATATTGGCGCTGGGCGACATGCTATTGATCAGAGCCAAAAATAAAGTTTATGAAGTATGCTACACGCACACATACATAGAAGCAAAGTAGTTCTATTAGTTTAGTTCTGTACCAATTGTCATTTTCTGGGGGAAAAAAAAAACAATAAAAATGACAATATTTTTATTTAATATAAAGAATACATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9553
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:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091205 | Essential Splice Site | 183 | 2120 | None | 46 |
ENSDART00000141238 | Essential Splice Site | 184 | 2095 | None | 44 |
ENSDART00000144164 | Missense | 183 | 199 | 4 | 4 |
ENSDART00000091205 | Essential Splice Site | 183 | 2120 | None | 46 |
ENSDART00000141238 | Essential Splice Site | 184 | 2095 | None | 44 |
ENSDART00000144164 | Missense | 183 | 199 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10523972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10656310 |
GRCz11 | 1 | 11340421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTAATGGGGAAAACAAAACCAGTCCTTCCATTTACCTGAGCATAGCAAG[T/A]AAGTTGTTTTGTCATTYATACTGTTTTGCTGTATTATTTAAATATATGTA
Long Flanking Sequence:
TTTTGTTGTGTTTTTCTTCAGCGAGTTATTTTTTGTAATCCTGTCCTCGAGAGATATAAAAATATCGGTCGGGAAAGTGACAAAAGCCTCGGTTAATGTAAGTGGATGTGCGCGCGTGTTTGTGCATGTTCATTTTCCACGTATTGATTTGCGCACGTGTGCTGAATGAGTAATTATCACATTGCCCTCCCGATGATGAGAAACCAGCCAGAACTAAAACAATACAACGCTCTTGTGCTTTACTTCTGGCTCAGTTTTACAAGTGAACAGATTCAGTACAGTTCACCCTTAGATTATGAAGGAAATGACAACACAAATGGATGATCTTGCACATCATTTTTACATGTGTTTTTTTCTAATTTCAGAGCTATAACGTTGGACAATCAGCTGGTGGTGTTGAGTACGGCAGCGGCAGATGCAGGGCGCTATTATGTACAGGCTGTTAATGAACGTAATGGGGAAAACAAAACCAGTCCTTCCATTTACCTGAGCATAGCAAG[T/A]AAGTTGTTTTGTCATTCATACTGTTTTGCTGTATTATTTAAATATATGTAAATGTGCGCGTGTGTGTGTGTGTGTGTGTGTCTGTACATGTGGCTAAGTTAGTGAAATGTCTTGTAGGCCTACATTTTAAAGTAGTTATACATGTTTCAGGCAAATTAGTCATTTTTTGTGATAGTGTGGTGTACAGTTTTTGGACACATTGGACTGATTGTGTTTTGTCTGTTGTGTATTTCACTTTACATTTGCTATTAAGGTGGTATGTTACAAATACAGAATGAGTGTATGTGTTACAAATGCAGTTGTGTACATAAATATATTGGCGCTGGGCGACATGCTATTGATCAGAGCCAAAAATAAAGTTTATGAAGTATGCTACACGCACACATACATAGAAGCAAAGTAGTTCTATTAGTTTAGTTCTGTACCAATTGTCATTTTCTGGGGGAAAAAAAAAACAATAAAAATGACAATATTTTTATTTAATATAAAGAATACATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19443
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091205 | Essential Splice Site | 810 | 2120 | 18 | 46 |
ENSDART00000141238 | Essential Splice Site | 809 | 2095 | 18 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10414142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10546480 |
GRCz11 | 1 | 11230591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTAAAAACATTTTGTGTTGGTCTTATTGTTCTTTGGCATCTTTTTAC[A/C]GCTGCTGGTGTGGCCTGAACACTGTCCGGATTGCATTACAATGGTGACCA
Long Flanking Sequence:
AAATCTTGAATAAAATCAGGCAATCTATGTATGAAGTTATATATATCTGATATATATCTCAGTAAGGACCTTCAGAATTCAGATATAAATAAAACTGTAAAGTTTATGTAAATATTGTTTAAGTGCTTGGTGAAGGAGCAAAAAAAAAAAAAACATTTTAAGAAAACCGCCTTTAAAAATGTGTACTTGGTCAACATCAGTAGTAGTGGTTAAGTGCACCGACACATAGCACTGAGGTGCTCACGGCGACCCAAGTTTGATTCTCTGTGATCCCTGTGTATTCCTATTTCAACTCTACTGTCCTATATAACAAAGGTGAAAAACCTACAAATATTTTTAAAAATATGCACTTTAATTTAATTCTACAGACATAATTTATAAAGATTTCTTTGCATTATACTGAAAAATAAATATTTATTTGCTTTGTTTTGCTTTAAATACTAGCAGTGTATGTTAAAAACATTTTGTGTTGGTCTTATTGTTCTTTGGCATCTTTTTAC[A/C]GCTGCTGGTGTGGCCTGAACACTGTCCGGATTGCATTACAATGGTGACCATTGCCCCCGAGTTCCACGGGTCACGTCATTATGGTTATGTTAGCAATTTAAGAAAGTTCACGTGGTATGAGACAGCGGTGCTTTGCTTCACCACTCCTGGAGATGGACCGGCCAGCACATCACAGCTCATCCAGACACATGTTGACAGTGAGTACATGAAAAAAAACACACGTTCACTCCAGCAAAAATTAAAGGGATATTTCACACAAAATATTAATATTTCACACATTTACTTAATATGCACACACCATGAAATGGTTCCAAATCTCTATGGATTTCCTTTTTTTTTTTGCTGATCACAAAAAAAGATATTTAGAATAATTTTGAAAACCTCTAATCGTTTACTTCCATAGGAGGAAAAATAGATACTATAGAAATCAATAGTTACAAGTTTCTAACATTTTCCAAAATATCTTTAAAAAAAATGCTGACACTTTTTTTATACTAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9945
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 |
---|---|---|---|---|---|
ENSDART00000091205 | Nonsense | 913 | 2120 | 20 | 46 |
ENSDART00000141238 | Nonsense | 910 | 2095 | 20 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10401000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10533338 |
GRCz11 | 1 | 11217449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATATCCCCTTTTCTMATTTTCGCCTCTCCATAGGTTACGTCTTGAGCT[G/A]GCAGGAGGCTGGTCAGAAYGAAACGCTCGTATCTCAGACTCTGTCCAACT
Long Flanking Sequence:
GTAGTTTTGGACAAAAGGGGTAAGTGCGAGTAATAGACGAAAGAACAGCATTTGCTGAATAGTATCTGCCATAGCGAACATCTATGTGACTATTCAGCTTCCTCCATTATGCTTGACTTGTTTACGGTTGGTTACTATATTATCACTACTACAGTGAACCACTCTAGCTTAATGGAAATGCCCCTAATTTGCATTTCAGATTTAATTTTGCTGTAAACTTTGAAAATATTTGCTTCACAATAAGATTGAAACAGACTTATGTTGCAATTACATACATTGAGGCAGCCTTCATGACTGAAATGATGCTATTTTTTAAAACTCAAGTCAAAAACGTACTTGCAGCACCTTTATGTATCGCATGAAAAACTAGAAATGGAAACAAAAAATTTCTAATAAGATGCATGTAGAGGACCCTAAAGAGTGCTTCAAATTAGCCAATGAAAAAGAAGGCAATATCCCCTTTTCTCATTTTCGCCTCTCCATAGGTTACGTCTTGAGCT[G/A]GCAGGAGGCTGGTCAGAACGAAACGCTCGTATCTCAGACTCTGTCCAACTCGACGCTGGCGTACAAAGTGACCGGGTTGACTTCTCTCACCACGTACGCTCTACAGGTGGCAGCAGTAACACAAGCTGGAGTCGGGGCTTCCACCTCATCCACCATCTCAACAGGACTGCCTCCAGGTGCCCGCACTCTCAAACAAACACACACTTCAGCACCAGCATCACTTTAATGCATCAAGTTCTCCCTTGGGGATCGGTGATAGTTGCCGTGTTGAAACTCTAAAGGAAATTCGGCACATGAAACTGGATGCCGCAGTGGGGCGCATATTTCACATAGACCAGCAATCCGAGACACAGTCAGTAAGACTGTAATACATCACACAGAGTCAGTATGATGCTCTTGGGGCCGCCGTTTGTGCGCGTGTGTGTGTGTTAGAGAGAACATGAAATAAATGATGATGACCAAAAGCCAAGCTACACTCATTATCTCCCACTGATATGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5935
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 |
---|---|---|---|---|---|
ENSDART00000091205 | Nonsense | 1029 | 2120 | 22 | 46 |
ENSDART00000141238 | Nonsense | 1026 | 2095 | 22 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10390815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10523153 |
GRCz11 | 1 | 11207264 |
KASP Assay ID:
554-3791.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGTGAYTGTGGGTGAGGAGGAAAAGGAGGCAGAATGGAAGGTTTTATA[T/G]GAGAGAGACAGTCCTCMAGCCTCAGACACACTGGAGATTCCCAATCTCAT
Long Flanking Sequence:
AAATGTATGTAATAATTATTATTTTATTATGTTAATAATTGTTTCATTTTATTATTATTACTTTTTTAAAAAGTCTCCCTCGCTGCTGGAATCAGCTTCCAGAAATGATCAGATGTGCTCAAATATCAGGCACATTCAAATTGAGACTGAAAACATACTGAATGAGCACTTTGCTACGTCCGACAGATCATACTATTATGTTTTTCTTTTCATTCTTTTATAACCTGTTTTACCTCATTTTAATCTATTTTTAATAATTTTTATTGTTTGTTTTTTATGTTCTTTTATGTTCACTTTGAATTGCCACTGTTTATGAAATGTGCTATATAAATAAACTTGCCTTGCCTTGCCTTACAGGTCAAAATCATTGCTGGTCTTGTTGCGTTTTTTCATGTCCAGTAAAGTATGCAGTCCCTTCTCCATTTCAGCTCATCCTCTGTATGTCCACAGGTGGTGATTGTGGGTGAGGAGGAAAAGGAGGCAGAATGGAAGGTTTTATA[T/G]GAGAGAGACAGTCCTCCAGCCTCAGACACACTGGAGATTCCCAATCTCATCCCCTTTACTCAATACAGGTCAGCCTTTCACTGAAAATCTCACGTTATCCAAATCACACCAAATGAAACATAAAGACCTTCACAAACCTGCCCAGTCTTTCAGTGTTGCTGTTTTCAGCCACTATTCTCTCTTTATAAATGTATTTGAGCCATTCATGACGGTTAATATTGATTAAACACTCATCACACTCTTTGCTCCTGCATTTTTTTTTTGTTTTTACTGTGTTTCATTCTCCTCTTCTCTCTCACTCTTTCTCTCATTCGCCATTTCTCTCTCTCCCTCTGTCTCTCCTTAATTGATTTTCTCAAGGTCCTGTGGAAAGATTGTCTTCTGATTCTCAGCACACTATCTTGTCCTAAAGGGATTACAGATGATCAGAGTCTGCAAAGATCTGTTATCCTGTCCAAAATCGCCTGTCCTCCTACTACTCTAGAGCAAGATCGGGGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24835
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 |
---|---|---|---|---|---|
ENSDART00000091205 | Nonsense | 1054 | 2120 | 23 | 46 |
ENSDART00000141238 | Nonsense | 1051 | 2095 | 23 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10390260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10522598 |
GRCz11 | 1 | 11206709 |
KASP Assay ID:
554-7602.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTGTTTTCGTTCTCGTTCTCTCCTCTTTTATATGGCTTCTAGGTTC[A/T]GAATGAAGCAGGTGAACATTGTTGGTTCGAGCCCCTTTAGTGAGTCCTCC
Long Flanking Sequence:
TTTACTCAATACAGGTCAGCCTTTCACTGAAAATCTCACGTTATCCAAATCACACCAAATGAAACATAAAGACCTTCACAAACCTGCCCAGTCTTTCAGTGTTGCTGTTTTCAGCCACTATTCTCTCTTTATAAATGTATTTGAGCCATTCATGACGGTTAATATTGATTAAACACTCATCACACTCTTTGCTCCTGCATTTTTTTTTTGTTTTTACTGTGTTTCATTCTCCTCTTCTCTCTCACTCTTTCTCTCATTCGCCATTTCTCTCTCTCCCTCTGTCTCTCCTTAATTGATTTTCTCAAGGTCCTGTGGAAAGATTGTCTTCTGATTCTCAGCACACTATCTTGTCCTAAAGGGATTACAGATGATCAGAGTCTGCAAAGATCTGTTATCCTGTCCAAAATCGCCTGTCCTCCTACTACTCTAGAGCAAGATCGGGGAATTAAAAATGTTGTTTTCGTTCTCGTTCTCTCCTCTTTTATATGGCTTCTAGGTTC[A/T]GAATGAAGCAGGTGAACATTGTTGGTTCGAGCCCCTTTAGTGAGTCCTCCCGATTGATGCAGACCCTGCAGTCCAGTCCAGATGTGGCCCCGACTGAGCTTGTCGTGTTTTCAGCCAGTGAAACCAGCCTGAGGATTCGCTGGGAGGTTAGAAAGACATACACACACAATCTGCAAACATTTACACTTAAGTTCACAGCTAATGTAGATTTTCTGCAGGTAAATGTGATTCTGGGTTATGGACTGTACTTGTATTCAGTAAGGAGATTTCTAAAGAATAAGGACTAGAGGAATGTCTGCTAAAATGTTTTAGTAATAGATCAAAGTTCTTGGTGTTTCACTGTACCATTGATTAAAGTGAAGTTTATTTATGAACTAATTTCGAGAGGATCGTGTACTTATGATTGCTTGCAGCCGGTCCCGCATTATTCAATTTATAATAATTTACCAATCAGATGATTCCTAAGCCACTATAAATACCCTAAGTTCCATATAACAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11705
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091205 | Nonsense | 1094 | 2120 | 23 | 46 |
ENSDART00000141238 | Nonsense | 1091 | 2095 | 23 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10390140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10522478 |
GRCz11 | 1 | 11206589 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCCAGTCCAGATGTGGCCCCGACTGAGCTTGTCGTGTTTWCAGCCAGT[G/T]AAACCAGCCTGAGGATTCGCTGGGAGGTTAGAAAGACATACACACACAAT
Long Flanking Sequence:
TTCTCTCTTTATAAATGTATTTGAGCCATTCATGACGGTTAATATTGATTAAACACTCATCACACTCTTTGCTCCTGCATTTTTTTTTTGTTTTTACTGTGTTTCATTCTCCTCTTCTCTCTCACTCTTTCTCTCATTCGCCATTTCTCTCTCTCCCTCTGTCTCTCCTTAATTGATTTTCTCAAGGTCCTGTGGAAAGATTGTCTTCTGATTCTCAGCACACTATCTTGTCCTAAAGGGATTACAGATGATCAGAGTCTGCAAAGATCTGTTATCCTGTCCAAAATCGCCTGTCCTCCTACTACTCTAGAGCAAGATCGGGGAATTAAAAATGTTGTTTTCGTTCTCGTTCTCTCCTCTTTTATATGGCTTCTAGGTTCAGAATGAAGCAGGTGAACATTGTTGGTTCGAGCCCCTTTAGTGAGTCCTCCCGATTGATGCAGACCCTGCAGTCCAGTCCAGATGTGGCCCCGACTGAGCTTGTCGTGTTTTCAGCCAGT[G/T]AAACCAGCCTGAGGATTCGCTGGGAGGTTAGAAAGACATACACACACAATCTGCAAACATTTACACTTAAGTTCACAGCTAATGTAGATTTTCTGCAGGTAAATGTGATTCTGGGTTATGGACTGTACTTGTATTCAGTAAGGAGATTTCTAAAGAATAAGGACTAGAGGAATGTCTGCTAAAATGTTTTAGTAATAGATCAAAGTTCTTGGTGTTTCACTGTACCATTGATTAAAGTGAAGTTTATTTATGAACTAATTTCGAGAGGATCGTGTACTTATGATTGCTTGCAGCCGGTCCCGCATTATTCAATTTATAATAATTTACCAATCAGATGATTCCTAAGCCACTATAAATACCCTAAGTTCCATATAACAGCCATCTTCGTTCTGAAGAATCCCCCCTTCCACCCCTACTCCTCCGCTTTTCCTAGATGGGTGGCATGGTGGCCCAGTGATTAGCACTGTTGCCTCACAGCAAGACTGTCACACTGTAATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38249
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 |
---|---|---|---|---|---|
ENSDART00000091205 | Nonsense | 1299 | 2120 | 28 | 46 |
ENSDART00000141238 | Nonsense | 1303 | 2095 | 27 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10364248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10496586 |
GRCz11 | 1 | 11180697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGCTGATGTTTCCAGAAGTGCGTCTCTCGTCTGTCAGGGTCGTCTGG[C/T]AACCTCCGTCTGAGCCCAACGGCATCATTATGGGTACCAGAAAAATAAAT
Long Flanking Sequence:
CCGTCTTCCCCTTTGAAATGAGTGAGTGTGTTCATATGTGGACTGTGGAGTCTTGCCAGCGGAATGACAAATGCCCTCTTTCTGTCATTTTTCTTAATCGGCTCAATGGAGCAACATTCGTATACGGAAATGTAGAAGGAAACCAGATACTCACACACACTCACATACACACAAAACTAGTGGATTACCAGCGCTGTTGGCCTAGTGTCCACTGGCAGAGTTAAATGTGTTTGATGAGGGATTTACCAAACACTAATATTTATATTTATGGATTTAAGGAATTAGAAGTTTACATTGTGTGCGTGTGTGAAGAGATTAAAATGTCGTATTTATCGCGACCGAGATAAAAGCTTGTCCTCACAAGCAGATGTTTGAAGTGTGTATGAATGTAATCGGGTTTAAACGGCATGTTTTTTTTCCCTCTTTTCTCTGCAGTTCCTGGTCCACCTGTCAGGCTGATGTTTCCAGAAGTGCGTCTCTCGTCTGTCAGGGTCGTCTGG[C/T]AACCTCCGTCTGAGCCCAACGGCATCATTATGGGTACCAGAAAAATAAATGCTATTCCACCAGTCACATACACTTTTACCCTTAGTGACAGGAGAGAAGATGTGTCATTGACATATGCTAGGTTAGATATAGAAGGATAATTATAGACACTGGACACTACATTTAAAACATAGATTTAATAAAAGTTCTACAGCTATTACATTTACTGTAGTGTTTTAGTAATAAATATTGAATTTATCTTTATAAATTAATAATTTTGCATTATTAAAAATGTTTTGCAATTTAAAAATTTTTTAACTGAAAATTGAAGCAATTTTTTTAAACATTTAATAATATAACTTAGATGAATAATAATAATAATCTGAAGTATTTTATGGCAAATCTGAGCAATAATAAAAATAAAATAAAATAAAAATATTTTTATATAAATAATTTAATTATTTACCTAAAATTATACTTAATATTTTTATTAGTTACAAATGTTCTGTTAAATTGTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39560
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 |
---|---|---|---|---|---|
ENSDART00000091205 | Nonsense | 1312 | 2120 | 29 | 46 |
ENSDART00000141238 | Nonsense | 1316 | 2095 | 28 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10353659)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10485997 |
GRCz11 | 1 | 11170108 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAAAAACAATGCACTCCAGCTGTTTTGACTTTTGTTTCTGCAGGTTAT[C/T]AGATTTCTTACCGTCTTGATATCAACGACCCCAACAAGTTCACCACGGTT
Long Flanking Sequence:
GATATATAATTTGTATCATCTGCATAAATATTTTATATCTAAGTATATACATTTTCTCAAATAAATCCATGCATGTGTGTAAATAAATATTTATATACTGTATACAGCAGGAAAAAATAAGTATTGAACACATCACCACTTTTCTTAGAAAGCATATTTCTAATGGTGCTATTGACTTGAAATTATCACCGGATGTTGGTAAACAATGTTCTATAAACAAATTTAATTAGTTTACAAATGAAGTTATGTGTAGTAAAATGAAATGACGCAGGGAAAAAGTATTGAACACATGAAGAAAGGGAGGTCCAGAAAGGCATTGAAAGCTTAGACAGCACCTGAAATCTCTCAGTAGTTCTCCAGCAACCCTCTGTCTTTCTTCAGTGTAAATAAATATCAGCTGCTTCAGTCCAACATCTACATTATCAGGATGATGAAGATGAAACCAGGGTGGACAAAAACAATGCACTCCAGCTGTTTTGACTTTTGTTTCTGCAGGTTAT[C/T]AGATTTCTTACCGTCTTGATATCAACGACCCCAACAAGTTCACCACGGTTGAGGTGGGCTCCAACGCCCGGCAGTTCACAGTCACGGGTCTGATGCCAGAGTCTGCGTATGTGTTCCAGATCACGGCGCGCACTTTACAGGGCTGGGGGCCCGCAGACGAGGCCATCGTCATCACCACTGAGAAAAGAGGTACGTTTAAGTCAGGGCTGTCCAAACTCGGTCCTGGAGGGCTGGTGTCCTGCATAGTTTAGCTCCAACTCTCTTCAACACACCTCCCTGGATGTTTCTAGCTTACCCAGAAAGAGCTAGATTAGCTGGTTCAGGTGTGTTTAAATGGGGTTGGTCCAGGACCGAGGTTTGAGTCATTACTTCACTTCCAGAATCGAAACGAAATACTGATCATTTACTCGCCCTTTATCATCCAAGTTGTTAATTTCTTCGTAGTTTCCTCCATATAGTGAACCTCAGTGATGCTCAGTGGTTTGAACTTCTGAATTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17607
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091205 | Essential Splice Site | 1988 | 2120 | 44 | 46 |
ENSDART00000141238 | Essential Splice Site | 1963 | 2095 | 42 | 44 |
ENSDART00000144164 | None | None | 199 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 10311973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 10444311 |
GRCz11 | 1 | 11128422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGACATCTGAACGTGAAGAGCTCTTTCCTCAAGAAGAATGGAACAAG[G/A]TAAGGCTTCATTGAACTGCGGTTAAAGCGTTTTGATGCTCTTTACACTTT
Long Flanking Sequence:
AAACCCAACTATAACTGTAAATTATTCCCAAAATCAGAGAGAAATAACAGATGGATAGCAATCATGTAGAAGTACATGACCCTAACCGTAAGATAAACTTAACATAAAGAGTAAACCTATCCTTTAATTCTGATTGGCTGATTGAAATGTTGTTCCAGGATCAACAAAGATGTTAATCCAGGAGCAAGTCCTTCTTGAAGTCAGGTTAGCGGGTATGGTTAGTTATCTATAGGTTTAAAATAGCTCTTACGTTTCATTCCACTGTATGTCCACACATGTAGCAGAATGACAATAAAGCTCAACTTGACTTGATAGAGTATCAGTCGACGAGGCTTGTCTTTGTTGGTATCACTCAGATGTTTTTTTTTTTTTCTCACAGGGAAGCACATCAGTACTGTCGAAGAATCGGTGACCCTTGACAATGGCGGCTTCACGGCCCTCGAGCTGAACAGCAGACATCTGAACGTGAAGAGCTCTTTCCTCAAGAAGAATGGAACAAG[G/A]TAAGGCTTCATTGAACTGCGGTTAAAGCGTTTTGATGCTCTTTACACTTTCTACTTCGTTAAGTGTGTAGTGTTACTGTTTGAGTGTTAAAAAAAGATCTGCAAAGTTCACTATGAAGCTCAAAGTCTACTCCAAAGAGAGTTATGAGTCACTATAATAGAAAACACTGATTCAAATGCTTCTTAGTCCTGATTTATTTATTTATTTTTATTATTTCATTTTATTTTTTTGTATATGTGTGAATGCAATGAAACATCAAAATATACATTTTATGATTATGTTATGATATTATGTTATGTTATGATATACTATGTAATTTACATTTTATCACCAGATTTTTTTTCTTCATGTAAATCCTAAATATAAATATGTCTTTATAGGAAATGTGTATGCAGTTTGTATAATGGAATGTTAATGTTGTTGTTTGGTCCACAGGTCTCCTCCACGGCCCAGTCCGGGTGGGCTGCACTACTCTGATGAAGACATCTGCAACAACTACA
Associated Phenotype:
Not determined