ZMP
si:ch211-69i14.4
Ensembl ID:
ZFIN ID:
Description:
Myosin-Ic [Source:UniProtKB/Swiss-Prot;Acc:A5PF48]
Human Orthologue:
MYO1C
Human Description:
myosin IC [Source:HGNC Symbol;Acc:7597]
Mouse Orthologue:
Myo1c
Mouse Description:
myosin IC Gene [Source:MGI Symbol;Acc:MGI:106612]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16308 | Nonsense | Available for shipment | Available now |
| sa20485 | Nonsense | Available for shipment | Available now |
| sa33658 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38492 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25307 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30862 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40512 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45215 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16308
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Nonsense | 58 | 1026 | 2 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39395881)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37195565 |
| GRCz11 | 5 | 37795718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAGACATATATTGGGTCGGTGCTGGTGTCGGTGAATCCTTACAAGGAGT[T/A]GGAGATTTACTCTAAACAGAACATGGAGCGCCACAGAGGAGTGAACTTCT
Long Flanking Sequence:
ATATAATATTAATTCTTTTCCCTCTGCACCATGACTTCATATTCTATACTGTACATTATTTCTTTTAAGAGACAAGACATTTTTTTTTCTATTTTTAAATGTGTTATCTTTCTATTTCTAAAGATGTTTGGTGACTAAAATACTGTCTGTTTAATACATATGCTATGTTTAAATGCACTAAAATATATTACATTTTCACTGAGAAATGGGTAAAAATATTCATTTTGGGATGTTCTGATTTATGCGGAGCACTGTAACTGTTTTACTTATTAATATATATATATATTTTTACAGTTTTTAAATGGTTAATGTTATTCATTTTAATACAGCCTAGGTAAATGTATCATATAAAGCTCCATAAACTCCAAAAAAAAAAAAGTTTACTTTGTAATTTTCTACTTTTATTTAACTTTCATTCTGTCTTTCCTCCTCAATCTATCTCTATCTCTATAAGACATATATTGGGTCGGTGCTGGTGTCGGTGAATCCTTACAAGGAGT[T/A]GGAGATTTACTCTAAACAGAACATGGAGCGCCACAGAGGAGTGAACTTCTATGAGATCTCACCTCACATGTGAGTGTTAAGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGGTCGTGAGAATCCCTGAGAACATTCCGCCAATTCTCCTATTATGACTCACTTTCCTGGAGATTCCGGAGATTGGACTGTTCAACTTTCCACTTCCACACACATTCACACCCTCACCATTAAAAAAACATGAAATCCATGCTCACACACAAGCTATTCCAAACTGTTTGGCAGAGTTAAAAAAAAATATATATTATTATTAGTATATTATATATTTTTGTATATTAGTATATTATTTAGTATATTATAGCGTATTAGTATATTATTACACGTTTTGTAAATTCACATTCTGCTGCTAGTGCTAATATTCTCTTAAACTTAAGAAGAATTACCTTTAGCATGTAAAAGTGCATTTACAGATTCTTTTCTCATCAATGTACATAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20485
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Nonsense | 335 | 1026 | 9 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39402688)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37202372 |
| GRCz11 | 5 | 37802525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAGATGCAGTCTGTATGTCTGTGTTTGATTTCAGATGATCAGTCCCT[T/A]GAGTTTAGAACAGGCTCTCTCTGCTCGAGACTCTTTTGCCAAAGCCATAT
Long Flanking Sequence:
CAAGCACCTTTTAAACTTTAGATTTATAGCCAACTGAGGCTGTACGGGTGCTGATAGTACTTAAATATATCACGGCTATCAGCCAATCAGATTCGAGAACCAGACAAAACTGTTGAACTATACTATAGAACTGACAGAACTATATATATATATATATATATAAATTCCAAAATATTATATATATATCAAAAAGTTGAAATAACACTTCTCAGTGATAACCCCTTGTCAGATTTGTTCTTGTTGATTTACACACATACAAAAGCACAGGGAATGTGCTGTAATGTTTTGTTCTATCAACAGCTGCTGGGTGTGGATGGCTCTGTCCTGAAAGCAGCTCTTACTCACAAGAAAATAGTTGCCAAAGGGGAGGAGGTAATATTACAATCTCTCTCTGTCTGTTCTCTTTCTGCATGCTTGATCTTTGCTAATCTCCACACTCATTGAGTCCAGCAGTAGATGCAGTCTGTATGTCTGTGTTTGATTTCAGATGATCAGTCCCT[T/A]GAGTTTAGAACAGGCTCTCTCTGCTCGAGACTCTTTTGCCAAAGCCATATATGGTCGTGCCTTTACCTGGCTTGTCCAGAAGTTGAACCGATCACTGGCCTTTAAGGTGTGCTCCTTCTGTCTGTCAATGTCCTTTTGTTTTATCAAAGTGGGCTTACTTGTTGTGACAGAATTGTTGTCTATGAACTGGAGCTTAATGTGCCCTCTAGTGGAAGATGTTTTGAAGATGATTATGCTTTTGTGTTTCACAGGATGAGATTTACTACTCCAGTAAATGTTCGTCTGTTATTGGTTTGCTGGACATATATGGATTTGAGGTCTTCCAGCACAACAGGTTGTTTACTCTTTGTCTGTGAATGTGAATGATTGTAAATGTAGACAATTAATCATTAATTTGTTATTGGAGAAATACAGTAATCATGTTTTTGGAATATTGGTGATTAGTATAGCCACATCTTTACTACAAATACCATAGTTAAACTAGGTCAGTGCAGTAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33658
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Nonsense | 585 | 1026 | 17 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39405940)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37205624 |
| GRCz11 | 5 | 37805777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGCTCAGTTTGGCTAAACTGATGGATATTCTGATGTCTAAGGAACCAT[C/A]ATATGTTCGCTGTATAAAACCCAATGATGGTAAACAGCCAGGTGAGAATT
Long Flanking Sequence:
AATTGGTCGGGAGGAGTTTAGACTGGTACACTATGCTGGAGAGGTCAACTATAACGTCAATGGTGAGGATAAAAAAAAAAATCAACAATTTATATGTTCATCCATAGTTGATTCTTCTGGTGCCATGACTTTTAATCTTTCTCCAATTTTTGTAGGGTTTCTGGACAAAAACAATGACCTGCTATACAGGCACTTGAAGGAGGTACAGTGTGTTTACAAAGAGTGGGTGAGCTGTTACGACTGAACAATGTGTGTTTCTAAACCCGCTGTGTCTCATTGCAGGTGCTGTGTCAGTCCACCAATCACATTGTGAGTCAATGTTTCCATGCAGATGAGCTGATGGACCAGAGAAGACCTGAAACGGTTAGATGAACACAAACACATACAGTACAGAGGCCTGAATTAAACTGAATTAAATTTTGTTGTCTCTGCTCAGGCTGCCACTCAGTTCAAGCTCAGTTTGGCTAAACTGATGGATATTCTGATGTCTAAGGAACCAT[C/A]ATATGTTCGCTGTATAAAACCCAATGATGGTAAACAGCCAGGTGAGAATTCATTTTTTTCTTATTTATTTTAATTGGTTTATCTTACTGAATTTACTCTGTAAATACAATAAGAATACTATAGATAGTATGTATACTACACAAACACCATAAAACTACTAGTTCAATTCAACAAAAAGAAAAAAACATATACACTCACTGGCCATTTTATTAGGTACACATTACTAGTATCGGGTTGAACCCACTTTTGCCTTCAGAGCTGCCTTAATCCATCGTGGCACAGATTTAACAAGGTACTGGAAATATTCCTCAGAGATTTTGGTCCATATTGACATGATAGCATCACGCCGTTGCTGTCGGCTACATATCCATGATGCAAATCTCCCGTTCCACCACATCCCAAAGGTGCTCTATTGAATTAAGTTCTGGTGACTGTGGAGGCCATTTGAGTACAGTGAAGTCATTGTCATGTTCAAGAAACCAGTCTGAGATGATTCGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38492
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Essential Splice Site | 724 | 1026 | 21 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39410270)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37209954 |
| GRCz11 | 5 | 37810107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGAGGCTACAGAGAGAGAGCCAATTACCATCGCATCCGTCATGCAG[G/A]TCGGCTTTACAAATAGACTGAAAACAGACAGACAATTGTAAGAAGAAAAT
Long Flanking Sequence:
ATAAAATTATTGAAAATTTCCAACGAGGAATGGAAAATGAACTTCCAGTTTAATAGCTGCTATAAGTAAATATAATTATGCATCTCTTATTTTAACAATAATTAATCTGTTTAGTTAAATTAAGACACAAAATTTATGTAAGAAATATCCTAGAATCAGAAAGTGGAAGAGCTGGCACAATAATGATCATAATTGAAAAATACATTTATTTGTTTTCTCTATAGGTCCAAAATCTTCATCCGCTTCCCAAGGACTCTGTTTATTACTGAGGATGCACTTGAGGCCCAGAAGCAAACTATCGGTAAGACCATGATGAGTTGACTTGAAATTGAGTATTCTTCTACTTCTGCTGAGTATTACTGTTTGCATTTCTTATAAATGACCTCATGAAAATTTGATCATTAAAAAAATAACTGGATTGTTTTTTTAAGCCGTCACTCTGCAGAAATCTTGGAGAGGCTACAGAGAGAGAGCCAATTACCATCGCATCCGTCATGCAG[G/A]TCGGCTTTACAAATAGACTGAAAACAGACAGACAATTGTAAGAAGAAAATGCAGCAGCATACCTGTTTTGTCTTTTTTATCTTGCAGTAATTGTCATCCAGTCATGGTGGAGAGGCGTCAAAGGCCGTAGGAAAGCCAAGCACCGTAGACAAGCTGCTGACACTATTCGCAAGTAGGAAACAACTTCTTTTACTTTTATGTGAACGAGTTAGTAGGTGATGCGGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGTTCGAGCCTCTGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGCTCGCGTGGGTTTCCTCCGGGTGATCCGGTTTCCACCACAGTCCAAAGACATGCGGTACAGGTGAGTGGGTAGGCTAAATTGTCAGTATGGTATGAGTGTGAATGAGTCTGTATGGATGTTTCCCAGAGATGGGTTGCAGCTGGAAGGGCGGTTCATTCCGCTGTGGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25307
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000053511 | Essential Splice Site | 725 | 1026 | 21 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39410271)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37209955 |
| GRCz11 | 5 | 37810108 |
KASP Assay ID:
554-7706.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGAGGCTACAGAGAGAGAGCCAATTACCATCGCATCCGTCATGCAGG[T/A]CGGCTTTACAAATAGACTGAAAACAGACAGACAATTGTAAGAAGAAAATG
Long Flanking Sequence:
TAAAATTATTGAAAATTTCCAACGAGGAATGGAAAATGAACTTCCAGTTTAATAGCTGCTATAAGTAAATATAATTATGCATCTCTTATTTTAACAATAATTAATCTGTTTAGTTAAATTAAGACACAAAATTTATGTAAGAAATATCCTAGAATCAGAAAGTGGAAGAGCTGGCACAATAATGATCATAATTGAAAAATACATTTATTTGTTTTCTCTATAGGTCCAAAATCTTCATCCGCTTCCCAAGGACTCTGTTTATTACTGAGGATGCACTTGAGGCCCAGAAGCAAACTATCGGTAAGACCATGATGAGTTGACTTGAAATTGAGTATTCTTCTACTTCTGCTGAGTATTACTGTTTGCATTTCTTATAAATGACCTCATGAAAATTTGATCATTAAAAAAATAACTGGATTGTTTTTTTAAGCCGTCACTCTGCAGAAATCTTGGAGAGGCTACAGAGAGAGAGCCAATTACCATCGCATCCGTCATGCAGG[T/A]CGGCTTTACAAATAGACTGAAAACAGACAGACAATTGTAAGAAGAAAATGCAGCAGCATACCTGTTTTGTCTTTTTTATCTTGCAGTAATTGTCATCCAGTCATGGTGGAGAGGCGTCAAAGGCCGTAGGAAAGCCAAGCACCGTAGACAAGCTGCTGACACTATTCGCAAGTAGGAAACAACTTCTTTTACTTTTATGTGAACGAGTTAGTAGGTGATGCGGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGTTCGAGCCTCTGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGCTCGCGTGGGTTTCCTCCGGGTGATCCGGTTTCCACCACAGTCCAAAGACATGCGGTACAGGTGAGTGGGTAGGCTAAATTGTCAGTATGGTATGAGTGTGAATGAGTCTGTATGGATGTTTCCCAGAGATGGGTTGCAGCTGGAAGGGCGGTTCATTCCGCTGTGGTGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30862
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Nonsense | 730 | 1026 | 22 | 31 |
| ENSDART00000053511 | Nonsense | 730 | 1026 | 22 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39410373)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37210057 |
| GRCz11 | 5 | 37810210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCATACCTGTTTTGTCTTTTTTATCTTGCAGTAATTGTCATCCAGT[C/A]ATGGTGGAGAGGCGTCAAAGGCCGTAGGAAAGCCAAGCACCGTAGACAAG
Long Flanking Sequence:
AATCTGTTTAGTTAAATTAAGACACAAAATTTATGTAAGAAATATCCTAGAATCAGAAAGTGGAAGAGCTGGCACAATAATGATCATAATTGAAAAATACATTTATTTGTTTTCTCTATAGGTCCAAAATCTTCATCCGCTTCCCAAGGACTCTGTTTATTACTGAGGATGCACTTGAGGCCCAGAAGCAAACTATCGGTAAGACCATGATGAGTTGACTTGAAATTGAGTATTCTTCTACTTCTGCTGAGTATTACTGTTTGCATTTCTTATAAATGACCTCATGAAAATTTGATCATTAAAAAAATAACTGGATTGTTTTTTTAAGCCGTCACTCTGCAGAAATCTTGGAGAGGCTACAGAGAGAGAGCCAATTACCATCGCATCCGTCATGCAGGTCGGCTTTACAAATAGACTGAAAACAGACAGACAATTGTAAGAAGAAAATGCAGCAGCATACCTGTTTTGTCTTTTTTATCTTGCAGTAATTGTCATCCAGT[C/A]ATGGTGGAGAGGCGTCAAAGGCCGTAGGAAAGCCAAGCACCGTAGACAAGCTGCTGACACTATTCGCAAGTAGGAAACAACTTCTTTTACTTTTATGTGAACGAGTTAGTAGGTGATGCGGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGTTCGAGCCTCTGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGCTCGCGTGGGTTTCCTCCGGGTGATCCGGTTTCCACCACAGTCCAAAGACATGCGGTACAGGTGAGTGGGTAGGCTAAATTGTCAGTATGGTATGAGTGTGAATGAGTCTGTATGGATGTTTCCCAGAGATGGGTTGCAGCTGGAAGGGCGGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAGGGATTAAACCGAAAAGAAAATGAATGAACGAATAAACGAATGAATGAAAGAGTTAGGACACTATGAATCCAATCTTTCCATATTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40512
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Nonsense | 730 | 1026 | 22 | 31 |
| ENSDART00000053511 | Nonsense | 730 | 1026 | 22 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39410373)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37210057 |
| GRCz11 | 5 | 37810210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCATACCTGTTTTGTCTTTTTTATCTTGCAGTAATTGTCATCCAGT[C/A]ATGGTGGAGAGGCGTCAAAGGCCGTAGGAAAGCCAAGCACCGTAGACAAG
Long Flanking Sequence:
AATCTGTTTAGTTAAATTAAGACACAAAATTTATGTAAGAAATATCCTAGAATCAGAAAGTGGAAGAGCTGGCACAATAATGATCATAATTGAAAAATACATTTATTTGTTTTCTCTATAGGTCCAAAATCTTCATCCGCTTCCCAAGGACTCTGTTTATTACTGAGGATGCACTTGAGGCCCAGAAGCAAACTATCGGTAAGACCATGATGAGTTGACTTGAAATTGAGTATTCTTCTACTTCTGCTGAGTATTACTGTTTGCATTTCTTATAAATGACCTCATGAAAATTTGATCATTAAAAAAATAACTGGATTGTTTTTTTAAGCCGTCACTCTGCAGAAATCTTGGAGAGGCTACAGAGAGAGAGCCAATTACCATCGCATCCGTCATGCAGGTCGGCTTTACAAATAGACTGAAAACAGACAGACAATTGTAAGAAGAAAATGCAGCAGCATACCTGTTTTGTCTTTTTTATCTTGCAGTAATTGTCATCCAGT[C/A]ATGGTGGAGAGGCGTCAAAGGCCGTAGGAAAGCCAAGCACCGTAGACAAGCTGCTGACACTATTCGCAAGTAGGAAACAACTTCTTTTACTTTTATGTGAACGAGTTAGTAGGTGATGCGGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGTTCGAGCCTCTGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGCTCGCGTGGGTTTCCTCCGGGTGATCCGGTTTCCACCACAGTCCAAAGACATGCGGTACAGGTGAGTGGGTAGGCTAAATTGTCAGTATGGTATGAGTGTGAATGAGTCTGTATGGATGTTTCCCAGAGATGGGTTGCAGCTGGAAGGGCGGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAGGGATTAAACCGAAAAGAAAATGAATGAACGAATAAACGAATGAATGAAAGAGTTAGGACACTATGAATCCAATCTTTCCATATTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45215
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 |
|---|---|---|---|---|---|
| ENSDART00000053511 | Nonsense | 929 | 1026 | 27 | 31 |
Genomic Location (Zv9):
Chromosome 5 (position 39414278)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 37213962 |
| GRCz11 | 5 | 37814115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCTGGTCCAGGAAGCAAAAATCAAACAACGTATCGACTACGGTGCAT[T/A]GCTGGGTAATGTTACTGTAATACAGCTCTCTCTATTGTTGGCTAACAATA
Long Flanking Sequence:
TTCATATAATCTTTGCCCAACAAAACAAAACCTTAGTCATTTTAAATGCCAATTGGGAATCGATATATTACTTAGTTTAATGATGGGTCACACTGTAGTTTTCATTAAAGTCTGTGATAAATAGGGTTGAGTTGAAACTTTTTGAAGCAATTTAAATCATAAAATCTAAAGGTTGTGGCTGATCACAAGAAGAGTGCACACACATACCCCAAAAAACAAACATTTCAAAATAGAAACAAAAAAAATGAACCAGCGTATGATGGAAAAAGTCAGTATTAATCAACAGGAACTATTCTAGTCAATATAATTCAATTACAAAAAGGTAATCTACTGATTATCTTGTGTTGTTTATTCTCCTCATCTTTTTCAGTATGGGATAGCGGTCACCAAGTACGATCGACATGGTTTTCGCCCACGTGTGCGGCAGCTGCTGTTGACCACTTCATCTGCTGTGCTGGTCCAGGAAGCAAAAATCAAACAACGTATCGACTACGGTGCAT[T/A]GCTGGGTAATGTTACTGTAATACAGCTCTCTCTATTGTTGGCTAACAATACTGTACCACAACTAAGCCTATTAAAGTTGCATAGTCTCGTTTTTCACCATATCTAACTCTTGGCTAATCATGCTCTTTACTAGTACTCCGCTCATAAATTCTCATTAGTGTCTTGTATTCATTGTTGGTTTGTTTATTTCTTGTAGGTATCTCTGTTAGTTCTCTCAGTGATGGATTTTTTGTTCTGCATATTCCCACTGCTGACAGTAAGCAGAAGGTGAGAGTTTTTTGTTCTTTCTTATTGACCTTATTGTTCAGTTGGAGCTCTGAGGTTTCACTATATGTCTTTTGACTGTTAGGGTGACCTGGTGCTGCAGTGTGATCATGTGATTGAGGCTGTCACCAAGCTGGCTATCATGGCAGACAAAATACACAATGTCAACATCAGCCAGGACAGGTGTGTACTGTGTACAGTATGTGTGTGCGCACACGGGCAAATGGTTTTGGCAG
Associated Phenotype:
Not determined