ZMP
si:ch73-194h10.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO7B
Human Description:
myosin VIIB [Source:HGNC Symbol;Acc:7607]
Mouse Orthologue:
Myo7b
Mouse Description:
myosin VIIB Gene [Source:MGI Symbol;Acc:MGI:107709]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40701 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40702 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40703 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15693 | Splice Site, Nonsense | Available for shipment | Available now |
sa10082 | Essential Splice Site | Available for shipment | Available now |
sa20714 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40701
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 |
---|---|---|---|---|---|
ENSDART00000065268 | Essential Splice Site | 192 | 2179 | 5 | 49 |
ENSDART00000143218 | None | None | 1419 | None | 30 |
Genomic Location (Zv9):
Chromosome 6 (position 27771339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28072550 |
GRCz11 | 6 | 28063111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTCCTGGATTGAGCAGCAAGTTCTAGAGGCCAACCCTATCTTAGAAGG[T/C]ACAGTTACATACACTTACATCTTCCTTATATTTCCTCCAGTAAACATTTC
Long Flanking Sequence:
GTTGCGTTGTTCTAAAAATAGCAACACGTCAGGGCAAACAAGTCTTGCACCTTATTGCGCCGGGAGTATGATAGGGCCCCTTGATTTGACGTTTCTGAAAACAAAACCGTATCTTTCTCTTGTCTTGAAAATGCGTCTTGATTTAAGTATTTTTAGATATTTGGACTATAAACAAGACAAAAACTGGTAAGAAAAGCATTTTTCATAGACTGTAAATCTCAGGTTTTCTGTACAGTTGGCAGCTGTGCAAACATCATTCCAAAATGAACTTGCCATTTATGTTGACAACCTCAGTCTCACTCTGACATCTGTCATGCATTGTTGGTGTAATCTGTTTGATGCATTCTGAGAGCGCCTGCATGTGTTGTGTTTTTCAGTGGGGAGTCTGGAGCAGGGAAAACAGAGAGTACCAAACTCATGCTGCAGTTTCTTGCAGCCGTGAGTGGTCAGCGCTCCTGGATTGAGCAGCAAGTTCTAGAGGCCAACCCTATCTTAGAAGG[T/C]ACAGTTACATACACTTACATCTTCCTTATATTTCCTCCAGTAAACATTTCAGGGTCACACTGTATTTTAATGGTTCATTTGTTGAATTAATATTACATTGCATCTATATGCCAACTAATTCTCATTAGATTATAAGTAAACTGTTAGGTTGGGTTTAGGGTTAGTGTAAGTTGACATGTACTTGCAAAGTGTTTTTTTAATAGTCAATTAAATGTCTGTTAAAGGAGCAGAATCAACAAATATTACGCAGACAGTCTACTAATACTCAAATGGACCATTAAAATAAAGTGTTACCCATTTTAGTGCTATCATAAATTTTTATTTTGCAGCCTTTGGTAATGCAAAAACCATCCGCAATGACAACTCCAGCCGCTTCGGAAAATACATCGACATCCACTTTAATAAAAGTGGAGCAATAGAGGGTGCTCGCATTGAACAGTACCTACTCGAAAAGTCACGTGTTTGCCGACAGGTAAAGCACAATGATATGAGATTATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40702
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065268 | Essential Splice Site | 596 | 2179 | 15 | 49 |
ENSDART00000143218 | None | None | 1419 | None | 30 |
Genomic Location (Zv9):
Chromosome 6 (position 27778813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28080024 |
GRCz11 | 6 | 28070585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGATTTAAATTACTTTGATTTGCATTCCCTTTTGTTTCTCACCCCATC[A/T]GCAAACAGCAGACACAAAGAAGCAAGTTCCAACATTAACTGGTCAGTTTC
Long Flanking Sequence:
CACAGTTTGGAATCCGGCATTTTGCTGGAGTTGTCCACTATGACTCCAAAGGTACTCTGACTTCACATCTTTGTGTTTTTTTTTTTTTTTTTTTTTGCGTTTAAATGATCTATGTCTATGAAATTTACTGTGCATATAGGTTTCCTTGAGAAGAACCGAGATGCTCTGAGTAGTGACATCATCCAGTTGATACACACATCTTCCAATAAGCTCCTGAAGCAGATATTCCACAGTGAGATCAGCACCATAGAGGGGAAAACTAGCATCAACCACACCATCGTCACCCCAAAAAGCTCACTTCGGGTAGGTTAACAGCAGCTTAAGGCTATATGGATATAAATATGGGTTGTTTATTAACATTTGGGTCAGTAATTAATATCAAGATAGCAGCTCAAAACCATGGATAAATATTGGTCATCCTTTATCTTTTGCCACAATTAACACATTTACTCTGATTTAAATTACTTTGATTTGCATTCCCTTTTGTTTCTCACCCCATC[A/T]GCAAACAGCAGACACAAAGAAGCAAGTTCCAACATTAACTGGTCAGTTTCGCCAGTCGCTTGACTCTTTGATGAAGACTCTAACTGCCTGTCAGCCTTTCTTCATTCGCTGCATTAAACCCAACGACTTCAAGAAGCCTATGGTGGGTTCAGTTCATCATTTAATCTGTTCTTCCACAGTATACATGCCTCAATTTTCTCTGAATGACCCACTTTTCTATCTTTGCTTCAGCTCTTTGACAGGGAGCTGTGTATCCGTCAGCTTCGTTACTCAGGAATGATGGAGACTATCCGCATCAGGAAGGCTGGATATCCCATCCGCCACACATTTGATGAGTTTCTGGAGCGTTACCGTGTGCTGCTCAAGTCCACTGTTTGTGATCCCCAAACTGTGAGAGTTGTTTTAAGTAGTTTTTAATGTTTTTTTTGAAAGACATTGGTGTTGCAGTTGTTTAATTCACCATGTCACAGGTTTTAAAGTTATTTTAAAGTTTAAAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40703
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065268 | Nonsense | 1754 | 2179 | 39 | 49 |
ENSDART00000143218 | Splice Site | None | 1419 | None | 30 |
Genomic Location (Zv9):
Chromosome 6 (position 27804614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28105825 |
GRCz11 | 6 | 28096386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGTTGGCGTGCACCTATTTTGAAGTATATGGGTGATTATCCCACCAGA[C/T]AGGTTCAGAGCCCTCTGGAGCTCACAGATCAGATCTTTGGCCCACCTACA
Long Flanking Sequence:
AACGATCAAAAACATAAATCTGACAGAAACAAAGCTAGTTGAATTGAGCATAGTGCAACCTACACAATGTTCCTTCACAAGACGGTGACAAACAGCCTAAAACAGTGGTGTGAGACAAGCAGATGCATATGAATGTGGATATAAGAATATGGATGTGAACGTAGACCTATTCACTGATGGTTAAGATGATTCGAAGTTCCAGGATGATCCTGTGTTGTTCAGCAGTTGTTATCTGGAAATAACATACCGTGGAATGTTGCAACTGACCAATAAGAATATTCCAGACAGACATCTAATAAGTATTGTTATCATATATTTAATCATCCTTTATTGTCATAATAGTGGGTTATCCCTTATTTTTAACTGATACATATCCAAATGACTTATAAGTGAGACTTGCCAGGGAAACTGGTTATTGGATGCAACCCCAGACAGTGCGGATTCCTTGACTAAGTTGGCGTGCACCTATTTTGAAGTATATGGGTGATTATCCCACCAGA[C/T]AGGTTCAGAGCCCTCTGGAGCTCACAGATCAGATCTTTGGCCCACCTACACAAAATGAGGAGCTCCGAGATGAGATCTACTGCCAGATCATGAAGCAAATGACCAGCAATAACAACCGGTAAACAGCATATTACTTGCTTTAATGTCATATGCTACTATTCAAGCTTTTCAAGTTTGTTTTCCTTTCAAAAGAGTTTTTGGGAGTAGTCTCTTGTACTTTTCAGACAAGGGTGCGGTTACTTAATAAAAAATGCTGTAAAACATTATTATTACATATACATAAATATTATTAGTTTCAAATTGCTTTGAAATTAATGTAATGACAAAGATAAGTTTGCACTACTTTAAATCAGTTTAATGTGCTGATTCTATGATTATGAAATGTTTCTTGTCATTTTCAAAGTTGTTTCAAAGCCAATGTTTTTGCGAAAGCTGCGATGTATATTTTGTCAGGGCTTATTAATAATTGGAAAGTTCAATCTTGCTACAAAAATACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15693
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065268 | Splice Site, Nonsense | 1918 | 2179 | 42 | 49 |
ENSDART00000143218 | Splice Site, Nonsense | 1155 | 1419 | 22 | 30 |
Genomic Location (Zv9):
Chromosome 6 (position 27814656)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28115867 |
GRCz11 | 6 | 28106428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGYTGTCCACAGCTGAAGGTTTCAGCCTCTTCAWGAAAACTCCTGAY[A/T]AGGTTTGTTCCTARTSTACCATGATTTATATTTAACAGCCAGGACTGTGT
Long Flanking Sequence:
AGCAGCTCCCAAAGATTCTGTTTTCTTTTCCATTGAGCACTGCTGCAGCTCCGCAGTTTCTATTCCATACTATATATAGCCTGTATTAACTGCAGTATTTATAGTAACTGAAATGTGTCAATAATATGCCACCAGTATTTTGGTACTGATGTGTGAATATTACCAGGAGAGCCAGTCTTGTCATTTTACAGTAATTACCAGGATTTCATTTTGATCGTTTTTGCCCAATGGCCATGTTTTAGATTTTTGTTTTTCAGCTTGGCGCTAGTGCTTTTTATCTACTCTCTAGTGTTCAAAATGCTGAAAATAATAGCAGTTGGATTTGATACCATTGTAACTCTTTGTTTATTCTAAACTTTGCTTTTTTTACTACTTACCCTTCTGGACAGATATTTGAGGTGGCAACCAATACTAAGATCAGAGACCTGGTCCGGACCATTGCTAATAAACTCATGCTGTCCACAGCTGAAGGTTTCAGCCTCTTCATGAAAACTCCTGAT[A/T]AGGTTTGTTCCTAGTGTACCATGATTTATATTTAACAGCCAGGACTGTGTGCTTCTATTAATGAACAGTTTCTGGAATATTGTGGAAAAAGGGGTATTCCAGACATTGAAAGTCTGGGAAATGTGTATTATTTGTCTATAATTCATTTTATATTTGTATTATGAATATTATTCTGATCTCAAGAATCATTGGTCTCAATTGACCTCTTAACCATTTAAAAAAATCCTATTTGATGCACAAATTACTTAAAGTAATCAGGGTAAACTAAATGGTTAAAATCTCTTTAACAATACTATTAGAAAAATCATGTTTTATTATACTAATAAAAATTATACTCATTTTTTACAAAGATGCAAATTGCTTAAAACTGGAAAAATGCCTAATAGCATGTAGTGGCTTTTGTAGATGCACGACTGCTCATTTGTAAGACAACTCAGACATTGTTGCACATTGGATAAGCGCTTTATAAACCAAACATAATGTGTCCTGAAAGGCCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10082
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065268 | Essential Splice Site | 1984 | 2179 | 44 | 49 |
ENSDART00000143218 | Essential Splice Site | 1221 | 1419 | 24 | 30 |
Genomic Location (Zv9):
Chromosome 6 (position 27815621)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28116832 |
GRCz11 | 6 | 28107393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCCCTGGGAGAGATGTGGAGGCAGATCTCATCTTCCATTACCCACAGG[T/A]ACTGAAATGTATGGTAAAATTCCCATGTAAGCTTTCYAAAAATATCTACA
Long Flanking Sequence:
TATAAACCAAACATAATGTGTCCTGAAAGGCCAAAATGTGCCAGAAATCTAATCTTAATTATATTGCAAGCTCATCTAAATTTTGTGTCATTTGCTTGGTTTTGTGTTAAATTCAGTATCACAGAATAGCAAAATTTAGGAAGGACTCCTCAAAAATTCTTATTTTTATTACCCTAAATGATCATTAATAACTGTTCTGCCATTTTCTATTTGTCAGGTTCTGAGTTTGAATGAAACAGACTACTTCTTTGACAGCCTCAGACAGATTACTGATTGGTCCAAAAGAGCAAAGAGAGTGAATCAAGGTAAGTCTGTTTGTTTTCTTTTAAATGGAACAGGTTTGAACTTAAATTCAAAGCAGTTGACATTGCTGATACTGTTTTAAACAGCAGGGGCTCCAGTGAATGTGTCCTACACTGTTTTCTTTATGAGGAAGCTATGGTTCAACATTATCCCTGGGAGAGATGTGGAGGCAGATCTCATCTTCCATTACCCACAGG[T/A]ACTGAAATGTATGGTAAAATTCCCATGTAAGCTTTCTAAAAATATCTACACTCATCTCGAAGAAGACCATTTTGTTAAGTTGATAAAATAGAACATTGAAGACATGCATACTACTCCAGATTGTTACATACACACAATTATATAATACAAATATATGTATAATATTCCCCCTTTCTATTCGTTAAAGAACGTTAATACAAATGGGGTTCACAGTACTATTAAGGTGCATAGCTGTCAATAATGAAAATTTGGACTTGAGCATCAAATCAGCATATTGCATTGATTTCTAAATTACTGTGGCATTGAAGAATTCTGAAAATTTTAGACTGTTGGAATTTCATTGACAAAGATCTGAATAAGTGAATGATGATAACTTGTTCACACTTTACAATAAGGTTCATTAGTTAATGTTAATTAATGTATTTACTAACTTGAACAAACAATGAACAATACATTTACTACTGTATTTGTTCATGTTAATTTACGTTAGTTAATGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20714
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 |
---|---|---|---|---|---|
ENSDART00000065268 | Nonsense | 2068 | 2179 | 46 | 49 |
ENSDART00000143218 | Nonsense | 1305 | 1419 | 26 | 30 |
Genomic Location (Zv9):
Chromosome 6 (position 27817484)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 28118695 |
GRCz11 | 6 | 28109256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACAACAAGCAAACGGGCATGACTGTGGAAGAGGCAATGATCGGCTTTT[T/A]GAAGATTGTCTATAAATGGCCCACATTTGGATGTGCCTTTTTTGATGTCA
Long Flanking Sequence:
GAGTAAATGATGACATAATTGACATTTTTGGGTGACCCATCCTTTAAAATTTAATATTATTTTCCCCCTTCTGTTTTTTATGGGCAATTTAATCCCATATATACAATCATGAATTCTTTTTAATACTATTGTTACATTTTCCCCATTTTTTTCACATCATCTAGGAGTTGCCGAAATACTTGAGAGGTTATCATCGTTGTACCAAAGAAGAAATGGTGATGCTCGGCGCACTCCTCTTCAGGGTGAAGGTGAACAATGATAAAACTCAGTTTCCCATGATTCCTAAGATGCTGAAGGATCTGGTGCCAAATGACCAGCTTAAAGCCCTGTCCGCTGATGAGTGGAAGAAGGTCAGTTTCTGCACACTGGAGATATTGCAGTGTATATGTAACTATACCCTTCTAAAGTGGTTTTGTACTCAAAAATTTGTCAACAGAGCATTTTTGCAGAGTACAACAAGCAAACGGGCATGACTGTGGAAGAGGCAATGATCGGCTTTT[T/A]GAAGATTGTCTATAAATGGCCCACATTTGGATGTGCCTTTTTTGATGTCAAAGTAAACAACTCGACTGTTATATTTTAGGTATTGTTACTTGACAAATGGTTTATAAGATTATGCTTGAAATTACAGCAAACGTCAGAGCCCAATTTCCCGGACATTGTGAGGATGGCCATCAGTAAGCAAGGCATCACCATCATTAATCCCAAAACAAAGGTATCGTCAATTCATATTTTGTTAGATGCTTAGATTTGTTTTCAGGTGTTCCTCTAAACATGAATGTGAAATTTCATTGTTTAAAATATGCTTTGTGTATCATAACTTCATAATGTTTGTCTAAGTTTGATTTTTTTAACTAATTGAATTGTTCTATTTAAGGATGCTCTGGCCATTCATCCATATAACAAGATTGCAAACTGGTGCAGTGGAAGCACATACTTCCACATGACTGTAGGAAACCTTGTCAAAGGCAACAAAATCCTCTGCGAAACTTCCTTGGTAAGTG
Associated Phenotype:
Not determined