ZMP
myo7bb
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myosin VIIA (MYO7A) [Source:UniProtKB/TrEMBL;Acc:B0S8H4]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19737 | Essential Splice Site | Available for shipment | Available now |
sa17781 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19737
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 |
---|---|---|---|---|---|
ENSDART00000109515 | Essential Splice Site | 664 | 2089 | None | 51 |
ENSDART00000136179 | None | None | 457 | None | 12 |
ENSDART00000139747 | None | None | 363 | None | 7 |
ENSDART00000141621 | None | None | 565 | None | 12 |
ENSDART00000144928 | Essential Splice Site | 40 | 323 | None | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 22371530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23258235 |
GRCz11 | 2 | 22913886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTGTGAGGACGCTTTTAAGATGACGTTTTCTCTTTATTTTCCTCATC[A/C]GGTTTTTAACAGAGAGCTCTGCATGCAGCAACTTCGCTACTCTGGAATGC
Long Flanking Sequence:
CCACCAGACCCGGAGATTGGCTAAATGAATTAAAAAATGGTCGAATTCAAATGTTTAACTTGAGGAGAGTTGTTAAATGAGCCTTTTCTAAAAAAAAAAAGGGGGGAATGTTCATTTGAGGCATTTATGACCTTACTCCGTAAAGGAAAACCTTTTGACACCTTTACATGACCACATGCATTCTCGACTTCAGCATAATCAGATTGAGAGCATTCTGATCAATGCACTCAATGAAAATAGCTTTGAGATAAATTCTCTGTTTTGTCTTACACAGCAAGTTAACGAATCAAGGAGACAGATTTCCACTCTGAGCGGCCAGTTTCGCCAGTCTCTGGACTCTCTGATGAAGGCTCTTTCTCTCTGCCAACCCTTCTTCATACGCTGCTTCAAGCCAAACGATAAAAAGTTGCCCATGGTATCAATTCACTTCAACATCACTTACATCTTGAGCAGCTGTGAGGACGCTTTTAAGATGACGTTTTCTCTTTATTTTCCTCATC[A/C]GGTTTTTAACAGAGAGCTCTGCATGCAGCAACTTCGCTACTCTGGAATGCTGGAGACCATTCGAATACGCAAGTTGGGATATCCCATCCGTCACACCTTCAAGGACTTCCTGCATCGCTACCGAGCACTCTTGAAGTCCATTGACTGCGACCCCAACACTGTATGAGATAATAGGATTATATTATTAATATGTGAATGCCCAGGATTGTAGTTGATGATAGTTGCTTAATGCAGTAGAATTAAGTCTCTCACATTGTAAGAAATTTAATGACAAAAAGTCAAGACAACACATATTTTTATGTTGCTTATTTTAATAAGCTACTCCGGTTTCAACCTATTTTTTTTAAGTTATACAAAGTTTAAAATGTGTGCATTTACATTATAGTTTACTAAAAATTTAAAGTTTTGATATGTGAAAATGAGTAAAAGGCTGTATTTCGCATACCTGGCCAGTAGATGGTAATGTAGTTTTATAAAGAAACAAAAAGCCCCTGTGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17781
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 |
---|---|---|---|---|---|
ENSDART00000109515 | Nonsense | 1124 | 2089 | 30 | 51 |
ENSDART00000136179 | None | None | 457 | None | 12 |
ENSDART00000139747 | None | None | 363 | None | 7 |
ENSDART00000141621 | None | None | 565 | None | 12 |
ENSDART00000144928 | None | None | 323 | None | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 22357594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23244299 |
GRCz11 | 2 | 22899950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWGAAATTTATTGTCAGATCTGTAAGCAGCTGACAGGCAATAAAAACCGC[A/T]AAAGTGTAAACAGAGGCTGGATCCTTCTGTCCATCTGTCTTGGTATCTTT
Long Flanking Sequence:
AAATATTATTTAAGACAACTTAGATGAAAATGAACCAGTTGAAAAGATTTAGGCAAAAATTATGTAATGCATTACTTTTCTTAAAAAGTAGCTAAAGAACCCCTTAAGCCTCTCTTTTTAAAGAAGTAACACAAGATGGTAATGCATTATTTTTAAAAGTAACTTTCCCCAAACTGATCATAGCAGGCTACTATTAACCATGCTGATGAAATTTGCAGCCAGAAGAAGAACCAAAGTCTCAAATGGAGGCTGTTCAGGAGGAGCAGGTTGTGCTGTTTGGAGAGGGACCAACTTTTGATCGTCCAATGACACCCTTGGAGAAACTGCACATTATTGTGGGATATGCCATTGTCCGACCAGATATAAGGTTAATATGTCCTTTATGTTCTTCAAATTATGATTCCATAGCAGAATACATGATCTTTATGACCTTATGTATGTTTTTCAGAGATGAAATTTATTGTCAGATCTGTAAGCAGCTGACAGGCAATAAAAACCGC[A/T]AAAGTGTAAACAGAGGCTGGATCCTTCTGTCCATCTGTCTTGGTATCTTTTCCCCTACAGAACGCCTCACTAAGGTATGAATTACTGGTTTAAATTTAGTTCTTTTATTTATGAGCTAATTTATGCACTCGTTTGTAATAAACCTGACAAAGTGATCTGGAGCTTGGCATAAGGCATAACATGTTGTCTGCTGAATGTTTTATTGACTCGTCTATGTAGAAAATGATACAAACACAGTTTATCGCTCAGGTTAATTGTAATATAATGTGTTATTAATTGTAATATAACAAATATTAGGCTGTGTTATGTATGTAATGTTATTATGTATTGTTATGTTGTGTTGTTGTATGATGTTTAAAGCAATGTTTTGTTTAGAGTTATATGAAACGTCATTGCAGTGTTATGTCCTGTTATTTTGGTCATTACATTAGTAGTACGTTTCCCCTTTTATCCAAGAGATGCAGTTTCACATATCTAATACACTGTTACACAGGCAGTTT
Associated Phenotype:
Not determined