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 |
---|---|---|---|
sa32907 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19737 | Essential Splice Site | Available for shipment | Available now |
sa17781 | Nonsense | Available for shipment | Available now |
sa32906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32907
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 |
---|---|---|---|---|---|
ENSDART00000109515 | Nonsense | 556 | 2089 | 13 | 51 |
ENSDART00000136179 | None | None | 457 | None | 12 |
ENSDART00000139747 | None | None | 363 | None | 7 |
ENSDART00000141621 | Nonsense | 505 | 565 | 11 | 12 |
ENSDART00000144928 | None | None | 323 | None | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 22373218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23259923 |
GRCz11 | 2 | 22915574 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCATCGGATACATTTTGGTGTTCAACACTTTGCTGGGTTGGTTTATTA[T/A]GACTGCGAAGGTACAATTCATCGATTATTTACTGTCCCATGACATATGTA
Long Flanking Sequence:
CCAGTCCAATGGTTAAGTAACATTTAGATACTCTAACCATACTTTGAGAATAATTTCTCTTTTCCACTTTTGTCATTTAGTTTTGAACAGCTGTGCATCAATTTCGCCAATGAGCATCTGCAGCAGTTTTTTGTGAGGCACGTCTTCAAGCTGGAGCAGGACGAGTACACTAAAGAAGGCATTTCATGGAAACGCATTGCTTTCAATGACAACCAGAAAACCCTGGACCTACTAGCCCTTAAACCTCTCAACATACTGGCTCTGATTGATGAGGAGAGCCATTTTCCTAAGGTGAGCTTCGTACGCTATATGATAGAGTGACTTATTTGCTTTTTATAAGCTATTTATGCCTGCGCTGTCCTGTTTTTAACACAGGGGACAGATGCTACGATGCTAAACAAACTGAGCCAAGAACACAAAGGCAACAAACTTTACATTTCATCCAGGGGCGACCATCGGATACATTTTGGTGTTCAACACTTTGCTGGGTTGGTTTATTA[T/A]GACTGCGAAGGTACAATTCATCGATTATTTACTGTCCCATGACATATGTACTGCATTCCCAGCAGTTATTTTATAAATGAAACAAGTTCTGTTCTAAATGAGCAATGTTTTGGCAGGTTTTTTGGAGAAGAACAGAGATACTGTGAGCATGGACATCTTGGAGCTGATTCGGAAATCTTCCAACAAGTTGCTTAAGCAGATCTTTGAGAAAGAGATCAATGTAAACTCGGTGAAGAATTCGAACAAAATGAACAAAGCTGTCATGACGCCAAAGAATTCATTACGAGTAAGAGATATTTATAAAAATGTTGACTTTAACAATGATCACGTATTCATGCACACAAATATCATAATAACCTACATTAAGTTAACCTGTTGTCTTGTTTTACATGCAAACCAGTAACCCTGCAATGCAAGCCCACCTAAAAAATTCTATTATAATTTTTTAGTAAATACTATAGTGTTTTTATATCATACTGTAGATATTATTTGTAGTATTA
Associated Phenotype:
Not determined
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
Mutation Details
Allele Name:
sa32906
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 |
---|---|---|---|---|---|
ENSDART00000109515 | Nonsense | 1775 | 2089 | 43 | 51 |
ENSDART00000136179 | Nonsense | 146 | 457 | 4 | 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 22345499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23232204 |
GRCz11 | 2 | 22887855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTATTATTGCAATGTTTTTGCCCCTGCACAGTATTGAGGGAAGGAAGT[T/A]GCCTCCTCACCAGGTGGAAGTGGATGCCATTCAGAATAACAGCACTCAGA
Long Flanking Sequence:
GGAATGAGCAAGGAGAGCTAAGGAAGGAAAGTTTGAGGAGTCACTGACAACCAACAAAGAAATTGAAGAGTCCGTGGCCATCTAGTGACTGGTGTAGGTAGAGAGGTCTCCCTAATCTGTGAAACTACGTTTTTCCATTCTGGATGGCTATGCGTAATTGAGGAGTGAGCACACACCTGTAGTGGCCAGGAAACAAATAGGGTATTGGTGATTTGCTTAAATGCACCTCAATTATGAGTATTAAAGGTGGAGGAGAGCATTGTTCATTGACTCCCCCTTGATTTCATTCAAAACTTTTGCCAGTAAACATATTTCATCATTTTTACTCTCACTGTCTAAGAGCCAACTGGATCTGACCACAGCCAGTGATGTGCAAATATTGCTCAATTTTGGCCTGTTTTGTCACAAACTTTAGGCCCCAACATGGAATGATCAAAAAGGTGAAAGTTGACCTATTATTGCAATGTTTTTGCCCCTGCACAGTATTGAGGGAAGGAAGT[T/A]GCCTCCTCACCAGGTGGAAGTGGATGCCATTCAGAATAACAGCACTCAGATCTTCCATAAAGTCCATTTCCCCAATGATACATCTGAAGTAAGGAGTGACATGCTCAGCTTAACCATTGTTTCTTATTATTTTCTTCACTCAAATTAAAAGCTGTCTTTAATTTCAGATATTTGAGGTGACCACCACCACAAGGATCAAAGACTTGTGTCGCAACATTGCCAAAGACCTCCGTCTGTCCTCACCAGAGGGATACAGCCTGTTTGTGAAAACCTCCACAAAGGTTTTAGATATGATTTCTCCATTCTCTTTTTTATTCCTGCTGGAGGTGTGTTAAGTCAGAGCTAAACTTTACCACATCTGATATTTTCAGGTAGAGAGTATGAATTCTGAGGAGTACTTTTTTGACAACCTCAGGCAACTCACAGATGTTACCAAAAAAGGAAAGAAAGTCAGGGAAGGTGAGCTGTTTAGCTTATTAAACACTGTAATAAACGTGTTT
Associated Phenotype:
Not determined