ZMP
myo6b
Ensembl ID:
ZFIN ID:
Description:
myosin-VI [Source:RefSeq peptide;Acc:NP_001004110]
Human Orthologue:
MYO6
Human Description:
myosin VI [Source:HGNC Symbol;Acc:7605]
Mouse Orthologue:
Myo6
Mouse Description:
myosin VI Gene [Source:MGI Symbol;Acc:MGI:104785]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2929 | Essential Splice Site | F2 line generated | Not yet available |
sa42976 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18082 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2929
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000042203 | Essential Splice Site | 185 | 1255 | 7 | 32 |
ENSDART00000061762 | Essential Splice Site | 185 | 1267 | 6 | 33 |
ENSDART00000088801 | Essential Splice Site | 185 | 1267 | 7 | 34 |
ENSDART00000131566 | Essential Splice Site | 185 | 1255 | 7 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 36969364)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 36854261 |
GRCz11 | 17 | 36801846 |
KASP Assay ID:
554-3365.1 (used for ordering genotyping assays)
KASP Sequence:
ACCACATCTTACGGCACAGGCCAAGATATAGATGAGAGGATTGTTGAAGG[T/C]AAGTGTCTAGCACAGTACTGCATGYTCTTTTTTTGCATMTGATGCAAAAT
Long Flanking Sequence:
TTGTTAAGCACTAGTCTTTTAGCCACCACCATGCTTTGCATCAATGACTCTTGCATTGCCTGAAGTAGAGCAGATGTAATTTGTGAGACGCCAAAGATGGCACGGCATCTGGTGGAAAAGGTCTGCTGTAAGCTTTGGAGCACCAGTCAGTAGAAAACATTTTAAACAATGTTACATTAAACGATAAAAAATAGAATTACAATGTTGTTTAAAATTAAAAGTATTACTATATTTACTGTATATTGATCAAATAAATACTTTATTACTTAAAATACCTTGGTTAATTGAAATACGGTTTGTATAAAATATGATCAAAAACATTTTATAGTCCTCAATAATGTTACTGTTTTGCAAATTAGTTTGGGGGTTGTTTTGGGCCAGTTTGATTATTAATGTAATCATGTTTTAATACTGTAAGTGTTTTTTTTTTATTATTATTTCAGGTATTTAACCACATCTTACGGCACAGGCCAAGATATAGATGAGAGGATTGTTGAAGG[T/C]AAGTGTCTAGCACAGTACTGCATGTTCTTTTTTTGCATCTGATGCAAAATGTTTGTTTTTACAGTACATACTGTATATTTCTCTGCTGTGTTCAGCCAACCCCTTGCTTGAAGCTTTTGGAAATGCAAAGACGGTCAGGAACAACAACAGCAGCCGCTTTGGAAAGTTTGTGGAAATTCATTTTAATGAGAAGGTGAATTTAGTTTTATAGTCTAAAGACAAGAGTGTGAGTGTACAAGATTTCACGTAGGTATTATTAACTATGTGTGTTGTGTCTTGTGAACCGTGTCCAGAATGCAGTTGTGGGCGGTTTTGTCTCTCACTATCTGCTGGAGAAGTCTCGGATTTGCATGCAGAGTCAAGAAGAGCGAAACTATCATATATTTTATAGACTGTGCGCAGGGGCGTCAGAGGACATCAGGAACATGCTCCATCTCAACTCCCCCGACAGCTTCCGGGTCAGTTTCCTGTACATTGTGTGTCAGGAAAACCTGGAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42976
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 |
---|---|---|---|---|---|
ENSDART00000042203 | Nonsense | 1058 | 1255 | 29 | 32 |
ENSDART00000061762 | Nonsense | 1070 | 1267 | 30 | 33 |
ENSDART00000088801 | Nonsense | 1070 | 1267 | 31 | 34 |
ENSDART00000131566 | Nonsense | 1058 | 1255 | 30 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 36870252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 36755149 |
GRCz11 | 17 | 36702734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGCAGGCCAACAAGGTGGCAGCTGGGGTGAAGAAGTACGACCTGAGC[A/T]AGTGGAAGTACGCTGAGCTGCGAGACGCCATCAACACCTCCTGTGGTAAG
Long Flanking Sequence:
GCTGTGCCCATTGCCCCAAAGGCTTCAGTAAAAATACATTCCCTCCTCAGACTGGTTTACTGTGGGAGCCTGGGCTTAATGTGATCCCTGTGAAACCCTTACAGAGCTCACATGTGTGCCTCCCTATCGCTTAGCATTAACCATCGTTAACCGCCATTAACCACCCTCAGCGCTGCAACCTCAGTGTTGCCAAGGCTGCATCTAATTTGCTCAGTGAGGTGTTAATTTGGCATGATCCGTGCTATTTCCATGTCATTACAAGTTTCAGAGAGAATGTATCTCTACGTAAGCAGAAGGCCAATTAATTGTCTGATTGTGCTGTGGCCTAGGGAACGTTTAGCAGCTGGTAACGGGAGCTTAATAGATGCATCAGGGCCTTTGCCTGTGGAGAAATATGAAGCTAAGAAAAAGTCCAAATTGTTCTTCCACTCTGTAATCTCAGGGGTGCGCAGGTGCAGGCCAACAAGGTGGCAGCTGGGGTGAAGAAGTACGACCTGAGC[A/T]AGTGGAAGTACGCTGAGCTGCGAGACGCCATCAACACCTCCTGTGGTAAGAGCAATCAGTCTTCTCAATCTGATCCCAGAACTTCCTGCTGACCTCAAGCCGCTCTTGGCAAAAAAAAAAAAAAAAAAGCATGTCATTTTGGAGATGGGGGGCTAACATGCGTTATGTGGAAGATGGGGGAAATACAGTTTTTTTTTTAGAGGGACTGGTTTTAAAGCCTACTCTCAGTCCATTATTATTTTAAAAGTGAATTAATGATGTATTCTTCCTTTTTATTTGCAAGTCTCTTTGTTTATTTGTCTTATTTTCTGCTAATTGAGACTTCACTCACTTTTTTTTGCTTCGCCGACTTTCTGGGCTGTCATGTTGGTTTCATTTTTAGGTGTTTAGACTCAAAGGAATAGTTCATGCTAAATTAAGTCATAATTTAGTTGCTTTTGTGTTGTTTCAAATGTGGTTTTCCTTCTGAAGTATACAAAATCTGATGCTCAGGCTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18082
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042203 | Nonsense | 1137 | 1255 | 31 | 32 |
ENSDART00000061762 | Nonsense | 1149 | 1267 | 32 | 33 |
ENSDART00000088801 | Nonsense | 1149 | 1267 | 33 | 34 |
ENSDART00000131566 | Nonsense | 1137 | 1255 | 32 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 36856295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 36741192 |
GRCz11 | 17 | 36688777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCTGCTCCACCTGTCCCAGCCCGGCAACAAGAGATCGCGATGAAYCGA[C/T]AGCAGCGTTACTTCCGCATTCCCTTCATCCGSCCCGCAGACCAGTACAAA
Long Flanking Sequence:
ATTTTGTTTCACCTTTTGACTTGCATTAATTGCTTAGTTGCATCACTCTAGTTTTTGTCTTCATGCTCTGATTCGCTCTCTGAAACATCTAGAACAAAGTTAGGTGCCCAAACTCGGTCCTGGAAGGCCAGTGTCCTGCAAAGTTTAGTTCAAAGCCCAATCAGACACACCTGGGCTAGCTTATCGAGCTCTTAGTAGACTTTCTAGAAACATCCTTGCAGGTGTGTTGGGGCAAGATGGAGCTAAAATCTGCAGGACACCGGCCCTCTAGAACTGAGTTTGGACTCCCCTGACCTAGAACAACACATTTTGTAACAACATGCTATAAATGACATCTTCATCACAATCAGATTACCCTAGAATCTCAGCAGCAGGTTTTGAACAGACAAGCAGACACAATTTTTTTATATTTTTTTTAAATTTTATATATTTGTATTCCAGCCCAGCAAAACCCTGCTCCACCTGTCCCAGCCCGGCAACAAGAGATCGCGATGAACCGA[C/T]AGCAGCGTTACTTCCGCATTCCCTTCATCCGGCCCGCAGACCAGTACAAAGACCCCCAGAACAAGAAGAAAGGCTGGTGGTACGCTCACTTTGATGGACCCTGGATCGCTAGGCAGATGGAGCTTCATCCAGACAAGCAGCCGATCCTCTTGGTTGCAGGTACCAAATACTATGAAGTTAAATCAGTCATTTTCTCCAATCTATAAACAATTAATACGCCAGAAAAGAAGCTGGAATTGATAAAATAGCTGAAACTCTTAAAGGCGGTTAAATTAGGTATTGCACTCCTGGTTCAAAACACACGCAAGCACAGGTTGCTAGATTGGAGACAGAAGCGACTATCAAGCCTAAAGACTGATTTAGATTGTGTTCTAAATAAAAGCAATAACACATGATAGAGGAAATATTTACCATATTGAAAGGAGTTTTTGTCCTAACCAACACCTCGAATTGATATTTTAGAAAAAGCTTTTATTTCTCGCAGCTGAATAACAGGATAA
Associated Phenotype:
Not determined