ZMP
zgc:165344
Ensembl ID:
ZFIN IDs:
Description:
myosin-binding protein H-like [Source:RefSeq peptide;Acc:NP_001093607]
Human Orthologues:
MYBPH, MYBPHL
Human Descriptions:
myosin binding protein H [Source:HGNC Symbol;Acc:7552]
myosin binding protein H-like [Source:HGNC Symbol;Acc:30434]
myosin binding protein H-like [Source:HGNC Symbol;Acc:30434]
Mouse Orthologues:
Mybph, Mybphl
Mouse Descriptions:
myosin binding protein H Gene [Source:MGI Symbol;Acc:MGI:1858196]
myosin binding protein H-like Gene [Source:MGI Symbol;Acc:MGI:1916003]
myosin binding protein H-like Gene [Source:MGI Symbol;Acc:MGI:1916003]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33980 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa20826 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33980
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026359 | Essential Splice Site | 113 | 487 | 2 | 11 |
ENSDART00000122794 | Missense | 134 | 529 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 55011647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 55028949 |
GRCz11 | 6 | 55038762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCAGCGAGCCCCTGGAGCTTGGCGTAGAGGACGTAAATGACACCTCC[G/A]TCACCATCTCATGGAGACCTCCAGCAACCATCGGAAACTCCGGCCTGGAT
Long Flanking Sequence:
ACACCTGTGCAATTTAAGACTGGTTTTGTGGAATAAAAAGCAATGACAAAACAAATGAGGAAGATTTCATGATGACTTTAAAAAAAAAATTCTAATAATGAGCACATAAATGCATATGTTTTAAAGCTACTTGTTTGGGGGGGTAATATGCCAAAAGTTCCCCCAAGCTCTGATGTCATAATTAAACTAAAGCAAAGCTTGAAGCTCTATTATATGCTGCTTTTATTAATGTGCCCTGCTTATTTAACACCAGCTGATGCTGAAGCTCCACCAGCCGAGGAAATCAAAGCTCCTACACCACCACCACCTCCAGGTAAACACACACAAATATAAAGCTTTTCATATCAACAGTATTACTCTTATGTTGAGTGTCTTTTTTTGCAACGGAAGCTTCAGACAGAGTGCCTGATCTAAGTTTAAAGTATTAAATGTGTTATTCTCCTGCAGAGCCCACCAGCGAGCCCCTGGAGCTTGGCGTAGAGGACGTAAATGACACCTCC[G/A]TCACCATCTCATGGAGACCTCCAGCAACCATCGGAAACTCCGGCCTGGATGGATACGTTGTGGAGGTCTGCAAGGAAGGAAGTAAGTGCTTACAAATAAATACATCTTGACCATCTTTGTTGCATACTTGACATAAAAATAATGCAATAATTTACCAACATTCAATATAAATCAAGACAGGTTTAGTTTAGTTAAATTTATTAAACGTTTAATTTATTAAAAACAAAATTATTTAATGAAACAGGTTCAAATGAAAGCTTTTATTAATCACATGCAAAATAAAAGTATTTGTTTACATAAAGTTTCCTATGTATATATATGTGTGTAAATATGTTAAAGTATATGCAGTGGTCCCTTGTTTATCGGTGGAGTTACATTCTAAAAATAGCCTGCTATAGGCGGAATCTGCGAAGTAGTCAGCTTAATTTTTTATAACTATTACAGTGGTTTTAAGGCTGTAAAACCCCTCGCTACACACTTTATATACATTATACACATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20826
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026359 | Essential Splice Site | 205 | 487 | 6 | 11 |
ENSDART00000122794 | Essential Splice Site | 247 | 529 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 55031262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 55047575 |
GRCz11 | 6 | 55057388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTAGAGATACTAATTCACAGCTTCTCTTGTATTGTTTTCTTACCGGC[A/T]GGGAAAACCCCAGCCTGTTGTGTCATGGACAAAGGATGGCCAGCCTATTG
Long Flanking Sequence:
ACTAACACCACTTCCGGCAGCAACCTAGCTTTCCCATGTGGTCTCCAATCCAGGTACTGACTGGGCGCAGCCCTGCTTAGCTTCAGTGGGCGACCATGTGAGAGTTGCAGAGAGCTAGCTGCCGGCGCATAAAATAAAAGCTGAGAGTTTTTTTCCCACAATGCTGCCTCTTGTACAGCCTCATATTATGTTTAAGGAGAAGCCTGTATCATTTCTGGTCAAAAAGAAAAAACAATACTAGTTGAATGAACCTAACTTTAAGTCAGAATTTGCCAGGAGAATGAATAATTTCAGGCTTGACTGAATATGCCGCTTGGTGCAAGTTGGCTTAATGCTATTATTCAGAATATTTAAACTATAGAAAATAGAAAAAATACAGAACAATAAGTGAATTCTGAGTAAAAAAATATCATATATAAATCTACTTTGTACCGTTTGGATCTACATTAGGACTTAGAGATACTAATTCACAGCTTCTCTTGTATTGTTTTCTTACCGGC[A/T]GGGAAAACCCCAGCCTGTTGTGTCATGGACAAAGGATGGCCAGCCTATTGACACTAAAAAGGTGAACATCCGCAACAGCGACAAGGACAGCATTTTCTTCATCCGTGCCGCTGAGAGAGTCGACTCCGGAGTGTATGAGATGTGTGTGAAAGTGGACAGCTTTGAGGACAAGGCCCAGCTAACTCTGCAGATTATCGGTGAGTGGTAGAATTGGATGCTAAATAAAAGTAAATCAACATGCTCCACAAGATAAGATTGGTGCTGTGAACAAATTAATTTTTTTTAATTATCATAATTGTGTTTTAACAATACAAACATATTAATCATAACAATGGATGACATCAAGTCAATAGTAAATAAGTATTTTTTTTAATAATACTTATTATTAAAATTATACTTAGTACAGAGGCAAATTATCAAATTAAATAATATTCACAAAGTCCTTCTAAAATTTCACAGTTTTAACACTTCTTTTGCTGTAAACGTTTTGTTAAGTAGTA
Associated Phenotype:
Not determined