ZMP
si:ch211-120k19.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYH14
Human Description:
myosin, heavy chain 14, non-muscle [Source:HGNC Symbol;Acc:23212]
Mouse Orthologue:
Myh14
Mouse Description:
myosin, heavy polypeptide 14 Gene [Source:MGI Symbol;Acc:MGI:1919210]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15579 | Essential Splice Site | Available for shipment | Available now |
sa17178 | Nonsense | Available for shipment | Available now |
sa16888 | Nonsense | Available for shipment | Available now |
sa22798 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15579
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 |
---|---|---|---|---|---|
ENSDART00000047409 | Essential Splice Site | 175 | 2020 | 4 | 42 |
ENSDART00000142155 | Essential Splice Site | 175 | 2007 | 5 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18938522)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16968845 |
GRCz11 | 16 | 16876822 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTTCATGTNATKCTAATGTCCTTCCTCTTTCTGTTTTTTTTTTYACTC[A/T]GACCGAGAAGATCAGTCTATCCTCTGCACGTGAGTTTCCACTGCCTRYGC
Long Flanking Sequence:
TAAAAGAATGGTGATTTGTCAGCACTTCACTGAAAAAAGTGAAACTACTGTGTCTTTCATTCAAATGACATTTTTATTTTAAAAAATGTTTTTTGATTTTAACCTATTTCATTCAACTTGCCCTAAAGAGAACAAATTTAAACAAACCCCCTAGGAAAAAGCAAACTGAAAAAGAAATAATTGATTGGATTTACTACCTTTTTTAAGGTAAGTGGTGGCAAACAATTTATATGGACTGGATTGAAACAAACAGATTAAATGTAGTAAAGTTTAACTTAAAGTGTTTGTCTTTGATTCAGCCAATATAAATTTTTTACAAACAATTTCCTTAATAACTTTAGTTAATCCAATGAATCTTATTTTCTGTGTAGTATTTTTACTTTAAACCTGCAGTTTTCATATCATGTGACCACATGAAAAAGTTGCTGTTTATGTGCTATTTGGTTTTTATGTGTTCATGTATTCTAATGTCCTTCCTCTTTCTGTTTTTTTTTTCACTC[A/T]GACCGAGAAGATCAGTCTATCCTCTGCACGTGAGTTTCCACTGCCTGTGCCCATTGTATACATTTACTGACTTTTATTAGCACATGTCTAATTTTGTTCCAAATGTTTTCTTTTAAGTCACCTGCCAGTATTTGTTTTAAGAACTCTGAAAATAGTCCGATCAGGTTTTACAGCAGAAGGTCATTTATTTGTTCTGTTTGTGTATATGTGTGTGCAGAGGGGAATCCGGTGCAGGAAAAACAGAAAACACCAAAAAAGTGATTCAGTATTTGGCACATGTGGCATCTTCACACAAGTCTGGTACTCTGGGGCGACCCAAAGACACTGTTGTACAGGTGAGGACTGCCGTCTTTTGGGAGCAAAACTCTAAACTCTAAACTTTTGGGTGCATAAAAGCAACAGTTCCTGCTTTTCTGAAACAAGCCAGCATACCTATTTTTTGAGTTATTGCTTCTCTTTCTTTCATTCTATAATAATAACTAAAGCATCTGTTACGGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17178
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 |
---|---|---|---|---|---|
ENSDART00000047409 | Nonsense | 236 | 2020 | 7 | 42 |
ENSDART00000142155 | Nonsense | 232 | 2007 | 7 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18945051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16975374 |
GRCz11 | 16 | 16883351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RGCTATTCTTCTTTTGTTGTGCYTAGGGGGAGCTGGAAAKACAGTTACTG[C/T]AAGCAAACCCCAKTCTTGAGGCCTTCGGMAAYGCCAAGACTGTCAAAAAC
Long Flanking Sequence:
TAGAAAGTGAAATTTAGGACATTATAAGAGATTTAAAAACCGGGCCAGACGAGAAGGTCTCGCGGGCACAGAAAAAAAACTGGTAAACAAGAGATTTTCTTCTACTTAATTGATTGCTGATGTTTGGCTATATAGAGTGGATATATATGTATATGGCTAAAAAAAACAACTAGATCTCAGAACTAGTTTATCCACCCACACGCAACCTTACAATGCATCTGCACTCCTTTAGGAGATTCTTCCCACACTTTAAAAAGCACTGAGTTAATATTTGGGTTATGATTAGTGTAGAGTAATCTCATATTAACAGAAGTAATAAGTCTCTAGTTAGAGTGTGTGTGTGTGTGTGTGTGTGTTTGAGAAAGAGTGTGAGGGTCTGCTTGGCTGCAGTCATACAGTATGCTGATGCTGGGCTTTTAGCTGAATGTGAGTTATATTCTTGCACTGAAGGGCTATTCTTCTTTTGTTGTGCCTAGGGGGAGCTGGAAAGACAGTTACTG[C/T]AAGCAAACCCCATTCTTGAGGCCTTCGGCAACGCCAAGACTGTCAAAAACGATAACTCTTCCAGATTTGTAAGCCCTGAATCGCCACAGCTAACACACAGAGTTAGATCTTGAGTTTGTGATTTGCTCTGAACTGACATGTATTTTTTATTTGTTACAGGGCAAATTCATCAGAATCAATTTTGATGTTGCTGGATATATTGTTGGTGCTAATATTGAGACTTGTATCCTTCATAATCCCTAAAATTCATTTAAACAGCTGATAATTGCAGAAAAGTTGCAAAATAATGTAGTTGTGAGAAAAGTACTGGCATTTTTGTTGCAGGTACTGCTATAATTATTTTGCCCGTACTATGTTTGTTTACAGATGTTACTTTATATTTTTTGATAAAATACCAAAATGCTAAGAAAGAATTTAAGGCCATTCTGCTGTATTTTTAATGTAAATTATTAGTATTTTGCTAAAAATTAGTTTTATGAAAAGCTTTAGTTTTAGTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16888
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 |
---|---|---|---|---|---|
ENSDART00000047409 | Nonsense | 831 | 2020 | 20 | 42 |
ENSDART00000142155 | Nonsense | 827 | 2007 | 20 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 18968434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16998757 |
GRCz11 | 16 | 16906734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGMACCGTATTTTAACGAYTATGTTTTTCAGGGCATTCCATAAGAAGCAG[C/T]AGCAGCTTAGTGCTCTGCGGGTGATGCAGAGAAATTGTGCTGCRTATCTG
Long Flanking Sequence:
GTACAGTGCTCAGCATAATTGAGTACAGCCAATCTTGAAATTTTTTTATTCATTTTTCAGTGAATGTACACAATGCATTTTGATGCATTTAAACAAAACACATTTATTGAACAGATATACTTATTAACCTAATATTTTAGTCACCAAACATATTGAGAAATTAAAATTAAATTCAAGCAAAATCTTGCAAAAAAAAAAAGACTATTTTAACTAAATTATTACATTGTATGCTTCTCTTGATATCTCCTCGTTTTAAATTTGTATTTGATATTTTTCTATAACATTAATTTGGTTGTACTAGTTTTTTGACCGTTATCGTATTGTTAGATAAGATCCAGATTTGGCTTCAGTACTGCCTAATCTAATGTATATGCATAAATATAATATTGTATAGCTTCCTATTAAAATATGAATTTAAAAGGTTTGTGAGGGGTGTACTTATATATGCTGAGAACCGTATTTTAACGATTATGTTTTTCAGGGCATTCCATAAGAAGCAG[C/T]AGCAGCTTAGTGCTCTGCGGGTGATGCAGAGAAATTGTGCTGCATATCTGAAGCTCAGAAACTGGCAGTGGTGGAGACTCTTCACCAAGGTAACACAAATTACTACACAAGGTTATAAACATAAAATTAGTAATGGGCTTAGTAAAGAAATGTATCTTTATTAGTTAGAGTATATGACAGTAATTTTTTACATTGCAAAAATGCTTTTCGTATTTAAAGGTTTTGTCTTGTTTTTTAGTCCAAATATCTAACAATTCTTCAATCAAGAAGCATTTTTTAGATGATCAACAATATTGCTTACCCCATTGGCAGATTATTTTTCTTGTTTTAAGTAAAAACTAATTTAAATGTAAAAAAACTTAACTTTGACATTATGTTTATGAAAACAAGACAATAAAATGTTTCTTGATTTAAGACTTTTTTAGATATTAGGGCTAAAAAAAAACTAAGAAAGGCATTTTTTGCAGTGTATTTATTGTCTCATTGCATATTCAGAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22798
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047409 | Essential Splice Site | 1949 | 2020 | 40 | 42 |
ENSDART00000142155 | Essential Splice Site | 1945 | 2007 | 40 | 41 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 18996330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17026653 |
GRCz11 | 16 | 16934630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATGCAGAGCATGAACCGCGAGCTCAACACTCTCCGCTCCCAACTCAG[G/A]TAAGGACAATGACAGTTATGACTGTGTGTTCGCCGTTTTGTGTATGGAGC
Long Flanking Sequence:
GCTGCATAAAACATGTGCTGGATAAGTTGGCGGTTTATTCCGCAGTGGCGACCCCAGATTATTAAAGGAACTTAGCCGAAAAGAAAACGAATTAATGAATATTAAGTTTGTTTGTTTGAATAAATTTGACCAAGTCATCTAGTTTGAGTTCAATCGCATTAAAATAATCAACTCAAATTAACAGATTATAACTTCTTAAAAAAAATGGACTCATTCCACAATCCCTTACAAATGATTTCTTTGCTATGTACCTAATCTTATATAGTCAACTTGGCTGTGGTTACACTTGGAGCATTTTTACATTATAAAATCTCTCTATTTTTGTAGTTGGATAAGTCTATGGGGCGCCTCCGTCAACTGAAGAGGCAGCTAGAGGAGGTAGAAGAAGAGAACTCTCGCTCCAATGCCCAGCGCAGGAAACTACAGCGAGAGCTGGAGGAAATGAGCGACAGCATGCAGAGCATGAACCGCGAGCTCAACACTCTCCGCTCCCAACTCAG[G/A]TAAGGACAATGACAGTTATGACTGTGTGTTCGCCGTTTTGTGTATGGAGCAAAAACAAACAACAACTAGCTAGCTTTTTTTAGCTGACTCAGGCTCATAATTTCCTGATATACAAGGGAATATATTGTGTATATGATGTTTAATAGTATTTAAAAATATAAATAAATATCTATATATATATATATATATATATATATATATATATTTATATAGTTAAATTTTTTCAGATTCGTCAAACGGCTATAAAAACAAACATACCTACTTTTCAGAGTCTACTGTATATGATAAATCTTATCAGATCTAGATCATCACTAGATCCAAAATTGCTTGCCGCTGGAATTTGATACATTAAATGTTTTCGTGTGAAACTTTTGTTGTTGTTTTAAATAAATTTACTATTAGTGAATTTCATGTTTTACTGCATGTTTATTCACTCACTTACTCATTTAATGTGTCTGATTGTGTGTCCATCTATATTTGTGCGTTTGTCTCCTACACCC
Associated Phenotype:
Not determined