Busch Lab

ZMP

MYO19

Ensembl ID:
ENSDARG00000075544
Description:
myosin XIX [Source:HGNC Symbol;Acc:26234]
Human Orthologue:
MYO19
Human Description:
myosin XIX [Source:HGNC Symbol;Acc:26234]
Mouse Orthologue:
Myo19
Mouse Description:
myosin XIX Gene [Source:MGI Symbol;Acc:MGI:1913446]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa20332 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa20332
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112144 Nonsense 35 162 1 5
Genomic Location (Zv9):
Chromosome 5 (position 3985587)
Other Location(s):
Assembly Chromosome Position
GRCz11 5 3975445
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCAACTTCTTCTCAGAGGTGCCAGGACACTGTAGAAAGGATAGAAAAA[C/T]GAGTACTGGACTCCAACCCTGTCATGGAGGCTTTTGGTAAGAAATCCAGA
Long Flanking Sequence:
ACAGTCGCAATTTTAATGCAAACAAATATGTTCATGATATTTGTGTAATAGTAGGCACTAAGTTACAAACAAATACTTTTTTTTTTTTTTTTTTGCATTGTTATCCATGATTCAGTAGTATTGTTTATTTAACCATGAGTTACATGAGGCAAACAAGCACATATTATGTTTAATGCCTATATAAAAACAACAGTAATTTGAATGCAAACAAATATGTGCATGATATTTGTGTAAGAGTAGGCACTAATTTACACACAAATAAGTGTTTTTGCATTATGTTAGTTATGTTAATTAGTAACTATTATGTTAGTCAAGAATAAATATAAAATATTTTGAGCACATGTTTTCTTTAAAACAGATTTTTTCAGTGTTTTTGATGCAAATTTAGTCTCTAAATTTATTCTCTCCAGACATGGACGTCGCGCTGTCTGATGAAATATTATGCCACTGTGGCAACTTCTTCTCAGAGGTGCCAGGACACTGTAGAAAGGATAGAAAAA[C/T]GAGTACTGGACTCCAACCCTGTCATGGAGGCTTTTGGTAAGAAATCCAGAGGCAAAAATGACCACCGAATTAATACTTAAGCATAACTCTCTTTCTTAATCCATTGTTTTCCTCTTCCTCAGGCAATGCATGCACATTACGCAACAACAACAGCAGTCGCTTCGGAAAATACATTCAGCTTCAGCTCAACAGGTCAGGCTTTTTTTGTTTTATTGACTTTAGGCATATAAACTTAAAGCATCTTGTGATTGGTTTAAGTATTTGTGATTTTATAATGCAGTTCTCAGTTGCTGGTTGGAGCATCAGTGCAGACGTATCTTTTGGAGAAGACCAGAGTGGCTTTCCAAGCACCAAATGAGAGAAATTTCCACATATTCTACCAGGTAAATTATTTACACAACCTTATAAAAATACTTTTTATGTAATTTTTACTGAAATTACAAATAATATAACAATATATTTCATGCTGATGCTTATTTAACTTGGTCAAGTTAACATTC
Associated Phenotype:
Not determined