Busch Lab

ZMP

LOC100331557

Ensembl ID:
ENSDARG00000089850
Human Orthologue:
MYOM2
Human Description:
myomesin (M-protein) 2, 165kDa [Source:HGNC Symbol;Acc:7614]
Mouse Orthologue:
Myom2
Mouse Description:
myomesin 2 Gene [Source:MGI Symbol;Acc:MGI:1328358]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa13314 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa13314
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125593 Nonsense 209 391 4 8
Genomic Location (Zv9):
Chromosome 13 (position 9571760)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 9699851
GRCz11 13 7007228
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCTCTCTTCTGTATTGTGACGGGGAATCCATGGTGCTCAACTGGAAG[C/T]AGCCCATCCATTCTGGAGGAGCAGAGGTCACCGATTATTACATTGACAAA
Long Flanking Sequence:
AATTAGTTGTCATGTAGATGCAATGTACCTTGAATTAAACAAACGGACCATCAAAATAAAGTGTGACCCAGTATTCTAAAATAAAGCTCTTACATGTTCAATATTCTAAATGCGTATCCATTTCCTTTACACTGCTTCTTCAGAAGGCAGCTGTTTATGTAGGCAGTAGACAGAAAGCAGCTCATTCTGTTTTCACTGTGAGTCCTACATTCTCTTGCTGAAAGCATTGCTATAATTTGAGCCTTATATTTATGTGCAACATTAAGATGCATTTCATCCTATTATATTACACCTCCAGGCGCAACATTTCCCTATGAAATGTGCATATTATAAGCCAGAGATGTGCCTTGCACGTCATTGCATGTTGCCCCGTGTAGAAGACATTGAGTAATGGCTACATCCAACTGAAGCAATCTGTCTTCTCCACAGAGTTGCCCTCTTCCCCTTATGACATCTCTCTTCTGTATTGTGACGGGGAATCCATGGTGCTCAACTGGAAG[C/T]AGCCCATCCATTCTGGAGGAGCAGAGGTCACCGATTATTACATTGACAAATGCAACGTGGCCAAGAAGACGTGGAAGGAGGTCAACATCCCGCCTGTTAAGGAAAGACTGCACAAGGTGGCCATGTATTGGTATTGCAGCATCCTGTGCATGCTGTTGTTGTATCAGCTAATGTTAATGGGTTTCTAATAAAATAGTGTGGTGTTATAATACTGTAATTGCTCAGATGAAATGTTCTTTCTGAAGGTTGGAGGTCTGACTGCTGGCTCAGTGTATCAGTTTAGGGTCTATGGTGCTAATGTGGTTGGAGTTGGTGATCCCTCGACCGCTAGCCCTTCCTTCAGATGTGACGCTTGGACCATGTCTGAACCCGGTAATGTGAAGTCTGCTAACACATTTAATGCTTAATGATTTGTTTTGTTCATTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGC
Associated Phenotype:
Not determined