Busch Lab

ZMP

LOC100331349

Ensembl ID:
ENSDARG00000091350
Human Orthologue:
MYO18B
Human Description:
myosin XVIIIB [Source:HGNC Symbol;Acc:18150]
Mouse Orthologue:
Myo18b
Mouse Description:
myosin XVIIIb Gene [Source:MGI Symbol;Acc:MGI:1921626]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa34992 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34992
Status:
Mutation detected in F1 DNA
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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
ENSDART00000124853 Essential Splice Site 79 670 2 16
Genomic Location (Zv9):
Chromosome 10 (position 45969073)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 45544241
GRCz11 10 45390853
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGAGTCCGTCTGAGGTGGTGTGTGCCATCGACCAACCAGGACTGCAGG[T/C]TTCACACACTCTCTACACACAGCAGATAAGTCACAGTCACTAATGCACTT
Long Flanking Sequence:
AAGTGGTGACGTGTTGGTGACGTATGTAATACTGTTTCCAGGTCCAAGCCGCCACATTTGTTTATGATCACTTTTAATTCCTATCACACATTAAAGTTAATTTTATATAAAATCCTAGTGTGCACAACAATCTCTGGGCTTGCTGCATCACAAATGCCAAAATTTTAACACTTTATAAAAAAATAAATCACTTTCTGGCCATCGGATATTAGGCATGGACATATATATTGCAATCTTGATTTACGTAAGTATTAAATTGCTTTGTAAACGTTAATTATTACCATTTTATGAGTCTCCCCATACAGTTGAATAGAGCACTTGGACCCGGAAGCCGCTTTGCGTGACGTCACACTTAACAAGCGGATAGTTATAATAGCTAGATTGAGATTATGAACATGTTTGTGTATGGTCTGTGCAGGAAGGAGTGCCTGTGGATTTCTCAGCCCCAGAGTCGAGTCCGTCTGAGGTGGTGTGTGCCATCGACCAACCAGGACTGCAGG[T/C]TTCACACACTCTCTACACACAGCAGATAAGTCACAGTCACTAATGCACTTCAGCTTCACAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTCTCAGGTTCGAGGGCCTGAAGCTGACTCTCGGGGTCTGCTGTGGGTTCTGGACGAAGAGTTGTCGACGGCGGGCTCCAGTGAGAGTGTGGTTCTAGAGAGAGTGTGTCAGTACTTCAGCAGCACAGGTGATCCGCCGTGTGTGTGTGTGTGGTCATCTCATATGTCTGCTGTGTGTGATATGTGTGTGGTCATCTCTCAACTATCTGCTGTGTGTGTGTGTGTGTGTGTGTTCAGTGCGTCAGTGTGAGCAGCCGCTGCAGTGTGAGATCGCTCATCTGATGGGTTCAGATGCGG
Associated Phenotype:
Not determined