zgc:171929

Ensembl ID:
ENSDARG00000079995
ZFIN ID:
ZDB-GENE-070820-19
Description:
hypothetical protein LOC100124596 [Source:RefSeq peptide;Acc:NP_001096093]
Human Orthologue:
AD001527.1
Human Description:
Putative transcription factor Ovo-like 2-like [Source:UniProtKB/Swiss-Prot;Acc:O00110]
Mouse Orthologue:
Ovol3
Mouse Description:
OVO homolog-like 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2388075]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa6153 Essential Splice Site Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa6153
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108918 Essential Splice Site 103 205 2 3
Genomic Location (Zv9):
Chromosome 10 (position 53536)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150440.1 192
GRCz11 KN150440.1 192
KASP Assay ID:
554-4631.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GGCTTYAAYGACACCTTYGACCTCAAGAGACACATGCGCACACACACGGG[T/A]GAGCTGAGACACAYGACAAACACACAMAYGCAAATACACACACAYACACA
Associated Phenotype:
Not determined

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