wu:fi13g07

Ensembl ID:
ENSDARG00000091387
ZFIN ID:
ZDB-GENE-030131-5694
Description:
Wu:fi13g07 protein [Source:UniProtKB/TrEMBL;Acc:Q6PH43]
Human Orthologue:
GRAMD3
Human Description:
GRAM domain containing 3 [Source:HGNC Symbol;Acc:24911]
Mouse Orthologue:
Gramd3
Mouse Description:
GRAM domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1914815]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa43756 Essential Splice Site Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa43756
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:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125779 Essential Splice Site 288 398 10 12
Genomic Location (Zv9):
Chromosome 22 (position 3252141)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 3248360
GRCz11 22 3267628
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTCAGTCAGTTCACCCACTGAAGACGACAGCGCTGATGATGAGCACACCG[G/A]TACGATTATGAATATTCATGACTGTGTAAACGAGTCTGCGATGACGCTGT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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