crygm2d4

Ensembl ID:
ENSDARG00000087164
ZFIN ID:
ZDB-GENE-060918-3
Description:
crystallin, gamma M2d3 [Source:RefSeq peptide;Acc:NP_001073530]
Human Orthologues:
CRYGA, CRYGB, CRYGC, CRYGD
Human Descriptions:
crystallin, gamma A [Source:HGNC Symbol;Acc:2408]
crystallin, gamma B [Source:HGNC Symbol;Acc:2409]
crystallin, gamma C [Source:HGNC Symbol;Acc:2410]
crystallin, gamma D [Source:HGNC Symbol;Acc:2411]
Mouse Orthologues:
Cryga, Crygb, Crygc, Crygd, Cryge, Crygf
Mouse Descriptions:
crystallin, gamma A Gene [Source:MGI Symbol;Acc:MGI:88521]
crystallin, gamma B Gene [Source:MGI Symbol;Acc:MGI:88522]
crystallin, gamma C Gene [Source:MGI Symbol;Acc:MGI:88523]
crystallin, gamma D Gene [Source:MGI Symbol;Acc:MGI:88524]
crystallin, gamma E Gene [Source:MGI Symbol;Acc:MGI:88525]
crystallin, gamma F Gene [Source:MGI Symbol;Acc:MGI:88526]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa44704 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa44704
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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114943 Nonsense 150 173 3 3
Genomic Location (Zv9):
Chromosome 9 (position 23278091)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22433877
GRCz11 9 22244746
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTTATGACCAGCCCCACTACAGAGGCAGGATGTGGCACTTCGGTCCTGGA[C/T]AGTACAGGAACTTCAGCAATTATGGTGGCATGAGGTTCATGAGTATGAGG
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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