ZMP

crygm2d5

Ensembl ID:

ENSDARG00000069792

ZFIN ID:

ZDB-GENE-060918-4

Description:

crystallin, gamma M2d5 [Source:RefSeq peptide;Acc:NP_001038328]

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
sa7181	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7181

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000101845	Essential Splice Site	2	173	1	3

The following transcripts of ENSDARG00000069792 do not overlap with this mutation:

ENSDART00000146460

Genomic Location (Zv9):

Chromosome 9 (position 23266069)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	22421855
GRCz11	9	22232724

KASP Assay ID:

554-5182.1 (used for ordering genotyping assays)

KASP Sequence:

CAGCTTCTCCTTTGTGGAACCACTGAGGATCAGACAACGCAAACATGAAG[G/A]TAAACCTCATTTTAGCACCCATTCTATACAGTGAAACTTTWAAAATAAWT

Long Flanking Sequence:

TAGCAATGATTTGTATTTATTTAAATGATTTGCCATGAGATATTGCTTTGTTTGCGTATTTTGTTATTCGTGTGGTTCTGTGACTTTCAAAATGAATTTGTTTTATTTTCTCTAGTTCTTACCGTGGTTCATAGTGCTTTGTTGTGTGATGAATTTACAGAATGAGAACCATAAATAAACGTTGAATCATCAGTGGAAGACTTGTTTTTAACCAGGACACTACACGTGACCAATACAGAATTTTAAAAATGCATATGAAAACAAAGAAGAAAAGAAAGAGATAAATCTTAGAACTAAGAACTGCATAACCAGTAGTTCTTTGGCTAGAAAAATCTCTTTGACAACTTGCATAGTCAGAAACTGAGTAACAATAGGGACTGTGTAGTCTTTAGTCTTGGGCTTGTATAAAAAAGCAGGTGACAGCAGTCAGTCAACAGGCAGAATCAGCTTCAGCTTCTCCTTTGTGGAACCACTGAGGATCAGACAACGCAAACATGAAG[G/A]TAAACCTCATTTTAGCACCCATTCTATACAGTGAAACTTTTAAAATAATTATTTTAGTTTTTTAACTTTTCATAACAAAAACATTATACTTGATCTTTTTAGGTCACCTTCTTTGAGGACAGGAATTTTCAGGGTCGCTCTTATGAGTGTATGGGCGACTGTGGTGACATGCACTCTTACATGAGCCGCTGTCACTCTTGCAGAGTGGACAGTGGCTGCTGGATGATGTATGATCAGCCCAACTACATGGGCAGTGGATATTTCTTCAGGAGGGGAGAGTATGCTGATTACATGTCTATGTTTGGAATGAGCAACTGCATCAGGTCCTGCCGTATGATCCCCATGGTAATTTAAATTTTGAGGATTATAAGATAATAATTTTTTGACTGTTAAAATGTTGTTGTCTGATAAACTTGAAAGTAACAGACTCATGTTGCACTTCAGTACAGGGGATCCTACAGAATGAGGATCTACGAGAGGGAGAACTTCGGAGGTCAGAT

Associated Phenotype:

Not determined