ZMP

crygmxl2

Ensembl ID:

ENSDARG00000074001

ZFIN ID:

ZDB-GENE-050522-401

Description:

gamma crystallin-like [Source:RefSeq peptide;Acc:NP_001019598]

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 are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8929	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa8929

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075983	Nonsense	48	176	2	3
ENSDART00000146367	Nonsense	10	138	2	3

The following transcripts of ENSDARG00000074001 do not overlap with this mutation:

ENSDART00000133829

Genomic Location (Zv9):

Chromosome 12 (position 32530823)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	30728820
GRCz11	12	30843722

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACTGCTGTAACTCCATCCGTGTCATGGGAGGTCACTGGGTGGGTTACGAG[A/T]AGCCCAACTTCATGGGCTRTCAGTACGTCCTGGGCCGTGGGGAGTACCCT

Long Flanking Sequence:

TAAGGTCAAATTTACTCTGAGCCCCATTGACACTGCACTAGAAACACCTCGCATAAGTGGTAATTGTTTTTTTTATAATTTGAAGCAAAAATGATATAATACATTCATTAATACATATAATGTTCATATGTTTTTTTTTTTTTTTAATAATGAAGATATTAAACACTTTCAAGGATTTAAGATTAGGATGACTGTTAAACATCAGTCTTGTGAGAAAGCTCCATAACTTTGATCTTCTCTGAAGGTGGCAACTTCTAGCACTGATCCATCAAAATGCACTTGTTTACTGAATGAGTTTTGACAAACTGAATCAGGATAGCCTTTTCTTCCCACTGTACCTTCTCTAATCACCATCTTTCTGTGGTCAGATTGTCTTCTACGAAGGCCGCAACTTCCAGGGCCGCTCTTACGAGTGCTCCTCTGACTGCTCCGACACCTACAACTACTTCAACTGCTGTAACTCCATCCGTGTCATGGGAGGTCACTGGGTGGGTTACGAG[A/T]AGCCCAACTTCATGGGCTATCAGTACGTCCTGGGCCGTGGGGAGTACCCTGACTATCACCACTGGATGGGCTTCAACAACTGCATCAGATCTTGTCAGATGTTCCCCCCAGTAAGTCAATCAAACTGATGGGTTTCATTTCACACAGTTAAACACCTTCACACAAAAAAAGCAACGTCAATCAATCAGTCCTTTGAAGTATTTCATATATGCAGAGGGGGGAAAAAAACAGGTTCACAGGTCCGCCAGGAGATTTAGTTATTTGAAATGGAGCAAGACACACTCGGATGACTGCGCAGCTCATCATCATTCCATTCATCCCTGCTTTTTTTATTTTTTGGCAGAGGAAGAATCATGACACTGTCACTAGAGTTAGTTCGACGAAAAGTGACTAAACGTCTACTTGAAAATCTTTGAAAGTTGTAGGTTTACAGCAGGAAGTCATGTTCAAAGGCTCTGTTTTAAACAGCGGCGTCAAGAATGCAGAGCTTTGCCTCCCAA

Associated Phenotype:

Not determined