ZMP

crygmx

Ensembl ID:

ENSDARG00000053862

ZFIN ID:

ZDB-GENE-030131-7732

Description:

crystallin, gamma MX [Source:RefSeq peptide;Acc:NP_001013280]

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
sa35326	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35326

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
ENSDART00000105594	Essential Splice Site	84	175	2	3
ENSDART00000105596	Essential Splice Site	84	200	2	4
ENSDART00000105594	Essential Splice Site	84	175	2	3
ENSDART00000105596	Essential Splice Site	84	200	2	4

Genomic Location (Zv9):

Chromosome 12 (position 32528159)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	30726156
GRCz11	12	30841058

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTGGGCTGGATTCAACGACTGCATTCGCTCCTGCCGCGTGGTTCCTGCT[G/A]TGAGTACTGTACAGTCAGCTGTAGTAGAAAACAGTACTGATTGATACTTT

Long Flanking Sequence:

TATAAAAGAATAGAGATTAAAAAAAAAGATGGAGATGTTATTGTAAAATTATAAACTTAAAGCCACAACAGATATTACCAACAGACACTGATAGAAGCAGACAATCATTATACAACCTGAGAAGTACCAATTTAGCATGTCTAAACTGAATAATACAAGCTCCGAAAAATGTGTCCATTACTGTCTGTCAGAGTGTGATTAACCTTGAAAGCATACCTGTAATCCTGCGTTGTTCTTTCATTCTCATTGACCAACAGATTACTTTCTATGAAGAGAAGAACTTCCAGGGCCGTCACTATGATTGCACTGGAGACTGCGCTGACATGCAGTCCCACTTTAATCGCTGCAACTCCATCCGAGTAGACAGTGGTAGCTGGGTGGCTTATGAGAAGCCCAACTTTTCTGGATACCAGTACATGCTGTTCAAGGGTGAATACCCTGATTTCCAGCACTGGGCTGGATTCAACGACTGCATTCGCTCCTGCCGCGTGGTTCCTGCT[G/A]TGAGTACTGTACAGTCAGCTGTAGTAGAAAACAGTACTGATTGATACTTTTGAAACATTATTTCAATCAAAAAGCATGATGGTAATACGTTTACAATTTGCATCAAGTTTCAGATGAATTACATATAGCTCAAGTCGCTGCTTACTTTTTATTGCAGCTTTATTATTTAGTCTTAAGGAAAATCTGTTGTTTGCTATATTTGCATAATTTTCAGGGTTCATACGATCATGGAAAATCTGGAAAAGTCTTGGAATTTTGACATGGCATTTTCCAGGCCTGAAAAAGTTCTGGAAAAACAGAAAAACCCACAAAGTTTTGGAAAAGTCCTGGAAATTACATTTACATTTAGTCATTTAGCAAATGTTTTGTTTAAAGCAACTTAAGCTGCGGTCACACTAGAGCTTGTGCATGCAAAATTCTGTCTTATGGCGCTGCGAAAAGGGGTGATATTAAACAATATGATTAGACGTTAATAAAAGTGAGCGTTAATAAAAGTGCTC

Associated Phenotype:

Not determined