ZMP

si:ch211-212n6.8

Ensembl ID:

ENSDARG00000076693

ZFIN ID:

ZDB-GENE-081105-90

Description:

hypothetical protein LOC561929 [Source:RefSeq peptide;Acc:NP_001092713]

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
sa34623	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34623

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
ENSDART00000132890	Nonsense	36	173	2	3

The following transcripts of ENSDARG00000076693 do not overlap with this mutation:

ENSDART00000110933

Genomic Location (Zv9):

Chromosome 9 (position 23221082)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	22376868
GRCz11	9	22187737

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGGTGACTGTGGTGACTTCTCCTCCTACATGAGCCGCTGTCACTCTTGC[A/T]GAGTGGACAGTGGTTGCTGGATGATGTACGATCAGCCCAACTACATGGGA

Long Flanking Sequence:

TTACTTATCAGATTCCCAATGTTGTTGATCAGATTCACACGTTCTGACAAATATAAATTGTAAGAAAATGTTTTTTTTTGTACTAACAAATGTGAACACTAAGATCTACATGCCAAGCTTTAGCTAGAATAGCCTCTATGACAACTTGCACAGTCAGGAATTAACTAACAATAGCTACTATGTAGTCTTTAGTCTTGGTCTAGTATAAAGGTACGAGTGGCAGCAGTCAGTAAACAAGCAGAATCAGCTTCAGCTTCTCCTTTGTGGAACAACTGAGGATAGACCACTGCAAACATGAAGGTAAACCTCAATCCACCATTTCTAAACAGTTCACATAGCTGTATTTTTTCCACATATTTTACTTTACCTTAATTAAACTTAAATCTTCACCTTTTTTAAAGGTCACCTTTTTCGAGGACAGGAACTTCCAGGGTCGCTCTTATGAGTGTATGGGTGACTGTGGTGACTTCTCCTCCTACATGAGCCGCTGTCACTCTTGC[A/T]GAGTGGACAGTGGTTGCTGGATGATGTACGATCAGCCCAACTACATGGGAAGTGGATATTTCTTCAGGAGGGGAGAGTATGCTGATTACATGTCTATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATTCCCATGGTAGGTTCAATTTTGAGTTTGTTTAAGATCATGGTGAAGTTATTTAATTGTATTTTAAAAGTAACAGACTTATGTTCCACTACAGCACAGGGGATCCTACAGAATGAGGATCTACGAGAGGGACAACTTCATGGGTCAGATGTACGAGATGATGGATGACTGTGACAACATCATGGACCGTTACCGCATGTCTCACTGCCAGTCCTGCCATGTGATGGACGGCCACTGGCTCTTTTATGACCAGCCTAACTACAGAGGCAGAATGTGGCACTTCGGGCCTGGACAGTACAGGAACTTCAGCAATTATGGTGGCATGAGGTTCATGAGCATGAGGCGTATCATGGACTCCTGGTACTA

Associated Phenotype:

Not determined