ZMP

crygm2d3

Ensembl ID:

ENSDARG00000088823

ZFIN ID:

ZDB-GENE-060918-2

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
sa21472	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa21472

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000146319	Nonsense	55	173	2	3

The following transcripts of ENSDARG00000088823 do not overlap with this mutation:

ENSDART00000123763

Genomic Location (Zv9):

Chromosome 9 (position 23314528)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	22470314
GRCz11	9	22281183

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTGGCTGTTGGATGATGTACGATCAGCCCAACTACATGGGAAGTGGATA[T/A]TTCTTCAGGAGGGGAGAGTATGCTGATTACATGTCTATGTTTGGAATGAA

Long Flanking Sequence:

TTAATAATAAATCCTACTTCACTCTGCGCTTGGGTCCTTGCTCCTTTTTCCCTTTACCGGAACGTGACAATAGCTAGAAAGGTCTCTATGCCAACTTGCATAGTCAGGAATTGAGTAACAATAGGAGCTGTGTAGTCTTTAGTCTTGGTCTTGTATAAAAGGACAGGTGACAGCAGTCAGTCAACAGCCAGAATCAGCTTTAGCTTCTCCTTTGTGGAACCACTGACAGCACAAACATGAAGGTAAACCTCATACTAGCACCCATTCCATACAGTGAAACTCAAAAACAATTTTGCTTGGTTTAACTTTTCATAACAAAAACATTACATTTAAATTTTTTAGGTCACCTTCTTTGAGGACAGGAACTTCCAGGGTCGCTCTTATGAGTGTATGGGCGACTGTGGTGACTTCTCCTCCTACATGAGCCGTTGTCACTCTTGCAGAGTGGACAGTGGCTGTTGGATGATGTACGATCAGCCCAACTACATGGGAAGTGGATA[T/A]TTCTTCAGGAGGGGAGAGTATGCTGATTACATGTCTATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCTATGGTGAGCCCAATGTTAAGCTTATATAAGATACAGATGAATACATTTTTCTGCTTAAGATTTTCTGCCTTATAAACTTGAAAATAACAGACTTCTGTTTCACTACAGTACAGGGGATCCTACAGAATGAGGATCTACGAGAGGGAGAACTTTGGAGGTCAGATGTACGAGATGATGGATGACTGTGACAACATTATGGATCGTTACCGCATGTCTCACTGCCAGTCCTGCCATGTGATGGACGGCCACTGGCTCTTTTACGATCAGCCCCACTACAGAGGCAGGATGTGGCACTTCGGGCCTGGACAATACAGGAACTTCAGCAATTATGGTGGCATGAGGTTCATGAGCATGAGGCGTATCATGGACTCTTGGTACTAGCGTTTCAATAAAGTAATTTTTATGCAACACTAAAAAAT

Associated Phenotype:

Not determined