Busch Lab

ZMP

crygm2d7

Ensembl ID:
ENSDARG00000076572
ZFIN ID:
ZDB-GENE-060918-5
Description:
crystallin, gamma M2d7 [Source:RefSeq peptide;Acc:NP_001038572]
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9600 Essential Splice Site Available for shipment Available now
sa8656 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa9600
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113174 Essential Splice Site 2 173 1 3
ENSDART00000113174 Essential Splice Site 2 173 1 3

The following transcripts of ENSDARG00000076572 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23305352)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22461138
GRCz11 9 22272007
KASP Assay ID:
2260-1775.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCTTCTCCCTTGTGAAACCACTGAGAATAATCCARTGCAAACATGAAG[G/A]TAAATCTCATTCTATYACCCACTCCAAACAGTAAAACTAAAATGATAWAT
Long Flanking Sequence:
TTCTTATTTTGTTAATTACTAATATATATATTATATATTTGTTTTTACCTCTGATAAGAGGCTGTAGATAGATGATAGACTAAAAAGGATCCAACAAGGTTCTAGTGATTTCCTTCAAGTAGACCAAGACCAGACTTTCAAATGATTTCATAACTCCCTGTGATAGAAAACTGAACCATAAAAATATGAAAAAGAGAAATATTGTATTTATTGAATTGCACTATGATTTGCTAGAATAAATTAATTGTTTTTTCTAGCTAAATACCTCTTTAAATACTTTTAAAAATCCAAATAAATCAGAGTACTGAGAACTACATACCAAGCCTTAACTAGAAAGGTCTCTATACCAACTTGCATAGTCAGGAACTAAGCAACAATAGGAGCTGTGTAGTCTTTAGTCTTGGTCTTGTATAAAAGGACAGTTGACAGTAGTCAGTCAACAGCCAGAATCAGCTTCTCCCTTGTGAAACCACTGAGAATAATCCAGTGCAAACATGAAG[G/A]TAAATCTCATTCTATCACCCACTCCAAACAGTAAAACTAAAATGATATATTTCAATTTGTTTAAATTTTCATAACAAAAACATTATATTTGAAATTTTTAGGTCACCTTCTTTGAGGACAGAAACTTCCAGGGTCGCTCCTATGAGTGTATGGGCGACTGTGGTGACTTCTCCTCCTACATGAGCCGCTGTCACTCTTGCAGAGTGGACAGTGGTTGCTGGATGATGTACGATCAGCCCAACTACATGGGAAGTGGATATTTCTTCAGGAGGGGAGAGTATGCTGATTATATGTCTATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCCATGGTGAGTTAAAGTTTAAGCTTATATTAGATACAAATAAATCCCCCTTTTTGTGCATAAAATGTTCTGCTTAATAAACTTGAAAATGATGAACTCTTCCACTACAGCACAGGGGATCCTACAGAATGAGGATCTATGAGAGGGAGAACTTCGGAGGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8656
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113174 Essential Splice Site 2 173 1 3
ENSDART00000113174 Essential Splice Site 2 173 1 3

The following transcripts of ENSDARG00000076572 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23305352)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22461138
GRCz11 9 22272007
KASP Assay ID:
2260-1775.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCTTCTCCCTTGTGAAACCACTGAGAATAATCCARTGCAAACATGAAG[G/A]TAAATCTCATTCTATYACCCACTCCAAACAGTAAAACTAAAATGATAWAT
Long Flanking Sequence:
TTCTTATTTTGTTAATTACTAATATATATATTATATATTTGTTTTTACCTCTGATAAGAGGCTGTAGATAGATGATAGACTAAAAAGGATCCAACAAGGTTCTAGTGATTTCCTTCAAGTAGACCAAGACCAGACTTTCAAATGATTTCATAACTCCCTGTGATAGAAAACTGAACCATAAAAATATGAAAAAGAGAAATATTGTATTTATTGAATTGCACTATGATTTGCTAGAATAAATTAATTGTTTTTTCTAGCTAAATACCTCTTTAAATACTTTTAAAAATCCAAATAAATCAGAGTACTGAGAACTACATACCAAGCCTTAACTAGAAAGGTCTCTATACCAACTTGCATAGTCAGGAACTAAGCAACAATAGGAGCTGTGTAGTCTTTAGTCTTGGTCTTGTATAAAAGGACAGTTGACAGTAGTCAGTCAACAGCCAGAATCAGCTTCTCCCTTGTGAAACCACTGAGAATAATCCAGTGCAAACATGAAG[G/A]TAAATCTCATTCTATCACCCACTCCAAACAGTAAAACTAAAATGATATATTTCAATTTGTTTAAATTTTCATAACAAAAACATTATATTTGAAATTTTTAGGTCACCTTCTTTGAGGACAGAAACTTCCAGGGTCGCTCCTATGAGTGTATGGGCGACTGTGGTGACTTCTCCTCCTACATGAGCCGCTGTCACTCTTGCAGAGTGGACAGTGGTTGCTGGATGATGTACGATCAGCCCAACTACATGGGAAGTGGATATTTCTTCAGGAGGGGAGAGTATGCTGATTATATGTCTATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCCATGGTGAGTTAAAGTTTAAGCTTATATTAGATACAAATAAATCCCCCTTTTTGTGCATAAAATGTTCTGCTTAATAAACTTGAAAATGATGAACTCTTCCACTACAGCACAGGGGATCCTACAGAATGAGGATCTATGAGAGGGAGAACTTCGGAGGTC
Associated Phenotype:
Not determined