Busch Lab

ZMP

crygm2d12

Ensembl ID:
ENSDARG00000069801
ZFIN ID:
ZDB-GENE-070822-19
Description:
crystallin, gamma M2d12 [Source:RefSeq peptide;Acc:NP_001093912]
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
sa21471 Essential Splice Site Available for shipment Available now
sa15843 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21471
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101869 Essential Splice Site 2 173 1 3
Genomic Location (Zv9):
Chromosome 9 (position 23238854)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22394640
GRCz11 9 22205509
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGCTTCACCTTCTATCTTGTGGAAGCACAGGCAGAGCAAACATGAAGG[T/A]AAACCTCACATCAGAACCCATTTCCATGTTAATCAGATTTTCGATTTGGT
Long Flanking Sequence:
ATTTTTAAAGATAACATAATTTGTGGTTTAAAAATATTAAGTAAAAGCATATTTAATCCCCAAACCCAATCAAACACACCTTAAGCAGGTAATGCATGTTTTCAGGTTTTCTTGATAATTACAGGCAGGTTTGCTGGAACAAAGTTGAAACTGAAACATGCAGTATGTATCCCTCCAGAACTAGTGTTGGTAATCTCTACTGTAAATTATCACTGACATTTCTCATTGTTTGTCAGATTCACAACATTCTTCTAAGCAATATCAATTTCAGAGAAAATAGTCTTTTGTACTAACAAATGTGAACACTAAGATCTACATAACAAGCTTTAGCCAGAAAGCACTTTGTGCCAATGTGCACAGTCAGGAACTTACCAACAATAGGGGCTGTGTAGTCATTAGTCTTGGTCTAGTATAAAGGTATGGATGACAGCAGTCAGTAAACAAGCAGAATTAGCTTCACCTTCTATCTTGTGGAAGCACAGGCAGAGCAAACATGAAGG[T/A]AAACCTCACATCAGAACCCATTTCCATGTTAATCAGATTTTCGATTTGGTATATTTCACTTTAAATCGCTAAAATATTTACTTTGCATTTTCAGGTCACATTTTACGAGGACAGGAACTTCCAGGGTCGCTCTTATGATTGTATGGGCGACTGTGGTGACTTCTCCTCCTACATGAGCCGCTGTCACTCTTGCAGAGTGGAGAGCGGCTGCTGGATGATGTACGATCAGCCCAACTACATGGGAAATCAGTATTTCTTCAGAAGGGGAGAGTATGCTGATTACATGTCTATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCTATGGTGAGCTCAATACAACATACAAAACTAAAAATATATACTTTATTTGAATCTGTAATGCTAAATCACAGTACTGGCTTTTCTTCCACTACAGCACAGGGGATCCTACAGAATGAGGATCTACGAGAGGGAGAACTTCGGAGGTCAGATGTACGAGATGATGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15843
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101869 Nonsense 103 173 3 3
Genomic Location (Zv9):
Chromosome 9 (position 23238366)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22394152
GRCz11 9 22205021
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTACAGAATGAGGATCTACGAGAGGGAGAACTTYGGAGGTCAGATGTA[C/A]GAGATGATGGATGACTGTGACAGYATCATGGACCGTTACCGCATGTCTCA
Long Flanking Sequence:
CAAACATGAAGGTAAACCTCACATCAGAACCCATTTCCATGTTAATCAGATTTTCGATTTGGTATATTTCACTTTAAATCGCTAAAATATTTACTTTGCATTTTCAGGTCACATTTTACGAGGACAGGAACTTCCAGGGTCGCTCTTATGATTGTATGGGCGACTGTGGTGACTTCTCCTCCTACATGAGCCGCTGTCACTCTTGCAGAGTGGAGAGCGGCTGCTGGATGATGTACGATCAGCCCAACTACATGGGAAATCAGTATTTCTTCAGAAGGGGAGAGTATGCTGATTACATGTCTATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCTATGGTGAGCTCAATACAACATACAAAACTAAAAATATATACTTTATTTGAATCTGTAATGCTAAATCACAGTACTGGCTTTTCTTCCACTACAGCACAGGGGATCCTACAGAATGAGGATCTACGAGAGGGAGAACTTCGGAGGTCAGATGTA[C/A]GAGATGATGGATGACTGTGACAGCATCATGGACCGTTACCGCATGTCTCACTGTATGTCCTGCAATGTGATGGACGGCCACTGGCTCTTTTATGACCAGCCCCACTATAGAGGCAGAATGTGGTACTTCAGGCCTGGAGAGTACAGAAGCTTCAGCAATTTTGGTGGCATGAGGTTCATGAGCATGAGGCGTATCATGGACTCTTGGTACTAATGTTCTTTAATAAAACAATGTTCATACAACAACAAGTTCTGTTCTGTAATTAAATCCAAACATTTATTAAAATGTAAAAAGAAAAAATAATATGTTTAGGAGAAATTTCAACAATTAAATTTTTCACACATACTGCAATGTATAAAAGAATAAGAAATGAGTGAATGGTTAAAATACTACAAAAGATGTAATGGTCTGTAAAGATATTTTGTAAATGTCCTACTGTAAAAATTTCAAAACTCATTCATTTTCTTGTCAGCTTAGTCCCTTTATTAATCTGGGGTTGC
Associated Phenotype:
Not determined