Busch Lab

ZMP

crygm2d11

Ensembl ID:
ENSDARG00000069827
ZFIN ID:
ZDB-GENE-071004-42
Description:
crystallin, gamma M2d11 [Source:RefSeq peptide;Acc:NP_001103328]
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
sa41405 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21469 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa41405
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101923 Essential Splice Site 86 175 3 3

The following transcripts of ENSDARG00000069827 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23132339)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22288125
GRCz11 9 22098994
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTTCTGCCATGATCAATGTGAAAATAACAGACTTCTCTTCCAATACA[G/T]TACAGGGGATCCTACAGAATGAGGATCTATGAGAGGGACAACTTTGGAGG
Long Flanking Sequence:
AACCAGAATCAGCTTTAGCTTCTCCTCTGTAGAACCACAGAAGACCAGCAAGTGCAACCATGATGGGAAAGGTAAAACTTCTCTCCAGCTCACAAGTTGAATTCAAATGAAAATTAAAGTAGACAAAAGTAAAAATACTAAAACTTGAATTTTCAGGTCGTCTTCTACGAGGATAGGAACTTCCAGGGTCGCTCTTATGAGTGTATGGGCGACTGTGGTGACTTTTCCTCCTACATGAGCCGTTGTCACTCATGCAGAGTGGAGAGTGGCTGCTGGATGATGTATGACCAAACCAACTACATGGGTAATGGGTATTTCTTTAGGAGGGGAGAGTATGCTGATTACATGTCGATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCCATGGTAAGCTGATTACACATAATATCTGTATATTTAGGCCTATATGCTTCTTTTTTATTTCTGCCATGATCAATGTGAAAATAACAGACTTCTCTTCCAATACA[G/T]TACAGGGGATCCTACAGAATGAGGATCTATGAGAGGGACAACTTTGGAGGTCAAATGTACGAGATGATGGATGACTGTGACAACATCATGGACCGTTACCGCATGTCTCACTGCCAGTCCTGCCATGTGATGGACGGCCACTGGCTCTTTTATGACCAGCCCCACTACAGAGGCAGGATGTGGCACTTCGGACCTGGACAGTACAGAAACTTCAGCAATTATGGTGGCATGAGATTCATGAGCATGAGGCGCATCATGGACTCTTGGTACTAGAGTTTCAATAAACCTTTTTCTCTACCACACTAAACATTGTGCATGTAAAATTTGATCATTAATGTATGCAAGTTTAACCAATCAAAAGTAAACAAACACAGCACATACGTTTATTATATTATATTATACAAATAACATATTTTGTTAGGAGAACTCCCCTGAGAATTTTATAGCTTGATAAATACAGGCAGGAGCACAAAGACCATCATCATCCCAAAAAGATGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21469
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101923 Nonsense 146 175 3 3

The following transcripts of ENSDARG00000069827 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23132156)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 22287942
GRCz11 9 22098811
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGGCCACTGGCTCTTTTATGACCAGCCCCACTACAGAGGCAGGATGTG[G/A]CACTTCGGACCTGGACAGTACAGAAACTTCAGCAATTATGGTGGCATGAG
Long Flanking Sequence:
CAGGGTCGCTCTTATGAGTGTATGGGCGACTGTGGTGACTTTTCCTCCTACATGAGCCGTTGTCACTCATGCAGAGTGGAGAGTGGCTGCTGGATGATGTATGACCAAACCAACTACATGGGTAATGGGTATTTCTTTAGGAGGGGAGAGTATGCTGATTACATGTCGATGTTTGGAATGAACAACTGCATCAGGTCCTGCCGTATGATCCCCATGGTAAGCTGATTACACATAATATCTGTATATTTAGGCCTATATGCTTCTTTTTTATTTCTGCCATGATCAATGTGAAAATAACAGACTTCTCTTCCAATACAGTACAGGGGATCCTACAGAATGAGGATCTATGAGAGGGACAACTTTGGAGGTCAAATGTACGAGATGATGGATGACTGTGACAACATCATGGACCGTTACCGCATGTCTCACTGCCAGTCCTGCCATGTGATGGACGGCCACTGGCTCTTTTATGACCAGCCCCACTACAGAGGCAGGATGTG[G/A]CACTTCGGACCTGGACAGTACAGAAACTTCAGCAATTATGGTGGCATGAGATTCATGAGCATGAGGCGCATCATGGACTCTTGGTACTAGAGTTTCAATAAACCTTTTTCTCTACCACACTAAACATTGTGCATGTAAAATTTGATCATTAATGTATGCAAGTTTAACCAATCAAAAGTAAACAAACACAGCACATACGTTTATTATATTATATTATACAAATAACATATTTTGTTAGGAGAACTCCCCTGAGAATTTTATAGCTTGATAAATACAGGCAGGAGCACAAAGACCATCATCATCCCAAAAAGATGTTTAAAACATCTGGCCAACATATGAACATGTTCAAAAGATGACCAATACTTTACAGTGTGCACATGCCAGAAAATCATATCTGATTTAAAGCTTGCAATATATAAATGCACACCTGATCACTTTATGTAGCATATACTGTATGTAAACTCTGTCTGGAATAATCAATTAGAATAGTTTGATTCCAG
Associated Phenotype:
Not determined