Busch Lab

ZMP

NP_001007792.1

Ensembl ID:
ENSDARG00000008219
Description:
crystallin, gamma M4 [Source:RefSeq peptide;Acc:NP_001007792]
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
sa613 Essential Splice Site Available for shipment Available now
sa33782 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa613
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122957 Essential Splice Site 3 174 1 3
Genomic Location (Zv9):
Chromosome 6 (position 25797)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 53999
GRCz11 6 72050
KASP Assay ID:
554-0523.1 (used for ordering genotyping assays)
KASP Sequence:
AAAAGCGGCAGCGGCGCATCAGTCCTGCACAGATCCAGCCATGAACAAGG[T/C]AAGCTCCACAACCCTTTACACACAATGCTGAACACAGCAGCCCTTTACAG
Long Flanking Sequence:
GTGAAGGCCTGGTCCTGCTCAAGCTGATCTCTGTCCGTCAAAGTGTCCCTTGAAGTGCTTAAAACACTTTCTGCCGCATCCTTCTGATTATTTCTGATTATACGTTTTCCCCAAGTTGTATTAATGTACCTGAATGATTCTAGGCTGTGATCTACTGTATAAGACTCACACATTGCTCTGACTGATGCAGGACTCGGATATTTTCATCAGGTGAATGTTTTCCCACACAGTGATGCGCGAGTGTGTGCTGCAGGCCTCTGAATGTCTGTAAAGACCTAAATAAATAATCAAACTTCTGAACACATTCAGGCACAAACTGCCTTCAATGCAGAATAGTTTTTGTTGTAGGACGCCTGAGATAGACACAGAAATGAACAGAAAACTCCTCTTGCTTGTTCATCAGCTTTGATGATTTAAATAACAAAAGCTATAGCGCGGCTTATCAAGTATAAAAGCGGCAGCGGCGCATCAGTCCTGCACAGATCCAGCCATGAACAAGG[T/C]AAGCTCCACAACCCTTTACACACAATGCTGAACACAGCAGCCCTTTACAGCCGCCCGTTTCACTGCTGTATAATGGCTCAGAAACACTATTGCATTACTATGATGCTATAATATCCAGACCCAAACTCAGACGGTTTGACAGACGAGTGCTCTTCACAGCAGAACACACTGCTGTAGTTGAATGAGTGTAATTTTGGCGTTTGTGTGTTTTAGATTGTTTTCTACGAGGACAGAAACTTCCAGGGCCGCTCCTATGAGACCAGCAGTGACTGTCCGGAGCTCAGCCAGTTTCTGAGCCGCTGCAGCTCCTGCCGGGTGGAGAACGGTTGCTTCATGATCTACGATCGCTCCAACTTCATGGGAAACCAGTTCTTCCTGCGGCGCGGCGAGTATGCGGACTGCAAGAGGATGGGTTTGAGCGACTCTATCAGATCCTGCCGTACCATTCCTCAGGTGAGGCTCTGCGGCCTTCTGTCTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa33782
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122957 Nonsense 23 174 2 3
Genomic Location (Zv9):
Chromosome 6 (position 26070)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 54272
GRCz11 6 72323
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGAGGACAGAAACTTCCAGGGCCGCTCCTATGAGACCAGCAGTGACTG[T/A]CCGGAGCTCAGCCAGTTTCTGAGCCGCTGCAGCTCCTGCCGGGTGGAGAA
Long Flanking Sequence:
ACCTAAATAAATAATCAAACTTCTGAACACATTCAGGCACAAACTGCCTTCAATGCAGAATAGTTTTTGTTGTAGGACGCCTGAGATAGACACAGAAATGAACAGAAAACTCCTCTTGCTTGTTCATCAGCTTTGATGATTTAAATAACAAAAGCTATAGCGCGGCTTATCAAGTATAAAAGCGGCAGCGGCGCATCAGTCCTGCACAGATCCAGCCATGAACAAGGTAAGCTCCACAACCCTTTACACACAATGCTGAACACAGCAGCCCTTTACAGCCGCCCGTTTCACTGCTGTATAATGGCTCAGAAACACTATTGCATTACTATGATGCTATAATATCCAGACCCAAACTCAGACGGTTTGACAGACGAGTGCTCTTCACAGCAGAACACACTGCTGTAGTTGAATGAGTGTAATTTTGGCGTTTGTGTGTTTTAGATTGTTTTCTACGAGGACAGAAACTTCCAGGGCCGCTCCTATGAGACCAGCAGTGACTG[T/A]CCGGAGCTCAGCCAGTTTCTGAGCCGCTGCAGCTCCTGCCGGGTGGAGAACGGTTGCTTCATGATCTACGATCGCTCCAACTTCATGGGAAACCAGTTCTTCCTGCGGCGCGGCGAGTATGCGGACTGCAAGAGGATGGGTTTGAGCGACTCTATCAGATCCTGCCGTACCATTCCTCAGGTGAGGCTCTGCGGCCTTCTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTTTGTTTCTCTATGTGTGTGTCTGTCTGTGTATGCTTATGTTTATCTCTGTCTGTCTGTCTCTTTGTGATTGTATTGCAATGTGAACTTCAGAAGTGCCCTAGTGTCAGCCTCACTAGTCTGCATGTCTTGAGCAGCACCGCGGAGCCTTCAGGATGCGGATCTATGAGAAAGAAAACTTTGGCGGGATGAGCTATGAGCTGACGGAGGACTGCGAGTCAACGGCGGACCGGTTCCGGC
Associated Phenotype:
Not determined