ZMP
crygm2d11
Ensembl ID:
ZFIN ID:
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]
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]
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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