ZMP
cry-dash
Ensembl ID:
ZFIN ID:
Description:
Cryptochrome DASH [Source:UniProtKB/Swiss-Prot;Acc:Q4KML2]
Human Orthologues:
CRY1, CRY2
Human Descriptions:
cryptochrome 1 (photolyase-like) [Source:HGNC Symbol;Acc:2384]
cryptochrome 2 (photolyase-like) [Source:HGNC Symbol;Acc:2385]
cryptochrome 2 (photolyase-like) [Source:HGNC Symbol;Acc:2385]
Mouse Orthologues:
Cry1, Cry2
Mouse Descriptions:
cryptochrome 1 (photolyase-like) Gene [Source:MGI Symbol;Acc:MGI:1270841]
cryptochrome 2 (photolyase-like) Gene [Source:MGI Symbol;Acc:MGI:1270859]
cryptochrome 2 (photolyase-like) Gene [Source:MGI Symbol;Acc:MGI:1270859]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30747 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24478 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30747
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035992 | Nonsense | 48 | 520 | 2 | 14 |
ENSDART00000139329 | Nonsense | 49 | 521 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 20815583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20062712 |
GRCz11 | 24 | 20207131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATAATACCGCTGTACTGCTTCGACCCGCGCCATTACCAGGGCACATA[T/A]CACTACAACTTCCCCAAAACTGGCCCCTTCCGGCTGCGCTTCCTCCTAGA
Long Flanking Sequence:
CAGCGATCAGTTGGTTTACTAACCCTGATTTTCAGCCACAACAAAAGAAAATATTTATTATTTTGACCATTTATAATTTTTGCCCTTCCCAGAGATGGGTTGCAGCTAATAGGGCATCCGCTGTGTAAAAACGTGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGCGACCCTGGATTAATAAAGGGACTAAGCAGAAAAGAAAATGAATGGATGAATGATTTTTGCCCCCCCAAAAAATTATTGAAATTCCATATTTGAAATCAATGTTATCAGGCCTGCCTAGAAGAAAATACAAATGCTGAACTAGACTGTGTAAATAAGCAGTGACTTTCTGAAATGCCGTGCTGGCTTTGACAAGTTGAGTTTTGTTGAAGTTCTTAAAGAAACATGAGAAACCGGTTTTCCTACATTCATTTAGGTGTTTCACTGGGCTCAGAGGAATGCAGAGCACATAATACCGCTGTACTGCTTCGACCCGCGCCATTACCAGGGCACATA[T/A]CACTACAACTTCCCCAAAACTGGCCCCTTCCGGCTGCGCTTCCTCCTAGACAGTGTAAAAGACCTGAGGGCCTTGCTGAAGAAACACGGCAGGTACGGCTCTCAGTAAACACTTCCTCTACTCATACTTGTATTCTATCACACATATACTGTGTACAGTACTGATCAAATGTCTGGAATGAGGACTTTTTATTGTTTTGCAAAGTCTTCTGTGAAATATTATTTACTTTTAAAATAACTGATTTTCATTTGTTTCATAAAGTAATTAATTTGCTCCAATGTCACAGTGTCCTTAGTGTCACTTGATTATTCAAAAATCAGTATAATAAACTGATTTACTGTTATGATCAATCATTATTGGTACTCAATACCTAATAAAGCATTTTATAAATGTCGATGATGAAAATTGTCAATGATGTTTTTTCCCGTGATACTTTTTACTTTTTAGGCATCTTTGATGAAGAAATAACAGAATTTGTTTTAATTAAAATCTTCTCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24478
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035992 | Nonsense | 461 | 520 | 13 | 14 |
ENSDART00000139329 | Nonsense | 462 | 521 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 20804650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20051779 |
GRCz11 | 24 | 20196198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATGTTCACACACCATGGACCCTCAGCAACTCAGCGCTGTCACACGCA[C/T]AGGTCTCACTCAACCAAACATACCCTTGTCCCATCATCACCGCACCCGAG
Long Flanking Sequence:
AAACTCTAAAGATATATTAATATATTTTAAATATCAAATCATTGTTTTGGTTAGAATAGACAATCAATAGATTATTATTTAAAAATTACAGCCTACTGTACAAATAAATAAATAAAAACAACAAAATAAATGCATTTTTCAAGTTTTTATTTAAATTGTATCTATTATCATTAATTATTTGAGAGTTTAAATTAATAAAATGATTACAATAAATGAACCGCTTTATTTTGCACCTTTGAATGCTCTTTATCATCACTTCAGTGAGCTGCTTCTACTGTGAATGCAAATGTAAATATAGAAAGGAGAAGTTAAACGTGAGTGCACAGAAGTGTCAGGAGAGATTAATGCACCATGATAAAGCCTTTTCCTGCACAGATCTGACACTTGATGTATTTCTGAAGGGCGACTATGTCCGTCAGTGGGTTCCTGAGCTTCGAGGTATTAAAGGTGGAGATGTTCACACACCATGGACCCTCAGCAACTCAGCGCTGTCACACGCA[C/T]AGGTCTCACTCAACCAAACATACCCTTGTCCCATCATCACCGCACCCGAGTGGAGTCGACACGTCAATAACAAATCAGTAAGATCACTAACTAGTAGTGTTGTCGCAATACTTGATCTTTAAGTATATCAATACTTGATACCAATTTTAAAATCACTGGGAAATATTACCAAAGCATTCATTCAATTTACAATATTAATGAACATCTAAGTTTTTTCTTTTGCCAGAGGTAAAACCTCAAAAATGATTAACTTTTTAAGTTCAGATTTTCACTTGCCATGACATCATTTTTACTGGCCTTGTTGAAAAAATATAGGAGTAAAATAATTGTATAATAATCTTTTTTTTACCATGAAACAGTGTAAAACATTATATGCCATGCAGTATTTTAATACATTTTACATTTCGTAATTCAAATTTAATATTTTATATTATTGCTATACTTCGAATAGTAAAACATTACACTGGCTCAGCAAAAAATAATAAATAGATAAGAGTAAG
Associated Phenotype:
Not determined