ZMP
Q6NY49_DANRE
Ensembl ID:
Description:
LOC407663 protein [Source:UniProtKB/TrEMBL;Acc:Q6NY49]
Human Orthologues:
RDH11, RDH12
Human Descriptions:
retinol dehydrogenase 11 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:17964]
retinol dehydrogenase 12 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:19977]
retinol dehydrogenase 12 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:19977]
Mouse Orthologues:
Rdh11, Rdh12
Mouse Descriptions:
retinol dehydrogenase 11 Gene [Source:MGI Symbol;Acc:MGI:102581]
retinol dehydrogenase 12 Gene [Source:MGI Symbol;Acc:MGI:1925224]
retinol dehydrogenase 12 Gene [Source:MGI Symbol;Acc:MGI:1925224]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34093 | Nonsense | Available for shipment | Available now |
sa20973 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34093
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 |
---|---|---|---|---|---|
ENSDART00000002075 | Nonsense | 148 | 331 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 31520101)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29912443 |
GRCz11 | 7 | 30183593 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTATTACATTTATTTTTCTGCCAACAGGGGTAATGATGTGCCCAAAGTG[G/A]CATACAGATGAAGGTTTTGAGATGCAGATTGGAGTAAACCACTTGGGCCA
Long Flanking Sequence:
GCTGCAGAGGAGATTAGGAAGAGGAGTGGAAATGAGAATGTGACTGTGAAAATGCTGGATCTGGCCTCTTTGCAGTCTGTCCGAGATCTGGTCAAAGATGTACAGCAGTCTGAACAAAGACTGGATATCCTCATTAATAATGCTGGTAAGAAATGTCATGCAAATTATTATGCTAAAGAGTATTGTATGAAAGCATTTCATTTTTTAGCTATCAAATTGCAAACCATCAATGTATTTTTTTCATTTGTATTTATTTATTCAGTTGTTTACTCATTAATGTTTATGCAAATTTTTTCCCGGTATTAAATTGTAATTTTATTATATGTTATGTTATCATATTTATTGTCTTTGTTCCTTATTATGTTTTATATTAACAGTTAAATCATAAATATTTATTTCTCCCATTTATGTTTATTTGTGCATTAATTTATTCATTTGTTTTTACTTTTATCTATTACATTTATTTTTCTGCCAACAGGGGTAATGATGTGCCCAAAGTG[G/A]CATACAGATGAAGGTTTTGAGATGCAGATTGGAGTAAACCACTTGGGCCACTTCCTGCTTACAAACTTGCTTCTGGACCTGTTGAAGAAGTCAGCACCCAGTCGTATTGTCAATGTGGCTAGCGTGGCCCATGAGAGAGGTGTGAAACACAAAATGTTTTTAACTGAAATACTCATAACATATCACACTTGTTTGTATTCCTAAATAGTCTTTAATTTATTGTAAGCATTAATTACCCAGGAACGGCACTAGGCATGTATGTAAAATCTAACTTTTATTTAATTTTTCTTTTGTATGATTTGTGATTCTATAAAAGCAGTCTAAGGCGGATCTGTGTTGAGAAACGGATCAGTCTAGGGTGCATTTCCAAAAACCATCGTTAGCCAACTAATGTCACAAGTTCCATCGTTGCGAACATACTTCATTGAATAGGCATTTCCCAAATACATCAATTCAAGGAACATTCACAAACTGCGTCGCAAACTTGGACCTCTGGAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20973
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002075 | Essential Splice Site | 234 | 331 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 31523613)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29915955 |
GRCz11 | 7 | 30187105 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTGGCTAATGTTCTGTTTACCCGTGAACTAGCTATCAAGCTAAGAGG[T/A]AAACCATAAACAAATGTTCTTCACTCTAATAGTTTAAAAAAAAAAACATA
Long Flanking Sequence:
AAAAAACCCCACTAAACATACTTGGGCGGCTGTTAATATACCTGGGAGGCCCACCCAAGTAAAGTATATGTGAGAGAAGCACTGCTTTTGCTATTCTTTCATTCAATTGTTTGAATTTTACAATGTATGTGCCTCCTAACCCCAACCCCAAAAATTGCCCACCTGGGATTTCTATCAAGCCACCACTCCGTGATTGGCAAAAACCGGGCCTGATTGTACCGCCTTATCAAACTCCTTGGCATGATGTTCAGTTTTGACAAAATGTGACAAAGTAGGTCAAAGTGCAGTCATTGTATTACTTCATAATGTAAATATTTATGTAAAATTTTTATTTCGGAGCATGTAACCCACTGAACCTTTCATCTTTGTGTGTGTTTGACAGGCAAGATTAACTTTAATGACATAAACATGGATAAAGACTATGATCCATACCAGAGCTATTATCGGAGTAAACTGGCTAATGTTCTGTTTACCCGTGAACTAGCTATCAAGCTAAGAGG[T/A]AAACCATAAACAAATGTTCTTCACTCTAATAGTTTAAAAAAAAAAACATAGATGTCACACTGAACCATACTGCGTTTAAAGATTCTCTCTGTATATTATTCAGACACAGGAGTGACCACTTATGCTCTCCATCCTGGCGTAATCCGTACTGAGCTTGGACGACACGTTTTCTCCAATCTGTGGAGGAAGCTCATAATCCTTCCCTTTTATTTCTTCTTCAAAAACCCTTGGCAGGGAGCTCAGACTACTATCTACTGCGCAGTGGACGAGAGTCTAAAGCACAGCAGTGGTCTTTACTACAGGTCAGTAGCTCTAACTGGGATTTTGGAAGTTTTTTGCTTATCACGGCATGTGTAAATGTGTGACCGTGTAATGGACAACATCGTAATTATACGCAGAGATATGGTAAAACATTCTGTCTATTTTATGGTCAAATTGTTTGACATTTTATTCTGTTTTTGTTCATAAATTATATGCATAACTGAGTAGAATCAACTTTT
Associated Phenotype:
Not determined