ZMP

zgc:153441

Ensembl ID:

ENSDARG00000054797

ZFIN ID:

ZDB-GENE-060825-39

Description:

retinol dehydrogenase 13 [Source:RefSeq peptide;Acc:NP_001038920]

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]

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]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa39258	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39258

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000077042	Essential Splice Site	234	336	6	7

Genomic Location (Zv9):

Chromosome 19 (position 43940730)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	42850532
GRCz11	19	42419969

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATAACTAATTACTGCATCAGACTTGTTTAATTGCTCTGTGCTTTAACTC[A/G]GGCTCTGGTGTGTCAGTGTTCTCTCTTCACCCTGGAGTGATCCGTACTGA

Long Flanking Sequence:

GTTTTGTACCAGTTGTAATTTATAAAGAGTTTTTTTAGAGAGGCCAAACGGAAGGGAATTACAGTAATCTAGCCCTTCCAGCTACAACCCAGTGTGTGCGTGAGCGTGTATGGGTGTTTCCAAGTACTGTGGCTGGAAGGGCATCCGCTGCGTAAATCTACTGTGGTGTCCCCTGATTTTTAACCCAACATGATAATCTATTGTGCATCTCTTTTCCATTCTGACATGCATGAGCCTGCTCTTATTCATACTAAATATTCCCATCTGATGCTCTTTCCTACAGGAAAGATCCACTTTGATGATCTTAACTTCAACAAAGCACCGTACGATTCATTGGTGAGCTACCGGCAGAGCAAACTCGCCAACCTGCTGTTCACTCGAGAGTTAGCCAGAAGGATTAAAGGTTTGTGCGCTCAATTCCAGTCCAGCAGAAACACAGAAACAGCTTTAAATAACTAATTACTGCATCAGACTTGTTTAATTGCTCTGTGCTTTAACTC[A/G]GGCTCTGGTGTGTCAGTGTTCTCTCTTCACCCTGGAGTGATCCGTACTGAACTGGGGCGATACGTGCAGACACGACACCCTTTGCTCAGCGGCCTGCTTTCTATTCCTGCTCTGCTACTCATGAAAACACCCTATCAAGGTGCTCAGACGTCCATCTACTGCGCCACGGCTGATGGTCTGGAGATTCACAGCGGCTGCTATTTCAGGTATACGACTACAGATTACACTGGTAAAAATGAAGAGTTGTAAATGTATTTACTTTTTAATTTAGTATTTAATTTAATTGATTGTAAAGGGGACCTATTTTGCAAAAATCGCTTTTGTAAGGGGTTTAAACACAGTTGTGTGGCAACAGTGTGTGAATATGGCAAAAATATGTTCATGGTATCAAATAATGAATTCCAGTTTTTATAATGACACTTGATAAACAGTCCGCAGAAACACTTTGATTGACATTTTCCCTTCGTACATGTCATCAGAGGGGATAAGCCCCGCCCACT

Associated Phenotype:

Not determined