ZMP

rdh12

Ensembl ID:

ENSDARG00000018069

ZFIN ID:

ZDB-GENE-040718-9

Description:

retinol dehydrogenase 12 [Source:RefSeq peptide;Acc:NP_001002325]

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
sa42241	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42241

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045484	Nonsense	216	319	5	7
ENSDART00000137315	Nonsense	217	320	5	7

Genomic Location (Zv9):

Chromosome 13 (position 33286048)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	32931996
GRCz11	13	33062446

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCGGACTTGCCTACTGCCAGAGCAAACTCGCTAACGTGCTTTTCACTCGT[G/T]AGCTGGCGCGCAGACTCCAGGGTAACTCAAATAATGATTCGACATGAATA

Long Flanking Sequence:

CCTGTAAATTTCACTTTAAGCTGTATAGAAGTTTCTTGAAAAATATTTAGTAAAATATTATGTACTGTCATCATGGCAAAGATAAAATAAACCAGTTATTAGAAATGAATTACTAAAACTGTTATGATTAGAAATTTGTTGAAAAATCAACAGAAATTGGGAAAAAAATTTATACAGGGGGCTAATAATTTTGACTTCAACTGTATATTAACAAATGACCAAAAAATAAAATAAAACTAGCATTACATGAGCACATTTCAGCATATAAAAATTATGACAAAAATATTGTAAATAATCCTTTTTTTCATCCAGGTCACTACCTGCTGACGTATCTCCTCATTGGTCTGCTGAAGCGTAGCGCTCCTTCACGAATCGTGGTCGTTTCCTCCCTGGCACATAACTTCGGGTGGATTCGATTCCACGACCTGCACAGTCAGGGCAGCTACAACAGCGGACTTGCCTACTGCCAGAGCAAACTCGCTAACGTGCTTTTCACTCGT[G/T]AGCTGGCGCGCAGACTCCAGGGTAACTCAAATAATGATTCGACATGAATAACTGAAATGGTACCTGCAGAAAATGTGAGTTTGACTTGTATGTGATGATCAGGGTCGAATGTGACTGTGAACTCTGTGCATCCTGGAACGGTGAGGTCAGAGCTGGTGCGTCATTCTACGCTGATGTCCCTGCTGTTCGCTTTCTTCTCGATGTTCCTGAAATCCCCGAAAGAAGGCGCTCAGACCTCCATCTACTGCGCCGTCGCTGAGGAGCTCCAGTCAATCTCAGGCAAACATTTCAGGTACGGCAAACTCCAGAACGCTTGTCATGGAAGACACACATTATTTAACACATGCTGGATATTAATAAACTGTATCAGCAAGGGTGCGGTTATTAAAACAGCAGTTCTCAACTTTTACATAGTAGTGCATACAATATAAAATGGACCCTTTTCACATTTCCAGGTTTCTCAGTAGCGGAGGTCATCATAGTCGCATTACCTTTGAGCG

Associated Phenotype:

Not determined