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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RDH8 ENSG00000080511

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Description

retinol dehydrogenase 8 (all-trans) [Source:HGNC Symbol;Acc:14423]

Gene Synonyms

PRRDH, SDR28C2

Location

Chromosome 19: 10,123,925-10,132,955 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 4 transcripts (splice variants) and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000591589.1	RDH8-001	1715	331aa	ENSP00000466058.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS12223	K7ELF7	-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000171214.1	RDH8-201	1714	311aa	ENSP00000171214.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q9NYR8	NM_015725.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000587782.1	RDH8-002	702	79aa	ENSP00000465773.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000589570.1	RDH8-003	430	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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