Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Ensembl protein families
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  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
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External references
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ID History
- Gene history

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Gene: Rdh19 ENSMUSG00000054052

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Description

retinol dehydrogenase 19 [Source:MGI Symbol;Acc:MGI:2678390]

Gene Synonyms

RDH-S, Rdhs

Location

Chromosome 10: 127,849,928-127,861,176 forward strand.

GRCm38:CM001003.2

About this gene

This gene has 1 transcript (splice variant), 382 orthologues and 31 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
Rdh19-201	ENSMUST00000077530.2	1889	318aa	ENSMUSP00000076735.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS24253	G5E8H9	<p>TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA.</p><p>The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript.</p>TSL:1, The GENCODE set is the gene set for human and mouse. <a href="/Help/Glossary?id=500" class="popup">GENCODE Basic</a> is a subset of representative transcripts (splice variants).GENCODE basic, <p>APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS.</p><p>APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene.</p>APPRIS P1,

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Summary

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Gene-based displays