Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Rwdd2b ENSRNOG00000001599

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Description

RWD domain containing 2B [Source:RGD Symbol;Acc:1305062]

Gene Synonyms

LOC304132, RGD1305062

Location

Primary_assembly 11: 40,152,147-40,167,656 reverse strand.

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000142675.1	Rwdd2b-202	2333	321aa	ENSRNOP00000111707.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000050902.5	Rwdd2b-201	2145	290aa	ENSRNOP00000039159.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JL75 F7F829	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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. APPRIS P1,

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Summary

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