Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
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: Rwdd1 ENSRNOG00000042916

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Description

RWD domain containing 1 [Source:RGD Symbol;Acc:631337]

Location

Primary_assembly 20: 26,493,672-26,510,295 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 3 transcripts (splice variants), 251 orthologues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000068777.5	Rwdd1-201	1045	243aa	ENSRNOP00000062656.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QX02 A6K3S3	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,
ENSRNOT00000098026.2	Rwdd1-203	868	232aa	ENSRNOP00000091822.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACH0	-
ENSRNOT00000095504.2	Rwdd1-202	835	221aa	ENSRNOP00000085613.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q99ND9	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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