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: Biological process
- GO: Molecular function
- GO: Cellular component
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: Washc5 ENSRNOG00000009739

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Description

WASH complex subunit 5 [Source:RGD Symbol;Acc:1564420]

Gene Synonyms

LOC362919, RGD1564420

Location

Primary_assembly 7: 92,773,625-92,825,532 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000105175.2	Washc5-202	3728	1161aa	ENSRNOP00000091567.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AFP0	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,
ENSRNOT00000013315.10	Washc5-201	4161	1159aa	ENSRNOP00000013315.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M1B3	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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