Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Wasf3 ENSRNOG00000048898

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Description

WASP family member 3 [Source:RGD Symbol;Acc:1592807]

Gene Synonyms

LOC682937

Location

Primary_assembly 12: 13,675,645-13,774,559 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 267 orthologues, 3 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000071567.4	Wasf3-201	5065	502aa	ENSRNOP00000065380.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K1D0 M0R7F3	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, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000119900.2	Wasf3-202	5056	499aa	ENSRNOP00000081893.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G8L2	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,

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Paralogues

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