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

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Gene: WIPF2 ENSBTAG00000038126

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Description

WAS/WASL interacting protein family member 2 [Source:VGNC Symbol;Acc:VGNC:36940]

Location

Primary_assembly 19: 40,511,307-40,526,914 forward strand.

ARS-UCD1.3:CM008186.2

About this gene

This gene has 2 transcripts (splice variants), 266 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000013695.5	WIPF2-201	1645	439aa	ENSBTAP00000013695.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1B777	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,
ENSBTAT00000068851.2	WIPF2-202	871	181aa	ENSBTAP00000058831.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LPA0	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,

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Summary

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