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

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Gene: WNT2 ENSG00000105989

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Description

wingless-type MMTV integration site family member 2 [Source:HGNC Symbol;Acc:12780]

Gene Synonyms

INT1L1, IRP

Location

Chromosome 7: 116,916,685-116,963,343 reverse strand.

GRCh37:CM000669.1

About this gene

This gene has 4 transcripts (splice variants) and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000265441.3	WNT2-002	2907	360aa	ENSP00000265441.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5771	A4D0V1 P09544	NM_003391.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000491214.1	WNT2-004	513	153aa	ENSP00000419466.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9JUI2	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000449446.1	WNT2-001	1768	110aa	ENSP00000389643.1	Nonsense mediated decay		F8WDR1	-	-
ENST00000461427.1	WNT2-003	571	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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