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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	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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