Gene: Wnt2 ENSMUSG00000010797

Description

wingless-type MMTV integration site family, member 2 [Source:MGI Symbol;Acc:MGI:98954]

Gene Synonyms

2610510E18Rik, Int1l1, Irp, Mirp, Wnt-2, Wnt2a, m-irp

Location

Chromosome 6: 17,985,468-18,031,892 reverse strand.

GRCm39:CM000999.3

About this gene

This gene has 8 transcripts (splice variants), 208 orthologues, 18 paralogues and is associated with 15 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000010941.7	Wnt2-201	3563	360aa	ENSMUSP00000010941.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS19928	P21552	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000501702.1	Wnt2-208	7591	204aa	ENSMUSP00000280065.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000501701.1	Wnt2-207	3298	207aa	ENSMUSP00000280064.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000501696.1	Wnt2-202	5728	130aa	ENSMUSP00000280059.1	Nonsense mediated decay		-	-
ENSMUST00000501697.1	Wnt2-203	5702	35aa	ENSMUSP00000280060.1	Nonsense mediated decay		-	-
ENSMUST00000501698.1	Wnt2-204	2218	110aa	ENSMUSP00000280061.1	Nonsense mediated decay		-	-
ENSMUST00000501700.1	Wnt2-206	2099	293aa	ENSMUSP00000280063.1	Nonsense mediated decay		-	-
ENSMUST00000501699.1	Wnt2-205	2040	35aa	ENSMUSP00000280062.1	Nonsense mediated decay		-	-

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Gene: Wnt2 ENSMUSG00000010797

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Gene: Wnt2 ENSMUSG00000010797

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