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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: WNT16 ENSG00000002745

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Description

wingless-type MMTV integration site family, member 16 [Source:HGNC Symbol;Acc:16267]

Location

Chromosome 7: 120,965,421-120,981,158 forward strand.

GRCh37:CM000669.1

About this gene

This gene has 2 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
ENST00000222462.2	WNT16-001	3147	365aa	ENSP00000222462.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5781	Q9UBV4	NM_057168.1	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,
ENST00000361301.2	WNT16-002	1230	355aa	ENSP00000355065.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5780	E9PH60	NM_016087.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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