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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: WNT8A ENSG00000061492

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Description

wingless-type MMTV integration site family, member 8A [Source:HGNC Symbol;Acc:12788]

Gene Synonyms

WNT8D

Location

Chromosome 5: 137,419,581-137,428,054 forward strand.

GRCh37:CM000667.1

About this gene

This gene has 4 transcripts (splice variants) and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000398754.1	WNT8A-002	1498	351aa	ENSP00000381739.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS43368	Q9H1J5	NM_058244.2	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,
ENST00000506684.1	WNT8A-004	1543	369aa	ENSP00000426653.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		D6RF47	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000504809.1	WNT8A-003	1193	360aa	ENSP00000424809.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		D6RF94	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000361560.2	WNT8A-001	1597	355aa	ENSP00000354726.2	Nonsense mediated decay		Q9H1J5	-	-

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Summary

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