Gene: WNT9B ENSG00000158955

Description

wingless-type MMTV integration site family, member 9B [Source:HGNC Symbol;Acc:12779]

Gene Synonyms

WNT14B, WNT15

Location

GRCh37:CM000679.1

About this gene

This gene has 3 transcripts (splice variants), 5 paralogues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000290015.2	WNT9B-001	1376	357aa	ENSP00000290015.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS11506	O14905	NM_003396.1	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,
ENST00000393461.2	WNT9B-002	2654	329aa	ENSP00000377105.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E7EPC3	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000575372.1	WNT9B-004	543	132aa	ENSP00000458192.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		I3L0L8	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

EMBL-EBI User Survey 2024