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: WNT9B ENSBTAG00000002664

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Description

Wnt family member 9B [Source:VGNC Symbol;Acc:VGNC:36967]

Location

Primary_assembly 19: 45,335,094-45,356,585 reverse strand.

ARS-UCD1.3:CM008186.2

About this gene

This gene has 2 transcripts (splice variants), 220 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000086580.2	WNT9B-201	2363	377aa	ENSBTAP00000061815.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M1A0	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,
ENSBTAT00000003449.6	WNT9B-202	2303	357aa	ENSBTAP00000003449.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N7G3	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,

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Summary

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