Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: WNT9B ENSOCUG00000021211

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Description

Wnt family member 9B [Source:HGNC Symbol;Acc:HGNC:12779]

Location

Chromosome 19: 45,782,094-45,834,267 reverse strand.

OryCun2.0:CM000808.1

About this gene

This gene has 2 transcripts (splice variants), 220 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000059490.1	WNT9B-202	2615	431aa	ENSOCUP00000045781.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000029313.3	WNT9B-201	1588	377aa	ENSOCUP00000016539.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1THX7	-

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Summary

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