Summary
Splice variantsTranscript comparisonGene allelesSequenceSecondary StructureComparative GenomicsOntologiesPhenotypesGenetic VariationGene expressionPathwayMolecular interactionsRegulationExternal referencesSupporting evidenceID History.
wingless-type MMTV integration site family, member 8B [Source:HGNC Symbol;Acc:12789]
Chromosome 10: 102,222,798-102,243,501 forward strand.
GRCh37:CM000672.1
This gene has 1 transcript (splice variant) and 5 paralogues.
.
WNT8B (HGNC Symbol)
This gene has proteins that correspond to the following UniProtKB identifiers: Q93098
This gene is a member of the Human CCDS set: CCDS7494.1
ENSG00000075290.7
This gene maps to 100,463,041-100,483,744 in GRCh38 coordinates.
Protein coding
Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.
This gene corresponds to the following database identifiers:
| Havana gene: |
OTTHUMG00000018912 (version 1) |
|---|
Go to Region in Detail for more tracks and navigation options (e.g. zooming)
The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Change track style:
URL to turn this track on
Copy the above url to force this track to be turned on
Click on the star to add/remove this track from your favourites
Click on the cross to turn the track off
Click to highlight/unhighlight this track
The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Change track style:
URL to turn this track on
Copy the above url to force this track to be turned on
Click on the star to add/remove this track from your favourites
Click on the cross to turn the track off
Click to highlight/unhighlight this track
URL to turn this track on
Copy the above url to force this track to be turned on
Click on the star to add/remove this track from your favourites
Click on the cross to turn the track off
Click to highlight/unhighlight this track
.
Expanded with labels