Description

forkhead box B2 [Source:HGNC Symbol;Acc:HGNC:23315]

Synonyms

bA159H20.4

Location
INSDC coordinates

chromosome:GRCh38:CM000671.2:77019655:77020953:1

About this gene

This gene has 1 transcript (splice variant), 70 orthologues, 23 paralogues, is a member of 1 Ensembl protein family and is associated with 46 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
FOXB2-001ENST000003767081299432aaENSP00000365898
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS35045Q5VYV0 NM_001013735
NP_001013757
TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays