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FOXB2 forkhead box B2 [ Homo sapiens (human) ]

Gene ID: 442425, updated on 12-Oct-2019

Summary

Official Symbol
FOXB2provided by HGNC
Official Full Name
forkhead box B2provided by HGNC
Primary source
HGNC:HGNC:23315
See related
Ensembl:ENSG00000204612
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
bA159H20.4
Orthologs

Genomic context

See FOXB2 in Genome Data Viewer
Location:
9q21.2
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (77019655..77020953)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (79634571..79635869)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene prune homolog 2 with BCH domain Neighboring gene prostate cancer associated 3 Neighboring gene LYPLA2 pseudogene 3 Neighboring gene uncharacterized LOC105376096 Neighboring gene ATP synthase membrane subunit f pseudogene 3 Neighboring gene replication factor C 5 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
DNA-binding transcription factor activity, RNA polymerase II-specific IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
DNA-binding transcription factor activity, RNA polymerase II-specific ISA
Inferred from Sequence Alignment
more info
 
sequence-specific DNA binding IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
anatomical structure morphogenesis IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
cell differentiation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
nuclear chromatin ISA
Inferred from Sequence Alignment
more info
 
nucleus IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

NCBI Reference Sequences (RefSeq)

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001013735.1NP_001013757.1  forkhead box protein B2

    See identical proteins and their annotated locations for NP_001013757.1

    Status: VALIDATED

    Source sequence(s)
    AL353637
    Consensus CDS
    CCDS35045.1
    UniProtKB/Swiss-Prot
    Q5VYV0
    Related
    ENSP00000365898.1, ENST00000376708.1
    Conserved Domains (1) summary
    smart00339
    Location:13101
    FH; FORKHEAD

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    77019655..77020953
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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