FOXP2

GENERAL INFORMATION

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Gene name

FOXP2

Gene description

Forkhead box P2

Protein class

Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

13
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Tissue enhanced (colon)

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous nuclear expression.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 3 antibodies.
HPA000382 , HPA000383 , CAB011488
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (colon)

Organ

Expression



GENE INFORMATION

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Gene name

FOXP2 (HGNC Symbol)

Synonyms

CAGH44, SPCH1, TNRC10

Description

Forkhead box P2 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]

Chromosome

7

Cytoband

q31.1

Chromosome location (bp)

114086327 - 114693772

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000128573 (version 78.38)

Entrez gene

93986

UniProt

O15409 (UniProt - Evidence at protein level)

neXtProt

NX_O15409

Antibodypedia

FOXP2 antibodies


PROTEIN BROWSER

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ENST00000350908
 
ENST00000360232
 
ENST00000378237
 
ENST00000390668
 
ENST00000393489
 
ENST00000393491
 
ENST00000393494
 
ENST00000393495
 
ENST00000393498
 
ENST00000403559
 
ENST00000408937
 
ENST00000452963
 
ENST00000462331
 
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PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

FOXP2-001 ENSP00000265436
ENST00000350908
O15409
Show all »
Show » Show » 715 79.9 No 0
FOXP2-004 ENSP00000386200
ENST00000408937
O15409
Show all »
Show » Show » 740 82.6 No 0
FOXP2-005 ENSP00000377135
ENST00000393498
A8MUV4
Show all »
Show » Show » 694 77.2 No 0
FOXP2-007 ENSP00000418100
ENST00000462331
Q75MZ5
Show all »
Show » 67 7.2 No 0
FOXP2-010 ENSP00000367482
ENST00000378237
O15409
Show all »
Show » Show » 365 41 No 0
FOXP2-014 ENSP00000377132
ENST00000393494
O15409
Show all »
Show » Show » 715 79.9 No 0
FOXP2-015 ENSP00000409826
ENST00000452963
C9JQP8
Show all »
Show » 205 23.7 No 0
FOXP2-016 ENSP00000375084
ENST00000390668
Q8N6B5
Show all »
Show » 456 51.3 No 0
FOXP2-017 ENSP00000353367
ENST00000360232
O15409
Show all »
Show » Show » 432 48.8 No 0
FOXP2-018 ENSP00000377133
ENST00000393495
A8MTU2
Show all »
Show » 171 18.5 No 0
FOXP2-020 ENSP00000377129
ENST00000393489
O15409
Show all »
Show » Show » 623 70.1 No 0
FOXP2-201 ENSP00000377130
ENST00000393491
Q0PRL4
Show all »
Show » Show » 530 59.9 No 0
FOXP2-202 ENSP00000385069
ENST00000403559
O15409
Show all »
Show » Show » 732 81.8 No 0