FOXC1

GENERAL INFORMATION

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Gene name

FOXC1

Gene description

Forkhead box C1

Protein class

Disease related genes
Plasma proteins
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (salivary gland)
GTEx:Tissue enhanced (salivary gland)

Protein evidence

Evidence at protein level

Protein localization

Nuclear and cytoplasmic expression in a majority of the tissues with highest expression in salivary gland and CNS.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Uncertain based on 1 antibody.
HPA040670
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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
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Salivary gland

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (salivary gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (salivary gland)

Organ

Expression



GENE INFORMATION

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Gene name

FOXC1 (HGNC Symbol)

Synonyms

ARA, FKHL7, FREAC3, IGDA, IHG1, IRID1

Description

Forkhead box C1 (HGNC Symbol)

Entrez gene summary

This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly. [provided by RefSeq, Jul 2008]

Chromosome

6

Cytoband

p25.3

Chromosome location (bp)

1609972 - 1613897

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000054598 (version 78.38)

Entrez gene

2296

UniProt

Q12948 (UniProt - Evidence at protein level)

neXtProt

NX_Q12948

Antibodypedia

FOXC1 antibodies


PROTEIN BROWSER

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ENST00000380874
 
 
 
 


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)

FOXC1-001 ENSP00000370256
ENST00000380874
Q12948
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