FANCC

GENERAL INFORMATION

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Gene name

FANCC

Gene description

Fanconi anemia, complementation group C

Protein class

Cancer-related genes
Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues displayed moderate cytoplasmic positivity, combined with cases of nuclear staining. Strong staining was observed in gall bladder and renal tubuli. Lymphoid tissues were generally negative or weakly stained.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
CAB017793
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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

Skin



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

FANCC (HGNC Symbol)

Synonyms

FA3, FAC, FACC

Description

Fanconi anemia, complementation group C (HGNC Symbol)

Entrez gene summary

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group C. [provided by RefSeq, Jul 2008]

Chromosome

9

Cytoband

q22.32

Chromosome location (bp)

95099054 - 95317709

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000158169 (version 78.38)

Entrez gene

2176

UniProt

Q00597 (UniProt - Evidence at protein level)

neXtProt

NX_Q00597

Antibodypedia

FANCC antibodies


PROTEIN BROWSER

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ENST00000289081
 
ENST00000375305
 
ENST00000433829
 
ENST00000490972
 
 
 
 


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)

FANCC-001 ENSP00000289081
ENST00000289081
Q00597
Show all »
Show » Show » 558 63.4 No 0
FANCC-002 ENSP00000364454
ENST00000375305
Q00597
Show all »
Show » Show » 558 63.4 No 0
FANCC-004 ENSP00000406908
ENST00000433829
B1ALR7
Show all »
Show » Show » 150 17.3 No 0
FANCC-201 ENSP00000479931
ENST00000490972
B1ALR7
Show all »
Show » Show » 492 56.1 No 0