FANCA

GENERAL INFORMATION

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Gene name

FANCA

Gene description

Fanconi anemia, complementation group A

Protein class

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

Predicted localization

Intracellular,Membrane

Number of transcripts

10
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Tissue enriched (testis)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (testis)

Organ

Expression



GENE INFORMATION

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Gene name

FANCA (HGNC Symbol)

Synonyms

FA-H, FAA, FACA, FAH, FANCH

Description

Fanconi anemia, complementation group A (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 A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008]

Chromosome

16

Cytoband

q24.3

Chromosome location (bp)

89737549 - 89816657

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000187741 (version 78.38)

Entrez gene

2175

UniProt

O15360 (UniProt - Evidence at protein level)

neXtProt

NX_O15360

Antibodypedia

FANCA antibodies


PROTEIN BROWSER

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ENST00000389301
 
ENST00000389302
 
ENST00000534992
 
ENST00000543736
 
ENST00000561722
 
ENST00000563673
 
ENST00000564475
 
ENST00000564870
 
ENST00000567879
 
ENST00000568369
 
 
 
 


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)

FANCA-001 ENSP00000373952
ENST00000389301
O15360
Show all »
Show » Show » 1455 162.8 No 1
FANCA-002 ENSP00000456829
ENST00000568369
O15360
Show all »
Show » Show » 1424 159.1 No 1
FANCA-003 ENSP00000373953
ENST00000389302
O15360
Show all »
Show » Show » 297 33 No 0
FANCA-004 ENSP00000443409
ENST00000543736
Q0VAP4
Show all »
Show » 265 29.2 No 0
FANCA-006 ENSP00000456443
ENST00000563673
H3BRX3
Show all »
Show » 316 35 No 0
FANCA-026 ENSP00000457006
ENST00000567879
H3BT40
Show all »
Show » 214 23.8 No 1
FANCA-027 ENSP00000456608
ENST00000561722
H3BSA3
Show all »
Show » 195 21.4 No 0
FANCA-028 ENSP00000454977
ENST00000564475
Show » 240 26.6 No 0
FANCA-030 ENSP00000456481
ENST00000564870
Show » 153 17.2 No 0
FANCA-201 ENSP00000443675
ENST00000534992
F5H8D5
Show all »
Show » 302 33.4 No 0