FANCB

GENERAL INFORMATION

? »

Gene name

FANCB

Gene description

Fanconi anemia, complementation group B

Protein class

Disease related genes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Mixed
GTEx:Not detected

Protein evidence

Evidence at protein level

Protein localization

Exocrine pancreas showed a strong cytoplasmic staining. Glandular cells in salivary glands, gastrointestinal tract, hepatocytes and renal tubules were moderately positive. Remaining normal tissues were weakly stained or negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA003124
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
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

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Not detected

Organ

Expression



GENE INFORMATION

? »

Gene name

FANCB (HGNC Symbol)

Synonyms

FAAP95, FAB, FLJ34064

Description

Fanconi anemia, complementation group B (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 B. Alternative splicing results in two transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]

Chromosome

X

Cytoband

p22.2

Chromosome location (bp)

14843407 - 14873069

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000181544 (version 78.38)

Entrez gene

2187

UniProt

Q8NB91 (UniProt - Evidence at protein level)

neXtProt

NX_Q8NB91

Antibodypedia

FANCB antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000324138
 
ENST00000398334
 
ENST00000452869
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

FANCB-001 ENSP00000326819
ENST00000324138
Q8NB91
Show all »
Show » Show » 859 97.7 No 0
FANCB-002 ENSP00000397849
ENST00000452869
C9J5X9
Show all »
Show » 818 93.1 No 0
FANCB-201 ENSP00000381378
ENST00000398334
Q8NB91
Show all »
Show » Show » 859 97.7 No 0