FLCN

GENE INFORMATION

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Gene name

FLCN (HGNC Symbol)

Synonyms

BHD, MGC17998, MGC23445

Description

folliculin (HGNC Symbol)

Entrez gene summary

This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

Chromosome

17 (Chromosome progress)

Cytoband

p11.2

Chromosome location (bp)

17115526 - 17140502

Ensembl

ENSG00000154803 (version 73.37)

Entrez gene

201163

UniProt

Q8NFG4 (UniProt - Evidence at protein level)

neXtProt

NX_Q8NFG4

Antibodypedia

FLCN antibodies
 

PROTEIN VIEW

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FLCN-001
 
FLCN-002
 
FLCN-006
 
FLCN-008
 
 
 
 
 

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)

FLCN-001 ENSP00000285071
ENST00000285071
Q8NFG4
Show all »
Show » Show » 579 64.5 No 0
FLCN-002 ENSP00000373821
ENST00000389169
Q8NFG4
Show all »
Show » Show » 342 37.7 No 0
FLCN-006 ENSP00000410410
ENST00000417064
C9J4C4
Show all »
Show » 153 17.2 No 0
FLCN-008 ENSP00000463970
ENST00000461699
J3QQZ7
Show all »
Show » 37 4 No 0