FLCN gene homepage

General information
Gene symbol FLCN
Gene name folliculin
Chromosome 17
Chromosomal band p11.2
Imprinted Unknown
Genomic reference LRG_325
Transcript reference NM_144606.5, NM_144997.5
Associated with diseases BHD, PSP
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 191
Unique public DNA variants reported 60
Individuals with public variants 210
Hidden variants 0
Date created May 20, 2020
Date last updated November 15, 2020
Version FLCN:201115

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 27310
Entrez Gene 201163
PubMed articles FLCN
OMIM - Gene 607273
OMIM - Diseases BHD (Birt-Hogg-Dube syndrome)
PSP (Pneumothorax, primary spontaneous)

Active transcripts




NCBI ID     

NCBI Protein ID     

00000087 17 transcript variant 1 NM_144997.5 NP_659434.2 191
00000088 17 transcript variant 2 NM_144606.5 NP_653207.1 167

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