FLCN folliculin

Information
Symbol
FLCN
Type
protein-coding
Description
folliculin
Entrez Gene ID
201163
Genome
hg19
Position
chr17:17,115,526-17,140,482
Genome
hg38
Position
chr17:17,212,212-17,237,168
MIM
607273 OMIM
HGNC
HGNC:27310 HGNC
Ensembl
ENSG00000154803 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 9 612
Likely pathogenic 1 152
Benign 4 186
Likely benign 1 1,478
Conflicting classifications of pathogenicity 0 370
not provided 8 2
Uncertain significance 16 1,832
Ranking
ClinVar
0
0
1,526
2,498
98
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM BHD
SYNONYM DENND8B
SYNONYM FLCL
MIM 607273 OMIM
HGNC HGNC:27310 HGNC
Ensembl ENSG00000154803 Ensembl
AllianceGenome HGNC:27310
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000389169.9 hg38 chr17 17,221,171 17,237,139 15,969
ENST00000285071.9 hg38 chr17 17,212,212 17,237,168 24,957
ENST00000285071.9 hg19 chr17 17,115,526 17,140,482 24,957
ENST00000389169.9 hg19 chr17 17,124,485 17,140,453 15,969
KeyValue
strand-
UniProtTSG
start17,115,526
Gene SymbolFLCN
Entrez GeneId201,163
Chr Band17p11.2
end17,140,501
chrchr17
Namefolliculin
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