FIGLA folliculogenesis specific bHLH transcription factor

Information
Symbol
FIGLA
Type
protein-coding
Description
folliculogenesis specific bHLH transcription factor
Entrez Gene ID
344018
Genome
hg19
Position
chr2:71,004,442-71,017,775
Genome
hg38
Position
chr2:70,777,310-70,790,643
MIM
608697 OMIM
HGNC
HGNC:24669 HGNC
Ensembl
ENSG00000183733 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 4
Benign 6 38
Likely benign 0 16
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 38
Ranking
ClinVar
0
0
18
74
8
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 BHLHC8
SYNONYM FIGALPHA
SYNONYM POF6
MIM 608697 OMIM
HGNC HGNC:24669 HGNC
Ensembl ENSG00000183733 Ensembl
AllianceGenome HGNC:24669
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000332372.6 hg38 chr2 70,777,310 70,790,643 13,334
ENST00000332372.6 hg19 chr2 71,004,442 71,017,775 13,334
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