FEM1B fem-1 homolog B

Information
Symbol
FEM1B
Type
protein-coding
Description
fem-1 homolog B
Entrez Gene ID
10116
Genome
hg19
Position
chr15:68,570,083-68,588,200
Genome
hg38
Position
chr15:68,277,745-68,295,862
MIM
613539 OMIM
HGNC
HGNC:3649 HGNC
Ensembl
ENSG00000169018 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
28
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
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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 F1A-ALPHA
SYNONYM F1AA
SYNONYM FEM1-beta
MIM 613539 OMIM
HGNC HGNC:3649 HGNC
Ensembl ENSG00000169018 Ensembl
AllianceGenome HGNC:3649
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000306917.5 hg38 chr15 68,277,745 68,295,862 18,118
ENST00000306917.5 hg19 chr15 68,570,083 68,588,200 18,118
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