SEMA4F ssemaphorin 4F

Information
Symbol
SEMA4F
Type
protein-coding
Description
ssemaphorin 4F
Entrez Gene ID
10505
Genome
hg19
Position
chr2:74,881,374-74,910,968
Genome
hg38
Position
chr2:74,654,247-74,683,841
MIM
603706 OMIM
HGNC
HGNC:10734 HGNC
Ensembl
ENSG00000135622 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 94
Ranking
ClinVar
0
0
0
104
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
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 M-SEMA
SYNONYM PRO2353
SYNONYM S4F
SYNONYM SEMAM
SYNONYM SEMAW
SYNONYM m-Sema-M
MIM 603706 OMIM
HGNC HGNC:10734 HGNC
Ensembl ENSG00000135622 Ensembl
AllianceGenome HGNC:10734
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000611975.4 hg38 chr2 74,654,228 74,683,853 29,626
ENST00000357877.7 hg38 chr2 74,654,247 74,683,841 29,595
ENST00000339773.9 hg38 chr2 74,654,280 74,680,441 26,162
ENST00000611975.4 hg19 chr2 74,881,355 74,910,980 29,626
ENST00000357877.7 hg19 chr2 74,881,374 74,910,968 29,595
ENST00000339773.9 hg19 chr2 74,881,407 74,907,568 26,162
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