F9 coagulation factor IX

Information
Symbol
F9
Type
protein-coding
Description
coagulation factor IX
Entrez Gene ID
2158
Genome
hg19
Position
chrX:138,612,898-138,645,618
Genome
hg38
Position
chrX:139,530,739-139,563,459
MIM
300746 OMIM
HGNC
HGNC:3551 HGNC
Ensembl
ENSG00000101981 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 340
Likely pathogenic 0 154
Benign 0 80
Likely benign 0 358
Benign; association 0 2
Conflicting classifications of pathogenicity 0 16
not provided 6 0
Uncertain significance 0 126
Ranking
ClinVar
0
36
96
754
140
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 F9 p22
SYNONYM FIX
SYNONYM HEMB
SYNONYM P19
SYNONYM PTC
SYNONYM THPH8
MIM 300746 OMIM
HGNC HGNC:3551 HGNC
Ensembl ENSG00000101981 Ensembl
AllianceGenome HGNC:3551
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000218099.7 hg38 chrX 139,530,739 139,563,459 32,721
ENST00000394090.2 hg38 chrX 139,530,765 139,562,071 31,307
ENST00000218099.7 hg19 chrX 138,612,898 138,645,618 32,721
ENST00000394090.2 hg19 chrX 138,612,924 138,644,230 31,307
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