FAM9C family with sequence similarity 9 member C

Information
Symbol
FAM9C
Type
protein-coding
Description
family with sequence similarity 9 member C
Entrez Gene ID
171484
Genome
hg19
Position
chrX:13,053,831-13,062,721
Genome
hg38
Position
chrX:13,035,712-13,044,602
MIM
300479 OMIM
HGNC
HGNC:18405 HGNC
Ensembl
ENSG00000187268 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 7 0
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
20
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
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 TEX39C
MIM 300479 OMIM
HGNC HGNC:18405 HGNC
Ensembl ENSG00000187268 Ensembl
AllianceGenome HGNC:18405
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000333995.7 hg38 chrX 13,035,712 13,044,602 8,891
ENST00000380625.8 hg38 chrX 13,035,617 13,044,620 9,004
ENST00000542843.5 hg38 chrX 13,035,618 13,044,682 9,065
ENST00000380625.8 hg19 chrX 13,053,736 13,062,739 9,004
ENST00000542843.5 hg19 chrX 13,053,737 13,062,801 9,065
ENST00000333995.7 hg19 chrX 13,053,831 13,062,721 8,891
Genome browser