FAM199X family with sequence similarity 199, X-linked

Information
Symbol
FAM199X
Type
protein-coding
Description
family with sequence similarity 199, X-linked
Entrez Gene ID
139231
Genome
hg19
Position
chrX:103,411,134-103,440,583
Genome
hg38
Position
chrX:104,166,453-104,195,902
HGNC
HGNC:25195 HGNC
Ensembl
ENSG00000123575 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
10
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 CXorf39
HGNC HGNC:25195 HGNC
Ensembl ENSG00000123575 Ensembl
AllianceGenome HGNC:25195
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000493442.2 hg38 chrX 104,166,453 104,195,902 29,450
ENST00000493442.2 hg19 chrX 103,411,134 103,440,583 29,450
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