FAM223B family with sequence similarity 223 member B

Information
Symbol
FAM223B
Type
ncRNA
Description
family with sequence similarity 223 member B
Entrez Gene ID
286967
Genome
hg19
Position
chrX:153,860,736-153,861,445
Genome
hg38
Position
chrX:154,632,470-154,633,182
HGNC
HGNC:34048 HGNC
Ensembl
ENSG00000272681 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
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 CXorf52
SYNONYM CXorf52B
SYNONYM LINC00204B
SYNONYM NCRNA00204B
HGNC HGNC:34048 HGNC
Ensembl ENSG00000272681 Ensembl
AllianceGenome HGNC:34048
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598177.2 hg38 chrX 154,632,470 154,633,182 713
ENST00000598177.2 hg19 chrX 153,860,736 153,861,445 710
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