CXorf58 chromosome X open reading frame 58

Information
Symbol
CXorf58
Type
protein-coding
Description
chromosome X open reading frame 58
Entrez Gene ID
254158
Genome
hg19
Position
chrX:23,926,123-23,957,626
Genome
hg38
Position
chrX:23,908,006-23,939,509
HGNC
HGNC:26356 HGNC
Ensembl
ENSG00000165182 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
8
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
HGNC HGNC:26356 HGNC
Ensembl ENSG00000165182 Ensembl
AllianceGenome HGNC:26356
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000379211.8 hg38 chrX 23,908,006 23,939,509 31,504
ENST00000648352.1 hg38 chrX 23,908,054 23,939,509 31,456
ENST00000379211.8 hg19 chrX 23,926,123 23,957,626 31,504
ENST00000648352.1 hg19 chrX 23,926,171 23,957,626 31,456
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