CXorf38 chromosome X open reading frame 38

Information
Symbol
CXorf38
Type
protein-coding
Description
chromosome X open reading frame 38
Entrez Gene ID
159013
Genome
hg19
Position
chrX:40,486,173-40,506,813
Genome
hg38
Position
chrX:40,626,921-40,647,561
MIM
301117 OMIM
HGNC
HGNC:28589 HGNC
Ensembl
ENSG00000185753 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
2
4
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
MIM 301117 OMIM
HGNC HGNC:28589 HGNC
Ensembl ENSG00000185753 Ensembl
AllianceGenome HGNC:28589
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378426.5 hg38 chrX 40,626,921 40,647,554 20,634
ENST00000327877.10 hg38 chrX 40,626,921 40,647,561 20,641
ENST00000378421.1 hg38 chrX 40,629,937 40,647,521 17,585
ENST00000378426.5 hg19 chrX 40,486,173 40,506,806 20,634
ENST00000327877.10 hg19 chrX 40,486,173 40,506,813 20,641
ENST00000378421.1 hg19 chrX 40,489,189 40,506,773 17,585
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