XYLT2 xylosyltransferase 2

Information
Symbol
XYLT2
Type
protein-coding
Description
xylosyltransferase 2
Entrez Gene ID
64132
Genome
hg19
Position
chr17:48,423,487-48,438,546
Genome
hg38
Position
chr17:50,346,126-50,361,185
MIM
608125 OMIM
HGNC
HGNC:15517 HGNC
Ensembl
ENSG00000015532 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 10
Benign 0 88
Likely benign 0 292
Conflicting classifications of pathogenicity 0 18
Uncertain significance 0 316
Ranking
ClinVar
0
0
120
580
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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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 PXYLT2
SYNONYM SOS
SYNONYM XT-II
SYNONYM XT2
SYNONYM xylT-II
MIM 608125 OMIM
HGNC HGNC:15517 HGNC
Ensembl ENSG00000015532 Ensembl
AllianceGenome HGNC:15517
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000017003.7 hg38 chr17 50,346,126 50,361,185 15,060
ENST00000507602.5 hg38 chr17 50,346,135 50,363,138 17,004
ENST00000017003.7 hg19 chr17 48,423,487 48,438,546 15,060
ENST00000507602.5 hg19 chr17 48,423,496 48,440,499 17,004
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