SLC2A10 solute carrier family 2 member 10

Information
Symbol
SLC2A10
Type
protein-coding
Description
solute carrier family 2 member 10
Entrez Gene ID
81031
Genome
hg19
Position
chr20:45,338,288-45,364,986
Genome
hg38
Position
chr20:46,709,649-46,736,347
MIM
606145 OMIM
HGNC
HGNC:13444 HGNC
Ensembl
ENSG00000197496 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 38
Likely pathogenic 0 38
Benign 0 86
Likely benign 0 396
Conflicting classifications of pathogenicity 0 106
not provided 1 10
Uncertain significance 0 560
Ranking
ClinVar
0
0
322
746
6
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 ATORS
SYNONYM ATS
SYNONYM GLUT10
MIM 606145 OMIM
HGNC HGNC:13444 HGNC
Ensembl ENSG00000197496 Ensembl
AllianceGenome HGNC:13444
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000359271.4 hg38 chr20 46,709,649 46,736,347 26,699
ENST00000486000.2 hg38 chr20 46,709,699 46,710,437 739
ENST00000359271.4 hg19 chr20 45,338,288 45,364,986 26,699
ENST00000486000.2 hg19 chr20 45,338,338 45,339,076 739
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