SLC2A13 solute carrier family 2 member 13

Information
Symbol
SLC2A13
Type
protein-coding
Description
solute carrier family 2 member 13
Entrez Gene ID
114134
Genome
hg19
Position
chr12:40,148,827-40,499,883
Genome
hg38
Position
chr12:39,755,025-40,106,081
MIM
611036 OMIM
HGNC
HGNC:15956 HGNC
Ensembl
ENSG00000151229 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 2 0
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
64
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 HMIT
MIM 611036 OMIM
HGNC HGNC:15956 HGNC
Ensembl ENSG00000151229 Ensembl
AllianceGenome HGNC:15956
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380858.1 hg38 chr12 39,949,490 40,106,089 156,600
ENST00000280871.9 hg38 chr12 39,755,025 40,106,081 351,057
ENST00000280871.9 hg19 chr12 40,148,827 40,499,883 351,057
ENST00000380858.1 hg19 chr12 40,343,292 40,499,891 156,600
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