SLC5A12 solute carrier family 5 member 12

Information
Symbol
SLC5A12
Type
protein-coding
Description
solute carrier family 5 member 12
Entrez Gene ID
159963
Genome
hg19
Position
chr11:26,688,567-26,743,607
Genome
hg38
Position
chr11:26,667,020-26,722,060
MIM
612455 OMIM
HGNC
HGNC:28750 HGNC
Ensembl
ENSG00000148942 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 64
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 SMCT2
MIM 612455 OMIM
HGNC HGNC:28750 HGNC
Ensembl ENSG00000148942 Ensembl
AllianceGenome HGNC:28750
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000396005.8 hg38 chr11 26,667,020 26,722,060 55,041
ENST00000280467.10 hg38 chr11 26,691,658 26,721,999 30,342
ENST00000396005.8 hg19 chr11 26,688,567 26,743,607 55,041
ENST00000280467.10 hg19 chr11 26,713,205 26,743,546 30,342
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