SLC16A13 solute carrier family 16 member 13

Information
Symbol
SLC16A13
Type
protein-coding
Description
solute carrier family 16 member 13
Entrez Gene ID
201232
Genome
hg19
Position
chr17:6,939,334-6,943,436
Genome
hg38
Position
chr17:7,036,015-7,040,117
HGNC
HGNC:31037 HGNC
Ensembl
ENSG00000174327 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
36
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 :
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 MCT13
HGNC HGNC:31037 HGNC
Ensembl ENSG00000174327 Ensembl
AllianceGenome HGNC:31037
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308027.7 hg38 chr17 7,036,015 7,040,117 4,103
ENST00000308027.7 hg19 chr17 6,939,334 6,943,436 4,103
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