SLC16A11 solute carrier family 16 member 11

Information
Symbol
SLC16A11
Type
protein-coding
Description
solute carrier family 16 member 11
Entrez Gene ID
162515
Genome
hg19
Position
chr17:6,944,940-6,947,411
Genome
hg38
Position
chr17:7,041,621-7,044,092
MIM
615765 OMIM
HGNC
HGNC:23093 HGNC
Ensembl
ENSG00000174326 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 78
Ranking
ClinVar
0
0
0
82
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 MCT 11
SYNONYM MCT11
MIM 615765 OMIM
HGNC HGNC:23093 HGNC
Ensembl ENSG00000174326 Ensembl
AllianceGenome HGNC:23093
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000574600.3 hg38 chr17 7,041,621 7,044,092 2,472
ENST00000662352.3 hg38 chr17 7,041,621 7,044,092 2,472
ENST00000673828.2 hg38 chr17 7,041,621 7,044,092 2,472
ENST00000574600.3 hg19 chr17 6,944,940 6,947,411 2,472
ENST00000662352.3 hg19 chr17 6,944,940 6,947,411 2,472
ENST00000673828.2 hg19 chr17 6,944,940 6,947,411 2,472
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