SLC16A6 solute carrier family 16 member 6

Information
Symbol
SLC16A6
Type
protein-coding
Description
solute carrier family 16 member 6
Entrez Gene ID
9120
Genome
hg19
Position
chr17:66,263,167-66,287,257
Genome
hg38
Position
chr17:68,267,026-68,291,116
MIM
603880 OMIM
HGNC
HGNC:10927 HGNC
Ensembl
ENSG00000108932 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
58
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 MCT6
SYNONYM MCT7
MIM 603880 OMIM
HGNC HGNC:10927 HGNC
Ensembl ENSG00000108932 Ensembl
AllianceGenome HGNC:10927
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000327268.8 hg38 chr17 68,267,026 68,291,116 24,091
ENST00000580666.6 hg38 chr17 68,267,026 68,291,127 24,102
ENST00000327268.8 hg19 chr17 66,263,167 66,287,257 24,091
ENST00000580666.6 hg19 chr17 66,263,167 66,287,268 24,102
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