SLC16A8 solute carrier family 16 member 8

Information
Symbol
SLC16A8
Type
protein-coding
Description
solute carrier family 16 member 8
Entrez Gene ID
23539
Genome
hg19
Position
chr22:38,474,144-38,480,191
Genome
hg38
Position
chr22:38,078,137-38,084,184
MIM
610409 OMIM
HGNC
HGNC:16270 HGNC
Ensembl
ENSG00000100156 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
not provided 0 2
Uncertain significance 0 86
Ranking
ClinVar
0
0
0
98
2
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 :
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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 MCT3
SYNONYM REMP
MIM 610409 OMIM
HGNC HGNC:16270 HGNC
Ensembl ENSG00000100156 Ensembl
AllianceGenome HGNC:16270
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000681075.2 hg38 chr22 38,078,137 38,084,184 6,048
ENST00000320521.10 hg38 chr22 38,078,134 38,083,355 5,222
ENST00000320521.10 hg19 chr22 38,474,141 38,479,362 5,222
ENST00000681075.2 hg19 chr22 38,474,144 38,480,191 6,048
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