SLC16A5 solute carrier family 16 member 5

Information
Symbol
SLC16A5
Type
protein-coding
Description
solute carrier family 16 member 5
Entrez Gene ID
9121
Genome
hg19
Position
chr17:73,085,033-73,102,246
Genome
hg38
Position
chr17:75,088,938-75,106,151
MIM
603879 OMIM
HGNC
HGNC:10926 HGNC
Ensembl
ENSG00000170190 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
74
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 :
Filtering :
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 MCT5
SYNONYM MCT6
MIM 603879 OMIM
HGNC HGNC:10926 HGNC
Ensembl ENSG00000170190 Ensembl
AllianceGenome HGNC:10926
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000450736.6 hg38 chr17 75,088,938 75,106,151 17,214
ENST00000538213.6 hg38 chr17 75,093,287 75,104,410 11,124
ENST00000329783.9 hg38 chr17 75,087,954 75,106,162 18,209
ENST00000580123.5 hg38 chr17 75,087,727 75,106,162 18,436
ENST00000580123.5 hg19 chr17 73,083,822 73,102,257 18,436
ENST00000329783.9 hg19 chr17 73,084,049 73,102,257 18,209
ENST00000450736.6 hg19 chr17 73,085,033 73,102,246 17,214
ENST00000538213.6 hg19 chr17 73,089,382 73,100,505 11,124
Genome browser