SLC22A8 solute carrier family 22 member 8

Information
Symbol
SLC22A8
Type
protein-coding
Description
solute carrier family 22 member 8
Entrez Gene ID
9376
Genome
hg19
Position
chr11:62,760,296-62,783,313
Genome
hg38
Position
chr11:62,992,824-63,015,841
MIM
607581 OMIM
HGNC
HGNC:10972 HGNC
Ensembl
ENSG00000149452 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 10
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
62
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 OAT3
MIM 607581 OMIM
HGNC HGNC:10972 HGNC
Ensembl ENSG00000149452 Ensembl
AllianceGenome HGNC:10972
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000311438.12 hg38 chr11 62,993,237 63,014,958 21,722
ENST00000535878.5 hg38 chr11 62,993,228 63,015,810 22,583
ENST00000336232.7 hg38 chr11 62,992,824 63,015,841 23,018
ENST00000430500.6 hg38 chr11 62,993,237 63,015,839 22,603
ENST00000545207.5 hg38 chr11 62,993,083 63,015,815 22,733
ENST00000336232.7 hg19 chr11 62,760,296 62,783,313 23,018
ENST00000545207.5 hg19 chr11 62,760,555 62,783,287 22,733
ENST00000535878.5 hg19 chr11 62,760,700 62,783,282 22,583
ENST00000311438.12 hg19 chr11 62,760,709 62,782,430 21,722
ENST00000430500.6 hg19 chr11 62,760,709 62,783,311 22,603
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