SLC22A10 solute carrier family 22 member 10

Information
Symbol
SLC22A10
Type
protein-coding
Description
solute carrier family 22 member 10
Entrez Gene ID
387775
Genome
hg19
Position
chr11:63,057,375-63,079,255
Genome
hg38
Position
chr11:63,289,903-63,311,783
MIM
607580 OMIM
HGNC
HGNC:18057 HGNC
Ensembl
ENSG00000184999 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
60
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 :
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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 OAT5
SYNONYM hOAT5
MIM 607580 OMIM
HGNC HGNC:18057 HGNC
Ensembl ENSG00000184999 Ensembl
AllianceGenome HGNC:18057
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000526800.1 hg38 chr11 63,290,308 63,311,101 20,794
ENST00000682643.1 hg38 chr11 63,268,022 63,311,221 43,200
ENST00000332793.11 hg38 chr11 63,289,903 63,311,783 21,881
ENST00000682643.1 hg19 chr11 63,035,494 63,078,693 43,200
ENST00000332793.11 hg19 chr11 63,057,375 63,079,255 21,881
ENST00000526800.1 hg19 chr11 63,057,780 63,078,573 20,794
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