SLC22A9 solute carrier family 22 member 9

Information
Symbol
SLC22A9
Type
protein-coding
Description
solute carrier family 22 member 9
Entrez Gene ID
114571
Genome
hg19
Position
chr11:63,137,257-63,177,766
Genome
hg38
Position
chr11:63,369,785-63,410,294
MIM
607579 OMIM
HGNC
HGNC:16261 HGNC
Ensembl
ENSG00000149742 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
46
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 HOAT4
SYNONYM OAT4
SYNONYM OAT7
SYNONYM UST3H
SYNONYM ust3
MIM 607579 OMIM
HGNC HGNC:16261 HGNC
Ensembl ENSG00000149742 Ensembl
AllianceGenome HGNC:16261
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000279178.4 hg38 chr11 63,369,785 63,410,294 40,510
ENST00000279178.4 hg19 chr11 63,137,257 63,177,766 40,510
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