SLC22A11 solute carrier family 22 member 11

Information
Symbol
SLC22A11
Type
protein-coding
Description
solute carrier family 22 member 11
Entrez Gene ID
55867
Genome
hg19
Position
chr11:64,323,413-64,340,347
Genome
hg38
Position
chr11:64,555,941-64,572,875
MIM
607097 OMIM
HGNC
HGNC:18120 HGNC
Ensembl
ENSG00000168065 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 66
Ranking
ClinVar
0
0
0
78
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 OAT4
SYNONYM hOAT4
MIM 607097 OMIM
HGNC HGNC:18120 HGNC
Ensembl ENSG00000168065 Ensembl
AllianceGenome HGNC:18120
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000301891.9 hg38 chr11 64,555,941 64,572,875 16,935
ENST00000377581.7 hg38 chr11 64,555,956 64,571,527 15,572
ENST00000377585.7 hg38 chr11 64,555,690 64,571,527 15,838
ENST00000377585.7 hg19 chr11 64,323,162 64,338,999 15,838
ENST00000301891.9 hg19 chr11 64,323,413 64,340,347 16,935
ENST00000377581.7 hg19 chr11 64,323,428 64,338,999 15,572
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