SLC22A7 solute carrier family 22 member 7

Information
Symbol
SLC22A7
Type
protein-coding
Description
solute carrier family 22 member 7
Entrez Gene ID
10864
Genome
hg19
Position
chr6:43,265,998-43,273,276
Genome
hg38
Position
chr6:43,298,260-43,305,538
MIM
604995 OMIM
HGNC
HGNC:10971 HGNC
Ensembl
ENSG00000137204 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 54
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 NLT
SYNONYM OAT2
SYNONYM hOAT11
MIM 604995 OMIM
HGNC HGNC:10971 HGNC
Ensembl ENSG00000137204 Ensembl
AllianceGenome HGNC:10971
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372585.10 hg38 chr6 43,298,260 43,305,538 7,279
ENST00000372574.7 hg38 chr6 43,298,359 43,304,480 6,122
ENST00000372589.7 hg38 chr6 43,298,264 43,305,538 7,275
ENST00000372585.10 hg19 chr6 43,265,998 43,273,276 7,279
ENST00000372589.7 hg19 chr6 43,266,002 43,273,276 7,275
ENST00000372574.7 hg19 chr6 43,266,097 43,272,218 6,122
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