SLCO1B3 solute carrier organic anion transporter family member 1B3

Information
Symbol
SLCO1B3
Type
protein-coding
Description
solute carrier organic anion transporter family member 1B3
Entrez Gene ID
28234
Genome
hg19
Position
chr12:20,963,639-21,069,845
Genome
hg38
Position
chr12:20,810,705-20,916,911
MIM
605495 OMIM
HGNC
HGNC:10961 HGNC
Ensembl
ENSG00000111700 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 124
Likely benign 0 80
Conflicting classifications of pathogenicity 0 42
not provided 2 0
Uncertain significance 0 242
Ranking
ClinVar
0
0
72
360
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 HBLRR
SYNONYM LST-2
SYNONYM LST-3TM13
SYNONYM LST3
SYNONYM OATP-8
SYNONYM OATP1B3
SYNONYM OATP8
SYNONYM SLC21A8
MIM 605495 OMIM
HGNC HGNC:10961 HGNC
Ensembl ENSG00000111700 Ensembl
AllianceGenome HGNC:10961
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000381545.8 hg38 chr12 20,810,705 20,916,911 106,207
ENST00000261196.6 hg38 chr12 20,815,672 20,916,911 101,240
ENST00000381545.8 hg19 chr12 20,963,639 21,069,845 106,207
ENST00000261196.6 hg19 chr12 20,968,606 21,069,845 101,240
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