SLC10A2 solute carrier family 10 member 2

Information
Symbol
SLC10A2
Type
protein-coding
Description
solute carrier family 10 member 2
Entrez Gene ID
6555
Genome
hg19
Position
chr13:103,696,348-103,718,767
Genome
hg38
Position
chr13:103,043,998-103,066,417
MIM
601295 OMIM
HGNC
HGNC:10906 HGNC
Ensembl
ENSG00000125255 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 34
Likely benign 0 136
Conflicting classifications of pathogenicity 0 58
Uncertain significance 0 360
Ranking
ClinVar
0
0
128
388
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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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 ASBT
SYNONYM IBAT
SYNONYM ISBT
SYNONYM NTCP2
SYNONYM PBAM
SYNONYM PBAM1
MIM 601295 OMIM
HGNC HGNC:10906 HGNC
Ensembl ENSG00000125255 Ensembl
AllianceGenome HGNC:10906
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000245312.5 hg38 chr13 103,043,998 103,066,417 22,420
ENST00000245312.5 hg19 chr13 103,696,348 103,718,767 22,420
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