SLC15A3 solute carrier family 15 member 3

Information
Symbol
SLC15A3
Type
protein-coding
Description
solute carrier family 15 member 3
Entrez Gene ID
51296
Genome
hg19
Position
chr11:60,704,556-60,719,648
Genome
hg38
Position
chr11:60,937,084-60,952,176
MIM
610408 OMIM
HGNC
HGNC:18068 HGNC
Ensembl
ENSG00000110446 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
72
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 OCTP
SYNONYM PHT2
SYNONYM PTR3
SYNONYM hPHT2
MIM 610408 OMIM
HGNC HGNC:18068 HGNC
Ensembl ENSG00000110446 Ensembl
AllianceGenome HGNC:18068
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000227880.8 hg38 chr11 60,937,084 60,952,176 15,093
ENST00000681275.1 hg38 chr11 60,937,084 60,952,080 14,997
ENST00000681882.1 hg38 chr11 60,937,084 60,952,176 15,093
ENST00000681951.1 hg38 chr11 60,937,084 60,952,176 15,093
ENST00000681275.1 hg19 chr11 60,704,556 60,719,552 14,997
ENST00000681882.1 hg19 chr11 60,704,556 60,719,648 15,093
ENST00000681951.1 hg19 chr11 60,704,556 60,719,648 15,093
ENST00000227880.8 hg19 chr11 60,704,556 60,719,648 15,093
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