SLC46A3 solute carrier family 46 member 3

Information
Symbol
SLC46A3
Type
protein-coding
Description
solute carrier family 46 member 3
Entrez Gene ID
283537
Genome
hg19
Position
chr13:29,274,854-29,293,107
Genome
hg38
Position
chr13:28,700,717-28,718,970
MIM
616764 OMIM
HGNC
HGNC:27501 HGNC
Ensembl
ENSG00000139508 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
50
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
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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 FKSG16
MIM 616764 OMIM
HGNC HGNC:27501 HGNC
Ensembl ENSG00000139508 Ensembl
AllianceGenome HGNC:27501
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380814.4 hg38 chr13 28,700,717 28,718,970 18,254
ENST00000266943.11 hg38 chr13 28,700,080 28,718,970 18,891
ENST00000266943.11 hg19 chr13 29,274,217 29,293,107 18,891
ENST00000380814.4 hg19 chr13 29,274,854 29,293,107 18,254
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