SLC46A2 solute carrier family 46 member 2

Information
Symbol
SLC46A2
Type
protein-coding
Description
solute carrier family 46 member 2
Entrez Gene ID
57864
Genome
hg19
Position
chr9:115,641,200-115,653,156
Genome
hg38
Position
chr9:112,878,920-112,890,876
MIM
608956 OMIM
HGNC
HGNC:16055 HGNC
Ensembl
ENSG00000119457 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 1 0
Benign 0 8
Likely benign 0 4
Uncertain significance 0 66
Ranking
ClinVar
0
0
0
78
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
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 Ly110
SYNONYM TSCOT
MIM 608956 OMIM
HGNC HGNC:16055 HGNC
Ensembl ENSG00000119457 Ensembl
AllianceGenome HGNC:16055
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000374228.5 hg38 chr9 112,878,920 112,890,876 11,957
ENST00000374228.5 hg19 chr9 115,641,200 115,653,156 11,957
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