SLC43A2 solute carrier family 43 member 2

Information
Symbol
SLC43A2
Type
protein-coding
Description
solute carrier family 43 member 2
Entrez Gene ID
124935
Genome
hg19
Position
chr17:1,477,666-1,531,635
Genome
hg38
Position
chr17:1,574,372-1,628,341
MIM
610791 OMIM
HGNC
HGNC:23087 HGNC
Ensembl
ENSG00000167703 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
70
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
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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 LAT4
MIM 610791 OMIM
HGNC HGNC:23087 HGNC
Ensembl ENSG00000167703 Ensembl
AllianceGenome HGNC:23087
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000571650.5 hg38 chr17 1,574,372 1,628,341 53,970
ENST00000301335.10 hg38 chr17 1,569,268 1,628,834 59,567
ENST00000412517.3 hg38 chr17 1,575,501 1,605,085 29,585
ENST00000301335.10 hg19 chr17 1,472,562 1,532,128 59,567
ENST00000571650.5 hg19 chr17 1,477,666 1,531,635 53,970
ENST00000412517.3 hg19 chr17 1,478,795 1,508,379 29,585
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