SLC38A2 solute carrier family 38 member 2

Information
Symbol
SLC38A2
Type
protein-coding
Description
solute carrier family 38 member 2
Entrez Gene ID
54407
Genome
hg19
Position
chr12:46,751,971-46,766,556
Genome
hg38
Position
chr12:46,358,188-46,372,773
MIM
605180 OMIM
HGNC
HGNC:13448 HGNC
Ensembl
ENSG00000134294 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 6
Uncertain significance 0 30
Ranking
ClinVar
0
0
2
36
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 :
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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 :
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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 ATA2
SYNONYM PRO1068
SYNONYM SAT2
SYNONYM SNAT2
MIM 605180 OMIM
HGNC HGNC:13448 HGNC
Ensembl ENSG00000134294 Ensembl
AllianceGenome HGNC:13448
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000612232.1 hg38 chr12 46,361,111 46,370,789 9,679
ENST00000256689.10 hg38 chr12 46,358,188 46,372,773 14,586
ENST00000551374.5 hg38 chr12 46,359,385 46,365,307 5,923
ENST00000256689.10 hg19 chr12 46,751,971 46,766,556 14,586
ENST00000551374.5 hg19 chr12 46,753,168 46,759,090 5,923
ENST00000612232.1 hg19 chr12 46,754,894 46,764,572 9,679
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