SLC38A4 solute carrier family 38 member 4

Information
Symbol
SLC38A4
Type
protein-coding
Description
solute carrier family 38 member 4
Entrez Gene ID
55089
Genome
hg19
Position
chr12:47,158,544-47,219,780
Genome
hg38
Position
chr12:46,764,761-46,825,997
MIM
608065 OMIM
HGNC
HGNC:14679 HGNC
Ensembl
ENSG00000139209 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
38
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 ATA3
SYNONYM NAT3
SYNONYM PAAT
SYNONYM SNAT4
MIM 608065 OMIM
HGNC HGNC:14679 HGNC
Ensembl ENSG00000139209 Ensembl
AllianceGenome HGNC:14679
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000447411.5 hg38 chr12 46,764,761 46,825,997 61,237
ENST00000266579.9 hg38 chr12 46,764,761 46,825,997 61,237
ENST00000447411.5 hg19 chr12 47,158,544 47,219,780 61,237
ENST00000266579.9 hg19 chr12 47,158,544 47,219,780 61,237
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