SLC38A5 solute carrier family 38 member 5

Information
Symbol
SLC38A5
Type
protein-coding
Description
solute carrier family 38 member 5
Entrez Gene ID
92745
Genome
hg19
Position
chrX:48,316,920-48,328,565
Genome
hg38
Position
chrX:48,458,537-48,470,177
MIM
300649 OMIM
HGNC
HGNC:18070 HGNC
Ensembl
ENSG00000017483 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
not provided 6 0
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
32
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 JM24
SYNONYM SN2
SYNONYM SNAT5
SYNONYM pp7194
MIM 300649 OMIM
HGNC HGNC:18070 HGNC
Ensembl ENSG00000017483 Ensembl
AllianceGenome HGNC:18070
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000595796.5 hg38 chrX 48,458,537 48,470,177 11,641
ENST00000620913.5 hg38 chrX 48,458,544 48,470,260 11,717
ENST00000619100.4 hg38 chrX 48,458,539 48,467,493 8,955
ENST00000595796.5 hg19 chrX 48,316,920 48,328,565 11,646
ENST00000619100.4 hg19 chrX 48,316,922 48,325,880 8,959
ENST00000620913.5 hg19 chrX 48,316,927 48,328,648 11,722
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