SLC6A5 solute carrier family 6 member 5

Information
Symbol
SLC6A5
Type
protein-coding
Description
solute carrier family 6 member 5
Entrez Gene ID
9152
Genome
hg19
Position
chr11:20,621,154-20,680,831
Genome
hg38
Position
chr11:20,599,608-20,659,285
MIM
604159 OMIM
HGNC
HGNC:11051 HGNC
Ensembl
ENSG00000165970 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 60
Likely pathogenic 0 40
Benign 0 166
Likely benign 0 606
Conflicting classifications of pathogenicity 0 38
Uncertain significance 0 628
Ranking
ClinVar
0
0
156
1,310
12
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 :
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 GLYT-2
SYNONYM GLYT2
SYNONYM HKPX3
SYNONYM NET1
MIM 604159 OMIM
HGNC HGNC:11051 HGNC
Ensembl ENSG00000165970 Ensembl
AllianceGenome HGNC:11051
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000525748.6 hg38 chr11 20,599,608 20,659,285 59,678
ENST00000525748.6 hg19 chr11 20,621,154 20,680,831 59,678
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