SLC6A16 solute carrier family 6 member 16

Information
Symbol
SLC6A16
Type
protein-coding
Description
solute carrier family 6 member 16
Entrez Gene ID
28968
Genome
hg19
Position
chr19:49,792,895-49,828,448
Genome
hg38
Position
chr19:49,289,638-49,325,191
MIM
607972 OMIM
HGNC
HGNC:13622 HGNC
Ensembl
ENSG00000063127 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 12
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
84
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 :
Search word :
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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 NT5
SYNONYM NTT5
MIM 607972 OMIM
HGNC HGNC:13622 HGNC
Ensembl ENSG00000063127 Ensembl
AllianceGenome HGNC:13622
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000454748.7 hg38 chr19 49,289,765 49,325,185 35,421
ENST00000335875.9 hg38 chr19 49,289,638 49,325,191 35,554
ENST00000335875.9 hg19 chr19 49,792,895 49,828,448 35,554
ENST00000454748.7 hg19 chr19 49,793,022 49,828,442 35,421
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