SLC6A14 solute carrier family 6 member 14

Information
Symbol
SLC6A14
Type
protein-coding
Description
solute carrier family 6 member 14
Entrez Gene ID
11254
Genome
hg19
Position
chrX:115,567,774-115,592,625
Genome
hg38
Position
chrX:116,436,606-116,461,458
MIM
300444 OMIM
HGNC
HGNC:11047 HGNC
Ensembl
ENSG00000268104 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 4
not provided 6 0
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
60
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 BMIQ11
MIM 300444 OMIM
HGNC HGNC:11047 HGNC
Ensembl ENSG00000268104 Ensembl
AllianceGenome HGNC:11047
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598581.3 hg38 chrX 116,436,606 116,461,458 24,853
ENST00000598581.3 hg19 chrX 115,567,774 115,592,625 24,852
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