SLC7A6 solute carrier family 7 member 6

Information
Symbol
SLC7A6
Type
protein-coding
Description
solute carrier family 7 member 6
Entrez Gene ID
9057
Genome
hg19
Position
chr16:68,298,463-68,335,722
Genome
hg38
Position
chr16:68,264,560-68,301,819
MIM
605641 OMIM
HGNC
HGNC:11064 HGNC
Ensembl
ENSG00000103064 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 10
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
54
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 :
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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 LAT-2
SYNONYM LAT3
SYNONYM y+LAT-2
MIM 605641 OMIM
HGNC HGNC:11064 HGNC
Ensembl ENSG00000103064 Ensembl
AllianceGenome HGNC:11064
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000219343.11 hg38 chr16 68,264,526 68,301,819 37,294
ENST00000618043.4 hg38 chr16 68,264,516 68,301,823 37,308
ENST00000566454.5 hg38 chr16 68,264,560 68,301,819 37,260
ENST00000219343.11 hg19 chr16 68,298,429 68,335,722 37,294
ENST00000618043.4 hg19 chr16 68,298,419 68,335,726 37,308
ENST00000566454.5 hg19 chr16 68,298,463 68,335,722 37,260
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