SLC7A11 solute carrier family 7 member 11

Information
Symbol
SLC7A11
Type
protein-coding
Description
solute carrier family 7 member 11
Entrez Gene ID
23657
Genome
hg19
Position
chr4:139,085,251-139,163,503
Genome
hg38
Position
chr4:138,164,097-138,242,349
MIM
607933 OMIM
HGNC
HGNC:11059 HGNC
Ensembl
ENSG00000151012 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
68
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 CCBR1
SYNONYM xCT
MIM 607933 OMIM
HGNC HGNC:11059 HGNC
Ensembl ENSG00000151012 Ensembl
AllianceGenome HGNC:11059
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000280612.9 hg38 chr4 138,164,097 138,242,349 78,253
ENST00000280612.9 hg19 chr4 139,085,251 139,163,503 78,253
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