SLC7A4 solute carrier family 7 member 4

Information
Symbol
SLC7A4
Type
protein-coding
Description
solute carrier family 7 member 4
Entrez Gene ID
6545
Genome
hg19
Position
chr22:21,383,007-21,386,850
Genome
hg38
Position
chr22:21,028,718-21,032,561
MIM
603752 OMIM
HGNC
HGNC:11062 HGNC
Ensembl
ENSG00000099960 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 14
not provided 14 0
Uncertain significance 0 110
Ranking
ClinVar
0
0
0
128
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
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 CAT-4
SYNONYM CAT4
SYNONYM HCAT3
SYNONYM VH
MIM 603752 OMIM
HGNC HGNC:11062 HGNC
Ensembl ENSG00000099960 Ensembl
AllianceGenome HGNC:11062
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403586.5 hg38 chr22 21,028,718 21,032,549 3,832
ENST00000382932.3 hg38 chr22 21,028,718 21,032,561 3,844
ENST00000403586.5 hg19 chr22 21,383,007 21,386,838 3,832
ENST00000382932.3 hg19 chr22 21,383,007 21,386,850 3,844
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