SLC66A3 solute carrier family 66 member 3

Information
Symbol
SLC66A3
Type
protein-coding
Description
solute carrier family 66 member 3
Entrez Gene ID
130814
Genome
hg19
Position
chr2:11,295,593-11,318,982
Genome
hg38
Position
chr2:11,155,467-11,178,856
HGNC
HGNC:28503 HGNC
Ensembl
ENSG00000162976 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 0
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
34
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 :
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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 C2orf22
SYNONYM PQLC3
HGNC HGNC:28503 HGNC
Ensembl ENSG00000162976 Ensembl
AllianceGenome HGNC:28503
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000441908.6 hg38 chr2 11,155,372 11,178,870 23,499
ENST00000295083.8 hg38 chr2 11,155,467 11,178,856 23,390
ENST00000402361.5 hg38 chr2 11,155,535 11,178,024 22,490
ENST00000441908.6 hg19 chr2 11,295,498 11,318,996 23,499
ENST00000295083.8 hg19 chr2 11,295,593 11,318,982 23,390
ENST00000402361.5 hg19 chr2 11,295,661 11,318,150 22,490
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