SLC25A11 solute carrier family 25 member 11

Information
Symbol
SLC25A11
Type
protein-coding
Description
solute carrier family 25 member 11
Entrez Gene ID
8402
Genome
hg19
Position
chr17:4,840,425-4,843,341
Genome
hg38
Position
chr17:4,937,130-4,940,046
MIM
604165 OMIM
HGNC
HGNC:10981 HGNC
Ensembl
ENSG00000108528 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Benign 0 4
Likely benign 0 20
Uncertain significance 0 30
Ranking
ClinVar
0
0
4
48
10
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 :
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 OGC
SYNONYM PGL6
SYNONYM PPGL6
SYNONYM SLC20A4
MIM 604165 OMIM
HGNC HGNC:10981 HGNC
Ensembl ENSG00000108528 Ensembl
AllianceGenome HGNC:10981
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000544061.6 hg38 chr17 4,937,724 4,940,053 2,330
ENST00000225665.12 hg38 chr17 4,937,130 4,940,046 2,917
ENST00000225665.12 hg19 chr17 4,840,425 4,843,341 2,917
ENST00000544061.6 hg19 chr17 4,841,019 4,843,348 2,330
Genome browser