SLC25A39 solute carrier family 25 member 39

Information
Symbol
SLC25A39
Type
protein-coding
Description
solute carrier family 25 member 39
Entrez Gene ID
51629
Genome
hg19
Position
chr17:42,396,996-42,402,191
Genome
hg38
Position
chr17:44,319,628-44,324,823
MIM
610820 OMIM
HGNC
HGNC:24279 HGNC
Ensembl
ENSG00000013306 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
60
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 CGI-69
SYNONYM CGI69
MIM 610820 OMIM
HGNC HGNC:24279 HGNC
Ensembl ENSG00000013306 Ensembl
AllianceGenome HGNC:24279
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000590194.5 hg38 chr17 44,319,642 44,324,809 5,168
ENST00000537904.6 hg38 chr17 44,319,870 44,324,827 4,958
ENST00000586016.5 hg38 chr17 44,319,673 44,324,782 5,110
ENST00000377095.10 hg38 chr17 44,319,628 44,324,823 5,196
ENST00000225308.12 hg38 chr17 44,319,625 44,324,870 5,246
ENST00000225308.12 hg19 chr17 42,396,993 42,402,238 5,246
ENST00000377095.10 hg19 chr17 42,396,996 42,402,191 5,196
ENST00000586016.5 hg19 chr17 42,397,041 42,402,150 5,110
ENST00000537904.6 hg19 chr17 42,397,238 42,402,195 4,958
ENST00000590194.5 hg19 chr17 42,397,010 42,402,177 5,168
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