SLC25A42 solute carrier family 25 member 42

Information
Symbol
SLC25A42
Type
protein-coding
Description
solute carrier family 25 member 42
Entrez Gene ID
284439
Genome
hg19
Position
chr19:19,174,803-19,223,839
Genome
hg38
Position
chr19:19,063,994-19,113,030
MIM
610823 OMIM
HGNC
HGNC:28380 HGNC
Ensembl
ENSG00000181035 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 6
Benign 0 26
Likely benign 0 146
Uncertain significance 0 110
Ranking
ClinVar
0
0
36
254
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 :
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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 :
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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 MECREN
MIM 610823 OMIM
HGNC HGNC:28380 HGNC
Ensembl ENSG00000181035 Ensembl
AllianceGenome HGNC:28380
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000318596.8 hg38 chr19 19,063,994 19,113,030 49,037
ENST00000318596.8 hg19 chr19 19,174,803 19,223,839 49,037
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