STARD8 StAR related lipid transfer domain containing 8

Information
Symbol
STARD8
Type
protein-coding
Description
StAR related lipid transfer domain containing 8
Entrez Gene ID
9754
Genome
hg19
Position
chrX:67,867,508-67,945,678
Genome
hg38
Position
chrX:68,647,666-68,725,836
MIM
300689 OMIM
HGNC
HGNC:19161 HGNC
Ensembl
ENSG00000130052 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 24
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 108
Ranking
ClinVar
0
0
0
138
2
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 ARHGAP38
SYNONYM DLC3
SYNONYM STARTGAP3
MIM 300689 OMIM
HGNC HGNC:19161 HGNC
Ensembl ENSG00000130052 Ensembl
AllianceGenome HGNC:19161
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000374597.3 hg38 chrX 68,693,651 68,725,833 32,183
ENST00000374599.8 hg38 chrX 68,647,666 68,725,836 78,171
ENST00000252336.10 hg38 chrX 68,647,669 68,725,840 78,172
ENST00000374599.8 hg19 chrX 67,867,508 67,945,678 78,171
ENST00000252336.10 hg19 chrX 67,867,511 67,945,682 78,172
ENST00000374597.3 hg19 chrX 67,913,493 67,945,675 32,183
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