RGS9 regulator of G protein signaling 9

Information
Symbol
RGS9
Type
protein-coding
Description
regulator of G protein signaling 9
Entrez Gene ID
8787
Genome
hg19
Position
chr17:63,133,488-63,223,821
Genome
hg38
Position
chr17:65,137,370-65,227,703
MIM
604067 OMIM
HGNC
HGNC:10004 HGNC
Ensembl
ENSG00000108370 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 36
Likely pathogenic 0 28
Benign 0 40
Likely benign 0 414
Conflicting classifications of pathogenicity 0 18
Uncertain significance 0 464
Ranking
ClinVar
0
0
84
890
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 PERRS
SYNONYM PERRS1
SYNONYM RGS9L
MIM 604067 OMIM
HGNC HGNC:10004 HGNC
Ensembl ENSG00000108370 Ensembl
AllianceGenome HGNC:10004
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000449996.7 hg38 chr17 65,137,469 65,227,703 90,235
ENST00000635833.1 hg38 chr17 65,100,986 65,227,690 126,705
ENST00000262406.10 hg38 chr17 65,137,370 65,227,703 90,334
ENST00000443584.7 hg38 chr17 65,137,448 65,225,588 88,141
ENST00000635833.1 hg19 chr17 63,097,104 63,223,808 126,705
ENST00000262406.10 hg19 chr17 63,133,488 63,223,821 90,334
ENST00000443584.7 hg19 chr17 63,133,566 63,221,706 88,141
ENST00000449996.7 hg19 chr17 63,133,587 63,223,821 90,235
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