CTSG cathepsin G

Information
Symbol
CTSG
Type
protein-coding
Description
cathepsin G
Entrez Gene ID
1511
Genome
hg19
Position
chr14:25,042,724-25,045,456
Genome
hg38
Position
chr14:24,573,518-24,576,250
MIM
116830 OMIM
HGNC
HGNC:2532 HGNC
Ensembl
ENSG00000100448 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 2
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
36
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 :
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 CATG
SYNONYM CG
MIM 116830 OMIM
HGNC HGNC:2532 HGNC
Ensembl ENSG00000100448 Ensembl
AllianceGenome HGNC:2532
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000216336.3 hg38 chr14 24,573,518 24,576,250 2,733
ENST00000216336.3 hg19 chr14 25,042,724 25,045,456 2,733
Genome browser