Capg (GeneID: 297339) | Rattus norvegicus
Description: capping actin protein, gelsolin like [Source:RGD Symbol;Acc:1311724]
Synonyms:
Other ID(s): ENSRNOG00000013668
Protein Accession Numbers: XP_017448027, XP_006236724, XP_017448029, XP_017448026, XP_006236723, XP_017448028, XP_006236725, NP_001013104, XP_017448030
Statistics: ClinVar(15) COSMIC(299) PTM(27)
ClinVar Pathogenicity of Variations help
Benign
Others
67%33%10010090908080707060605050404030302020101000
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∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000263867 You are here now! ENST00000409275 ENST00000409670 You are here now! ENST00000409724 You are here now! ENST00000409921 ENST00000439385 ENST00000447219 ENST00000449030 ENST00000453973 NP_001243068 You are here now! NP_001243069 NP_001307661 You are here now! NP_001307662 You are here now! NP_001307663 NP_001738 You are here now!


import_contactsClinVar Data

healinggnomAD
10010090908080707060605050404030302020101000

placePost-translational Modifications (PTMs)
Acetylation
Phosphorylation
Ubiquitination
7%56%37%10010090908080707060605050404030302020101000
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blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Substitution - Coding Silent
Substitution - Missense
Substitution - Nonsense
Unknown
9%50%4%37%10010090908080707060605050404030302020101000
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format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00626 Gelsolin Gelsolin repeat 146-221 CL0092 ADF Homo sapiens
PF00626 Gelsolin Gelsolin repeat 28-107 CL0092 ADF Homo sapiens
PF00626 Gelsolin Gelsolin repeat 264-341 CL0092 ADF Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.616 0.655
Keloid Skin and Connective Tissue Diseases ; Pathological Conditions, Signs and Symptoms ; 0.616 0.655
Leukemia, Myelocytic, Acute Neoplasms ; 0.616 0.655
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.616 0.655
Acute Myeloid Leukemia, M1 Neoplasms ; 0.616 0.655
Adenocarcinoma of lung (disorder) Neoplasms ; Respiratory Tract Diseases ; 0.616 0.655
Conventional (Clear Cell) Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.616 0.655
Chromophobe Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.616 0.655
Sarcomatoid Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.616 0.655
Collecting Duct Carcinoma of the Kidney Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.616 0.655
Papillary Renal Cell Carcinoma Neoplasms ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; 0.616 0.655
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.616 0.655
NO RESULT FOUND
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