CASP7 (GeneID: 840) | Homo sapiens
Description: caspase 7 [Source:HGNC Symbol;Acc:HGNC:1508]
Synonyms: LICE2, CASP-7, ICE-LAP3, MCH3, CMH-1
Other ID(s): HGNC:1508, ENSG00000165806
Protein Accession Numbers: NP_001218, ENST00000369331, NP_203124, ENST00000369315, NP_001253986, ENST00000452490, NP_203126, ENST00000369321, NP_001307840, ENST00000345633, NP_001253985, ENST00000429617, NP_203125, ENST00000369318, NP_001253987
Statistics: ClinVar(2) gnomAD(248) COSMIC(111) PTM(21)
ClinVar Pathogenicity of Variations help

∙ 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.
ENST00000345633 ENST00000369315 ENST00000369318 ENST00000369321 ENST00000369331 ENST00000429617 ENST00000452490 You are here now! NP_001218 NP_001253985 NP_001253986 NP_001253987 You are here now! NP_001307840 NP_203124 NP_203125 NP_203126


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

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
PF00656 Peptidase_C14 Caspase domain 67-300 CL0093 Peptidase_CD Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.611 0.586
Leukemia, Myelocytic, Acute Neoplasms ; 0.611 0.586
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.611 0.586
Acute Myeloid Leukemia, M1 Neoplasms ; 0.611 0.586
Myocardial Reperfusion Injury Cardiovascular Diseases ; Pathological Conditions, Signs and Symptoms ; 0.611 0.586
Vitiligo Skin and Connective Tissue Diseases ; 0.611 0.586
Breast Carcinoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.611 0.586
Mammary Neoplasms, Human Neoplasms ; Skin and Connective Tissue Diseases ; 0.611 0.586
Mammary Neoplasms Neoplasms ; Skin and Connective Tissue Diseases ; 0.611 0.586
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.611 0.586
NO RESULT FOUND
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