KRT18 (GeneID: 3875) | Homo sapiens
Description: keratin 18 [Source:HGNC Symbol;Acc:HGNC:6430]
Synonyms: CK-18, K18, CYK18
Other ID(s): ENSG00000111057, HGNC:6430
Protein Accession Numbers: ENST00000388835.3, ENST00000550600, ENST00000388835, NP_954657, ENST00000388837, NP_000215
Statistics: ClinVar(40) gnomAD(884) COSMIC(474) PTM(114)
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.
ENST00000388835 You are here now! ENST00000388837 You are here now! ENST00000550600 NP_000215 You are here now! NP_954657 You are here now!


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
PF00038 Filament Intermediate filament protein 79-391 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 ; 0.557 0.552
Hepatitis, Toxic Digestive System Diseases ; Chemically-Induced Disorders ; 0.557 0.552
Liver Cirrhosis Digestive System Diseases ; 0.557 0.552
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.557 0.552
Liver neoplasms Neoplasms ; Digestive System Diseases ; 0.557 0.552
Necrosis Pathological Conditions, Signs and Symptoms ; 0.557 0.552
Liver Failure, Acute Digestive System Diseases ; 0.557 0.552
Fibrosis, Liver Digestive System Diseases ; 0.557 0.552
Cirrhosis, Cryptogenic Digestive System Diseases ; 0.557 0.552
Indian childhood cirrhosis Digestive System Diseases ; Respiratory Tract Diseases ; 0.557 0.552
Malignant neoplasm of liver Neoplasms ; Digestive System Diseases ; 0.557 0.552
Breast Carcinoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.557 0.552
Drug-Induced Liver Disease Digestive System Diseases ; Chemically-Induced Disorders ; 0.557 0.552
Mammary Neoplasms, Human Neoplasms ; Skin and Connective Tissue Diseases ; 0.557 0.552
Hepatitis, Drug-Induced Digestive System Diseases ; Chemically-Induced Disorders ; 0.557 0.552
Mammary Neoplasms Neoplasms ; Skin and Connective Tissue Diseases ; 0.557 0.552
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding) N/A 0.557 0.552
COPPER TOXICOSIS, IDIOPATHIC Digestive System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; 0.557 0.552
Cirrhosis, Familial Digestive System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.557 0.552
Copper-Overload Cirrhosis Digestive System Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Nutritional and Metabolic Diseases ; 0.557 0.552
Endemic Tyrolean Infantile Cirrhosis Pathological Conditions, Signs and Symptoms ; 0.557 0.552
Drug-Induced Acute Liver Injury Digestive System Diseases ; Chemically-Induced Disorders ; 0.557 0.552
Chemical and Drug Induced Liver Injury Digestive System Diseases ; Chemically-Induced Disorders ; 0.557 0.552
Chemically-Induced Liver Toxicity Digestive System Diseases ; Chemically-Induced Disorders ; 0.557 0.552
NO RESULT FOUND
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