Gene Gene information from NCBI Gene database.
Entrez ID 3880
Gene name Keratin 19
Gene symbol KRT19
Synonyms (NCBI Gene)
CK19K19K1CS
Chromosome 17
Chromosome location 17q21.2
Summary The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratin
miRNA miRNA information provided by mirtarbase database.
66
miRTarBase ID miRNA Experiments Reference
MIRT016304 hsa-miR-193b-3p Proteomics 21512034
MIRT016860 hsa-miR-335-5p Microarray 18185580
MIRT1101175 hsa-miR-1207-5p CLIP-seq
MIRT1101176 hsa-miR-1253 CLIP-seq
MIRT1101177 hsa-miR-1912 CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
3
Transcription factor Regulation Reference
ESR1 Activation 11026574
KLF4 Activation 10859317
SP1 Activation 10859317
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
GO ID Ontology Definition Evidence Reference
GO:0002009 Process Morphogenesis of an epithelium IBA
GO:0005198 Function Structural molecule activity IEA
GO:0005200 Function Structural constituent of cytoskeleton TAS 2448790
GO:0005515 Function Protein binding IPI 15846844, 16000376, 16189514, 20080707, 25416956, 25910212, 26871637, 29892012, 31515488, 32296183, 32814053
GO:0005829 Component Cytosol IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
148020 6436 ENSG00000171345
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P08727
Protein name Keratin, type I cytoskeletal 19 (Cytokeratin-19) (CK-19) (Keratin-19) (K19)
Protein function Involved in the organization of myofibers. Together with KRT8, helps to link the contractile apparatus to dystrophin at the costameres of striated muscle.
PDB 8XTN , 8XTO , 8Y3S , 8ZUG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00038 Filament 79 390 Intermediate filament protein Coiled-coil
Tissue specificity TISSUE SPECIFICITY: Expressed in a defined zone of basal keratinocytes in the deep outer root sheath of hair follicles. Also observed in sweat gland and mammary gland ductal and secretory cells, bile ducts, gastrointestinal tract, bladder urothelium, oral
Sequence
Sequence length 400
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Estrogen signaling pathway
Staphylococcus aureus infection
  Keratinization
Formation of the cornified envelope
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hereditary breast ovarian cancer syndrome Uncertain significance rs117671585 RCV001374482
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 15710986, 23348905, 24078426, 33832101, 34102222
Adenocarcinoma Stimulate 34706517
Adenocarcinoma Follicular Associate 17728499, 27171147, 34711014
Adenocarcinoma Mucinous Associate 21699710
Adenocarcinoma of Lung Associate 12192603, 18329483, 2414994, 25189096, 32519739, 35441736, 39522011
Adenocarcinoma Papillary Associate 36705380
Adenolymphoma Associate 22990554
Adenoma Associate 20565793
Adrenal Gland Neoplasms Associate 24322017
Alagille Syndrome Associate 8701983