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KRT19 (keratin 19)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3880
Gene nameGene Name - the full gene name approved by the HGNC.
Keratin 19
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
KRT19
SynonymsGene synonyms aliases
CK19, K19, K1CS
ChromosomeChromosome number
17
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q21.2
SummarySummary of gene provided in NCBI Entrez Gene.
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
miRNAmiRNA information provided by mirtarbase database.
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 factor Regulation Reference
ESR1 Activation 11026574
KLF4 Activation 10859317
SP1 Activation 10859317
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
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 TAS
GO:0005882 Component Intermediate filament IEA
GO:0005886 Component Plasma membrane IDA 23377137
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID 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
Sequence
Sequence length 400
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Estrogen signaling pathway
Staphylococcus aureus infection
  Keratinization
Formation of the cornified envelope
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Asthma Asthma rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 15478392
Autoimmune diseases Autoimmune Diseases rs41285370, rs869025224 25055964
Esophagus neoplasm Squamous cell carcinoma of esophagus rs28934578, rs121918714, rs1567556006, rs1575166666 21517111
Unknown
Disease name Disease term dbSNP ID References
Cholangitis Cholangitis 25055964
Copper-overload cirrhosis Copper-Overload Cirrhosis 22879914

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