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KRT10 (keratin 10)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3858
Gene nameGene Name - the full gene name approved by the HGNC.
Keratin 10
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
KRT10
SynonymsGene synonyms aliases
BCIE, BIE, CK10, EHK, EHK2, EHK2A, EHK2B, IHL, K10, KPP
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.
This gene encodes a member of the type I (acidic) cytokeratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along wi
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023292 hsa-miR-122-5p Proteomics 21750653
MIRT460670 hsa-miR-497-3p PAR-CLIP 20371350
MIRT077072 hsa-miR-3609 PAR-CLIP 20371350
MIRT077074 hsa-miR-548ah-5p PAR-CLIP 20371350
MIRT077067 hsa-miR-106a-5p PAR-CLIP 20371350
Transcription factors
Transcription factor Regulation Reference
HOXA7 Activation 11435435
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001533 Component Cornified envelope IDA 7543090
GO:0005515 Function Protein binding IPI 19627498
GO:0005615 Component Extracellular space HDA 23580065
GO:0005634 Component Nucleus HDA 21630459
GO:0005737 Component Cytoplasm IDA 22170488
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P13645
Protein name Keratin, type I cytoskeletal 10 (Cytokeratin-10) (CK-10) (Keratin-10) (K10)
Protein function Plays a role in the establishment of the epidermal barrier on plantar skin (By similarity). Involved in the maintenance of cell layer development and keratin filament bundles in suprabasal cells of the epithelium (By similarity). {ECO:0000250|Un
PDB 3ASW , 4F1Z , 4ZRY , 6E2J , 6EC0 , 6UUI
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00038 Filament
145 459
Intermediate filament protein
Coiled-coil
Sequence
MSVRYSSSKHYSSSRSGGGGGGGGCGGGGGVSSLRISSSKGSLGGGFSSGGFSGGSFSRG
SSGGGCFGGSSGGYGGLGGFGGGSFRGSYGSSSFGGSYGGIFGGGSFGGGSFGGGSFGGG
GFGGGGFGGGFGGGFGGDGGLLSGNEKVTMQNLNDRLASYLDKVRALEESNYELEGKIKE
WYEKHGNSHQGEPRDYSKYYKTIDDLKNQILNLTTDNANILLQIDNARLAADDFRLKYEN
EVALRQSVEADINGLRRVLDELTLTKADLEMQIESLTEELAYLKKNHEEEMKDLRNVSTG
DVNVEMNAAPGVDLTQLLNNMRSQYEQLAEQNRKDAEAWFNEKSKELTTEIDNNIEQISS
YKSEITELRRNVQALEIELQSQLALKQSLEASLAETEGRYCVQLSQIQAQISALEEQLQQ
IRAETECQNTEYQQLLDIKIRLENEIQTYRSLLEGEGSS
GGGGRGGGSFGGGYGGGSSGG
GSSGGGHGGGHGGSSGGGYGGGSSGGGSSGGGYGGGSSSGGHGGSSSGGYGGGSSGGGGG
GYGGGSSGGGSSSGGGYGGGSSSGGHKSSSSGSVGESSSKGPRY
Sequence length 584
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
Ichthyosis with epidermolytic hyperkeratosis Annular epidermolytic ichthyosis rs59075499, rs57837128
Carcinoma Squamous cell carcinoma rs121912654, rs555607708, rs786202962, rs1564055259 18572023
Congenital reticular ichthyosiform erythroderma Congenital reticular ichthyosiform erythroderma rs587776815, rs587776816, rs587776817, rs267607384, rs1555171158 7508181, 20798280
Dermatitis Contact Dermatitis rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 25724174
Unknown
Disease name Disease term dbSNP ID References
Arsenic encephalopathy Arsenic Encephalopathy 19953893
Conjunctival hamartoma Conjunctival hamartoma
Epidermolytic ichthyosis Autosomal dominant epidermolytic ichthyosis, Autosomal recessive epidermolytic ichthyosis
Exfoliative dermatitis Exfoliative dermatitis

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