ENSG00000186395


Homo sapiens

Features
Gene ID: ENSG00000186395
  
Biological name :KRT10
  
Synonyms : keratin 10 / KRT10 / P13645
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: -1
Band: q21.2
Gene start: 40818117
Gene end: 40822595
  
Corresponding Affymetrix probe sets: 207023_x_at (Human Genome U133 Plus 2.0 Array)   210633_x_at (Human Genome U133 Plus 2.0 Array)   213287_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000269576
Ensembl peptide - ENSP00000490524
NCBI entrez gene - 3858     See in Manteia.
OMIM - 148080
RefSeq - NM_000421
RefSeq - XM_005257343
RefSeq Peptide - NP_000412
swissprot - A0A1B0GVI3
swissprot - P13645
Ensembl - ENSG00000186395
  
Related genetic diseases (OMIM): 113800 - Epidermolytic hyperkeratosis, 113800
  607602 - Ichthyosis, cyclic, with epidermolytic hyperkeratosis, 607602
  609165 - Ichthyosis with confetti, 609165
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 cyt1ENSDARG00000092947Danio rerio
 cyt1lENSDARG00000036832Danio rerio
 krt1-19dENSDARG00000023082Danio rerio
 krt15ENSDARG00000036840Danio rerio
 krt17ENSDARG00000094041Danio rerio
 krt91ENSDARG00000036830Danio rerio
 krt92ENSDARG00000036834Danio rerio
 krt93ENSDARG00000044976Danio rerio
 krt94ENSDARG00000044975Danio rerio
 krt95ENSDARG00000014356Danio rerio
 krt96ENSDARG00000095147Danio rerio
 krt97ENSDARG00000000212Danio rerio
 krtt1c19eENSDARG00000090268Danio rerio
 si:ch211-156l18.7ENSDARG00000022334Danio rerio
 Krt10ENSMUSG00000019761Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
KRT24 / Q2M2I5 / keratin 24ENSG0000016791651
KRT12 / Q99456 / keratin 12ENSG0000018724248
KRT16 / P08779 / keratin 16ENSG0000018683247
KRT14 / P02533 / keratin 14ENSG0000018684747
KRT13 / P13646 / keratin 13ENSG0000017140145
KRT15 / P19012 / keratin 15ENSG0000017134645
KRT28 / Q7Z3Y7 / keratin 28ENSG0000017390844
KRT17 / Q04695 / keratin 17ENSG0000012842244
KRT27 / Q7Z3Y8 / keratin 27ENSG0000017144644
KRT26 / Q7Z3Y9 / keratin 26ENSG0000018639342
KRT25 / Q7Z3Z0 / keratin 25ENSG0000020489742
KRT19 / P08727 / keratin 19ENSG0000017134540


Protein motifs (from Interpro)
Interpro ID Name
 IPR001664  Intermediate filament protein
 IPR002957  Keratin, type I
 IPR018039  Intermediate filament protein, conserved site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0018149 peptide cross-linking IDA
 biological_processGO:0030216 keratinocyte differentiation IEP
 biological_processGO:0031424 keratinization TAS
 biological_processGO:0070268 cornification TAS
 cellular_componentGO:0001533 cornified envelope IDA
 cellular_componentGO:0005615 extracellular space HDA
 cellular_componentGO:0005634 nucleus HDA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005882 intermediate filament NAS
 cellular_componentGO:0016020 membrane HDA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0005198 structural molecule activity IEA
 molecular_functionGO:0030280 structural constituent of epidermis IDA


Pathways (from Reactome)
Pathway description
Keratinization
Formation of the cornified envelope


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000972 Palmoplantar hyperkeratosis "`Hyperkeratosis` (HP:0000962) affecting the palm of the hand and the sole of the foot." [HPO:probinson]
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 HP:0000982 Palmoplantar keratoderma 
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 HP:0000992 Photosensitivity "An increased sensitivity of the skin to light. Photosensitivity may result in a rash upon exposure to the sun (which is known as photodermatosis). Photosensitivity can be diagnosed by phototests in which light is shone on small areas of skin." [HPO:curators]
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 HP:0000998 Hypertrichosis "Hypertrichosis is increased hair growth that is abnormal in quantity or location." [HPO:curators]
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 HP:0001019 Erythroderma "An inflammatory exfoliative dermatosis involving nearly all of the surface of the skin. Erythroderma develops suddenly. A patchy erythema may generalize and spread to affect most of the skin. Scaling may appear in 2-6 days and be accompanied by hot, red, dry skin, malaise, and fever." [HPO:probinson]
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 HP:0001217 Clubbing "Non-edematous swelling/broadening of the soft tissue of the fingertips in all dimensions." [HPO:curators]
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 HP:0001824 Weight loss 
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 HP:0004396 Poor appetite 
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 HP:0007475 Epidermolytic hyperkeratosis 
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 HP:0008066 Abnormal blistering of the skin 
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 HP:0010783 Erythema "Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin." [HPO:probinson]
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 HP:0025092 Epidermal acanthosis "Diffuse hypertrophy or thickening of the stratum spinosum of the epidermis (prickle cell layer of the skin)." []
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 HP:0040189 Scaling skin "Refers to the loss of the outer layer of the epidermis in large, scale-like flakes." []
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 HP:0100780 Conjunctival hamartomas 
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 HP:0200042 skin ulcer "A discontinuity of the skin exhibiting complete loss of the epidermis and often portions of the dermis and even subcutaneous fat." [HPO:SKOEHLER]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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