Details for: KRT17

Gene ID: 3872

Symbol: KRT17

Ensembl ID: ENSG00000128422

Description: keratin 17

Associated with

Cells (max top 100)

(Cell Significance Index and respective Thresholds are uniquely calculated using our advanced thresholding algorithms to reveal cell-specific gene markers)

  • Cell Name: embryonic stem cell (CL0002322)
    Fold Change: 68.7709
    Cell Significance Index: -28.3300
  • Cell Name: oral mucosa squamous cell (CL1001576)
    Fold Change: 63.1026
    Cell Significance Index: 542.2400
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: 13.1033
    Cell Significance Index: 356.6600
  • Cell Name: sebaceous gland cell (CL2000021)
    Fold Change: 10.8284
    Cell Significance Index: 14.0100
  • Cell Name: epithelial cell of urethra (CL1000296)
    Fold Change: 8.7198
    Cell Significance Index: 53.9700
  • Cell Name: epidermal cell (CL0000362)
    Fold Change: 7.9397
    Cell Significance Index: 17.9000
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 7.6061
    Cell Significance Index: 395.1200
  • Cell Name: basal epithelial cell of prostatic duct (CL0002236)
    Fold Change: 7.6016
    Cell Significance Index: 67.4800
  • Cell Name: cortical thymic epithelial cell (CL0002364)
    Fold Change: 4.7229
    Cell Significance Index: 39.0600
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 4.0587
    Cell Significance Index: 1794.4600
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 3.7776
    Cell Significance Index: 120.9900
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: 3.5538
    Cell Significance Index: 251.3400
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 2.9982
    Cell Significance Index: 368.6500
  • Cell Name: endothelial tip cell (CL0000704)
    Fold Change: 2.7022
    Cell Significance Index: 11.6200
  • Cell Name: prostate gland microvascular endothelial cell (CL2000059)
    Fold Change: 2.0134
    Cell Significance Index: 14.4600
  • Cell Name: lactocyte (CL0002325)
    Fold Change: 1.6691
    Cell Significance Index: 215.6300
  • Cell Name: luminal hormone-sensing cell of mammary gland (CL4033058)
    Fold Change: 1.3340
    Cell Significance Index: 8.2100
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: 1.3173
    Cell Significance Index: 98.1800
  • Cell Name: basal-myoepithelial cell of mammary gland (CL0002324)
    Fold Change: 1.2453
    Cell Significance Index: 9.2200
  • Cell Name: umbrella cell of urothelium (CL4030056)
    Fold Change: 1.2336
    Cell Significance Index: 11.3600
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 1.2104
    Cell Significance Index: 218.2100
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: 1.1916
    Cell Significance Index: 56.0100
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.4409
    Cell Significance Index: 83.9200
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: 0.4375
    Cell Significance Index: 12.5400
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.4113
    Cell Significance Index: 224.6200
  • Cell Name: mammary gland epithelial cell (CL0002327)
    Fold Change: 0.3736
    Cell Significance Index: 1.7200
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: 0.2105
    Cell Significance Index: 9.1500
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.1892
    Cell Significance Index: 170.8500
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1529
    Cell Significance Index: 15.1300
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.0984
    Cell Significance Index: 16.0100
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: 0.0716
    Cell Significance Index: 54.1600
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: 0.0364
    Cell Significance Index: 22.7000
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.0056
    Cell Significance Index: 1.1200
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: -0.0009
    Cell Significance Index: -0.0900
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: -0.0057
    Cell Significance Index: -10.4300
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: -0.0060
    Cell Significance Index: -11.2500
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: -0.0078
    Cell Significance Index: -12.0100
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0096
    Cell Significance Index: -6.1100
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0106
    Cell Significance Index: -7.8500
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0192
    Cell Significance Index: -10.8400
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.0202
    Cell Significance Index: -0.7100
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: -0.0223
    Cell Significance Index: -30.2800
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.0240
    Cell Significance Index: -0.6700
  • Cell Name: endothelial cell of venule (CL1000414)
    Fold Change: -0.0246
    Cell Significance Index: -0.2800
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: -0.0264
    Cell Significance Index: -0.3600
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0293
    Cell Significance Index: -21.4500
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0344
    Cell Significance Index: -5.8700
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.0377
    Cell Significance Index: -1.7600
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0558
    Cell Significance Index: -25.3500
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.0594
    Cell Significance Index: -1.7100
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: -0.0599
    Cell Significance Index: -21.4800
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.0607
    Cell Significance Index: -1.5600
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.0614
    Cell Significance Index: -7.0400
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0691
    Cell Significance Index: -14.5500
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.0729
    Cell Significance Index: -10.0100
  • Cell Name: vascular lymphangioblast (CL0005022)
    Fold Change: -0.0770
    Cell Significance Index: -1.3600
  • Cell Name: odontoblast (CL0000060)
    Fold Change: -0.0856
    Cell Significance Index: -10.9700
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.1135
    Cell Significance Index: -6.9600
  • Cell Name: slow muscle cell (CL0000189)
    Fold Change: -0.1177
    Cell Significance Index: -1.7600
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: -0.1302
    Cell Significance Index: -25.8300
  • Cell Name: extravillous trophoblast (CL0008036)
    Fold Change: -0.1336
    Cell Significance Index: -0.8300
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.1345
    Cell Significance Index: -6.1000
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: -0.1412
    Cell Significance Index: -3.5300
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.1490
    Cell Significance Index: -21.6600
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: -0.1565
    Cell Significance Index: -10.8300
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.1693
    Cell Significance Index: -19.7300
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.1721
    Cell Significance Index: -19.6400
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.1759
    Cell Significance Index: -3.8100
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: -0.1770
    Cell Significance Index: -10.6300
  • Cell Name: T-helper 17 cell (CL0000899)
    Fold Change: -0.2136
    Cell Significance Index: -1.6300
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.2150
    Cell Significance Index: -4.4600
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.2210
    Cell Significance Index: -22.5800
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.2213
    Cell Significance Index: -13.9500
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.2424
    Cell Significance Index: -25.2400
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.2431
    Cell Significance Index: -28.6700
  • Cell Name: keratinocyte (CL0000312)
    Fold Change: -0.2592
    Cell Significance Index: -6.4800
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.2878
    Cell Significance Index: -17.6900
  • Cell Name: luminal epithelial cell of mammary gland (CL0002326)
    Fold Change: -0.3347
    Cell Significance Index: -4.3100
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.3363
    Cell Significance Index: -8.9800
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.3406
    Cell Significance Index: -11.1500
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: -0.3519
    Cell Significance Index: -23.6700
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.3560
    Cell Significance Index: -13.0700
  • Cell Name: epithelial cell of esophagus (CL0002252)
    Fold Change: -0.3691
    Cell Significance Index: -2.4500
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.3736
    Cell Significance Index: -24.1000
  • Cell Name: peg cell (CL4033014)
    Fold Change: -0.4246
    Cell Significance Index: -9.8100
  • Cell Name: L5/6 near-projecting glutamatergic neuron (CL4030067)
    Fold Change: -0.4641
    Cell Significance Index: -2.4300
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: -0.4717
    Cell Significance Index: -13.8900
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.4749
    Cell Significance Index: -26.6500
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.5144
    Cell Significance Index: -27.0100
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.5191
    Cell Significance Index: -18.1900
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.5441
    Cell Significance Index: -17.3300
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: -0.5627
    Cell Significance Index: -8.0100
  • Cell Name: helper T cell (CL0000912)
    Fold Change: -0.5722
    Cell Significance Index: -8.1300
  • Cell Name: basal cell of epithelium of trachea (CL1000348)
    Fold Change: -0.6114
    Cell Significance Index: -5.2600
  • Cell Name: skeletal muscle myoblast (CL0000515)
    Fold Change: -0.6375
    Cell Significance Index: -6.9300
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: -0.6491
    Cell Significance Index: -28.7100
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: -0.6540
    Cell Significance Index: -13.6900
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.6576
    Cell Significance Index: -22.8500
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.7508
    Cell Significance Index: -15.9900
  • Cell Name: secretory cell (CL0000151)
    Fold Change: -0.7571
    Cell Significance Index: -5.2500

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Other Information

**Key Characteristics:** 1. **Expression Pattern:** KRT17 is predominantly expressed in epithelial cells, including myoepithelial cells of the mammary gland, basal cells of prostate epithelium, and epithelial cells of the urethra, trachea, and bladder. 2. **Structural Role:** KRT17 forms part of the intermediate filament cytoskeleton, providing mechanical strength and resistance to stress in epithelial cells. 3. **Differentiation and Cell Growth:** KRT17 is involved in the regulation of cell growth, differentiation, and proliferation, particularly in the context of epithelial cell development and maintenance. 4. **Positive Regulation:** KRT17 acts as a positive regulator of various cellular processes, including hair follicle development, positive regulation of translation, and protein binding. **Pathways and Functions:** 1. **Cytoskeleton Organization:** KRT17 contributes to the formation and maintenance of the intermediate filament cytoskeleton, which provides structural support and stability to epithelial cells. 2. **Epithelial Cell Differentiation:** KRT17 plays a crucial role in the differentiation of epithelial cells, particularly in the development of the cornified envelope. 3. **Hair Follicle Morphogenesis:** KRT17 is involved in the regulation of hair follicle development and morphogenesis. 4. **Cell Growth and Proliferation:** KRT17 acts as a positive regulator of cell growth and proliferation, contributing to the maintenance of epithelial homeostasis. **Clinical Significance:** 1. **Cancer and Tumorigenesis:** Alterations in KRT17 expression have been observed in various types of cancer, including breast, prostate, and bladder cancers, suggesting its potential role in tumorigenesis. 2. **Skin Disorders:** Abnormalities in KRT17 expression have been linked to skin disorders, such as epidermolysis bullosa simplex, highlighting its importance in skin health. 3. **Mucous Membrane Diseases:** KRT17 expression has been found to be altered in mucous membrane diseases, such as laryngopharyngeal reflux, underscoring its role in maintaining mucosal integrity. 4. **Thymic Epithelial Cell Function:** KRT17 expression is critical for the function of thymic epithelial cells, which are essential for the development and maturation of T cells. In conclusion, Keratin 17 is a vital component of the intermediate filament cytoskeleton, playing a crucial role in maintaining epithelial cell integrity, differentiation, and growth. Its dysregulation has been implicated in various human diseases, highlighting the importance of further research into the mechanisms underlying KRT17 function and its potential as a therapeutic target.

Genular Protein ID: 2384205657

Symbol: K1C17_HUMAN

Name: Keratin, type I cytoskeletal 17

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 1281771

Title: Characterization of the human gene encoding cytokeratin 17 and its expression pattern.

PubMed ID: 1281771

PubMed ID: 1372562

Title: Interferon-gamma regulates expression of a novel keratin class I gene.

PubMed ID: 1372562

DOI: 10.1002/eji.1830220415

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 7539673

Title: Keratin 16 and keratin 17 mutations cause pachyonychia congenita.

PubMed ID: 7539673

DOI: 10.1038/ng0395-273

PubMed ID: 2481679

Title: Patterns of expression of keratin 17 in human epithelia: dependency on cell position.

PubMed ID: 2481679

DOI: 10.1242/jcs.93.3.419

PubMed ID: 10651700

Title: Keratin expression in the normal nail unit: markers of regional differentiation.

PubMed ID: 10651700

DOI: 10.1046/j.1365-2133.2000.03246.x

PubMed ID: 10844551

Title: Keratin 17 expression in the hard epithelial context of the hair and nail, and its relevance for the pachyonychia congenita phenotype.

PubMed ID: 10844551

DOI: 10.1046/j.1523-1747.2000.00986.x

PubMed ID: 15795121

Title: HLA DR B1*04, *07-restricted epitopes on Keratin 17 for autoreactive T cells in psoriasis.

PubMed ID: 15795121

DOI: 10.1016/j.jdermsci.2005.01.001

PubMed ID: 15608502

Title: Interferon-gamma-dependent in vitro model for the putative keratin 17 autoimmune loop in psoriasis: exploration of pharmaco- and gene-therapeutic effects.

PubMed ID: 15608502

DOI: 10.1159/000081685

PubMed ID: 17081983

Title: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.

PubMed ID: 17081983

DOI: 10.1016/j.cell.2006.09.026

PubMed ID: 16713453

Title: Altered keratin 17 peptide ligands inhibit in vitro proliferation of keratinocytes and T cells isolated from patients with psoriasis.

PubMed ID: 16713453

DOI: 10.1016/j.jaad.2006.02.033

PubMed ID: 18691976

Title: Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.

PubMed ID: 18691976

DOI: 10.1016/j.molcel.2008.07.007

PubMed ID: 18669648

Title: A quantitative atlas of mitotic phosphorylation.

PubMed ID: 18669648

DOI: 10.1073/pnas.0805139105

PubMed ID: 20068231

Title: Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.

PubMed ID: 20068231

DOI: 10.1126/scisignal.2000475

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 22006917

Title: Type I keratin 17 protein is phosphorylated on serine 44 by p90 ribosomal protein S6 kinase 1 (RSK1) in a growth- and stress-dependent fashion.

PubMed ID: 22006917

DOI: 10.1074/jbc.m111.302042

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 25218447

Title: Uncovering global SUMOylation signaling networks in a site-specific manner.

PubMed ID: 25218447

DOI: 10.1038/nsmb.2890

PubMed ID: 25114211

Title: Mapping of SUMO sites and analysis of SUMOylation changes induced by external stimuli.

PubMed ID: 25114211

DOI: 10.1073/pnas.1413825111

PubMed ID: 25772364

Title: SUMO-2 orchestrates chromatin modifiers in response to DNA damage.

PubMed ID: 25772364

DOI: 10.1016/j.celrep.2015.02.033

PubMed ID: 28112733

Title: Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation.

PubMed ID: 28112733

DOI: 10.1038/nsmb.3366

PubMed ID: 9008238

Title: Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex.

PubMed ID: 9008238

DOI: 10.1111/1523-1747.ep12335315

PubMed ID: 9767294

Title: Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.

PubMed ID: 9767294

DOI: 10.1046/j.1365-2133.1998.02413.x

PubMed ID: 10571744

Title: Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.

PubMed ID: 10571744

DOI: 10.1046/j.1523-1747.1999.00762.x

PubMed ID: 11348474

Title: Novel keratin 17 mutations in pachyonychia congenita type 2.

PubMed ID: 11348474

DOI: 10.1046/j.1523-1747.2001.01335.x

PubMed ID: 11886499

Title: Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.

PubMed ID: 11886499

DOI: 10.1046/j.0022-202x.2001.01565.x

PubMed ID: 11874497

Title: A novel point mutation in the keratin 17 gene in a Japanese case of pachyonychia congenita type 2.

PubMed ID: 11874497

DOI: 10.1046/j.0022-202x.2001.01701.x

PubMed ID: 15102078

Title: A novel mutation in the second half of the keratin 17 1A domain in a large pedigree with delayed-onset pachyonychia congenita type 2.

PubMed ID: 15102078

DOI: 10.1111/j.0022-202x.2004.22408.x

PubMed ID: 15795125

Title: Identification of a recurrent mutation in keratin 17 in a Japanese family with pachyonychia congenita type 2.

PubMed ID: 15795125

DOI: 10.1016/j.jdermsci.2004.12.022

PubMed ID: 16250206

Title: The genetic basis of pachyonychia congenita.

PubMed ID: 16250206

DOI: 10.1111/j.1087-0024.2005.10204.x

PubMed ID: 16620218

Title: Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity.

PubMed ID: 16620218

DOI: 10.1111/j.1346-8138.2006.00037.x

PubMed ID: 17719747

Title: A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.

PubMed ID: 17719747

DOI: 10.1016/j.jdermsci.2007.07.003

PubMed ID: 18547302

Title: A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb.

PubMed ID: 18547302

DOI: 10.1111/j.1365-2133.2008.08684.x

PubMed ID: 19470054

Title: Novel missense mutation of keratin in Chinese family with steatocystoma multiplex.

PubMed ID: 19470054

DOI: 10.1111/j.1468-3083.2009.03180.x

PubMed ID: 21326300

Title: A large mutational study in pachyonychia congenita.

PubMed ID: 21326300

DOI: 10.1038/jid.2011.20

PubMed ID: 23278621

Title: A novel mutation of keratin 17 gene in a pedigree with pachyonychia congenita type 2.

PubMed ID: 23278621

DOI: 10.1111/j.1365-4632.2010.04667.x

PubMed ID: 23855588

Title: Novel mutation (p.L91P, c.272T>C) of keratin 17 in a case with pachyonychia congenita type 2.

PubMed ID: 23855588

DOI: 10.1111/1346-8138.12212

PubMed ID: 34686882

Title: Formation of keto-type ceramides in palmoplantar keratoderma based on biallelic KDSR mutations in patients.

PubMed ID: 34686882

DOI: 10.1093/hmg/ddab309

Sequence Information:

  • Length: 432
  • Mass: 48106
  • Checksum: 35B429243F47EB5C
  • Sequence:
  • MTTSIRQFTS SSSIKGSSGL GGGSSRTSCR LSGGLGAGSC RLGSAGGLGS TLGGSSYSSC 
    YSFGSGGGYG SSFGGVDGLL AGGEKATMQN LNDRLASYLD KVRALEEANT ELEVKIRDWY 
    QRQAPGPARD YSQYYRTIEE LQNKILTATV DNANILLQID NARLAADDFR TKFETEQALR 
    LSVEADINGL RRVLDELTLA RADLEMQIEN LKEELAYLKK NHEEEMNALR GQVGGEINVE 
    MDAAPGVDLS RILNEMRDQY EKMAEKNRKD AEDWFFSKTE ELNREVATNS ELVQSGKSEI 
    SELRRTMQAL EIELQSQLSM KASLEGNLAE TENRYCVQLS QIQGLIGSVE EQLAQLRCEM 
    EQQNQEYKIL LDVKTRLEQE IATYRRLLEG EDAHLTQYKK EPVTTRQVRT IVEEVQDGKV 
    ISSREQVHQT TR

Genular Protein ID: 2823457695

Symbol: Q14666_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 2442723

Title: Effects of UV, 4-NQO and TPA on gene expression in cultured human epidermal keratinocytes.

PubMed ID: 2442723

DOI: 10.1093/nar/15.15.5945

Sequence Information:

  • Length: 266
  • Mass: 30838
  • Checksum: 0F39A8D9AC5A01BE
  • Sequence:
  • DEFRTKFETD QALRLSVEAD INGLRRVLDE LTLARADLEM QIENLKEELA YLKKNHEEEM 
    NALRGQVGGE INVEMDAAPG VDLSRILNEM RDQYEKMAEK NRKDAEDWFF SKTEELNREV 
    ATNSELVQSG KSEISELRRT MQALEIELQS QLSMKASLEG NLAETENRYC VQLSQIQGLI 
    GSVEEQLAQL RCEMEQQNQE YKILLDVKTR LEQEIATYRR LLEGEDAHLT QYKKEPVTTR 
    QVRTIVEEVQ DGKVISSREQ VHQTTR

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.