Details for: KRT13

Gene ID: 3860

Symbol: KRT13

Ensembl ID: ENSG00000171401

Description: keratin 13

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: polychromatophilic erythroblast (CL0000550)
    Fold Change: 152.1422
    Cell Significance Index: -23.6700
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 108.6762
    Cell Significance Index: -27.5700
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 21.3998
    Cell Significance Index: -26.3900
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 9.0859
    Cell Significance Index: 253.9200
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 8.6721
    Cell Significance Index: 1066.3200
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 7.9551
    Cell Significance Index: 1434.0500
  • Cell Name: epithelial cell of esophagus (CL0002252)
    Fold Change: 6.3679
    Cell Significance Index: 42.2700
  • Cell Name: epithelial cell of urethra (CL1000296)
    Fold Change: 5.0462
    Cell Significance Index: 31.2300
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 5.0336
    Cell Significance Index: 261.4800
  • Cell Name: umbrella cell of urothelium (CL4030056)
    Fold Change: 5.0333
    Cell Significance Index: 46.3500
  • Cell Name: epithelial cell of prostate (CL0002231)
    Fold Change: 1.9320
    Cell Significance Index: 11.9200
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 1.7632
    Cell Significance Index: 44.0800
  • Cell Name: epithelial cell of stratum germinativum of esophagus (CL1000447)
    Fold Change: 0.7075
    Cell Significance Index: 5.7800
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: 0.5622
    Cell Significance Index: 15.3000
  • Cell Name: oral mucosa squamous cell (CL1001576)
    Fold Change: 0.5097
    Cell Significance Index: 4.3800
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.5057
    Cell Significance Index: 96.2500
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: 0.4844
    Cell Significance Index: 358.8200
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.2935
    Cell Significance Index: 29.0400
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.2853
    Cell Significance Index: 257.5800
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 0.1986
    Cell Significance Index: 6.3600
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: 0.1943
    Cell Significance Index: 109.6100
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.1406
    Cell Significance Index: 22.8600
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: 0.0681
    Cell Significance Index: 0.9700
  • Cell Name: endothelial cell of venule (CL1000414)
    Fold Change: 0.0634
    Cell Significance Index: 0.7200
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: 0.0377
    Cell Significance Index: 23.5300
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 0.0322
    Cell Significance Index: 0.4400
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: 0.0105
    Cell Significance Index: 7.9800
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: 0.0000
    Cell Significance Index: 0.0000
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -0.0064
    Cell Significance Index: -0.1300
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0152
    Cell Significance Index: -8.3100
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: -0.0167
    Cell Significance Index: -25.6900
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0231
    Cell Significance Index: -3.9500
  • Cell Name: primitive red blood cell (CL0002355)
    Fold Change: -0.0239
    Cell Significance Index: -0.2700
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.0259
    Cell Significance Index: -0.9100
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.0272
    Cell Significance Index: -3.1700
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.0308
    Cell Significance Index: -1.8900
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: -0.0386
    Cell Significance Index: -17.0600
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0444
    Cell Significance Index: -20.1700
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.0451
    Cell Significance Index: -1.3000
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: -0.0479
    Cell Significance Index: -5.2100
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.0955
    Cell Significance Index: -4.3300
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: -0.1180
    Cell Significance Index: -23.4300
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: -0.1183
    Cell Significance Index: -8.1800
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: -0.1584
    Cell Significance Index: -31.7800
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.1648
    Cell Significance Index: -18.8100
  • Cell Name: odontoblast (CL0000060)
    Fold Change: -0.1733
    Cell Significance Index: -22.2100
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.1951
    Cell Significance Index: -25.2100
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.1971
    Cell Significance Index: -20.1300
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.2016
    Cell Significance Index: -27.6900
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.2306
    Cell Significance Index: -26.4200
  • Cell Name: epithelial cell of lacrimal sac (CL1000436)
    Fold Change: -0.2348
    Cell Significance Index: -1.6900
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.2420
    Cell Significance Index: -5.0200
  • Cell Name: mucosal invariant T cell (CL0000940)
    Fold Change: -0.2807
    Cell Significance Index: -3.2300
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.2945
    Cell Significance Index: -6.3800
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: -0.3118
    Cell Significance Index: -18.7200
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.3171
    Cell Significance Index: -14.9100
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.3462
    Cell Significance Index: -8.9000
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.3468
    Cell Significance Index: -25.8500
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: -0.4342
    Cell Significance Index: -12.7900
  • Cell Name: proerythroblast (CL0000547)
    Fold Change: -0.4780
    Cell Significance Index: -6.8500
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: -0.5299
    Cell Significance Index: -23.0400
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.5306
    Cell Significance Index: -11.3000
  • Cell Name: keratinocyte (CL0000312)
    Fold Change: -0.5341
    Cell Significance Index: -13.3400
  • Cell Name: squamous epithelial cell (CL0000076)
    Fold Change: -0.5467
    Cell Significance Index: -6.6500
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.5481
    Cell Significance Index: -20.1200
  • Cell Name: slow muscle cell (CL0000189)
    Fold Change: -0.5935
    Cell Significance Index: -8.8800
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.6344
    Cell Significance Index: -29.5800
  • Cell Name: thymocyte (CL0000893)
    Fold Change: -0.7075
    Cell Significance Index: -8.9400
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.7126
    Cell Significance Index: -24.9700
  • Cell Name: obsolete epithelial cell of alveolus of lung (CL0010003)
    Fold Change: -0.7956
    Cell Significance Index: -19.8400
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: -0.8356
    Cell Significance Index: -22.3900
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.8412
    Cell Significance Index: -22.4600
  • Cell Name: fallopian tube secretory epithelial cell (CL4030006)
    Fold Change: -0.8487
    Cell Significance Index: -13.1300
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.8688
    Cell Significance Index: -27.6700
  • Cell Name: T-helper 17 cell (CL0000899)
    Fold Change: -0.8715
    Cell Significance Index: -6.6500
  • Cell Name: taste receptor cell (CL0000209)
    Fold Change: -0.8736
    Cell Significance Index: -10.1600
  • Cell Name: urothelial cell (CL0000731)
    Fold Change: -0.8762
    Cell Significance Index: -6.1100
  • Cell Name: neutrophil progenitor cell (CL0000834)
    Fold Change: -0.8931
    Cell Significance Index: -23.8900
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: -0.8972
    Cell Significance Index: -13.5200
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.9038
    Cell Significance Index: -29.5900
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: -0.9056
    Cell Significance Index: -25.9600
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: -0.9302
    Cell Significance Index: -24.4600
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: -0.9417
    Cell Significance Index: -20.6200
  • Cell Name: epithelial cell (CL0000066)
    Fold Change: -0.9669
    Cell Significance Index: -10.2000
  • Cell Name: erythrocyte (CL0000232)
    Fold Change: -0.9675
    Cell Significance Index: -24.6500
  • Cell Name: pro-T cell (CL0000827)
    Fold Change: -0.9705
    Cell Significance Index: -24.7900
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -1.0024
    Cell Significance Index: -25.0100
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -1.0391
    Cell Significance Index: -17.3900
  • Cell Name: CD14-positive, CD16-negative classical monocyte (CL0002057)
    Fold Change: -1.0832
    Cell Significance Index: -20.0200
  • Cell Name: peg cell (CL4033014)
    Fold Change: -1.0994
    Cell Significance Index: -25.4000
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -1.1813
    Cell Significance Index: -23.0600
  • Cell Name: myeloid dendritic cell (CL0000782)
    Fold Change: -1.1871
    Cell Significance Index: -9.3100
  • Cell Name: hepatoblast (CL0005026)
    Fold Change: -1.2557
    Cell Significance Index: -21.1200
  • Cell Name: seromucus secreting cell (CL0000159)
    Fold Change: -1.2678
    Cell Significance Index: -26.4400
  • Cell Name: basal cell (CL0000646)
    Fold Change: -1.2782
    Cell Significance Index: -15.2100
  • Cell Name: nasal mucosa goblet cell (CL0002480)
    Fold Change: -1.2981
    Cell Significance Index: -13.2400
  • Cell Name: CD14-positive monocyte (CL0001054)
    Fold Change: -1.3313
    Cell Significance Index: -26.0300
  • Cell Name: paneth cell of colon (CL0009009)
    Fold Change: -1.3421
    Cell Significance Index: -20.1100
  • Cell Name: epithelial cell of pancreas (CL0000083)
    Fold Change: -1.3575
    Cell Significance Index: -22.3700
  • Cell Name: megakaryocyte (CL0000556)
    Fold Change: -1.3744
    Cell Significance Index: -22.2600

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:** Keratin 13 exhibits several key characteristics that distinguish it from other keratin proteins. Its high expression in stratified epithelial cells, particularly in the epidermis, highlights its role in keratinization, a process crucial for maintaining the barrier function of the skin. Additionally, KRT13's ability to interact with other proteins and form complexes with intermediate filaments underscores its importance in maintaining the structural integrity of epithelial cells. Its involvement in the formation of the cornified envelope, a feature characteristic of stratified epithelial cells, further emphasizes its critical role in epithelial differentiation. **Pathways and Functions:** Keratin 13 is involved in various cellular processes, including: 1. **Cytoskeleton Organization:** KRT13 contributes to the organization and stability of the intermediate filament cytoskeleton, which is essential for maintaining cellular shape and structure. 2. **Protein Binding:** KRT13 interacts with other proteins, including keratins, intermediate filament-associated proteins, and cytoskeletal proteins, to form complexes that regulate cellular processes. 3. **Formation of the Cornified Envelope:** KRT13 plays a critical role in the formation and maintenance of the cornified envelope, a feature characteristic of stratified epithelial cells. 4. **Stress Response:** KRT13 is involved in regulating the response to cellular stress, including heat shock and oxidative stress. 5. **Epithelial Cell Differentiation:** KRT13 contributes to the differentiation of epithelial cells, particularly in the development of stratified epithelial tissues. **Clinical Significance:** Dysregulation of KRT13 has been implicated in various diseases, including: 1. **Psoriasis:** Mutations in the KRT13 gene have been associated with psoriasis, a chronic inflammatory skin disease characterized by abnormal keratinization. 2. **Cancer:** Alterations in KRT13 expression have been observed in various types of cancer, including squamous cell carcinoma and basal cell carcinoma. 3. **Epidermolysis Bullosa:** Mutations in the KRT13 gene have been associated with epidermolysis bullosa, a group of genetic disorders characterized by blistering skin lesions. In conclusion, Keratin 13 is a critical component of epithelial cell structure and integrity, playing a pivotal role in maintaining the structural integrity and differentiation of stratified epithelial cells. Its involvement in various cellular processes, including cytoskeleton organization, protein binding, and stress response, underscores its significance in maintaining epithelial cell homeostasis. Dysregulation of KRT13 has been implicated in various diseases, highlighting the importance of this gene in maintaining human health.

Genular Protein ID: 939079087

Symbol: K1C13_HUMAN

Name: Keratin, type I cytoskeletal 13

UniProtKB Accession Codes:

P13646 Q53G54 Q6AZK5 Q8N240

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 2 CTD 1 ChiTaRS 1 DMDM 1 DNASU 1 DisGeNET 1 EMBL 9 Ensembl 2 ExpressionAtlas 1 GO 11 Gene3D 3 GeneCards 1 GeneTree 1 GeneWiki 1 GenomeRNAi 1 GlyConnect 1 GlyCosmos 1 GlyGen 1 HGNC 1 HOGENOM 1 HPA 1 InParanoid 1 IntAct 1 InterPro 3 KEGG 1 MANE-Select 1 MIM 3 MINT 1 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 1 OrthoDB 1 PANTHER 2 PIR 2 PRIDE 1 PRINTS 1 PRO 1 PROSITE 2 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 1 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 3 RNAct 1 Reactome 2 RefSeq 2 SMART 1 SMR 1 STRING 1 SUPFAM 1 SignaLink 1 SwissPalm 1 TreeFam 1 UCSC 1 UniProtKB 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1 neXtProt 1

Citations:

PubMed ID: 2475110

Title: Sequence of a human keratin 13 specific cDNA encompassing coil 1B through the 3' end.

PubMed ID: 2475110

DOI: 10.1016/0006-291x(89)90847-4

PubMed ID: 2477803

Title: The N-, but not the C-terminal domains of human keratins 13 and 15 are closely related.

PubMed ID: 2477803

DOI: 10.1093/nar/17.19.7984

PubMed ID: 2483837

Title: Synthesis of cytokeratin 13, a component characteristic of internal stratified epithelia, is not induced in human epidermal tumors.

PubMed ID: 2483837

DOI: 10.1111/j.1432-0436.1989.tb00612.x

PubMed ID: 9714826

Title: Isolation, sequence and expression of the gene encoding human keratin 13.

PubMed ID: 9714826

DOI: 10.1016/s0378-1119(98)00297-2

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: 2474541

Title: Cytokeratin 13 contains O-glycosidically linked N-acetylglucosamine residues.

PubMed ID: 2474541

DOI: 10.1016/s0021-9258(18)71636-0

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: 19369195

Title: Large-scale proteomics analysis of the human kinome.

PubMed ID: 19369195

DOI: 10.1074/mcp.m800588-mcp200

PubMed ID: 20068231

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

PubMed ID: 20068231

DOI: 10.1126/scisignal.2000475

PubMed ID: 21406692

Title: System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.

PubMed ID: 21406692

DOI: 10.1126/scisignal.2001570

PubMed ID: 23186163

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

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 24129315

Title: Immunoaffinity enrichment and mass spectrometry analysis of protein methylation.

PubMed ID: 24129315

DOI: 10.1074/mcp.o113.027870

PubMed ID: 7493031

Title: Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus.

PubMed ID: 7493031

DOI: 10.1038/ng1295-453

PubMed ID: 10561721

Title: Identification of two novel mutations in keratin 13 as the cause of white sponge naevus.

PubMed ID: 10561721

DOI: 10.1111/j.1601-0825.1999.tb00097.x

PubMed ID: 11379896

Title: A novel mutation in the keratin 13 gene causing oral white sponge nevus.

PubMed ID: 11379896

DOI: 10.1177/00220345010800031401

PubMed ID: 14600690

Title: Constitutional mutation of keratin 13 gene in familial white sponge nevus.

PubMed ID: 14600690

DOI: 10.1016/s1079-2104(03)00372-x

PubMed ID: 18616775

Title: A de novo missense mutation in the keratin 13 gene in oral white sponge naevus.

PubMed ID: 18616775

DOI: 10.1111/j.1365-2133.2008.08716.x

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 25606422

Title: Keratin 13 mutations associated with oral white sponge nevus in two Chinese families.

PubMed ID: 25606422

DOI: 10.1016/j.mgene.2014.04.008

PubMed ID: 29476668

Title: Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus.

PubMed ID: 29476668

DOI: 10.4317/medoral.21437

Sequence Information:

  • Length: 458
  • Mass: 49588
  • Checksum: A51AECFD6195ACB4
  • Sequence:
    • MSLRLQSSSA SYGGGFGGGS CQLGGGRGVS TCSTRFVSGG SAGGYGGGVS CGFGGGAGSG 
FGGGYGGGLG GGYGGGLGGG FGGGFAGGFV DFGACDGGLL TGNEKITMQN LNDRLASYLE 
KVRALEEANA DLEVKIRDWH LKQSPASPER DYSPYYKTIE ELRDKILTAT IENNRVILEI 
DNARLAADDF RLKYENELAL RQSVEADING LRRVLDELTL SKTDLEMQIE SLNEELAYMK 
KNHEEEMKEF SNQVVGQVNV EMDATPGIDL TRVLAEMREQ YEAMAERNRR DAEEWFHTKS 
AELNKEVSTN TAMIQTSKTE ITELRRTLQG LEIELQSQLS MKAGLENTVA ETECRYALQL 
QQIQGLISSI EAQLSELRSE MECQNQEYKM LLDIKTRLEQ EIATYRSLLE GQDAKMIGFP 
SSAGSVSPRS TSVTTTSSAS VTTTSNASGR RTSDVRRP

Genular Protein ID: 3242151711

Symbol: A1A4E9_HUMAN

Name: N/A

UniProtKB Accession Codes:

A1A4E9

Database IDs:

ARBA 2 AlphaFoldDB 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 5 GO 4 Gene3D 3 IntAct 1 InterPro 3 KEGG 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PRINTS 1 PROSITE 4 PeptideAtlas 1 Pfam 1 PharmGKB 1 RefSeq 1 RuleBase 1 SAM 2 SMART 1 SMR 1 SUPFAM 1

Citations:

PubMed ID: 11181995

Title: The sequence of the human genome.

PubMed ID: 11181995

DOI: 10.1126/science.1058040

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

Sequence Information:

  • Length: 458
  • Mass: 49586
  • Checksum: 9E033A247CD2B106
  • Sequence:
    • MSLRLQSSSA SYGGGFGGGS CQLGGGRGVS TCSTRFVSGG SAGGYGGGVS CGFGGGAGSG 
FGGGYGGGLG GGYGGGLGGG FGGGFAGGFV DFGACDGGLL TGNEKITMQN LNDRLASYLE 
KVRALEEANA DLEVKIRDWH LKQSPASPER DYSPYYKTIE ELRDKILTAT IENNRVILEI 
DNARLAVDDF RLKYENELAL RQSVEADING LRRVLDELTL SKTDLEMQIE SLNEELAYMK 
KNHEEEMKEF SNQVVGQVNV EMDATPGIDL TRVLAEMREQ YEAMAERNRR DAEEWFHAKS 
AELNKEVSTN TAMIQTSKTE ITELRRTLQG LEIELQSQLS MKAGLENTVA ETECRYALQL 
QQIQGLISSI EAQLSELRSE MECQNQEYKM LLDIKTRLEQ EIATYRSLLE GQDAKMIGFP 
SSAGSVSPRS TSVTTTSSAS VTTTSNASGR RTSDVRRP

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.