Human Gene NOTCH1 (ENST00000651671.1_7) from GENCODE V47lift37
  Description: notch receptor 1 (from RefSeq NM_017617.5)
Gencode Transcript: ENST00000651671.1_7
Gencode Gene: ENSG00000148400.13_14
Transcript (Including UTRs)
   Position: hg19 chr9:139,388,885-139,440,500 Size: 51,616 Total Exon Count: 34 Strand: -
Coding Region
   Position: hg19 chr9:139,390,523-139,440,238 Size: 49,716 Coding Exon Count: 34 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesGeneReviewsModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr9:139,388,885-139,440,500)mRNA (may differ from genome)Protein (2555 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedReactome
UniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: NOTC1_HUMAN
DESCRIPTION: RecName: Full=Neurogenic locus notch homolog protein 1; Short=Notch 1; Short=hN1; AltName: Full=Translocation-associated notch protein TAN-1; Contains: RecName: Full=Notch 1 extracellular truncation; Contains: RecName: Full=Notch 1 intracellular domain; Short=NICD; Flags: Precursor;
FUNCTION: Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. May be important for normal lymphocyte function. In altered form, may contribute to transformation or progression in some T-cell neoplasms. Involved in the maturation of both CD4+ and CD8+ cells in the thymus. May be important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, may function as a receptor for neuronal DNER and may be involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May enhance HIF1A function by sequestering HIF1AN away from HIF1A (By similarity).
SUBUNIT: Heterodimer of a C-terminal fragment N(TM) and an N- terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with DNER, DTX1, DTX2 and RBPJ/RBPSUH. Also interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH1. The activated membrane-bound form interacts with AAK1 which promotes NOTCH1 stabilization. Forms a trimeric complex with FBXW7 and SGK1. Interacts with HIF1AN. HIF1AN negatively regulates the function of notch intracellular domain (NICD), accelerating myogenic differentiation (By similarity).
INTERACTION: Q13526:PIN1; NbExp=9; IntAct=EBI-636374, EBI-714158; Q06330:RBPJ; NbExp=2; IntAct=EBI-636374, EBI-632552; Q13573:SNW1; NbExp=3; IntAct=EBI-636374, EBI-632715;
SUBCELLULAR LOCATION: Cell membrane; Single-pass type I membrane protein (By similarity).
SUBCELLULAR LOCATION: Notch 1 intracellular domain: Nucleus (By similarity). Note=Following proteolytical processing NICD is translocated to the nucleus (By similarity).
TISSUE SPECIFICITY: In fetal tissues most abundant in spleen, brain stem and lung. Also present in most adult tissues where it is found mainly in lymphoid tissues.
PTM: Synthesized in the endoplasmic reticulum as an inactive form which is proteolytically cleaved by a furin-like convertase in the trans-Golgi network before it reaches the plasma membrane to yield an active, ligand-accessible form. Cleavage results in a C- terminal fragment N(TM) and a N-terminal fragment N(EC). Following ligand binding, it is cleaved by TNF-alpha converting enzyme (TACE) to yield a membrane-associated intermediate fragment called notch extracellular truncation (NEXT). Following endocytosis, this fragment is then cleaved by presenilin dependent gamma-secretase to release a notch-derived peptide containing the intracellular domain (NICD) from the membrane (By similarity).
PTM: Phosphorylated (By similarity).
PTM: O-glycosylated on the EGF-like domains. Contains both O- linked fucose and O-linked glucose.
PTM: Ubiquitinated; undergoes 'Lys-29'-linked polyubiquitination catalyzed by ITCH. Monoubiquitination at Lys-1759 is required for activation by gamma-secretase cleavage, it promotes interaction with AAK1, which stabilizes it. Deubiquitination by EIF3F is necessary for nuclear import of activated Notch.
PTM: Hydroxylated at Asn-1955 by HIF1AN. Hydroxylated at Asn-2022 by HIF1AN (By similarity). Hydroxylation reduces affinity for HI1AN and may thus indirectly modulate negative regulation of NICD (By similarity).
DISEASE: Defects in NOTCH1 are a cause of aortic valve disease 1 (AOVD1) [MIM:109730]. A common defect in the aortic valve in which two rather than three leaflets are present. It is often associated with aortic valve calcification and insufficiency. In extreme cases, the blood flow may be so restricted that the left ventricle fails to grow, resulting in hypoplastic left heart syndrome.
SIMILARITY: Belongs to the NOTCH family.
SIMILARITY: Contains 5 ANK repeats.
SIMILARITY: Contains 36 EGF-like domains.
SIMILARITY: Contains 3 LNR (Lin/Notch) repeats.
WEB RESOURCE: Name=Atlas of Genetics and Cytogenetics in Oncology and Haematology; URL="http://atlasgeneticsoncology.org/Genes/NOTCH1ID30ch9q34.html";

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: NOTCH1
Diseases sorted by gene-association score: adams-oliver syndrome 5* (1330), aortic valve disease 1* (1030), left ventricular outflow tract obstruction* (500), familial bicuspid aortic valve* (368), adams-oliver syndrome* (235), tetralogy of fallot* (149), oliver syndrome (49), invasive bladder transitional cell carcinoma (22), hypoplastic left heart syndrome (20), nodular regenerative hyperplasia (18), acute lymphocytic leukemia (15), lacrimal gland adenoid cystic carcinoma (15), substernal goiter (15), alagille syndrome 1 (14), c-p angle neurinoma (14), subclavian steal syndrome (14), kleefstra syndrome (13), actg2 (13), richter's syndrome (12), lymphoblastic lymphoma (12), splenic diffuse red pulp small b-cell lymphoma (11), lymphoblastic leukemia (10), aplasia cutis congenita (10), carcinoid tumors, intestinal (9), cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 (9), tetraploidy (9), ossifying fibroma (9), tympanic membrane disease (9), hajdu-cheney syndrome (8), petroclival meningioma (8), mucocele of salivary gland (8), sciatic neuropathy (7), aortic disease (7), aortic valve disease 2 (7), granulomatous gastritis (7), plasmablastic lymphoma (7), acrocallosal syndrome (7), nerve compression syndrome (6), spondylocostal dysostosis 3, autosomal recessive (6), pyomyositis (6), radial neuropathy (6), long qt syndrome 13 (6), breast cancer (6), deafness, autosomal recessive 79 (6), tongue squamous cell carcinoma (6), lung adenoma (6), johanson-blizzard syndrome (6), plexopathy (6), tibial neuropathy (6), tarsal tunnel syndrome (6), frontal sinusitis (6), cervical adenosquamous carcinoma (5), brachial plexus neuritis (5), aortic coarctation (5), polyradiculopathy (5), squamous cell carcinoma (5), discrete subaortic stenosis (5), hard palate cancer (5), bone squamous cell carcinoma (5), optic disk drusen (5), aortic valve insufficiency (5), diabetes mellitus, insulin-dependent, 11 (5), deafness, autosomal recessive 33 (4), tricuspid valve stenosis (4), chorioangioma (4), dowling-degos disease (4), jervell and lange-nielsen syndrome (4), dystonia-1, torsion (4), precursor t-cell acute lymphoblastic leukemia (4), chorioretinal scar (4), poland syndrome (4), spinal cord astrocytoma (4), cd45 deficiency (4), lacrimal gland adenocarcinoma (4), chronic lymphocytic leukemia (4), spinal cord ependymoma (4), granulomatous angiitis (4), carotid artery dissection (4), skull base meningioma (4), sialolithiasis (3), hallermann-streiff syndrome (3), serotonin syndrome (3), intrahepatic cholangiocarcinoma (3), leukemia, acute lymphoblastic (2), endometrial cancer (2), heart disease (2), pancreatic cancer (2), bone cancer (2), hematologic cancer (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -148.00262-0.565 Picture PostScript Text
3' UTR -588.101638-0.359 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR002110 - Ankyrin_rpt
IPR020683 - Ankyrin_rpt-contain_dom
IPR024600 - DUF3454_notch
IPR000742 - EG-like_dom
IPR001881 - EGF-like_Ca-bd
IPR013032 - EGF-like_CS
IPR000152 - EGF-type_Asp/Asn_hydroxyl_site
IPR018097 - EGF_Ca-bd_CS
IPR008297 - Notch
IPR022362 - Notch_1
IPR000800 - Notch_dom
IPR010660 - Notch_NOD_dom
IPR011656 - Notch_NODP_dom

Pfam Domains:
PF00008 - EGF-like domain
PF00023 - Ankyrin repeat
PF00066 - LNR domain
PF06816 - NOTCH protein
PF07645 - Calcium-binding EGF domain
PF07684 - NOTCH protein
PF12661 - Human growth factor-like EGF
PF12796 - Ankyrin repeats (3 copies)
PF13606 - Ankyrin repeat
PF13637 - Ankyrin repeats (many copies)
PF13857 - Ankyrin repeats (many copies)

SCOP Domains:
140860 - Pseudo ankyrin repeat-like
48403 - Ankyrin repeat
57196 - EGF/Laminin
57184 - Growth factor receptor domain
90193 - Notch domain

Protein Data Bank (PDB) 3-D Structure
MuPIT help
1PB5 - NMR MuPIT 1TOZ - NMR MuPIT 1YYH - X-ray MuPIT 2F8X - X-ray MuPIT 2F8Y - X-ray MuPIT 2HE0 - X-ray MuPIT 2VJ3 - X-ray MuPIT 3ETO - X-ray MuPIT 3I08 - X-ray 3L95 - X-ray MuPIT 3NBN - X-ray MuPIT 3V79 - X-ray MuPIT


ModBase Predicted Comparative 3D Structure on P46531
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The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGDEnsembl   
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0001047 core promoter binding
GO:0001190 transcriptional activator activity, RNA polymerase II transcription factor binding
GO:0003682 chromatin binding
GO:0003700 transcription factor activity, sequence-specific DNA binding
GO:0004857 enzyme inhibitor activity
GO:0004888 transmembrane signaling receptor activity
GO:0005112 Notch binding
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0019899 enzyme binding
GO:0031490 chromatin DNA binding
GO:0038023 signaling receptor activity
GO:0043565 sequence-specific DNA binding
GO:0046872 metal ion binding
GO:0046982 protein heterodimerization activity

Biological Process:
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001525 angiogenesis
GO:0001701 in utero embryonic development
GO:0001708 cell fate specification
GO:0001837 epithelial to mesenchymal transition
GO:0001889 liver development
GO:0001947 heart looping
GO:0002040 sprouting angiogenesis
GO:0002052 positive regulation of neuroblast proliferation
GO:0002437 inflammatory response to antigenic stimulus
GO:0003157 endocardium development
GO:0003160 endocardium morphogenesis
GO:0003162 atrioventricular node development
GO:0003169 coronary vein morphogenesis
GO:0003180 aortic valve morphogenesis
GO:0003181 atrioventricular valve morphogenesis
GO:0003184 pulmonary valve morphogenesis
GO:0003192 mitral valve formation
GO:0003197 endocardial cushion development
GO:0003198 epithelial to mesenchymal transition involved in endocardial cushion formation
GO:0003203 endocardial cushion morphogenesis
GO:0003207 cardiac chamber formation
GO:0003208 cardiac ventricle morphogenesis
GO:0003209 cardiac atrium morphogenesis
GO:0003213 cardiac right atrium morphogenesis
GO:0003214 cardiac left ventricle morphogenesis
GO:0003219 cardiac right ventricle formation
GO:0003222 ventricular trabecula myocardium morphogenesis
GO:0003241 growth involved in heart morphogenesis
GO:0003256 regulation of transcription from RNA polymerase II promoter involved in myocardial precursor cell differentiation
GO:0003264 regulation of cardioblast proliferation
GO:0003270 Notch signaling pathway involved in regulation of secondary heart field cardioblast proliferation
GO:0003273 cell migration involved in endocardial cushion formation
GO:0003344 pericardium morphogenesis
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0006367 transcription initiation from RNA polymerase II promoter
GO:0006955 immune response
GO:0006959 humoral immune response
GO:0007050 cell cycle arrest
GO:0007219 Notch signaling pathway
GO:0007221 positive regulation of transcription of Notch receptor target
GO:0007275 multicellular organism development
GO:0007283 spermatogenesis
GO:0007368 determination of left/right symmetry
GO:0007386 compartment pattern specification
GO:0007409 axonogenesis
GO:0007420 brain development
GO:0007440 foregut morphogenesis
GO:0007492 endoderm development
GO:0007507 heart development
GO:0008284 positive regulation of cell proliferation
GO:0008285 negative regulation of cell proliferation
GO:0008544 epidermis development
GO:0008593 regulation of Notch signaling pathway
GO:0009912 auditory receptor cell fate commitment
GO:0010001 glial cell differentiation
GO:0010468 regulation of gene expression
GO:0010629 negative regulation of gene expression
GO:0010718 positive regulation of epithelial to mesenchymal transition
GO:0010812 negative regulation of cell-substrate adhesion
GO:0010832 negative regulation of myotube differentiation
GO:0014031 mesenchymal cell development
GO:0014807 regulation of somitogenesis
GO:0021515 cell differentiation in spinal cord
GO:0021915 neural tube development
GO:0030154 cell differentiation
GO:0030182 neuron differentiation
GO:0030216 keratinocyte differentiation
GO:0030279 negative regulation of ossification
GO:0030324 lung development
GO:0030326 embryonic limb morphogenesis
GO:0030334 regulation of cell migration
GO:0030335 positive regulation of cell migration
GO:0030513 positive regulation of BMP signaling pathway
GO:0030514 negative regulation of BMP signaling pathway
GO:0030900 forebrain development
GO:0031069 hair follicle morphogenesis
GO:0031100 animal organ regeneration
GO:0031960 response to corticosteroid
GO:0032495 response to muramyl dipeptide
GO:0032496 response to lipopolysaccharide
GO:0035116 embryonic hindlimb morphogenesis
GO:0035148 tube formation
GO:0035914 skeletal muscle cell differentiation
GO:0035924 cellular response to vascular endothelial growth factor stimulus
GO:0042127 regulation of cell proliferation
GO:0042246 tissue regeneration
GO:0043065 positive regulation of apoptotic process
GO:0043086 negative regulation of catalytic activity
GO:0045070 positive regulation of viral genome replication
GO:0045165 cell fate commitment
GO:0045596 negative regulation of cell differentiation
GO:0045603 positive regulation of endothelial cell differentiation
GO:0045607 regulation of auditory receptor cell differentiation
GO:0045608 negative regulation of auditory receptor cell differentiation
GO:0045618 positive regulation of keratinocyte differentiation
GO:0045662 negative regulation of myoblast differentiation
GO:0045665 negative regulation of neuron differentiation
GO:0045668 negative regulation of osteoblast differentiation
GO:0045687 positive regulation of glial cell differentiation
GO:0045747 positive regulation of Notch signaling pathway
GO:0045892 negative regulation of transcription, DNA-templated
GO:0045893 positive regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0045955 negative regulation of calcium ion-dependent exocytosis
GO:0045967 negative regulation of growth rate
GO:0046427 positive regulation of JAK-STAT cascade
GO:0046533 negative regulation of photoreceptor cell differentiation
GO:0046579 positive regulation of Ras protein signal transduction
GO:0048103 somatic stem cell division
GO:0048663 neuron fate commitment
GO:0048708 astrocyte differentiation
GO:0048709 oligodendrocyte differentiation
GO:0048711 positive regulation of astrocyte differentiation
GO:0048715 negative regulation of oligodendrocyte differentiation
GO:0048754 branching morphogenesis of an epithelial tube
GO:0048845 venous blood vessel morphogenesis
GO:0050678 regulation of epithelial cell proliferation
GO:0050679 positive regulation of epithelial cell proliferation
GO:0050767 regulation of neurogenesis
GO:0050768 negative regulation of neurogenesis
GO:0050793 regulation of developmental process
GO:0055008 cardiac muscle tissue morphogenesis
GO:0060038 cardiac muscle cell proliferation
GO:0060045 positive regulation of cardiac muscle cell proliferation
GO:0060253 negative regulation of glial cell proliferation
GO:0060271 cilium assembly
GO:0060317 cardiac epithelial to mesenchymal transition
GO:0060411 cardiac septum morphogenesis
GO:0060412 ventricular septum morphogenesis
GO:0060528 secretory columnal luminar epithelial cell differentiation involved in prostate glandular acinus development
GO:0060548 negative regulation of cell death
GO:0060740 prostate gland epithelium morphogenesis
GO:0060768 regulation of epithelial cell proliferation involved in prostate gland development
GO:0060842 arterial endothelial cell differentiation
GO:0060843 venous endothelial cell differentiation
GO:0060948 cardiac vascular smooth muscle cell development
GO:0060956 endocardial cell differentiation
GO:0060979 vasculogenesis involved in coronary vascular morphogenesis
GO:0060982 coronary artery morphogenesis
GO:0061314 Notch signaling involved in heart development
GO:0061384 heart trabecula morphogenesis
GO:0061419 positive regulation of transcription from RNA polymerase II promoter in response to hypoxia
GO:0070374 positive regulation of ERK1 and ERK2 cascade
GO:0070986 left/right axis specification
GO:0071372 cellular response to follicle-stimulating hormone stimulus
GO:0072017 distal tubule development
GO:0072044 collecting duct development
GO:0072144 glomerular mesangial cell development
GO:0072602 interleukin-4 secretion
GO:0090051 negative regulation of cell migration involved in sprouting angiogenesis
GO:0090090 negative regulation of canonical Wnt signaling pathway
GO:0097150 neuronal stem cell population maintenance
GO:1901201 regulation of extracellular matrix assembly
GO:1902263 apoptotic process involved in embryonic digit morphogenesis
GO:1903849 positive regulation of aorta morphogenesis
GO:2000737 negative regulation of stem cell differentiation
GO:2000811 negative regulation of anoikis
GO:2000974 negative regulation of pro-B cell differentiation
GO:2001027 negative regulation of endothelial cell chemotaxis

Cellular Component:
GO:0000139 Golgi membrane
GO:0001669 acrosomal vesicle
GO:0002193 MAML1-RBP-Jkappa- ICN1 complex
GO:0005576 extracellular region
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0005794 Golgi apparatus
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005912 adherens junction
GO:0009986 cell surface
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
GO:0031410 cytoplasmic vesicle
GO:0043235 receptor complex
GO:0071944 cell periphery


-  Descriptions from all associated GenBank mRNAs
  BC046127 - Homo sapiens, clone IMAGE:4938771, mRNA.
BC063597 - Homo sapiens cDNA clone IMAGE:4754960, partial cds.
BC039147 - Homo sapiens Notch homolog 1, translocation-associated (Drosophila), mRNA (cDNA clone IMAGE:4746828), with apparent retained intron.
AK000012 - Homo sapiens cDNA FLJ20005 fis, clone ADKA02526.
BC049843 - Homo sapiens Notch homolog 1, translocation-associated (Drosophila), mRNA (cDNA clone IMAGE:4448593), with apparent retained intron.
BC013208 - Homo sapiens Notch homolog 1, translocation-associated (Drosophila), mRNA (cDNA clone IMAGE:4156263).
DI450742 - KR 1020140111673-A/11: COMBINATION THERAPY FOR TREATING HEARING AND BALANCE DISORDERS.
HW767457 - JP 2014528704-A/11: Double-Stranded Oligonucleotide Compounds And Methods Of Use Thereof For Treating Hearing And Balance Disorders.
JB837400 - Sequence 11 from Patent WO2013106494.
JE566451 - Sequence 12 from Patent EP2853595.
JE828145 - Sequence 12 from Patent WO2015043768.
LF807178 - JP 2016528161-A/11: COMBINATION THERAPY FOR TREATING HEARING AND BALANCE DISORDERS.
LZ947776 - JP 2016533190-A/12: NOTCH 1 specific siRNA molecules.
AB209873 - Homo sapiens mRNA for notch1 preproprotein variant protein.
JD038001 - Sequence 19025 from Patent EP1572962.
JD120910 - Sequence 101934 from Patent EP1572962.
JD129691 - Sequence 110715 from Patent EP1572962.
JD389358 - Sequence 370382 from Patent EP1572962.
JD271309 - Sequence 252333 from Patent EP1572962.
JD230516 - Sequence 211540 from Patent EP1572962.
JD144098 - Sequence 125122 from Patent EP1572962.
JD561777 - Sequence 542801 from Patent EP1572962.
CR457221 - Homo sapiens full open reading frame cDNA clone RZPDo834G108D for gene NOTCH1, Notch homolog 1, translocation-associated (Drosophila); complete cds, incl. stopcodon.
JD158181 - Sequence 139205 from Patent EP1572962.
JD227855 - Sequence 208879 from Patent EP1572962.
JD280706 - Sequence 261730 from Patent EP1572962.
JD094637 - Sequence 75661 from Patent EP1572962.
JD436551 - Sequence 417575 from Patent EP1572962.
JD062348 - Sequence 43372 from Patent EP1572962.
JD396318 - Sequence 377342 from Patent EP1572962.
JD365715 - Sequence 346739 from Patent EP1572962.
JD348431 - Sequence 329455 from Patent EP1572962.
JD239420 - Sequence 220444 from Patent EP1572962.
JD089215 - Sequence 70239 from Patent EP1572962.
JD339486 - Sequence 320510 from Patent EP1572962.
JD171100 - Sequence 152124 from Patent EP1572962.
CQ873737 - Sequence 156 from Patent WO2004076622.
DD413574 - Regulation of Mammalian Cells.
AF308602 - Homo sapiens NOTCH 1 (N1) mRNA, complete cds.
M73980 - Human TAN-1 mRNA (homologue of Drosophila Notch gene), 5' end.
DL491593 - Novel nucleic acids.
DD356919 - Method of Screening for Compound Regulating Translation of Specific mRNA.

-  Biochemical and Signaling Pathways
  BioCarta from NCI Cancer Genome Anatomy Project
h_hesPathway - Segmentation Clock
h_ps1Pathway - Presenilin action in Notch and Wnt signaling
h_notchpathway - Proteolysis and Signaling Pathway of Notch

Reactome (by CSHL, EBI, and GO)

Protein P46531 (Reactome details) participates in the following event(s):

R-HSA-157353 NEXT1 is cleaved to produce NICD1
R-HSA-157632 Complex of NOTCH1 with its ligand is cleaved to produce NEXT1
R-HSA-2666278 NOTCH1 t(7;9)(NOTCH1:M1580_K2555) is cleaved to produce NEXT1
R-HSA-2730752 NOTCH1 HD domain mutants are cleaved to produce NEXT1 irrespective of ligand binding
R-HSA-157926 NICD1 traffics to nucleus
R-HSA-2220988 NEXT1 PEST domain mutants are cleaved to produce NICD1 PEST domain mutants
R-HSA-1912388 NICD1 displaces co-repressor complex from RBPJ (CSL)
R-HSA-1912396 NICD1 binds HIF1A
R-NUL-2064264 NICD1 displaces NCOR co-repressor complex from CSL
R-HSA-1912385 Phosphorylated NICD1 binds FBXW7
R-HSA-1912391 NICD1 is phosphorylated by CDK8
R-HSA-1912349 Fucosylation of Pre-NOTCH by POFUT1
R-HSA-1980042 NOTCH1 binds JAG1
R-HSA-1980044 NOTCH1 binds JAG2
R-HSA-1980122 DTX binds NOTCH1
R-HSA-1980128 NOTCH1 associates with negative regulators NUMB and ITCH
R-HSA-1980130 NOTCH1 binds DLK1
R-HSA-1980138 NOTCH1 binds DLL/JAG ligand in cis
R-NUL-2076711 rDll1 binds NOTCH1 in cis
R-HSA-1912394 NICD1 in complex with RBPJ (CSL) recruits MAML
R-HSA-212356 Formation of CSL-NICD coactivator complex
R-HSA-1912353 Glucosylation of Pre-NOTCH by POGLUT1
R-HSA-1912355 Glycosylation of Pre-NOTCH by FRINGE
R-HSA-1912369 NOTCH precursor cleaved to form mature NOTCH
R-HSA-1852623 Ubiquitination of NICD1 by FBWX7
R-HSA-1912378 Sialylation of Pre-NOTCH
R-HSA-1912352 Galactosylation of Pre-NOTCH
R-HSA-1912372 Fringe-modified Pre-NOTCH is cleaved by FURIN
R-HSA-2220971 CDK8 phosphorylates NICD1 PEST domain mutants
R-HSA-2220944 ADAM10/17 cleaves ligand-bound NOTCH1 PEST domain mutants to produce NEXT1 PEST domain mutants
R-HSA-2220976 NOTCH1 HD+PEST domain mutants are cleaved by ADAM10/17 irrespective of ligand binding
R-HSA-2769015 NICD1 PEST domain mutants translocate from cytosol to nucleus
R-HSA-2220982 NICD1 PEST domain mutants displace co-repressor complex from RBPJ (CSL)
R-HSA-1912386 Ubiquitination of NOTCH1 by ITCH in the absence of ligand
R-HSA-373706 Contactin-1 (CNTN1) binds NOTCH1
R-HSA-1912398 NOTCH1 binds DNER
R-HSA-1980123 DTX recruits beta-arrestin (ARRB) to NOTCH
R-HSA-1980039 NOTCH1 binds DLL1
R-HSA-1980041 NOTCH1 binds DLL4
R-HSA-2691211 NOTCH1 HD domain mutants bind DLL4
R-HSA-2691214 NOTCH1 HD domain mutants bind JAG2
R-HSA-2691219 NOTCH1 HD domain mutants bind DLL1
R-HSA-2691226 NOTCH1 HD domain mutants bind JAG1
R-HSA-1912393 MAML in complex with NICD1 recruits CDK8
R-HSA-4396347 NOTCH1 Coactivator Complex binds HES1 promoter
R-HSA-4396371 NOTCH1 Coactivator Complex binds MYC promoter
R-HSA-4396379 NOTCH1 Coactivator Complex binds HES5 promoter
R-HSA-4396382 NOTCH1 Coactivator Complex binds promoters of HEY genes
R-HSA-8878220 RUNX3 binds the NOTCH1 coactivator complex
R-HSA-9017835 NOTCH1 coactivator complex binds NOTCH3 gene
R-HSA-2900743 NOTCH1 HD+PEST domain mutants bind JAG1
R-HSA-2900747 NOTCH1 HD+PEST domain mutants bind DLL4
R-HSA-2900748 NOTCH1 HD+PEST domain mutants bind DLL1
R-HSA-2900756 NOTCH1 HD+PEST domain mutants bind JAG2
R-HSA-2768993 NOTCH1 PEST domain mutants bind JAG2
R-HSA-2768999 NOTCH1 PEST domain mutants bind JAG1
R-HSA-2769000 NOTCH1 PEST domain mutants bind DLL4
R-HSA-2769008 NOTCH1 PEST domain mutants bind DLL1
R-HSA-2220964 NICD1 PEST domain mutants in complex with RBPJ (CSL) bind MAML
R-HSA-1980074 Ubiquitination of DLL/JAG ligands upon binding to NOTCH1
R-HSA-8878237 RUNX3:NOTCH1 coactivator complex binds the HES1 gene promoter
R-HSA-9021451 NOTCH1,NOTCH3 coactivator complex binds PLXND1 gene promoter
R-HSA-2220957 NOTCH1 PEST domain mutants coactivator complex binds CDK8:CCNC
R-HSA-4396392 NOTCH1 PEST domain mutants bind HES1 promoter
R-HSA-4396393 NOTCH1 PEST domain mutants bind MYC promoter
R-HSA-4396401 NOTCH1 PEST domain mutants bind HES5 promoter
R-HSA-4396402 NOTCH1 PEST domain mutants bind promoters of HEY genes
R-HSA-2737728 Ubiquitination of DLL/JAG ligands upon binding to NOTCH1 HD domain mutants
R-HSA-2900765 Ubiquitination of DLL/JAG ligands upon binding to NOTCH1 HD+PEST domain mutants
R-HSA-2769007 Ubiquitination of DLL/JAG ligands upon binding to NOTCH1 PEST domain mutants
R-HSA-1912408 Pre-NOTCH Transcription and Translation
R-HSA-157212 A third proteolytic cleavage releases NICD
R-HSA-2122948 Activated NOTCH1 Transmits Signal to the Nucleus
R-HSA-156988 Receptor-ligand binding initiates the second proteolytic cleavage of Notch receptor
R-HSA-2660826 Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant
R-HSA-2691232 Constitutive Signaling by NOTCH1 HD Domain Mutants
R-HSA-157052 NICD traffics to nucleus
R-HSA-2644606 Constitutive Signaling by NOTCH1 PEST Domain Mutants
R-HSA-2894862 Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
R-HSA-2122947 NOTCH1 Intracellular Domain Regulates Transcription
R-HSA-2644607 Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling
R-HSA-1912399 Pre-NOTCH Processing in the Endoplasmic Reticulum
R-HSA-1912422 Pre-NOTCH Expression and Processing
R-HSA-1980143 Signaling by NOTCH1
R-HSA-2660825 Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant
R-HSA-2691230 Signaling by NOTCH1 HD Domain Mutants in Cancer
R-HSA-2644602 Signaling by NOTCH1 PEST Domain Mutants in Cancer
R-HSA-2894858 Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer
R-HSA-350054 Notch-HLH transcription pathway
R-HSA-1912420 Pre-NOTCH Processing in Golgi
R-HSA-5083630 Defective LFNG causes SCDO3
R-HSA-2644605 FBXW7 Mutants and NOTCH1 in Cancer
R-HSA-157118 Signaling by NOTCH
R-HSA-2644603 Signaling by NOTCH1 in Cancer
R-HSA-8941856 RUNX3 regulates NOTCH signaling
R-HSA-212436 Generic Transcription Pathway
R-HSA-3906995 Diseases associated with O-glycosylation of proteins
R-HSA-162582 Signal Transduction
R-HSA-5663202 Diseases of signal transduction
R-HSA-9013508 NOTCH3 Intracellular Domain Regulates Transcription
R-HSA-8878159 Transcriptional regulation by RUNX3
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-3781865 Diseases of glycosylation
R-HSA-1643685 Disease
R-HSA-9012852 Signaling by NOTCH3
R-HSA-74160 Gene expression (Transcription)

-  Other Names for This Gene
  Alternate Gene Symbols: NM_017617, NOTC1_HUMAN, P46531, Q59ED8, Q5SXM3, TAN1, uc328tgs.1, uc328tgs.2
UCSC ID: ENST00000651671.1_7
RefSeq Accession: NM_017617.5
Protein: P46531 (aka NOTC1_HUMAN or NTC1_HUMAN)

-  GeneReviews for This Gene
  GeneReviews article(s) related to gene NOTCH1:
taa (Heritable Thoracic Aortic Disease Overview)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.