HCSGD entry for JAG1
1. General information
Official gene symbol | JAG1 |
---|---|
Entrez ID | 182 |
Gene full name | jagged 1 |
Other gene symbols | AGS AHD AWS CD339 HJ1 JAGL1 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
This gene isn't in PPI subnetwork.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0001525 | Angiogenesis | NAS | biological_process |
GO:0001709 | Cell fate determination | NAS | biological_process |
GO:0002011 | Morphogenesis of an epithelial sheet | IEA | biological_process |
GO:0003184 | Pulmonary valve morphogenesis | IMP | biological_process |
GO:0003215 | Cardiac right ventricle morphogenesis | IEA ISS | biological_process |
GO:0005112 | Notch binding | IEA NAS | molecular_function |
GO:0005198 | Structural molecule activity | NAS | molecular_function |
GO:0005509 | Calcium ion binding | IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005576 | Extracellular region | NAS | cellular_component |
GO:0005886 | Plasma membrane | IDA IEA TAS | cellular_component |
GO:0005887 | Integral component of plasma membrane | NAS | cellular_component |
GO:0007219 | Notch signaling pathway | IMP NAS TAS | biological_process |
GO:0007220 | Notch receptor processing | TAS | biological_process |
GO:0007399 | Nervous system development | NAS | biological_process |
GO:0008083 | Growth factor activity | NAS | molecular_function |
GO:0016020 | Membrane | TAS | cellular_component |
GO:0016021 | Integral component of membrane | IEA | cellular_component |
GO:0030097 | Hemopoiesis | NAS | biological_process |
GO:0030216 | Keratinocyte differentiation | NAS | biological_process |
GO:0030334 | Regulation of cell migration | NAS | biological_process |
GO:0032495 | Response to muramyl dipeptide | IEA | biological_process |
GO:0035909 | Aorta morphogenesis | IEA ISS | biological_process |
GO:0042127 | Regulation of cell proliferation | NAS | biological_process |
GO:0042491 | Auditory receptor cell differentiation | IEA | biological_process |
GO:0045177 | Apical part of cell | IEA | cellular_component |
GO:0045445 | Myoblast differentiation | NAS | biological_process |
GO:0045446 | Endothelial cell differentiation | NAS | biological_process |
GO:0045599 | Negative regulation of fat cell differentiation | IEA | biological_process |
GO:0045639 | Positive regulation of myeloid cell differentiation | IEA | biological_process |
GO:0045665 | Negative regulation of neuron differentiation | IEA | biological_process |
GO:0045747 | Positive regulation of Notch signaling pathway | IEA | biological_process |
GO:0045944 | Positive regulation of transcription from RNA polymerase II promoter | IEA IMP | biological_process |
GO:0060411 | Cardiac septum morphogenesis | IEA ISS | biological_process |
GO:0061156 | Pulmonary artery morphogenesis | IMP | biological_process |
GO:0061309 | Cardiac neural crest cell development involved in outflow tract morphogenesis | IEA ISS | biological_process |
GO:0061314 | Notch signaling involved in heart development | IC IEA IMP | biological_process |
GO:0061444 | Endocardial cushion cell development | IEA ISS | biological_process |
GO:0072017 | Distal tubule development | IEA | biological_process |
GO:0072070 | Loop of Henle development | IEA | biological_process |
GO:0097150 | Neuronal stem cell maintenance | IEP | biological_process |
GO:2000737 | Negative regulation of stem cell differentiation | IMP | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.0221452718 | 0.4158445842 | 0.3564166259 | 1.0000000000 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Down | -0.5956566339 |
GSE13712_SHEAR | Up | 0.1294248876 |
GSE13712_STATIC | Up | 0.1591007994 |
GSE19018 | Down | -0.7408273494 |
GSE19899_A1 | Up | 0.0284966626 |
GSE19899_A2 | Up | 0.2770987596 |
PubMed_21979375_A1 | Down | -0.5595285505 |
PubMed_21979375_A2 | Up | 0.2050965155 |
GSE35957 | Down | -1.0240134632 |
GSE36640 | Up | 0.3651445742 |
GSE54402 | Down | -0.1162829556 |
GSE9593 | Up | 0.0801096315 |
GSE43922 | Up | 0.5837655498 |
GSE24585 | Up | 0.1182239625 |
GSE37065 | Up | 0.2817703345 |
GSE28863_A1 | Up | 1.4163059446 |
GSE28863_A2 | Up | 0.4713083737 |
GSE28863_A3 | Up | 0.4593800568 |
GSE28863_A4 | Up | 0.2983740249 |
GSE48662 | Up | 0.2070122416 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-34a-5p | MIMAT0000255 | MIRT000074 | Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 20351093 |
hsa-miR-34a-5p | MIMAT0000255 | MIRT000074 | Flow//Immunoblot//Luciferase reporter assay//Microarray//qRT-PCR | Functional MTI | 19398721 |
hsa-miR-21-5p | MIMAT0000076 | MIRT000176 | Flow//Immunoblot//Luciferase reporter assay//Microarray//qRT-PCR | Functional MTI | 19398721 |
hsa-miR-21-5p | MIMAT0000076 | MIRT000176 | Luciferase reporter assay | Functional MTI | 22618231 |
hsa-miR-21-5p | MIMAT0000076 | MIRT000176 | Microarray | Functional MTI (Weak) | 18591254 |
hsa-miR-34b-3p | MIMAT0004676 | MIRT006291 | Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 22113133 |
hsa-miR-200c-3p | MIMAT0000617 | MIRT005457 | Immunohistochemistry//qRT-PCR | Functional MTI (Weak) | 21224848 |
hsa-miR-524-5p | MIMAT0002849 | MIRT006891 | Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 22871495 |
hsa-miR-375 | MIMAT0000728 | MIRT019703 | Microarray | Functional MTI (Weak) | 20215506 |
hsa-miR-98-5p | MIMAT0000096 | MIRT027545 | Microarray | Functional MTI (Weak) | 19088304 |
hsa-let-7b-5p | MIMAT0000063 | MIRT051999 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
- mirRecord
MicroRNA name | mirBase ID | Target site number | MiRNA mature ID | Test method inter | MiRNA regulation site | Reporter target site | Pubmed ID |
---|---|---|---|---|---|---|---|
hsa-miR-34a-5p | MIMAT0000255 | 1 | hsa-miR-34a | {Western blot} | {overexpression by miRNA precursor transfection} | 20351093 | |
hsa-miR-21-5p | MIMAT0000076 | NA | hsa-miR-21 | 19398721 | |||
hsa-miR-200c-3p | MIMAT0000617 | 1 | hsa-miR-200c | {Western blot} | {overexpression by miRNA mimics tranfection} | 21224847 | |
hsa-miR-141-3p | MIMAT0000432 | 1 | hsa-miR-141 | {Western blot} | {overexpression by miRNA mimics tranfection} | 21224847 |
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6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 7 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26650241 | Deregulated expression of Notch1 and Jagged1 is observed in colorectal cancer |
24950189 | Conversely, over-expression of Notch1 or Jagged1 prolonged the replicative lifespan of endothelial cells |
24445253 | Mutations in SAMHD1 cause Aicardi-Goutieres syndrome (AGS), an inflammatory disorder that shares phenotypic similarity with systemic lupus erythematosus, including activation of antiviral type 1 interferon (IFN) |
24445253 | To further define the pathomechanisms underlying autoimmunity in AGS due to SAMHD1 mutations, we investigated the physiological properties of SAMHD1 |
24445253 | RESULTS: We show that increased dNTP pools due to SAMHD1 deficiency cause genome instability in fibroblasts of patients with AGS |
24175851 | We exposed AGS, HGC-27 and GES-1 gastric cancer cell lines to IFN-gamma and found significantly reduced colony formation ability |
24164458 | We found that IGFBP5 (insulin-like growth factor binding protein 5), PLAT (plasminogen activator), SNAI2 (snail homolog 2), JAG1 (jagged 1), SPRY4 (Sprouty homolog 4), and CD44 were upregulated, whereas CFB (complement factor B), VCAM1 (vascular cell adhesion molecule 1), AQP1 (aquaporin 1), LOXL1 (lysyl oxidase-like 1), and RBPMS (RNA-binding protein with multiple splicing) were down- regulated in both radiation-damaged and old cells |
23104211 | Xenograft analyses using p53-functional AGS or -dysfunctional SNU601 cells displayed statistically significant tumor growth retardation by silencing MKRN1, which was reversed under depletion of p14ARF (AGS cells, MKRN1 knockdown tumors vs MKRN1 and p14ARF knockdown tumors: 164 |
20132052 | A neural crest origin was confirmed by increased colony-forming efficiency (CFE) in the presence of Jagged 1 and the expression of a number of neural crest markers within the developing colonies by ICC and serially passaged clones by Western blotting |
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