2024年12月24日 · ARTN (Artemin) is a Protein Coding gene. Diseases associated with ARTN include Burning Mouth Syndrome and Thyroid Carcinoma, Familial Medullary . Among its related pathways are MAPK family signaling cascades and Nervous system development .

Showing 25 of 4,067 results for ARTN Search Time: 0 ms in Aliases & Descriptions Drugs & Compounds Disorders Text-Mined Disorders Domains Expression in Human Tissues Function Genomics Localization Orthologs Paralogs Pathways Phenotypes Proteins Publications Summaries Transcripts Variants in category Protein Coding RNA Gene Functional Element ...

2024年12月25日 · Receptor for artemin (ARTN), a growth factor that supports the survival of sensory and sympathetic peripheral neurons (PubMed:31535977, 9883723). ARTN-binding leads to autophosphorylation and activation of the RET receptor (PubMed: 31535977 , 9883723 ).

2024年12月25日 · An important paralog of this gene is ARTN. UniProtKB/Swiss-Prot Summary for NRTN Gene Growth factor that supports the survival of sympathetic neurons in culture (PubMed: 8945474 ).

Showing 25 of 3,875 results for ARTN Search Time: 0 ms in NEW (Click on the icon in the table below to see search hit context) Showing of 3,875 Results for ARTN Search Time: 0 ms. Export Show: Symbol Description Category UniProt ID GIFtS GC id Score; 3676 ...

2024年12月25日 · GDNF ligands (GDNF, NRTN, ARTN, PSPN and GDF15) first bind their corresponding GDNFR coreceptors (GFRA1, GFRA2, GFRA3, GFRA4 and GFRAL, respectively), triggering RET autophosphorylation and activation, leading to activation of downstream signaling pathways, including the MAPK- and AKT-signaling pathways (PubMed:21994944, 23333276, …

Symbol Description Category UniProt ID GIFtS GC id Score; 1: ARMH1: Armadillo Like Helical Domain Containing 1: Protein Coding: Q6PIY5: 34: GC01P070085: 23.34: 2: TMEM53

2024年12月25日 · SLC2A1 (Solute Carrier Family 2 Member 1) is a Protein Coding gene. Diseases associated with SLC2A1 include Glut1 Deficiency Syndrome 2 and Glut1 Deficiency Syndrome 1.Among its related pathways are Metabolism of water-soluble vitamins and cofactors and glycolysis (BioCyc).Gene Ontology (GO) annotations related to this gene include identical …

2024年12月25日 · KDM4A (Lysine Demethylase 4A) is a Protein Coding gene. Diseases associated with KDM4A include Hyperoxaluria, Primary, Type I and Lung Sarcomatoid Carcinoma.Among its related pathways are NR1H2 and NR1H3-mediated signaling and HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA).Gene Ontology …

2024年12月24日 · ANGPT1 (Angiopoietin 1) is a Protein Coding gene. Diseases associated with ANGPT1 include Angioedema, Hereditary, 5 and Hereditary Angioedema With Normal C1inh Not Related To F12 Or Plg Variant.Among its related pathways are MIF Mediated Glucocorticoid Regulation and TGF-Beta Pathway.Gene Ontology (GO) annotations related to this gene …