2024年12月25日 · GLS2 (Glutaminase 2) is a Protein Coding gene. Diseases associated with GLS2 include Metabolic Acidosis and Juvenile Dermatitis Herpetiformis . Among its related pathways are Gene expression (Transcription) and Transmission across Chemical Synapses .

2024年12月25日 · Glutaminase (GLS) is an aminohydrolase enzyme, EC 3.5.1.2, which catalyzes the conversion of the amino acid glutamine to glutamate. Two GLS isoforms have been identified to date, GLS1 (KGA; kidney-type glutaminase) and GLS2 (LGA; liver-type glutaminase).

Showing 25 of 5,496 results for gls2 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24日 · ALDH4A1 (Aldehyde Dehydrogenase 4 Family Member A1) is a Protein Coding gene. Diseases associated with ALDH4A1 include Hyperprolinemia, Type Ii and Hyperprolinemia.Among its related pathways are Proline catabolism and Glyoxylate metabolism and glycine degradation.Gene Ontology (GO) annotations related to this gene include identical …

2024年12月25日 · SAT1 (Spermidine/Spermine N1-Acetyltransferase 1) is a Protein Coding gene. Diseases associated with SAT1 include Pediatric Systemic Lupus Erythematosus and Keratosis Follicularis Spinulosa Decalvans, X-Linked.Among its related pathways are Autodegradation of the E3 ubiquitin ligase COP1 and Metabolism.Gene Ontology (GO) annotations related to this …

Symbol Description Category UniProt ID GIFtS GC id Score; 1: GLS: Glutaminase: Protein Coding: O94925: 62: GC02P190880: 66.69: 2: LOC129935268: ATAC-STARR-Seq ...

2024年12月25日 · WNT7B (Wnt Family Member 7B) is a Protein Coding gene. Diseases associated with WNT7B include Microphthalmia, Syndromic 9 and Macs Syndrome.Among its related pathways are ncRNAs involved in Wnt signaling in hepatocellular carcinoma and Wnt Pathway.Gene Ontology (GO) annotations related to this gene include signaling receptor …

2024年12月25日 · SMAD2 (SMAD Family Member 2) is a Protein Coding gene. Diseases associated with SMAD2 include Loeys-Dietz Syndrome 6 and Congenital Heart Defects, Multiple Types, 8, With Or Without Heterotaxy.Among its related pathways are TGF-beta receptor signaling activates SMADs and Gastrulation.Gene Ontology (GO) annotations related to this …

Showing of 6,012 Results for GLS2 Search Time: 0 ms. Export Show: Symbol Description Category UniProt ID GIFtS GC id Score; 51: TFRC: Transferrin Receptor: Protein Coding: P02786: 63: GC03M196576: 0.20: 52: UGT1A1: UDP Glucuronosyltransferase Family 1 Member A1: Protein Coding: P22309 ...

2024年12月25日 · RHPN2 (Rhophilin Rho GTPase Binding Protein 2) is a Protein Coding gene. Diseases associated with RHPN2 include Blepharocheilodontic Syndrome 1 and Hereditary Mixed Polyposis Syndrome.Among its related pathways are Signaling by Rho GTPases and RHOC GTPase cycle.An important paralog of this gene is RHPN1.