2024年12月25日 · PXK (PX Domain Containing Serine/Threonine Kinase Like) is a Protein Coding gene. Diseases associated with PXK include Systemic Lupus Erythematosus and Lupus Erythematosus. Gene Ontology (GO) annotations related to this gene include transferase activity, transferring phosphorus-containing groups and nucleotide binding.

Showing 25 of 2,006 results for PXK 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 · PIM3 (Pim-3 Proto-Oncogene, Serine/Threonine Kinase) is a Protein Coding gene. Diseases associated with PIM3 include Spinocerebellar Ataxia, X-Linked 5 and Hepatic Flexure Cancer.Among its related pathways are Apoptosis and Autophagy and NF-kappaB Signaling.Gene Ontology (GO) annotations related to this gene include transferase activity, …

Showing of 2,007 Results for PXK Search Time: 0 ms. Export Show: Symbol Description Category UniProt ID GIFtS GC id Score; 1: A4GALT: Alpha 1,4-Galactosyltransferase (P1PK Blood Group) Protein Coding: Q9NPC4: 53: GC22M042692: 0.53: 2: A4GNT: Alpha-1,4-N-Acetylglucosaminyltransferase: Protein Coding ...

2024年12月25日 · LIMK1 (LIM Domain Kinase 1) is a Protein Coding gene. Diseases associated with LIMK1 include Non-Specific Early-Onset Epileptic Encephalopathy and Williams-Beuren Syndrome.Among its related pathways are Semaphorin interactions and Signaling by Rho GTPases.Gene Ontology (GO) annotations related to this gene include transferase activity, …

2024年12月25日 · RPP14 FAM107A PXK PDHB KCTD6 ACOX2 HTD2 ENSG00000243384 ENSG00000272182 HSALNG0026431: GH03J058462: Enhancer: 1: ENCODE CraniofacialAtlas: 19.80: 20.11-29.8: 5: 1.6: PBX2 MGA PRDM1 CTCF ZNF184 MYC CEBPB ZNF207 JUND NFIC: PDHB RPP14 PXK KCTD6 ACOX2 HTD2 ENSG00000243384 FAM107A piR-30188-113 …

2024年12月24日 · CTCFL (CCCTC-Binding Factor Like) is a Protein Coding gene. Diseases associated with CTCFL include Intellectual Developmental Disorder, Autosomal Dominant 21 and Testicular Cancer.Among its related pathways is Male infertility.Gene Ontology (GO) annotations related to this gene include nucleic acid binding and RNA polymerase II cis-regulatory region …

2024年12月25日 · FAT2 (FAT Atypical Cadherin 2) is a Protein Coding gene. Diseases associated with FAT2 include Spinocerebellar Ataxia 45 and Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7.Gene Ontology (GO) annotations related to this gene include calcium ion binding.An important paralog of this gene is FAT1.

2024年12月25日 · SIM1 (SIM BHLH Transcription Factor 1) is a Protein Coding gene. Diseases associated with SIM1 include Obesity Due To Sim1 Deficiency and Sim1-Related Prader-Willi-Like Syndrome.Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and obsolete signal transducer activity.An important paralog of this …

2024年12月25日 · FGGY (FGGY Carbohydrate Kinase Domain Containing) is a Protein Coding gene. Diseases associated with FGGY include Sporadic Amyotrophic Lateral Sclerosis and Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1.Gene Ontology (GO) annotations related to this gene include kinase activity and phosphotransferase activity, …