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61 Possible Causes for Gene, LCF

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  • Licofelone

    Rofecoxib only diminished COX-2 protein expression and MCP-1 gene expression in vascular atheroma. Prostaglandin E(2) in rabbit plasma was attenuated by both drugs.[ncbi.nlm.nih.gov] […] chemical compound LCF ML3000 edit Language Label Description Also known as English Licofelone chemical compound LCF ML3000 Statements instance of chemical compound 2 references[wikidata.org] Gene Name PLA2G2E Uniprot ID Q9NZK7 Uniprot Name Group IIE secretory phospholipase A2 Molecular Weight 15988.525 Da References Berman HM, Westbrook J, Feng Z, Gilliland G,[drugbank.ca]

  • T-cell Acute Lymphoblastic Leukemia

    KEYWORDS: T-ALL; ZBTB16-ABL1; fusion gene; gene mutation; transcriptome[ncbi.nlm.nih.gov] Asparaginase Given IM or IV Other Names: ASP-1 Asparaginase II Asparaginase-E.Coli Colaspase Elspar Kidrolase L-Asnase L-ASP L-Asparaginase L-Asparagine amidohydrolase Laspar Lcf-ASP[clinicaltrials.gov] The CBF complex appears to regulate a number of genes important for hematopoiesis.[ncbi.nlm.nih.gov]

  • Congenital Dyserythropoietic Anemia

    Future analysis of this locus may lead to the identification of a gene essential to normal erythropoiesis.[ncbi.nlm.nih.gov] 104950368 MZE: 101487300 (cdan1) OLA: 101174386 (cdan1) XMA: 102222516 (cdan1) PRET: 103458399 (cdan1) NFU: 107392091 (cdan1) KMR: 108239018 (cdan1) CSEM: 103380031 (cdan1) LCF[genome.jp] […] codanin 1 The CDAN1 gene provides instructions for making a protein called codanin-1.[ghr.nlm.nih.gov]

  • Spastic Paraplegia

    This is surprising as none of the other 72 genes for HSP are ion channel genes.[epilepsygenetics.net] 101169630 XMA: 102222538 (spart) 102233736 PRET: 103474976 103475563 (spg20) NFU: 107380233 107386908 (spg20) KMR: 108235971 108236876 (spart) CSEM: 103378171 103395225 (spg20) LCF[genome.jp] […] atlastin GTPase 1 alastin-1 atlastin spastic paraplegia 3a (autosomal dominant) spg3a gene ATL1 AD-FSP ATL-1 FSP1 SPG3 606439 11231 BSCL2, seipin lipid droplet biogenesis[ukgtn.nhs.uk]

  • Mitochondrial Disease

    NHS test for affected families Defective genes can be caused by mutations in either the maternally-inherited mitochondrial genome (mtDNA) or more frequently, the genes located[ncl.ac.uk] […] complex (PDC), which irreversibly decarboxylates pyruvate acetyl CoA, an intermediate that is also formed as a product of the β-oxidation of long-chain fatty acyl CoAs (LCF[aasmnet.org] The novel m.7539C T mt-tRNA(Asp) gene mutation extends the spectrum of pathogenic mutations in this gene, further supporting the notion that mt-tRNA(Asp) gene mutations are[ncbi.nlm.nih.gov]

  • Lattice Corneal Dystrophy Type 1

    RESULTS: AC -- T mutation at position 417 was detected in exon 4 of the kerato-epithelin gene, which is expected to cause an Arg124 -- Cys change.[ncbi.nlm.nih.gov] […] tgfbi) MZE: 101471060 (tgfbi) OLA: 101170658 (tgfbi) XMA: 102237987 (tgfbi) PRET: 103471784 (tgfbi) NFU: 107381089 (tgfbi) KMR: 108248951 (tgfbi) CSEM: 103390796 (tgfbi) LCF[genome.jp] Genes for Gene Perturbations dataset.[amp.pharm.mssm.edu]

  • Contiguous ABCD1 DXS1357E Deletion Syndrome (CADDS)

    B cell receptor associated protein 31 From NCBI Gene : This gene encodes a member of the B-cell receptor associated protein 31 superfamily.[ghr.nlm.nih.gov] MZE: 101484469 (bcap31) OLA: 101171812 (bcap31) XMA: 102234920 (bcap31) PRET: 103460516 (bcap31) NFU: 107397283 (bcap31) KMR: 108228463 (bcap31) CSEM: 103384412 (bcap31) LCF[genome.jp] Genes for Gene Perturbations dataset.[amp.pharm.mssm.edu]

  • Griscelli Syndrome, Type 3

    DnaJ heat shock protein family (Hsp40) member C21 From NCBI Gene : This gene encodes a member of the DNAJ heat shock protein 40 family of proteins that is characterized by[ghr.nlm.nih.gov] 101476799 (dnajc21) OLA: 101169715 (dnajc21) XMA: 102217838 (dnajc21) PRET: 103473872 (dnajc21) NFU: 107374694 (dnajc21) KMR: 108230883 (dnajc21) CSEM: 103390276 (dnajc21) LCF[genome.jp] Genes for Gene Perturbations dataset.[amp.pharm.mssm.edu]

  • X-Linked Deafness 6

    5 gene.[ghr.nlm.nih.gov] 108245526 108247736 (col4a5) 108249212 108249250 108251702 CSEM: 103378334 103378380 103386168 (col4a6) 103386192 (col4a5) 103392136 (col4a2) 103392140 103396029 103396079 LCF[genome.jp] Gene view The gene view histogram is a graphical view of mutations across COL4A6.[cancer.sanger.ac.uk]

  • Leber Congenital Amaurosis 16

    Genes known to cause other forms of hereditary retinal degeneration may be good candidates for genes causing RP.[spandidos-publications.com] NCC: 104953880 MZE: 101463874 (kcnn4) OLA: 101173735 XMA: 102231308 PRET: 103461032 103478481 (kcnn4) NFU: 107396721 (kcnn4) KMR: 108250012 (kcnn4) CSEM: 103388523 (kcnn4) LCF[kegg.jp] The results confirm that pupillometry is a useful objective measure for the assessment of therapeutic effect of gene therapy in patients with LCA.[wrap.warwick.ac.uk]

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