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14 Possible Causes for LCOR, gene

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  • Noma

    To catalog bacteria present in noma lesions and identify candidate noma-triggering organisms, we performed a cross-sectional sequencing study of 16S rRNA gene amplicons from[ncbi.nlm.nih.gov] Open in Google Maps 340 Florida Ave NE Washington, DC 20002 Developer: LCOR Expected Completion Date: Spring of 2017 Square Footage: N/A The Skinny: This mixed-use development[dc.curbed.com] In an attempt to better understand the microbiological events occurring during this disease, we used phylogenetic and low-density microarrays targeting the 16S rRNA gene to[ncbi.nlm.nih.gov]

  • Congenital Cerulean Cataract Type 5

    Cerulean cataracts may be caused by mutations in several genes, including the CRYBB2, CRYGD, and MAF genes, and are inherited in an autosomal dominant manner.[malacards.org] […] family member 16B KMT2A lysine (K)-specific methyltransferase 2A KPNB1 karyopherin (importin) beta 1 LALBA lactalbumin, alpha- LAMP2 lysosomal-associated membrane protein 2 LCOR[amp.pharm.mssm.edu] Affected Tissue/Organ Chromosome Gene Product Gene Symbol # of Mutation Entry Disease Name Curator eye 1 ATP-binding Transporter ABCR 24 Stargardt Disease Type 1 Keio Univ[mutationview.jp]

  • Lactococcus Lactis

    It was generated by deleting the alr gene, an alanine racemase encoding gene, in the progenitor strain MG1363.[mobitec.com] The genes lcoRS are involved in transcription regulation of lcoABC , the products of which confer copper resistance by lowering the accumulation of copper inside the lactococcal[journals.plos.org] The ureB gene was amplified by PCR from a H.pylori strain MEL-Hp27.[ncbi.nlm.nih.gov]

  • Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] Ligand-dependent corepressor (LCoR) recruitment by Kruppel-like factor 6 (KLF6) regulates expression of the cyclin-dependent kinase inhibitor CDKN1A gene.[academictree.org] […] osteolysis, nodulosis and arthropathy (MONA) spectrum disorder is a rare inherited progressive skeletal disorder caused by mutations in the matrix metalloproteinase 2 (MMP2) gene[clinicaltrials.gov]

  • Ring Chromosome 10

    Locus Gene 10q22-q24 Actin, Alpha, Smooth Muscle, Aortic 10q26.3 A Disintegrin And Metalloproteinase Domain 8 10q24.2-q24.3 Adducin 3 10q24-q26 Alpha-2a-adrenergic Receptor[okdb.appliedbioinfo.net] […] domain family member 5) (La-related protein 5) [KIAA0217] [LARP5] LBX1 10q24 P52954 LBX1_HUMAN 604255 Transcription factor LBX1 (Ladybird homeobox protein homolog 1) [LBX1H] LCOR[uniprot.org] Sometimes there is a mutation, a change in a gene or genes.[icdlist.com]

  • Ring Chromosome 4

    Therefore, interactions between a proposed 1/2 dose "ectrodactyly" gene on 4q33 and some 1/2 dosage genes on distal 4p (or disturbed cellular homeostasis due to a ring chromosome[ncbi.nlm.nih.gov] 7) (P-TEFb-interaction protein for 7SK stability) (PIP7S) [HDCMA18P] LCORL 4p15.32 Q8N3X6 LCORL_HUMAN 611799 Ligand-dependent nuclear receptor corepressor-like protein (LCoR-like[uniprot.org] The absence of seizures despite the absence of the specific 4p16.3 region with haploinsufficiency of the LETM1 gene is striking.[ncbi.nlm.nih.gov]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] LCOR G:607698 . . LCORL G:611799 . . LCP1 G:153430 . . LCP2 G:601603 . . LCS1 P:214900 . . LCT G:603202 . Lactase deficiency, congenital, 223000 (3) LDB1 G:603451 . .[usegalaxy.org] A-B: Genetic Testing by Individual Gene Gene Protein Associated Disease(s) AARS2 Alanyl-tRNA Synthetase 2, Mitochondrial Familial Hypertrophic Cardiomyopathy (HCM) ABCA1 ATP-Binding[bcm.edu]

  • Nestor-Guillermo Progeria Syndrome

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] LCOR G:607698 . . LCORL G:611799 . . LCP1 G:153430 . . LCP2 G:601603 . . LCS1 P:214900 . . LCT G:603202 . Lactase deficiency, congenital, 223000 (3) LDB1 G:603451 . .[usegalaxy.org] An inherited LMNA gene mutation in atypical Progeria syndrome. Am J Med Genet A 2012;158A(11):2881-7.[scholar.um5.ac.ma]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    The gene symbol is from the HUGO Gene Nomenclature Committee (HGNC) database.[dna.universeofatoms.com] LCOR G:607698 . . LCORL G:611799 . . LCP1 G:153430 . . LCP2 G:601603 . . LCS1 P:214900 . . LCT G:603202 . Lactase deficiency, congenital, 223000 (3) LDB1 G:603451 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    Below are the genes sequenced in this screen and the targeted disease(s) associated with each of these genes.[genepeeks.com] LCOR G:607698 . . LCORL G:611799 . . LCP1 G:153430 . . LCP2 G:601603 . . LCS1 P:214900 . . LCT G:603202 . Lactase deficiency, congenital, 223000 (3) LDB1 G:603451 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

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