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10 Possible Causes for LCN10, gene

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  • Hypogonadotropic Hypogonadism Type 19 with or without Anosmia

    NCBI LCN10 Members of the lipocalin family, such as LCN10, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding[lettersforcecilia.com] Below are the genes sequenced in this screen and the targeted disease(s) associated with each of these genes.[genepeeks.com] Gene view The gene view histogram is a graphical view of mutations across DUSP6.[cancer.sanger.ac.uk]

  • Anauxetic Dysplasia

    L1CAM, L2HGDH, L3MBTL1, LAMA1, LAMA2, LAMA3, LAMA4, LAMA5, LAMB1, LAMB2, LAMB3, LAMC1, LAMC2, LAMC3, LAMP2, LAMTOR2, LARGE, LARS2, LBP, LBR, LCA5, LCAT, LCE3B, LCE3C, LCE5A, LCN10[inteligene.com.br] RMRP related disorders - The RMRP gene encodes an RNA component of an enzyme involved in the processing of mitochondrial RNA.[ctgt.net] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.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] LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[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] LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[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] LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Premature Chromatid Separation Trait

    811 The long hunt for the Huntingtons chorea gene 240 positional cloning of an imprinted gene?[books.google.com] LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[usegalaxy.org] An important gene associated with Premature Chromatid Separation Trait is BUB1B (BUB1 Mitotic Checkpoint Serine/Threonine Kinase B).[malacards.org]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    Human Gene Mutation Database (HGMD) RMRP SNPedia medical, phenotypic, and genealogical associations of SNPs for RMRP SNP Genotyping and Copy Number Assay Products No data[genecards.org] LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[usegalaxy.org] gene; Usher syndrome type IIIA and retinitis pigmentosa-61 caused by mutations in the CLRN1 gene).[julesberman.blogspot.com]

  • AICA-Ribosiduria

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[usegalaxy.org] The outlier genes identified in the two HPRT deficient patients were different and none of these genes to our knowledge are disease associated.[ojrd.biomedcentral.com]

  • Colobomatous Microphthalmia - Rhizomelic Dysplasia Syndrome

    LCN10 G:612904 . . LCN12 G:612905 . . LCN2 G:600181 . . LCN6 G:609379 . . LCN8 G:612902 . . LCN9 G:612903 . . LCO G:165320 . . LCOR G:607698 . . LCORL G:611799 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] Frkp-Related MDDGC5 LGMD2I 607155 Genetic Test Registry Myopathy, Myofibrillar, 2 Alpha-B Crystallinopathy Myopathy, Desmin-Related, Associated With Mutation In The CRYAB Gene[ukgtn.nhs.uk]

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