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13 Possible Causes for DENND1C, gene

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  • Autosomal Recessive Myopia 18

    […] protein-coupled receptor 180 0.645871 SORCS3 sortilin-related VPS10 domain containing receptor 3 0.643909 UBASH3A ubiquitin associated and SH3 domain containing A 0.639391 DENND1C[amp.pharm.mssm.edu] Previous HGNC Symbols for ADAMTS18 Gene Previous GeneCards Identifiers for ADAMTS18 Gene GC16M068256 GC16M078287 GC16M077065 GC16M077106 GC16M077095 GC16M075873 GC16M063072[genecards.org] For example, for a particular gene, say the ability to roll your tongue, there is a dominant and a recessive gene.[sciencebrainwaves.com]

  • Hereditary Early-Onset Parkinson Disease

    […] spans 184 kb in chromosome 19p13.3 and contains 12 genes and predicted transcripts, namely: CLPP , ALKBH7 , PSPN , GTF2F1 , KHSRP , MIR3940 , SLC25A41 , SLC25A23 , CRB3 , DENND1C[journals.plos.org] Order single gene SNCA Order this gene as a single gene test.[invitae.com] The genes vs. environment debate has benefited research. J.[genomenewsnetwork.org]

  • Pallidopyramidal Syndrome

    […] spans 184 kb in chromosome 19p13.3 and contains 12 genes and predicted transcripts, namely: CLPP , ALKBH7 , PSPN , GTF2F1 , KHSRP , MIR3940 , SLC25A41 , SLC25A23 , CRB3 , DENND1C[journals.plos.org] Order single gene FBXO7 Order this gene as a single gene test.[invitae.com] F-box protein 7 From NCBI Gene : This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box.[ghr.nlm.nih.gov]

  • Hereditary Late-Onset Parkinson Disease

    […] spans 184 kb in chromosome 19p13.3 and contains 12 genes and predicted transcripts, namely: CLPP , ALKBH7 , PSPN , GTF2F1 , KHSRP , MIR3940 , SLC25A41 , SLC25A23 , CRB3 , DENND1C[journals.plos.org] Many mutations in the new recessive and X-chromosomal genes cause severe atypical juvenile Parkinsonism, but less devastating mutations in these genes may cause PD.[portal.research.lu.se] The question arises as to whether the PINK1 gene is also a candidate gene for late-onset forms of Parkinson's disease, similar to the suggested role of the Parkin gene.[jnrbm.biomedcentral.com]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    DENND1C G:613634 . . DENND4A G:600382 . . DENR G:604550 . . DEPDC1 G:612002 . . DEPDC5 G:614191 . . DEPDC7 G:612294 . . DEPTOR G:612974 . . DERL1 G:608813 . .[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

    DENND1C G:613634 . . DENND4A G:600382 . . DENR G:604550 . . DEPDC1 G:612002 . . DEPDC5 G:614191 . . DEPDC7 G:612294 . . DEPTOR G:612974 . . DERL1 G:608813 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.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

    DENND1C G:613634 . . DENND4A G:600382 . . DENR G:604550 . . DEPDC1 G:612002 . . DEPDC5 G:614191 . . DEPDC7 G:612294 . . DEPTOR G:612974 . . DERL1 G:608813 . .[usegalaxy.org] The gene symbol is from the HUGO Gene Nomenclature Committee (HGNC) database.[dna.universeofatoms.com] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    DENND1C G:613634 . . DENND4A G:600382 . . DENR G:604550 . . DEPDC1 G:612002 . . DEPDC5 G:614191 . . DEPDC7 G:612294 . . DEPTOR G:612974 . . DERL1 G:608813 . .[usegalaxy.org] Below are the genes sequenced in this screen and the targeted disease(s) associated with each of these genes.[genepeeks.com] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Premature Chromatid Separation Trait

    DENND1C G:613634 . . DENND4A G:600382 . . DENR G:604550 . . DEPDC1 G:612002 . . DEPDC5 G:614191 . . DEPDC7 G:612294 . . DEPTOR G:612974 . . DERL1 G:608813 . .[usegalaxy.org] 811 The long hunt for the Huntingtons chorea gene 240 positional cloning of an imprinted gene?[books.google.com] An important gene associated with Premature Chromatid Separation Trait is BUB1B (BUB1 Mitotic Checkpoint Serine/Threonine Kinase B).[malacards.org]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    DENND1C G:613634 . . DENND4A G:600382 . . DENR G:604550 . . DEPDC1 G:612002 . . DEPDC5 G:614191 . . DEPDC7 G:612294 . . DEPTOR G:612974 . . DERL1 G:608813 . .[usegalaxy.org] 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] gene; Usher syndrome type IIIA and retinitis pigmentosa-61 caused by mutations in the CLRN1 gene).[julesberman.blogspot.com]

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