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10,068 Possible Causes for CENPM, gene

  • Lynch Syndrome

    Germline genetic testing of the MSH2, MSH6, and EPCAM genes revealed full gene deletions.[ncbi.nlm.nih.gov] Its pathogenesis is thought to be closely related to germline mutations of mismatch repair (MMR) genes such as the MLH1, MSH2, PMS2 and MSH6 genes.[ncbi.nlm.nih.gov] The basis of the disease is believed to be the mismatch repair gene mutations.[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Essential Hypertension

    (GMDR) was used to analyze the gene-gene interaction and gene-smoking interaction.[ncbi.nlm.nih.gov] This study reports the association of E-selectin gene Leu554Phe polymorphism and the expression of E-selectin gene in patients with essential hypertension.[ncbi.nlm.nih.gov] The polymorphism of connexin (Cx) genes is found associated with the development of hypertension.[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Hemochromatosis

    We performed magnetic resonance imaging and liver biopsy in an asymptomatic patient with more than 1,000 µg/L of serum ferritin and studied the genes involved in this condition[ncbi.nlm.nih.gov] To assess the prevalence and clinical expression of the HFE gene, we conducted a population-based study in Busselton, Australia.[ncbi.nlm.nih.gov] There are four main classes of HH, as well as five individual molecular subtypes, caused by mutations in five genes, and the approaches implemented in the discovery of each[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Ichthyosis Vulgaris

    Abstract The aim of this study was to detect an 811 bp filaggrin (FLG) gene fragment known to carry a mutation 2282del4 which causes ichthyosis vulgaris.[ncbi.nlm.nih.gov] […] of this gene.[thenakedchemist.com] Abstract Ichthyosis vulgaris (OMIM 146700) is the most common inherited disorder of keratinization and one of the most frequent single-gene disorders in humans.[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Familial Adenomatous Polyposis

    The gene associated with FAP (APC) contains 15 coding exons.[ncbi.nlm.nih.gov] Jejunal carcinoma in patients with familial adenomatous polyposis has been rarely reported, and little is known about its association with genetic alterations of the APC gene[ncbi.nlm.nih.gov] In the Chinese population, most of the previously reported APC gene mutations are missense mutations.[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Familial Prostate Cancer

    CONCLUSIONS: Forty-three nonsense and shared, missense variants were identified in our candidate genes.[ncbi.nlm.nih.gov] Vitamin D acts via vitamin D receptor (VDR), and an association of genetic polymorphisms of the VDR gene has been reported.[ncbi.nlm.nih.gov] Abstract The RNASEL gene on chromosome 1q25 has been identified as a prostate cancer susceptibility gene.[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Escherichia Coli

    O’Malley Journal of the History of Biology (2018) Abiotic Gene Transfer: Rare or Rampant? Tadej Kotnik & James C.[doi.org] gene cassette was found to be the most prevalent.[ncbi.nlm.nih.gov] Plasmids can be transferred between bacteria, potentially spreading the resistance gene to other bacterial species.[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Hereditary Leiomyomatosis and Renal Cell Cancer

    Although the identification of germline mutations in the fumarate hydratase (FH) gene in European families supports it as the susceptibility gene for HLRCC, its role in families[ncbi.nlm.nih.gov] HLRCC is inherited in an autosomal dominant manner, and it is caused by heterozygous germline mutations in the FH gene, which encodes the fumarate hydratase enzyme.[ncbi.nlm.nih.gov] The clinical diagnosis of the autosomal dominant hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome was confirmed by identification of a fumarate hydratase gene[ncbi.nlm.nih.gov]

    Missing: CENPM
  • Retinitis Pigmentosa

    Progress in finding treatments is dependent on determining the genes and mutations causing these diseases, which includes both gene discovery and mutation screening in affected[ncbi.nlm.nih.gov] More than 70 causative genes are known to be responsible for RP.[ncbi.nlm.nih.gov] Gene data Gene symbol reports Gene group reports Tools BioMart HCOP Multi-symbol checker Search Downloads BioMart Custom downloads REST service Statistics and download files[genenames.org]

    Missing: CENPM
  • Lafora Disease

    The critical region for the Lafora gene has been localised to chromosome 6q24 flanked by the dinucleotide repeat markers D6S292 and D6S420.[ncbi.nlm.nih.gov] […] one other gene causing the disease.[ncbi.nlm.nih.gov] LD is caused by mutations in the EMP2A gene encoding a protein phosphatase.[ncbi.nlm.nih.gov]

    Missing: CENPM

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