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6 Possible Causes for CLC5

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  • Autosomal Recessive Infantile Hypercalcemia

    ClC5, FcRn, NaPi-IIa gene are related with metabolic renal disease.[oatext.com] NHE3 mutations show association with congenital sodium diarrhea, whereas ClC5 gene is related to renal failure or Dent disease.[oatext.com] The components of this transcytosis system are LRP2, AMN, CUBN, ARH, Dab2, GIPC, NHE3, ClC5, FcRn and NaPi-IIa, which mediate the reuptake of B complex vitamins, including[oatext.com]

  • Early Infantile Epileptic Encephalopathy 24

    Promotes ubiquitination and internalization of various plasma membrane channels such as ENaC, Nav1.2, Nav1.3, Nav1.5, Nav1.7, Nav1.8, Kv1.3, KCNH2, EAAT1 or CLC5.[string-db.org]

  • Encephalomyelitis

    Gena P, Calamita G, Guggino WB (2010) Cadmium impairs albumin reabsorption by down-regulating megalin and ClC5 channels in renal proximal tubule cells.[journals.plos.org]

  • Proteinuria

    […] endocytic vesicle is associated with albuminuria and low molecular weight proteinuria in patients with Dent disease, an X-linked recessive disorder due to a mutation of the CLC5[emedicine.medscape.com]

  • Orthostatic Proteinuria

    […] endocytic vesicle is associated with albuminuria and low molecular weight proteinuria in patients with Dent disease, an X-linked recessive disorder due to a mutation of the CLC5[emedicine.medscape.com]

  • Acoustic Neuritis

    […] due to Cl- channels kidney CLCKA and CLCKB anomaly Non-pore-loop channelopathy due to Cl- transporter Clc7anomaly Non-pore-loop channelopathy due to Cl- transporter kidney Clc5[orpha.net]

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