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Istanbul Faculty of Medicine (Istanbul University), ISTUNI_MEDGEN

General information

Istanbul Faculty of Medicine, ISTUNI_MEDGEN
Istanbul University
Millet Cad.,
Istanbul
Istanbul
Turkey - 34093

Organization ID: 507485

Personnel

Assertion criteria

Level: Assertion criteria not provided

    Summary of submissions to ClinVar

    Total submissions: 92

    Gene

    GeneSubmissionsLast Updated
    AARS22Apr 21, 2021
    ACTC11Sep 15, 2023
    ALG81Apr 21, 2021
    BEND41Nov 5, 2020
    BLTP11Aug 22, 2023
    BRIP11Mar 17, 2020
    COG61Aug 22, 2023
    COL1A15Apr 3, 2024
    COL1A23Oct 5, 2022
    CRLF12Apr 8, 2022
    CUL71Sep 17, 2021
    DCX1Jun 7, 2022
    DLK12Jun 23, 2023
    DNAH92Aug 22, 2023
    DNAJC211Jul 20, 2023
    EARS22Jun 30, 2020
    ECHS12Feb 24, 2023
    FANCA12Jun 7, 2022
    FANCE1Mar 17, 2020
    FANCF1Jun 7, 2022
    FREM21Nov 14, 2022
    GALT5Sep 3, 2022
    GHRHR1Apr 21, 2021
    GJD2-DT1Sep 15, 2023
    HEXA1Sep 8, 2022
    HSPG21Aug 22, 2023
    HTRA11Aug 26, 2020
    JAG15Aug 7, 2023
    KLHL401Aug 22, 2023
    KLHL72Aug 22, 2023
    LOC1096115891May 29, 2020
    LOC1268598711Jun 15, 2021
    LOC1299937341Apr 8, 2023
    LOC1300016831Jan 10, 2022
    LOC1300598371Jun 7, 2022
    LRRK21Jul 12, 2023
    NDUFAF61Apr 21, 2021
    NEB3Aug 22, 2023
    NOTCH34Aug 26, 2020
    OXCT12Apr 21, 2021
    P3H11Apr 1, 2024
    POLR1C2Apr 21, 2021
    PRKN1Jun 15, 2021
    PSAT11Aug 22, 2023
    RAPSN2Aug 22, 2023
    RELN1Jun 7, 2022
    RETREG11Apr 8, 2023
    RETREG1-AS11Apr 8, 2023
    RIF11Aug 22, 2023
    RUNX210Aug 28, 2020
    SMARCAL11Apr 21, 2021
    SUPT3H1May 29, 2020
    USP141Nov 18, 2021
    WASHC51Aug 22, 2023
    ZNF2761Mar 17, 2020

    Condition

    NameSubmissionsLast Updated
    3M syndrome 11Sep 17, 2021
    ALG8 congenital disorder of glycosylation1Apr 21, 2021
    Alagille syndrome due to a JAG1 point mutation5Aug 7, 2023
    Alkuraya-Kucinskas syndrome1Aug 22, 2023
    Arthrogryposis1Sep 15, 2023
    Arthrogryposis multiplex congenita 63Aug 22, 2023
    Autosomal recessive juvenile Parkinson disease 21Jun 15, 2021
    Bone marrow failure syndrome 31Jul 20, 2023
    CARASIL syndrome1Aug 26, 2020
    COG6-ongenital disorder of glycosylation1Aug 22, 2023
    Central precocious puberty2Jun 23, 2023
    Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 21Aug 26, 2020
    Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 13Aug 26, 2020
    Cleidocranial dysostosis10Aug 28, 2020
    Cold-induced sweating syndrome 12Apr 8, 2022
    Combined oxidative phosphorylation defect type 82Apr 21, 2021
    Congenital heart disease2Aug 22, 2023
    Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase5Sep 3, 2022
    Distal arthrogryposis and CNS involvement1Nov 18, 2021
    Familial acute necrotizing encephalopathy1Nov 5, 2020
    Fanconi anemia complementation group A12Jun 7, 2022
    Fanconi anemia complementation group E1Mar 17, 2020
    Fanconi anemia complementation group F1Jun 7, 2022
    Fanconi anemia complementation group J1Mar 17, 2020
    Fetal akinesia deformation sequence 22Aug 22, 2023
    Fraser syndrome 21Nov 14, 2022
    Interstitial pulmonary disease1Jul 12, 2023
    Isolated growth hormone deficiency, type 41Apr 21, 2021
    Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome2Jun 30, 2020
    Lissencephaly type 1 due to doublecortin gene mutation1Jun 7, 2022
    Mitochondrial complex 1 deficiency, nuclear type 171Apr 21, 2021
    Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency2Feb 24, 2023
    Nemaline myopathy 81Aug 22, 2023
    Neu-Laxova syndrome 21Aug 22, 2023
    Neuropathy, hereditary sensory and autonomic, type 2B1Apr 8, 2023
    Norman-Roberts syndrome1Jun 7, 2022
    Osteogenesis imperfecta type 81Apr 1, 2024
    Osteogenesis imperfecta with normal sclerae, dominant form1Oct 5, 2022
    Osteogenesis imperfecta, perinatal lethal7Apr 3, 2024
    PERCHING syndrome2Aug 22, 2023
    Ritscher-Schinzel syndrome 11Aug 22, 2023
    Schimke immuno-osseous dysplasia1Apr 21, 2021
    Schwartz-Jampel syndrome type 11Aug 22, 2023
    Succinyl-CoA acetoacetate transferase deficiency2Apr 21, 2021
    Tay-Sachs disease1Sep 8, 2022