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CTGA Database Listing
Arab Genomic Studies
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  • Complex I, Subunit ND5
    OMIM # 516005
    MTND5, NADH-Ubiquinone Oxidoreductase, Subunit ND5, NADH Dehydrogenase, Subunit 5
  • Mitochondrial Myopathy, Infantile, Transient
    OMIM # 500009
    MMIT, Mitochondrial Myopathy, Infantile, Transient, due to Respiratory Chain Deficiency, COX Defieiency Myopathy, Infantile, Transient, Respiratory Chain Deficiency, Infantile Transient
  • Transfer RNA, Mitochondrial, Alanine
    OMIM # 590000
    tRNA-ALA, Mitochondrial
  • Neurexin I
    OMIM # 600565
    NRXN1
  • Cortical Dysplasia, Complex, with Other Brain Malformations 2
    OMIM # 615282
    CDCBM2
  • Kinesin Family Member 5C
    OMIM # 604593
    KIFC2, Kinesin, Heavy Chain, Neuron-Specific, 2, NKHC2
  • Myosin, Heave Chain 14, Nonmuscle
    OMIM # 608568
    MYH14, Nonmuscle Myosin Heavy Chain IIC, NMHC IIC, KIAA2034,
  • Inositol 1,4,5-Triphosphate Receptor, Type 1
    OMIM # 147265
    ITPR1, IP3R, IP3R1
  • Spinocerebellar Ataxia 15
    OMIM # 606658
    SCA15, Spinocerebellar Ataxia 16, SCA16,
  • Phospholipase A2, Group VI
    OMIM # 603604
    PLA2G6, Phospholipase A2, Calcium-Independent, IPLA2, Patatin-Like Phospholipase Domain-Containing Protein 9, PNPLA9, Phospholipase A2, Calcium-Independent, Group VI, A, IPLA2-VIA
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