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CTGA Database Listing
Arab Genomic Studies
Records found: 2208 Sort by:
  • Syntaxin 11
    OMIM # 605014
    STX11
  • Transient Receptor Potential Cation Channel, Subfamily M, Member 1
    OMIM # 603576
    TRPM1, Melastatin 1, MLSN1,
  • Hemophagocytic Lymphohistiocytosis, Familial, 4
    OMIM # 603552
    FHL4, HPLH4, HLH4,
  • MADS Box Transcription Enhancer Factor 2, Polypeptide A
    OMIM # 600660
    MEF2A
  • Potassium Channel, Voltage-Gated, Shaker-Related Subfamily, Member 2
    OMIM # 176262
    KCNA2, MK2, Mouse, Homolog Of, KV1.2,
  • Nemaline Myopathy 3
    OMIM # 161800
    NEM3, Myopathy, Actin, Congenital, with Excess of Thin Myofilaments, Included, Nemaline Myopathy 3, with Intranuclear Rods, Included, Myopathy, Actin, Congenital, with Cores, Included,
  • Actin, Alpha, Skeletal Muscle 1
    OMIM # 102610
    ACTA1, ASMA,
  • Myocardial Infarction, Susceptibility to, 1
    OMIM # 608446
    MCI1, Myocardial Infarction, Early-Onset, Susceptibility to,
  • ALMS1 Gene
    OMIM # 606844
    ALMS1, KIAA0328,
  • Guanylate Cyclase 2D, Membrane
    OMIM # 600179
    GUCY2D, GUC2D, Guanylate Cyclase 2D, Retinal, GUCY2E, Mouse, Homolog of, Rod Outer Segment Membrane Guanylate Cyclase, ROSGC, RETGC, RETGC1
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