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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Jalili Syndrome
    OMIM # 217080
    Cone-Rod Dystrophy and Amelogenesis Imperfecta
  • Cyclin M4
    OMIM # 607805
    CNNM4, Ancient Conserved Domain Protein 4, ACDP4, KIAA1592
  • Inositol Polyphosphate-5-Phosphatase, 72-KD
    OMIM # 613037
    INPP5E
  • Joubert Syndrome 1
    OMIM # 213300
    JBTS1, Joubert Syndrome, JBTS, Joubert-Boltshauser Syndrome, Cerebelloparenchymal Disorder IV, CPD4, Cerebellooculorenal Syndrome 1, CORS1
  • CDK5 Regulatory Subunit-Associated Protein 2
    OMIM # 608201
    CDK5RAP2, Centrosomal Protein, 215-KD, CEP215, KIAA1633,
  • BUB1 Mitotic checkpoint Serine/Threonine Kinase B
    OMIM # 602860
    BUB1B, Budding Uninhibiting by Benzimidazoles 1, S. cerevisiae, Homolog of, Beta, BUB1, S. cerevisiae, Homolog of, Beta, Mitotic Checkpoint Gene BUB1B, BUBR1
  • Ribonuclease H2, Subunit C
    OMIM # 610330
    RNASEH2C, AYP1, FLJ20974
  • Aicardi-Goutieres Syndrome 3
    OMIM # 610329
    AGS3
  • Retinitis Pigmentosa 19
    OMIM # 601718
    RP19
  • ATPase, Class I, Type 8B, Member 1
    OMIM # 602397
    ATP8B1, FIC Gene 1, FIC1
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