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CTGA Database Listing
Arab Genomic Studies
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  • Tubulin Tyrosine Ligase-like Family, Member 5
    OMIM # 612268
    TTLL5
  • Transient Receptor Potential Cation Channel, Subfamily M, Member 1
    OMIM # 603576
    TRPM1, Melastatin 1, MLSN1,
  • Night Blindness, Congenital Stationary, Type 1C
    OMIM # 613216
    CSNB1C, CSNB, Complete, Autosomal Recessive,
  • Thiamine-Responsive Megaloblastic Anemia Syndrome
    OMIM # 249270
    TRMA, Thiamine Metabolism Dysfunction Syndrome 1 (Megaloblastic Anemia, Diabetes mellitus, and deafness Type), THMD1, Megaloblastic Anemia, Thiamine-Responsive, with Diabetes Mellitus and Sensorineural Deafness, Rogers Syndrome, Thiamine-Responsive Anemia Syndrome, Thiamine-Responsive Myelodysplasia,
  • Solute Carrier Family 19 (Thiamine Transporter), Member 2
    OMIM # 603941
    SLC19A2, Thiamine Transporter Protein 1, THTR1, THT1
  • Spermatogenesis-Associated Protein 7
    OMIM # 609868
    SPATA7, HSD3
  • Leber Congenital Amaurosis 3
    OMIM # 604232
    LCA3, Retinitis Pigmentosa, Juvenile, SPATA7-Related,
  • B-Raf Protooncogene, Serine/Threonine Kinase
    OMIM # 164757
    BRAF, V-RAF Murine Sarcoma Viral Oncogene Homolog B1, Oncogene BRAF, BRAF1, RAFB1
  • Matrix Metallopeptidase 1
    OMIM # 120353
    MMP1, Collagenase, Fibroblast , CLG, CLGN, Collagenase, Interstitial
  • Transmembrane Channel-Like protein 8
    OMIM # 605829
    EV Gene, EVER2, EV2
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