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  • G6PD: glucose-6-phosphate dehydrogenase
  • GAA: glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II)
  • GALC: galactosylceramidase
  • GALE: UDP-galactose-4-epimerase
  • GALK1: galactokinase 1
  • GALT: galactose-1-phosphate uridylyltransferase
  • GAMT: guanidinoacetate N-methyltransferase
  • GAN: giant axonal neuropathy (gigaxonin)
  • GARS: glycyl-tRNA synthetase
  • GBA: glucosidase, beta; acid (includes glucosylceramidase)
  • GCDH: glutaryl-Coenzyme A dehydrogenase
  • GCH1: GTP cyclohydrolase 1 (dopa-responsive dystonia)
  • GDAP1: ganglioside-induced differentiation-associated protein 1
  • GFAP: glial fibrillary acidic protein
  • GJB1: gap junction protein, beta 1, 32kDa
  • GJB2: gap junction protein, beta 2, 26kDa
  • GJB3: gap junction protein, beta 3, 31kDa
  • GJB6: gap junction protein, beta 6, 30kDa
  • GLA: galactosidase, alpha
  • GLDC: glycine dehydrogenase (decarboxylating)
  • GLI3: GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome)
  • GM2A: GM2 ganglioside activator
  • GNAS: GNAS complex locus
  • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
  • GNE: glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
  • GNMT: glycine N-methyltransferase
  • GPC3: glypican 3
  • GPR143: G protein-coupled receptor 143
  • GPR98: G protein-coupled receptor 98
  • GRHPR: glyoxylate reductase/hydroxypyruvate reductase
  • GSS: glutathione synthetase
  • GTF2I: general transcription factor II, i
  • GTF2IRD1: GTF2I repeat domain containing 1
 
 
Published: January 23, 2009