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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