GlyCosmos Portal

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
348654	GEN1 Holliday junction 5' flap endonuclease	GEN1
25929	gem nuclear organelle associated protein 5	GEMIN5
50628	gem nuclear organelle associated protein 4	GEMIN4
390637	GDP-D-glucose phosphorylase 1	GDPGP1
81544	glycerophosphodiester phosphodiesterase domain containing 5	GDPD5 GDE2 PP1665	acute myeloid leukemia breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer neuroblastoma neurodegenerative disease rheumatoid arthritis
220032	glycerophosphodiester phosphodiesterase domain containing 4	GDPD4 GDE6
79153	glycerophosphodiester phosphodiesterase domain containing 3	GDPD3 MGC4171	Fabry disease Wolman disease chylomicron retention disease lipid storage disease
54857	glycerophosphodiester phosphodiesterase domain containing 2	GDPD2 FLJ20207 GDE3 OBDPF osteoblast differentiation promoting factor
284161	glycerophosphodiester phosphodiesterase domain containing 1	GDPD1 FLJ37451 GDE4
2668	glial cell derived neurotrophic factor	GDNF
2661	growth differentiation factor 9	GDF9
151449	growth differentiation factor 7	GDF7
392255	growth differentiation factor 6	GDF6
8200	growth differentiation factor 5	GDF5
9573	growth differentiation factor 3	GDF3
2658	growth differentiation factor 2	GDF2
9518	growth differentiation factor 15	GDF15
10220	growth differentiation factor 11	GDF11
2662	growth differentiation factor 10	GDF10
2657	growth differentiation factor 1	GDF1
51573	glycerophosphodiester phosphodiesterase 1	GDE1 MIR16 membrane interacting protein of RGS16
9615	guanine deaminase	GDA CYPIN GAH cytoplasmic PSD-95 interactor guanase guanine aminohydrolase nedasin
2653	glycine cleavage system protein H	GCSH lipoic acid-containing protein	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome amino acid metabolic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease breast cancer breast carcinoma cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome early myoclonic encephalopathy embryoma epilepsy focal hand dystonia glycine encephalopathy intellectual disability learning disability lymphoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II multiple mitochondrial dysfunctions syndrome obsolete ymphosarcoma schizophrenia urea cycle disorder visual epilepsy
145781	GCOM1, MYZAP-POLR2M combined locus	GCOM1
140687	glucosaminyl (N-acetyl) transferase family member 7	GCNT7 dJ1153D9.2	colorectal cancer colorectal carcinoma large intestine cancer

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