GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **5901 - 5925** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
9679	family with sequence similarity 53 member B	FAM53B
9678	PHD finger protein 14	PHF14
9675	TELO2 interacting protein 1	TTI1
9672	syndecan 3	SDC3 N-syndecan SYND3 syndecan proteoglycan 3	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 breast fibrocystic disease cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis C hepatocellular carcinoma liver cancer microglandular adenosis muscular dystrophy nonpapillary renal cell carcinoma obesity pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma
9671	WSC domain containing 2	WSCD2
9669	eukaryotic translation initiation factor 5B	EIF5B DKFZp434I036 FLJ10524 IF2 KIAA0741 translation initiation factor IF2
9668	zinc finger protein 432	ZNF432
9667	scaffold attachment factor B2	SAFB2
9665	meiosis regulator and mRNA stability factor 1	MARF1
9663	lipin 2	LPIN2 KIAA0249	Chanarin-Dorfman syndrome Crohn's colitis Crohn's disease Diamond-Blackfan anemia SAPHO syndrome acne agranulocytosis allergic asthma anemia asthma autosomal recessive congenital ichthyosis 1 autosomal recessive osteopetrosis 7 cancer chronic recurrent multifocal osteomyelitis congenital dyserythropoietic anemia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypoplastic anemia congestive heart failure dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism familial mediterranean fever familial periodic paralysis fibromyalgia gastrointestinal system disease glomerulonephritis granular corneal dystrophy 2 ichthyosis inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrinsic asthma keratosis follicularis leukopenia lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy macrocytic anemia mevalonic aciduria microcytic anemia mongolian spot myoglobinuria myopathy myopia myositis nephritis neutropenia obesity obsolete congenital ichthyosiform erythroderma osteomyelitis osteopetrosis osteosclerosis prostate cancer prostate carcinoma proteinuria pseudoxanthoma elasticum relapsing fever rheumatoid arthritis severe congenital neutropenia synovitis tenosynovitis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue type 2 diabetes mellitus ulcerative colitis
9662	centrosomal protein 135	CEP135
9659	phosphodiesterase 4D interacting protein	PDE4DIP
9658	zinc finger protein 516	ZNF516
9656	mediator of DNA damage checkpoint 1	MDC1
9654	tubulin tyrosine ligase like 4	TTLL4
9653	heparan sulfate 2-O-sulfotransferase 1	HS2ST1 KIAA0448	benign mastocytoma extracutaneous mastocytoma hypereosinophilic syndrome indolent systemic mastocytosis mast cell neoplasm mastocytosis melanoma skin melanoma
9652	SKI3 subunit of superkiller complex	SKIC3
9651	phospholipase C eta 2	PLCH2 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 KIAA0450 PLC-eta2 PLCeta2 RP3-395M20.1	azoospermia intellectual disability learning disability schizophrenia
9650	mitochondrial fission regulator 1	MTFR1
9649	Ral GEF with PH domain and SH3 binding motif 1	RALGPS1
9648	GRIP and coiled-coil domain containing 2	GCC2
9647	protein phosphatase, Mg2+/Mn2+ dependent 1F	PPM1F
9645	microtubule associated monooxygenase, calponin and LIM domain containing 2	MICAL2
9644	SH3 and PX domains 2A	SH3PXD2A
9643	mortality factor 4 like 2	MORF4L2

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