GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4076 - 4100** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
9658	zinc finger protein 516	ZNF516
9659	phosphodiesterase 4D interacting protein	PDE4DIP
9662	centrosomal protein 135	CEP135
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
9665	meiosis regulator and mRNA stability factor 1	MARF1
9667	scaffold attachment factor B2	SAFB2
9668	zinc finger protein 432	ZNF432
9669	eukaryotic translation initiation factor 5B	EIF5B DKFZp434I036 FLJ10524 IF2 KIAA0741 translation initiation factor IF2
9671	WSC domain containing 2	WSCD2
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
9675	TELO2 interacting protein 1	TTI1
9678	PHD finger protein 14	PHF14
9679	family with sequence similarity 53 member B	FAM53B
9681	DEP domain containing 5, GATOR1 subcomplex subunit	DEPDC5
9683	NEDD4 binding protein 1	N4BP1
9684	leucine rich repeat containing 14	LRRC14
9685	clathrin interactor 1	CLINT1
9686	vestigial like family member 4	VGLL4
9687	growth regulating estrogen receptor binding 1	GREB1
9688	nucleoporin 93	NUP93
9690	ubiquitin protein ligase E3C	UBE3C
9693	Rap guanine nucleotide exchange factor 2	RAPGEF2
9694	ER membrane protein complex subunit 2	EMC2
9695	ER degradation enhancing alpha-mannosidase like protein 1	EDEM1 EDEM KIAA0212	cystic fibrosis depressive disorder hepatitis C major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia skin melanoma
9696	ciliary rootlet coiled-coil, rootletin	CROCC

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