GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5701 - 5725** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
10048	RAN binding protein 9	RANBP9
10047	cystatin 8	CST8
10046	mastermind like domain containing 1	MAMLD1
10040	target of myb1 like 1 membrane trafficking protein	TOM1L1
10039	poly(ADP-ribose) polymerase family member 3	PARP3 ADPRT3 ARTD3 IRT1 NAD+ ADP-ribosyltransferase 3 hPARP-3 pADPRT-3 poly(ADP-ribose) polymerase 3 poly(ADP-ribose) synthetase-3	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease cystic fibrosis embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma
10038	poly(ADP-ribose) polymerase 2	PARP2 ARTD2	arteriosclerotic cardiovascular disease atherosclerosis azoospermia breast cancer breast carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 coronary artery disease diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma epithelioid malignant peripheral nerve sheath tumor esophageal cancer esophageal carcinoma hepatitis A hepatitis hepatocellular carcinoma lipoatrophic diabetes mellitus lipodystrophy liver cancer lymphopenia malignant peripheral nerve sheath tumor neurilemmoma neuroblastoma neurofibrosarcoma obesity peritoneal carcinoma prostate cancer prostate carcinoma rheumatoid arthritis steatotic liver disease type 2 diabetes mellitus
10036	chromatin assembly factor 1 subunit A	CHAF1A
10026	phosphatidylinositol glycan anchor biosynthesis class K	PIGK GPI transamidase subunit GPI-anchor transamidase GPI8 GPI8 homolog (S. cerevisiae) PIG-K hGPI8	adult lymphoma cancer central nervous system lymphoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer lymphoma obsolete ymphosarcoma
10025	mediator complex subunit 16	MED16
10024	trophinin associated protein	TROAP
10021	hyperpolarization activated cyclic nucleotide gated potassium channel 4	HCN4
10020	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	GNE Uae1 bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	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 Bell's palsy GNE myopathy Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Paget's disease of bone Pick's disease Reye syndrome X-linked myopathy with excessive autophagy Zika fever amnestic disorder attention deficit hyperactivity disorder autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer cardiomyopathy cerebral degeneration cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital central hypoventilation syndrome congenital hypothyroidism dementia distal myopathy endomyocardial fibrosis epilepsy esophagitis facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis frontotemporal dementia gastroesophageal reflux disease hypertrophic cardiomyopathy hypothyroidism inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 inclusion body myositis inguinal hernia intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myopathy myositis myxedema neuromuscular disease nonpapillary renal cell carcinoma obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive sleep apnea oculopharyngeal muscular dystrophy pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma scoliosis sialuria sleep apnea thrombocytopenia tibial muscular dystrophy visual epilepsy
10015	programmed cell death 6 interacting protein	PDCD6IP
10013	histone deacetylase 6	HDAC6 FLJ16239 HD6 JM21 KIAA0901 PPP1R90 protein phosphatase 1, regulatory subunit 90
10011	steroid receptor RNA activator 1	SRA1
10010	TRAF family member associated NFKB activator	TANK
10009	zinc finger and BTB domain containing 33	ZBTB33
10008	potassium voltage-gated channel subfamily E regulatory subunit 3	KCNE3
10007	glucosamine-6-phosphate deaminase 1	GNPDA1 GNPDA GPI HLN KIAA0060 glucosamine-6-phosphate deaminase oscillin
10006	abl interactor 1	ABI1
10005	acyl-CoA thioesterase 8	ACOT8 NAP1 Nef (lentivirus myristoylated factor) associated protein 1 PTE-2 choloyl-CoA hydrolase hACTE-III hTE	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 Pick's disease Reye syndrome Thiel-Behnke corneal dystrophy acquired immunodeficiency syndrome bacterial sepsis cancer cerebral degeneration diabetes insipidus diarrhea embryoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypophosphatemia liver cancer low tension glaucoma lung cancer lung non-small cell carcinoma neurohypophyseal diabetes insipidus parapsoriasis psoriasis pustulosis of palm and sole
10004	N-acetylated alpha-linked acidic dipeptidase like 1	NAALADL1
10003	N-acetylated alpha-linked acidic dipeptidase 2	NAALAD2
10002	nuclear receptor subfamily 2 group E member 3	NR2E3
10000	AKT serine/threonine kinase 3	AKT3

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