GlyCosmos Portal

Displaying entries **8001 - 8025** of **16604** in total

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P37231	Peroxisome proliferator-activated receptor gamma	NR1C3 PPARG	1	0	Alzheimer's disease cardiovascular system disease carotid artery disease cognitive disorder colon cancer end stage renal disease familial partial lipodystrophy type 3 hypertension lipodystrophy obesity pancreatic cancer pre-eclampsia proliferative diabetic retinopathy type 2 diabetes mellitus
P37198	Nuclear pore glycoprotein p62	NUP62	101	2	primary biliary cholangitis striatonigral degeneration
P37173	TGF-beta receptor type-2	TGFBR2	7	12	Loeys-Dietz syndrome 2 Lynch syndrome Marfan syndrome colon cancer esophagus squamous cell carcinoma hereditary nonpolyposis colorectal cancer type 6 mismatch repair cancer syndrome pancreatic cancer
P37108	Signal recognition particle 14 kDa protein	SRP14	3	1
P37088	Amiloride-sensitive sodium channel subunit alpha	SCNN1 SCNN1A	5	3	Liddle syndrome bronchiectasis 2 pseudohypoaldosteronism
P37023	Activin receptor type-1-like	ACVRL1 ACVRLK1 ALK1	1	0	hereditary hemorrhagic telangiectasia pulmonary hypertension
P36980	Complement factor H-related protein 2	CFHL2 CFHR2 FHR2 HFL3	1	5
P36957	Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial	DLST DLTS	3	1	Alzheimer's disease paraganglioma
P36956	Sterol regulatory element-binding protein 1	BHLHD1 SREBF1 SREBP1	3	1	coronary artery disease disease of metabolism type 2 diabetes mellitus
P36955	Pigment epithelium-derived factor	PEDF PIG35 SERPINF1	6	56	brain edema corneal neovascularization diabetic retinopathy endometriosis leukostasis macular retinal edema metabolic dysfunction-associated steatohepatitis obesity osteogenesis imperfecta type 6 osteosarcoma ovarian hyperstimulation syndrome proliferative diabetic retinopathy retinal degeneration retinitis pigmentosa retinoblastoma sciatic neuropathy transient cerebral ischemia type 2 diabetes mellitus uveitis
P36952	Serpin B5	PI5 SERPINB5	5	1
P36941	Tumor necrosis factor receptor superfamily member 3	D12S370 LTBR TNFCR TNFR3 TNFRSF3	7	3
P36915	Guanine nucleotide-binding protein-like 1	GNL1 HSR1	1	0
P36897	TGF-beta receptor type-1	ALK5 SKR4 TGFBR1	3	2	Ferguson-Smith tumor Loeys-Dietz syndrome 1 Lynch syndrome colorectal cancer pancreatic ductal adenocarcinoma urinary bladder cancer
P36896	Activin receptor type-1B	ACVR1B ACVRLK4 ALK4	1	0	lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma pancreatic cancer stomach cancer
P36894	Bone morphogenetic protein receptor type-1A	ACVRLK3 ALK3 BMPR1A	1	0	hereditary mixed polyposis syndrome 2 intestinal disease juvenile polyposis syndrome
P36888	Receptor-type tyrosine-protein kinase FLT3	CD135 FLK2 FLT3 STK1	10	1	acute lymphoblastic leukemia acute myeloid leukemia acute myelomonocytic leukemia colorectal adenocarcinoma hepatocellular carcinoma prostate cancer
P36873	Serine/threonine-protein phosphatase PP1-gamma catalytic subunit	PPP1CC	1	0
P36871	Phosphoglucomutase-1	PGM1	1	1	congenital disorder of glycosylation It endometrial cancer teratoma
P36776	Lon protease homolog, mitochondrial	LONP1 PRSS15	1	0	CODAS syndrome
P36578	Large ribosomal subunit protein uL4	RPL1 RPL4	4	3
P36551	Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial	CPO CPOX CPX	1	1	hereditary coproporphyria liver disease
P36544	Neuronal acetylcholine receptor subunit alpha-7	CHRNA7 NACHRA7	3	0
P36543	V-type proton ATPase subunit E 1	ATP6E ATP6E2 ATP6V1E1	1	1	autosomal recessive cutis laxa type IIC
P36542	ATP synthase subunit gamma, mitochondrial	ATP5C ATP5C1 ATP5CL1 ATP5F1C	1	2

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