GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5626 - 5650** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
10199	M-phase phosphoprotein 10	MPHOSPH10
10198	M-phase phosphoprotein 9	MPHOSPH9
10197	proteasome activator subunit 3	PSME3
10195	ALG3 alpha-1,3- mannosyltransferase	ALG3 CDGS4 D16Ertd36e NOT56L Not56 carbohydrate deficient glycoprotein syndrome type IV dol-P-Man dependent alpha-1,3- mannosyltransferase dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	Alzheimer's disease Creutzfeldt-Jakob disease acute myeloid leukemia breast cancer breast carcinoma cancer celiac disease cerebral degeneration clubfoot coloboma congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation type I congenital disorder of glycosylation developmental and epileptic encephalopathy 36 diarrhea embryoma epilepsy esophagus squamous cell carcinoma head and neck squamous cell carcinoma hypertropia laryngeal squamous cell carcinoma mechanical strabismus microcephaly nonsyndromic congenital nail disorder 9 obsolete infantile epileptic encephalopathy ophthalmoplegia optic atrophy strabismus visual epilepsy
10194	teashirt zinc finger homeobox 1	TSHZ1
10189	Aly/REF export factor	ALYREF
10188	tyrosine kinase non receptor 2	TNK2
10180	RNA binding motif protein 6	RBM6
10179	RNA binding motif protein 7	RBM7
10178	teneurin transmembrane protein 1	TENM1
10174	sorbin and SH3 domain containing 3	SORBS3
10168	zinc finger protein 197	ZNF197
10165	solute carrier family 25 member 13	SLC25A13	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
10164	carbohydrate sulfotransferase 4	CHST4 HEC-GLCNAC-6-ST LSST	arthritis arthropathy cancer colitis colon cancer colon carcinoma colon mucinous adenocarcinoma colonic benign neoplasm colorectal cancer gastroenteritis ileitis ileocolitis large intestine cancer osteoarthritis
10163	WASP family member 2	WASF2
10162	lysophosphatidylcholine acyltransferase 3	LPCAT3 C3F LPLAT12 Lysophospholipid acyltransferase 5 lysophospholipid acyltransferase 12 nessy	allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis beta thalassemia cancer coronary artery disease essential hypertension hepatocellular carcinoma hyperglycemia hypertension intrinsic asthma liver cancer nutmeg liver sickle cell anemia thalassemia vascular disease
10161	lysophosphatidic acid receptor 6	LPAR6
10159	ATPase H+ transporting accessory protein 2	ATP6AP2 APT6M8-9 ATP6M8-9 M8-9 PRR RENR V-ATPase M8.9 subunit prorenin receptor renin receptor	Bartter disease Blau syndrome CAKUT Conn's syndrome Graves' disease Horner's syndrome Kawasaki disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Waterhouse-Friderichsen syndrome X-linked parkinsonism-spasticity syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction acute promyelocytic leukemia adamantinous craniopharyngioma adenocarcinoma adenoma age related macular degeneration agnosia alcoholic cardiomyopathy angioma serpiginosum aortic valve disease 2 aortic valve insufficiency aortic valve stenosis aplastic anemia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bacterial infectious disease breast cancer breast carcinoma bronchiolitis bronchus cancer bronchus carcinoma cancer capillary hemangioma carcinoma cardiovascular system disease cavernous hemangioma central nervous system cancer cerebral degeneration cerebrovascular disease chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation type II congenital disorder of glycosylation congestive heart failure coronary artery disease coronary thrombosis craniopharyngioma cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes insipidus diabetes mellitus diabetic angiopathy diabetic cataract diabetic ketoacidosis diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy dysthymic disorder echolalia eclampsia embryoma endometrial cancer endometrial carcinoma epilepsy essential hypertension extrinsic allergic alveolitis farmer's lung gallbladder disease gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glycogen storage disease II granular cell carcinoma granular cell tumor heart disease heart septal defect hepatocellular carcinoma high grade glioma hypertension hyperthyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease intellectual disability invasive ductal carcinoma kidney disease kidney failure large intestine cancer learning disability liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma macular degeneration major depressive disorder melancholic depression mixed glioma morbid obesity multiple sclerosis myocardial infarction nephritis nephrogenic diabetes insipidus nephrosis neurodegenerative disease neurohypophyseal diabetes insipidus neurotic disorder obesity obsolete melancholia obstructive sleep apnea pancreatic ductal adenocarcinoma papillary craniopharyngioma pneumocystosis postinflammatory pulmonary fibrosis pre-eclampsia primary hyperaldosteronism proliferative diabetic retinopathy prostate cancer prostate carcinoma pulmonary fibrosis pyoureter renal osteodystrophy scoliosis secondary Parkinson disease shigellosis silent myocardial infarction syndromic X-linked intellectual disability Hedera type syndromic X-linked intellectual disability thyrotoxicosis tubular adenocarcinoma type 2 diabetes mellitus uremia ureteral obstruction uterine corpus cancer viral infectious disease visual epilepsy
10155	tripartite motif containing 28	TRIM28
10154	plexin C1	PLXNC1
10152	abl interactor 2	ABI2
10150	muscleblind like splicing regulator 2	MBNL2
10149	adhesion G protein-coupled receptor G2	ADGRG2
10148	Epstein-Barr virus induced 3	EBI3
10147	SURP and G-patch domain containing 2	SUGP2

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