GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5551 - 5575** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
10376	tubulin alpha 1b	TUBA1B K-ALPHA-1 tubulin, alpha, ubiquitous
10371	semaphorin 3A	SEMA3A
10369	calcium voltage-gated channel auxiliary subunit gamma 2	CACNG2
10361	nucleophosmin/nucleoplasmin 2	NPM2
10352	tryptophanyl tRNA synthetase 2, mitochondrial	WARS2
10351	ATP binding cassette subfamily A member 8	ABCA8
10350	ATP binding cassette subfamily A member 9	ABCA9
10347	ATP binding cassette subfamily A member 7	ABCA7
10345	triadin	TRDN
10343	polycystin family receptor for egg jelly	PKDREJ
10342	trafficking from ER to golgi regulator	TFG
10333	toll like receptor 6	TLR6	aspergillosis asthma bacterial pneumonia infective endocarditis perinatal necrotizing enterocolitis rhinitis tuberculosis
10332	C-type lectin domain family 4 member M	CLEC4M
10331	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3	B3GNT3 B3GN-T3 B3GNT-3 HP10328 beta-1,3-N-acetylglucosaminyltransferase bGnT-3 beta3Gn-T3 putative type II membrane protein transmembrane protein 3	cancer cervical adenocarcinoma cervical cancer cervix carcinoma common wart embryoma influenza lung cancer lung non-small cell carcinoma neuroblastoma
10329	ribitol xylosyltransferase 1	RXYLT1 HP10481	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
10328	ER membrane protein complex subunit 8	EMC8
10327	aldo-keto reductase family 1 member A1	AKR1A1 ALR DD3 aldehyde reductase dihydrodiol dehydrogenase 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 B-cell lymphoma Barrett's esophagus Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prinzmetal angina Reye syndrome Stargardt disease Wernicke-Korsakoff syndrome acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy adult fibrosarcoma age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis amnestic disorder anaplastic astrocytoma anorectal stricture arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atrophy of testis autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome background diabetic retinopathy benign ependymoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma brain cancer brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis cardiovascular system disease cellular ependymoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood ependymoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential tremor exudative vitreoretinopathy familial periodic paralysis fibrillary astrocytoma fibrosarcoma gallbladder disease gastric cardia adenocarcinoma gemistocytic astrocytoma glucocorticoid-remediable aldosteronism glycogen storage disease II granular cell carcinoma granuloma annulare head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hypopharynx cancer immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macular degeneration major depressive disorder malaria malignant astrocytoma marasmus melancholic depression migraine myocardial infarction myopathy myxopapillary ependymoma neurodegenerative disease neuropathy neurotic disorder nicotine dependence non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete constipation obsolete eye and adnexa disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oral candidiasis osteoporosis osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary ependymoma papillary renal cell carcinoma perinatal necrotizing enterocolitis peripheral nervous system disease pharynx cancer pilocytic astrocytoma placental insufficiency polyneuropathy proliferative diabetic retinopathy prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma renal carcinoma renal cell carcinoma reticulosarcoma sarcomatoid renal cell carcinoma schizophrenia scurvy sensorineural hearing loss silent myocardial infarction squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tanycytic ependymoma tongue squamous cell carcinoma tracheal disease tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus urinary bladder cancer viral infectious disease vulvovaginal candidiasis
10326	signal regulatory protein beta 1	SIRPB1
10325	Ras related GTP binding B	RRAGB
10321	cysteine rich secretory protein 3	CRISP3
10320	IKAROS family zinc finger 1	IKZF1
10319	laminin subunit gamma 3	LAMC3
10317	beta-1,3-galactosyltransferase 5	B3GALT5 B3GalT-V B3T5 GLCT5 GlcNAc-beta-1,3-galactosyltransferase 5 beta3Gal-T5 homolog of C. elegans Bt toxin resistance gene bre-5	acute myeloid leukemia adenocarcinoma adenoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cribriform carcinoma granular cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer pancreatic cancer pancreatic carcinoma tubular adenocarcinoma
10316	neuromedin U receptor 1	NMUR1
10314	LanC like glutathione S-transferase 1	LANCL1

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