GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **201 - 225** of **1582** in total

« First

‹ Prev

…

5

6

7

8

9

10

11

12

13

…

Next ›

Last »
Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
131544	crystallin beta-gamma domain containing 3	CRYBG3 DKFZp667G2110	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
131375	lysozyme like 4	LYZL4 LYC4 MGC26768	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 cerebral degeneration
130749	carboxypeptidase O	CPO metallocarboxypeptidase C metallocarboxypeptidase O	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
130589	galactose mutarotase	GALM aldose 1-epimerase aldose mutarotase galactomutarotase	Crohn's colitis Crohn's disease classic galactosemia colitis colorectal cancer colorectal carcinoma galactokinase deficiency galactosemia gastroenteritis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease 2 inflammatory bowel disease large intestine cancer ulcerative colitis
130576	LY6/PLAUR domain containing 6B	LYPD6B CT116 LYPD7 cancer/testis antigen 116
130574	LY6/PLAUR domain containing 6	LYPD6 MGC52057	Gilles de la Tourette syndrome anxiety disorder generalized anxiety disorder phobic disorder
130367	sphingosine-1-phosphate phosphatase 2	SGPP2 FLJ39004 SPP2	cancer colitis embryoma gastroenteritis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease stomach cancer stomach carcinoma ulcerative colitis
130120	regenerating family member 3 gamma	REG3G LPPM429 PAP1B UNQ429	acute pancreatitis bronchus cancer bronchus carcinoma cancer colitis essential hypertension gastroenteritis head and neck cancer head and neck squamous cell carcinoma hypertension ileitis ileocolitis interstitial nephritis lung benign neoplasm lung cancer lung carcinoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pneumonia pyelitis pyelonephritis sciatic neuropathy steatotic liver disease type 2 diabetes mellitus visual epilepsy
129807	neuraminidase 4	NEU4	cancer embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	adrenoleukodystrophy
129530	lysozyme g1	LYG1 LYGA1 SALW1939	cancer
128869	phosphatidylinositol glycan anchor biosynthesis class U	PIGU GAB1 GPI and Actin Bar homolog (S. cerevisiae) GPI transamidase subunit PIGU PIG-U bA346K17.2	bladder carcinoma breast cancer breast carcinoma cancer carcinoma cerebral degeneration colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma differentiated thyroid gland carcinoma dysplastic nevus syndrome embryoma epilepsy hepatocellular carcinoma intellectual disability large intestine cancer learning disability liver cancer melanoma nasopharynx carcinoma papillary carcinoma sarcomatoid carcinoma scoliosis skin benign neoplasm skin cancer skin melanoma urinary bladder cancer visual epilepsy
127550	alpha 1,3-galactosyltransferase 2	A3GALT2 IGB3S IGBS3S iGb3 synthase isoglobotriaosylceramide synthase
127281	peroxiredoxin like 2B	PRXL2B MGC26818 prostamide/prostaglandin F synthase thioredoxin-type PGF synthase
126792	beta-1,3-galactosyltransferase 6	B3GALT6 beta-1,3-galactosyltransferase-6 beta3GalT6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease Hirschsprung's disease Laron syndrome Rothmund-Thomson syndrome achondroplasia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease bone disease cartilage disease cherubism chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate clubfoot collagen disease collecting duct carcinoma connective tissue disease cutis laxa enophthalmos exostosis heart septal defect hepatocellular carcinoma intellectual disability isolated cleft palate isolated ectopia lentis learning disability liver cancer mal de Meleda mitral valve insufficiency mitral valve prolapse myopia nonpapillary renal cell carcinoma obsolete exophthalmos orbital disease osteogenesis imperfecta osteoporosis papillary renal cell carcinoma paraplegia patent foramen ovale periarthritis renal carcinoma renal cell carcinoma restrictive dermopathy sarcomatoid renal cell carcinoma scoliosis spinal cord disease spondyloepimetaphyseal dysplasia with joint laxity type 1 tendinitis ventricular septal defect
126129	carnitine palmitoyltransferase 1C	CPT1C CATL1 CPT1P CPTIC FLJ23809	Henoch-Schoenlein purpura autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer congenital hypothyroidism embryoma giant cell glioblastoma glioblastoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 73 high grade glioma hypersensitivity vasculitis hypoglycemia hypothyroidism immune system disease lung benign neoplasm melanoma multiple myeloma myxedema neuropathy obesity papillary adenocarcinoma papillary renal cell carcinoma paraplegia peripheral nervous system disease polyneuropathy skin melanoma steatotic liver disease thyroid gland papillary carcinoma
125981	alkaline ceramidase 1	ACER1	alopecia
125972	calreticulin 3	CALR3 CRT2 CT93 FLJ25355 MGC26577 calsperin cancer/testis antigen 93	Parkinson's disease cardiomyopathy cataract endomyocardial fibrosis familial hypertrophic cardiomyopathy hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy vitiligo
125061	arylformamidase	AFMID DKFZp686F03259 KF kynurenine formamidase	colon cancer colonic benign neoplasm colorectal cancer large intestine cancer
124912	sperm acrosome associated 3	SPACA3 ALLP17 CT54 LYC3 LYZL3 SLLP1 cancer/testis antigen 54 sperm lyzozyme-like acrosomal protein 1	acute myeloid leukemia cancer hematologic cancer seminoma testicular cancer testis seminoma
124872	beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group)	B4GALNT2 Cad Sda	Duchenne muscular dystrophy 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 campomelic dysplasia cancer carcinoma cerebrotendinous xanthomatosis congenital muscular dystrophy coronary artery disease distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy 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 oculopharyngeal muscular dystrophy rippling muscle disease 2 sarcomatoid carcinoma
123904	neuritin 1 like	NRN1L MRCC2446 UNQ2446	epilepsy visual epilepsy
123876	acyl-CoA synthetase medium chain family member 2A	ACSM2A A-923A4.1 MGC150530	cerebral palsy hemiplegia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
123745	phospholipase A2 group IVE	PLA2G4E FLJ45651	nicotine dependence panic disorder
123099	delta 4-desaturase, sphingolipid 2	DEGS2 DES2 FADS8 dihydroceramide desaturase 2 sphingolipid delta(4)-desaturase 2	acquired immunodeficiency syndrome colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis disease of mental health human immunodeficiency virus infectious disease large intestine cancer neurodegenerative disease obesity psychotic disorder schizophrenia type 2 diabetes mellitus

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements