GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6601 - 6625** of **9988** in total

« First

‹ Prev

…

261

262

263

264

265

266

267

268

269

…

Next ›

Last »
Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
7936	negative elongation factor complex member E	NELFE
7932	olfactory receptor family 2 subfamily H member 2	OR2H2
7923	hydroxysteroid 17-beta dehydrogenase 8	HSD17B8 D6S2245E H2-KE6 HKE6 KE6 RING2 SDR30C1 short chain dehydrogenase/reductase family 30C, member 1	breast cancer breast carcinoma cancer hepatitis B rheumatoid arthritis tuberculosis
7922	solute carrier family 39 member 7	SLC39A7
7917	BAG cochaperone 6	BAG6
7916	proline rich coiled-coil 2A	PRRC2A
7915	aldehyde dehydrogenase 5 family member A1	ALDH5A1 SSADH SSDH succinate-semialdehyde dehydrogenase	Crohn's colitis Crohn's disease Rett syndrome X-linked dystonia-parkinsonism Zika fever age related macular degeneration agnosia anxiety disorder autistic disorder carcinoma degeneration of macula and posterior pole developmental coordination disorder dystonia 12 dystonia 16 dystonia 21 dystonia 25 dystonia 27 dystonia 5 dystonia epilepsy focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia generalized epilepsy with febrile seizures plus hypertropia idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability juvenile myoclonic epilepsy learning disability lingual-facial-buccal dyskinesia macular degeneration mechanical strabismus movement disease myoclonic dystonia 11 ophthalmoplegia ovarian cancer ovarian carcinoma psychotic disorder schizoaffective disorder schizophreniform disorder status epilepticus strabismus succinic semialdehyde dehydrogenase deficiency syndromic X-linked intellectual disability 94 torsion dystonia 13 torsion dystonia 17 torsion dystonia 1 torsion dystonia 2 torsion dystonia 4 torsion dystonia 6 torsion dystonia with onset in infancy tuberculosis ulcerative colitis visual epilepsy
7913	DEK proto-oncogene	DEK
7903	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	ST8SIA4 PST PST1 ST8Sia IV	Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Norum disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Tangier disease abetalipoproteinemia acne acute pancreatitis adrenoleukodystrophy alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alternating hemiplegia of childhood anal carcinoma in situ anaplastic astrocytoma ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma carotid artery thrombosis carotid stenosis central nervous system disease cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood leukemia cholecystolithiasis choledocholithiasis cholelithiasis choreaacanthocytosis chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma complement deficiency coronary artery disease depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea dysthymic disorder embryoma esophageal cancer esophageal carcinoma essential hypertension fibrillary astrocytoma fragile X syndrome gallbladder cancer gallbladder carcinoma gallbladder disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis gyrate atrophy hepatocellular carcinoma hereditary spherocytosis high grade glioma hypertension hypolipoproteinemia hypoparathyroidism juvenile pilocytic astrocytoma kidney disease large intestine cancer laryngeal squamous cell carcinoma leukemia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant astrocytoma melancholic depression muscular dystrophy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephritis nervous system disease neuroblastoma neurotic disorder nonpapillary renal cell carcinoma nutmeg liver obsolete melancholia pancreatitis papillary renal cell carcinoma papilloma periodontitis pilocytic astrocytoma pneumonia prostate cancer prostate carcinoma protoplasmic astrocytoma pseudohypoparathyroidism renal carcinoma renal cell carcinoma rhabdomyosarcoma rhinitis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sinusitis squamous cell carcinoma squamous cell papilloma steatotic liver disease subependymal giant cell astrocytoma substance abuse substance-related disorder systemic lupus erythematosus thyroid gland follicular carcinoma tongue squamous cell carcinoma type 2 diabetes mellitus uveoparotid fever
7879	RAB7A, member RAS oncogene family	RAB7A
7874	ubiquitin specific peptidase 7	USP7
7871	sarcolemma associated protein	SLMAP
7869	semaphorin 3B	SEMA3B
7866	interferon related developmental regulator 2	IFRD2
7862	bromodomain and PHD finger containing 1	BRPF1
7855	frizzled class receptor 5	FZD5
7852	C-X-C motif chemokine receptor 4	CXCR4
7850	interleukin 1 receptor type 2	IL1R2
7849	paired box 8	PAX8
7846	tubulin alpha 1a	TUBA1A B-ALPHA-1 FLJ25113 TUBA3 tubulin, alpha, brain-specific
7841	mannosyl-oligosaccharide glucosidase	MOGS CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	Japanese encephalitis Turner syndrome Zika fever acquired hyperkeratosis actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia adamantinoma agammaglobulinemia ameloblastoma blepharophimosis bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic monocytic leukemia chronic myelomonocytic leukemia congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIb congenital disorder of glycosylation cystic fibrosis dengue disease epilepsy gonadal dysgenesis holoprosencephaly 1 holoprosencephaly juvenile myelomonocytic leukemia keratoacanthoma lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma malaria melanoma obesity optic atrophy pleomorphic xanthoastrocytoma sensorineural hearing loss skin melanoma viral infectious disease visual epilepsy yellow fever
7840	ALMS1 centrosome and basal body associated protein	ALMS1
7837	peroxidasin	PXDN
7832	BTG anti-proliferation factor 2	BTG2
7827	NPHS2 stomatin family member, podocin	NPHS2

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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements