GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4201 - 4225** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
55130	outer dynein arm docking complex subunit 2	ODAD2
4952	OCRL inositol polyphosphate-5-phosphatase	OCRL Dent disease 2 Dent-2 OCRL1	Bartter disease Conn's syndrome Dent disease Ehlers-Danlos syndrome Fanconi anemia Fanconi syndrome Laron syndrome Waterhouse-Friderichsen syndrome achondroplasia amblyopia anemia angular cheilitis anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder autoimmune hemolytic anemia azoospermia blindness buphthalmos calcinosis calcium metabolism disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cheilitis chromosome 17p13.1 deletion syndrome chronic kidney disease chronic ulcer of skin congenital nystagmus cryptorchidism cystinosis dental caries dental enamel hypoplasia dentin caries depressive disorder diabetes insipidus dissociated nystagmus dysthymic disorder epilepsy esophagitis fetal erythroblastosis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma gingivitis glaucoma glioblastoma glomerulonephritis high grade glioma hydrocephalus hydrophthalmos hypercalcemia hyperparathyroidism hypertropia hypokalemia hypophosphatemia inguinal hernia intellectual disability isolated elevated serum creatine phosphokinase levels kidney failure learning disability lip disease lissencephaly listeriosis macrocytic anemia major depressive disorder mechanical strabismus melancholic depression microphthalmia neonatal anemia nephritis nephrocalcinosis nephrolithiasis neurohypophyseal diabetes insipidus neurotic disorder obsolete constipation obsolete melancholia oculocerebrorenal syndrome omphalocele ophthalmoplegia osteitis fibrosa osteoarthritis osteogenesis imperfecta osteomalacia otitis media pathologic nystagmus peptic esophagitis periodontitis phosphorus metabolism disease primary hyperaldosteronism proteinuria recurrent corneal erosion renal tubular acidosis rickets scoliosis skin benign neoplasm skin cancer spondyloepimetaphyseal dysplasia, Sponastrime type spontaneous ocular nystagmus stereotypic movement disorder strabismic amblyopia strabismus subcortical band heterotopia thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue umbilical hernia uremia uric acid nephrolithiasis visual epilepsy
100506658	occludin	OCLN
54940	OCIA domain containing 1	OCIAD1
4948	OCA2 melanosomal transmembrane protein	OCA2
729330	otoconin 90	OC90
23363	obscurin like cytoskeletal adaptor 1	OBSL1
84033	obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF	OBSCN
79596	ORC ubiquitin ligase 1	OBI1
4940	2'-5'-oligoadenylate synthetase 3	OAS3
4938	2'-5'-oligoadenylate synthetase 1	OAS1	primary immunodeficiency disease
221443	O-acyl-ADP-ribose deacylase 1	OARD1 MGC19570 TARG1 dJ34B21.3 terminal ADP-ribose protein glycohydrolase 1	acute myeloid leukemia neurodegenerative disease stomach cancer stomach carcinoma
220323	out at first homolog	OAF
60506	nyctalopin	NYX CLRP CSNB1A	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
57523	NYN domain and retroviral integrase containing	NYNRIN
57624	neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2	NYAP2
29107	nuclear transport factor 2 like export factor 1	NXT1
11247	neurexophilin 4	NXPH4
11248	neurexophilin 3	NXPH3
11249	neurexophilin 2	NXPH2
30010	neurexophilin 1	NXPH1
54827	neurexophilin and PC-esterase domain family member 4	NXPE4
91775	neurexophilin and PC-esterase domain family member 3	NXPE3
120406	neurexophilin and PC-esterase domain family member 2	NXPE2
120400	neurexophilin and PC-esterase domain family member 1	NXPE1

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