GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3851 - 3875** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
729	complement C6	C6
730	complement C7	C7
731	complement C8 alpha chain	C8A
732	complement C8 beta chain	C8B
735	complement C9	C9
722	complement component 4 binding protein alpha	C4BPA
725	complement component 4 binding protein beta	C4BPB
100293534	complement component 4B (Chido/Rodgers blood group), copy 2	C4B_2
629	complement factor B	CFB
3075	complement factor H	CFH
3078	complement factor H related 1	CFHR1
3080	complement factor H related 2	CFHR2
10878	complement factor H related 3	CFHR3
10877	complement factor H related 4	CFHR4
81494	complement factor H related 5	CFHR5
3426	complement factor I	CFI
5199	complement factor properdin	CFP
1147	component of inhibitor of nuclear factor kappa B kinase complex	CHUK
9382	component of oligomeric golgi complex 1	COG1 KIAA1381	Baraitser-Winter syndrome Burkitt lymphoma Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome anemia branchiootic syndrome cerebral degeneration cerebrocostomandibular syndrome chronic lymphocytic leukemia clubfoot congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIg cryptorchidism hematologic cancer hydronephrosis hypospadias kidney failure macrocytic anemia orofaciodigital syndrome I orofaciodigital syndrome X placental insufficiency primary pulmonary hypertension scoliosis sensorineural hearing loss thrombocytopenia
22796	component of oligomeric golgi complex 2	COG2	atrial fibrillation cardiovascular system disease congenital disorder of glycosylation type IIq congenital disorder of glycosylation coronary artery disease diabetes mellitus epilepsy familial hypercholesterolemia heart disease hypobetalipoproteinemia locked-in syndrome obsolete constipation quadriplegia rheumatoid arthritis stomach cancer stomach carcinoma type 2 diabetes mellitus visual epilepsy
83548	component of oligomeric golgi complex 3	COG3 SEC34	autosomal recessive limb-girdle muscular dystrophy type 2A breast cancer cancer congenital disorder of glycosylation type II
25839	component of oligomeric golgi complex 4	COG4 COD1 DKFZP586E1519	Laron syndrome Saul-Wilson syndrome X-linked nonsyndromic deafness achondroplasia agnosia agranulocytosis apraxia autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness blood coagulation disease cataract 5 multiple types cataract cerebral degeneration clubfoot cone-rod dystrophy congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIj congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness developmental coordination disorder dissociated nystagmus enophthalmos fundus albipunctatus microcephaly neutropenia night blindness obsolete autosomal recessive nonsyndromic deafness 105 obsolete exophthalmos obsolete inherited blood coagulation disease orbital disease pathologic nystagmus placental insufficiency retinitis pigmentosa 3 retinitis pigmentosa sensorineural hearing loss severe congenital neutropenia spontaneous ocular nystagmus thrombocytopenia
10466	component of oligomeric golgi complex 5	COG5 GTC90	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 Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy
57511	component of oligomeric golgi complex 6	COG6 COD2 KIAA1134	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
91949	component of oligomeric golgi complex 7	COG7	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease genetic disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss