GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **1551 - 1575** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
401494	3-hydroxyacyl-CoA dehydratase 4	HACD4 Em:AL662879.1 OTTHUMG00000021016 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer
402635	galectin-related inter-fiber protein	GRIFIN
414328	IDNK gluconokinase	IDNK bA522I20.2 hGntK
440138	ALG11 alpha-1,2-mannosyltransferase	ALG11 CDG1P GDP-Man:Man(3)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase KIAA0266	cerebral degeneration congenital disorder of glycosylation Ip congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia inherited metabolic disorder intellectual disability learning disability mechanical strabismus microcephaly ophthalmoplegia scoliosis sensorineural hearing loss strabismus visual epilepsy
441531	phosphoglycerate mutase family member 4	PGAM4 PGAM-B PGAM1 PGAM3 dJ1000K24.1	male infertility
442117	polypeptide N-acetylgalactosaminyltransferase like 6	GALNTL6 GALNT17 GalNAc-T6L polypeptide GalNAc transferase-like 6	nicotine dependence
493869	glutathione peroxidase 8 (putative)	GPX8 EPLA847 UNQ847
497190	C-type lectin domain family 18 member B	CLEC18B	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma
574537	UDP glucuronosyltransferase family 2 member A2	UGT2A2	ovarian cancer ovarian carcinoma
606495	cytochrome b5 reductase like	CYB5RL LOC606495
641371	acyl-CoA thioesterase 1	ACOT1 ACH2 CTE-1 LACH2	gastric adenocarcinoma hepatocellular carcinoma liver cancer
643664	solute carrier family 35 member G6	SLC35G6
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
646000	solute carrier family 35 member G4	SLC35G4
648791	protein phosphatase 1 regulatory subunit 3G	PPP1R3G	obesity steatotic liver disease
653308	N-acylsphingosine amidohydrolase 2B	ASAH2B ASAH2L bA449O16.3 bA98I6.3	breast cancer breast carcinoma
653509	surfactant protein A1	SFTPA1 COLEC4 SP-A SP-A1 surfactant, pulmonary-associated protein A1A	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 Hermansky-Pudlak syndrome Pick's disease Reye syndrome T cell deficiency X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amnestic disorder amyloidosis anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolitis obliterans bronchiolitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types cerebral degeneration cerebral infarction cerebrovascular disease chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cryptogenic organizing pneumonia cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential thrombocythemia extrinsic allergic alveolitis familial periodic paralysis gastroesophageal reflux disease granular cell carcinoma heart disease hematologic cancer hydrocephalus hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease interstitial lung disease interstitial nephritis intrinsic asthma keratoconus liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis macrocytic anemia mastitis myelodysplastic syndrome myopathy neurodegenerative disease newborn respiratory distress syndrome obesity obsolete T lymphocyte deficiency obstructive hydrocephalus obstructive lung disease osteomalacia otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis pulmonary alveolar proteinosis pulmonary edema pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory syncytial virus infectious disease retrograde amnesia rickets secondary hypertrophic osteoarthropathy senile degeneration of brain shigellosis sinusitis squamous cell carcinoma staphyloenterotoxemia systolic heart failure tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis viral infectious disease
654346	galectin 9C	LGALS9C	cancer
727936	glucoside xylosyltransferase 2	GXYLT2
728661	solute carrier family 35 member E2B	SLC35E2B
728819	C1GALT1 specific chaperone 1 like	C1GALT1C1L
729020	ribulose-5-phosphate-3-epimerase like 1	RPEL1
729201	sperm acrosome associated 5B	SPACA5B LYZL5B
729238	surfactant protein A2	SFTPA2 COLEC5 SP-A2 surfactant, pulmonary-associated protein A2A	Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cystic fibrosis embryoma esophagitis gastroesophageal reflux disease granular cell carcinoma heart disease hydrocephalus hypereosinophilic syndrome hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease interstitial nephritis intrinsic asthma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis newborn respiratory distress syndrome obesity obstructive hydrocephalus obstructive lung disease otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory failure respiratory syncytial virus infectious disease rheumatoid arthritis secondary hypertrophic osteoarthropathy senile degeneration of brain spondyloarthropathy spondylosis squamous cell carcinoma tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis
729920	CDP-L-ribitol pyrophosphorylase A	CRPPA 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis) D-ribitol-5-phosphate cytidylyltransferase IspD Nip hCG_1745121 notch1-induced protein	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia anemia 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 bilateral optic nerve hypoplasia cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly macrocytic anemia microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis nonpapillary renal cell carcinoma 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 papillary renal cell carcinoma persistent hyperplastic primary vitreous pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rippling muscle disease 2 sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy

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