GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2851 - 2875** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
258	ameloblastin	AMBN
51005	amidohydrolase domain containing 2	AMDHD2 CGI-14 N-acetylglucosamine-6-phosphate deacetylase	colorectal cancer colorectal carcinoma large intestine cancer
26	amine oxidase copper containing 1	AOC1
314	amine oxidase copper containing 2	AOC2
8639	amine oxidase copper containing 3	AOC3
9255	aminoacyl tRNA synthetase complex interacting multifunctional protein 1	AIMP1
275	aminomethyltransferase	AMT GCST NKH glycine cleavage system protein T nonketotic hyperglycinemia	Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome acute pancreatitis autism spectrum disorder autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome chromosome 9p deletion syndrome chylomicron retention disease colorectal cancer colorectal carcinoma corneal ulcer depressive disorder developmental and epileptic encephalopathy 3 disease of metabolism dysthymic disorder early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy familial lipoprotein lipase deficiency female reproductive organ cancer focal hand dystonia glaucoma glycine encephalopathy hemophilia B hyperlipoproteinemia type V inflammatory bowel disease 1 inflammatory bowel disease intellectual disability lactic acidosis large intestine cancer learning disability lymphoma major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II multiple sclerosis neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma pancreatitis ulcerative colitis urea cycle disorder visual epilepsy
9520	aminopeptidase puromycin sensitive	NPEPPS
81693	amnion associated transmembrane protein	AMN
374	amphiregulin	AREG
276	amylase alpha 1A	AMY1A	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition schizophrenia seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
277	amylase alpha 1B	AMY1B	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
278	amylase alpha 1C	AMY1C	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
279	amylase alpha 2A	AMY2A	acute interstitial pneumonia acute pancreatitis autoimmune pancreatitis cancer diabetic ketoacidosis glucose intolerance idiopathic interstitial pneumonia lung benign neoplasm lung carcinoma obsolete type 1 diabetes mellitus 9 pancreatitis prediabetes syndrome stomach cancer stomach carcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
280	amylase alpha 2B	AMY2B	autosomal recessive congenital ichthyosis 1 ichthyosis keratosis follicularis lung benign neoplasm lung carcinoma mongolian spot obsolete congenital ichthyosiform erythroderma pseudoxanthoma elasticum
178	amylo-alpha-1,6-glucosidase and 4-alpha-glucanotransferase	AGL GDE glycogen debranching enzyme glycogen storage disease type III	Duchenne muscular dystrophy Laron syndrome achondroplasia acute promyelocytic leukemia atrichia with papular lesions 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 bladder carcinoma cancer cardiomyopathy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital muscular dystrophy cystinuria disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial partial lipodystrophy familial periodic paralysis galactosemia giardiasis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis C hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung cancer lung non-small cell carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy nodular nonsuppurative panniculitis 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 panniculitis primary immunodeficiency disease rippling muscle disease 2 uremia urinary bladder cancer
325	amyloid P component, serum	APCS
333	amyloid beta precursor like protein 1	APLP1
334	amyloid beta precursor like protein 2	APLP2
351	amyloid beta precursor protein	APP
320	amyloid beta precursor protein binding family A member 1	APBA1
322	amyloid beta precursor protein binding family B member 1	APBB1
64682	anaphase promoting complex subunit 1	ANAPC1
367	androgen receptor	AR
154796	angiomotin	AMOT