GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **901 - 925** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
388512	C-type lectin domain containing 17A	CLEC17A FLJ45910 prolectin	Richter's syndrome chronic lymphocytic leukemia
6716	steroid 5 alpha-reductase 2	SRD5A2 3-oxo-5-alpha-steroid 4-dehydrogenase 2	Sertoli cell-only syndrome Turner syndrome Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 adenosarcoma alcohol dependence alcohol use disorder alopecia androgen insensitivity syndrome androgenic alopecia azoospermia breast cancer breast carcinoma cancer childhood acute lymphocytic leukemia cryptorchidism diabetes mellitus diabetic ketoacidosis disorder of sexual development embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis gallbladder disease gonadal dysgenesis hepatitis C hepatocellular carcinoma hermaphroditism hyperprolactinemia hypogonadotropic hypogonadism 23 with or without anosmia hypospadias liver cancer liver carcinoma liver disease nephroblastoma nodular prostate oligospermia ovarian cancer ovarian carcinoma pancreatitis peripheral artery disease phimosis polycystic ovary syndrome post-traumatic stress disorder prostate cancer prostate carcinoma prostate disease prostatic adenoma pseudohermaphroditism schizophrenia type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer
83639	testis expressed 101	TEX101 CT131 MGC4766 SGRG SPATA44 TES101-reactive protein TES101RP cancer/testis antigen 131 spermatogenesis associated 44	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma azoospermia basal cell carcinoma breast cancer breast ductal carcinoma cancer cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma liver cancer oligospermia tubular adenocarcinoma
5634	phosphoribosyl pyrophosphate synthetase 2	PRPS2 PRS II ribose-phosphate diphosphokinase 2	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 cancer embryoma oligospermia systemic lupus erythematosus
27159	chitinase acidic	CHIA AMCase CHIT2 TSA1902 acidic mammalian chitinase	Sjogren's syndrome allergic asthma allergic conjunctivitis allergic rhinitis asthma cryptococcosis dry eye syndrome eosinophilic esophagitis giant papillary conjunctivitis intrinsic asthma keratoconjunctivitis sicca silicosis sinusitis vasomotor rhinitis vernal conjunctivitis xerophthalmia
222	aldehyde dehydrogenase 3 family member B2	ALDH3B2	Sjogren-Larsson syndrome alcohol dependence alcohol use disorder
218	aldehyde dehydrogenase 3 family member A1	ALDH3A1 aldehyde dehydrogenase, dimeric NADP-preferring	Sjogren-Larsson syndrome allergic asthma arteriosclerosis asthma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cataract colon cancer colon carcinoma colonic benign neoplasm colorectal cancer depressive disorder dysthymic disorder embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma intrinsic asthma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression melanoma mucoepidermoid carcinoma neurotic disorder obsolete congenital ichthyosiform erythroderma obsolete melancholia placental insufficiency pleomorphic adenoma prostate cancer prostate carcinoma pterygium sarcomatoid carcinoma schizophrenia skin melanoma stomach cancer
2181	acyl-CoA synthetase long chain family member 3	ACSL3 ACS3 PRO2194	Sjogren-Larsson syndrome allergic asthma asthma breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer craniosynostosis embryoma familial hyperlipidemia gliosarcoma hepatitis C hepatocellular carcinoma high grade glioma intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma melanoma mixed glioma non-syndromic X-linked intellectual disability 63 non-syndromic X-linked intellectual disability ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma sarcoma skin melanoma syndactyly
221	aldehyde dehydrogenase 3 family member B1	ALDH3B1 aldehyde dehydrogenase 3B1 aldehyde dehydrogenase 7	Sjogren-Larsson syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma delusional disorder papillary renal cell carcinoma paranoid schizophrenia renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
2222	farnesyl-diphosphate farnesyltransferase 1	FDFT1 SQS squalene synthase	Smith-Lemli-Opitz syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acrodermatitis adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cardiovascular system disease cataract chondrodysplasia punctata cocaine abuse cocaine dependence cribriform carcinoma dermatitis embryoma epilepsy familial hyperlipidemia familial mediterranean fever giant cell glioblastoma glioblastoma granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma intellectual disability learning disability liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma melanoma mevalonic aciduria morbid obesity morphine dependence obesity phencyclidine abuse prostate cancer prostate carcinoma skin disease skin melanoma steatotic liver disease tubular adenocarcinoma visual cortex disease visual epilepsy
144423	glycosyltransferase 1 domain containing 1	GLT1D1 FLJ31978	St. Louis encephalitis allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis coronary artery disease intrinsic asthma
259230	sphingomyelin synthase 1	SGMS1 MGC17342 MOB SMS1 phosphatidylcholine:ceramide cholinephosphotransferase 1	St. Louis encephalitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bronchus cancer bronchus carcinoma cancer central nervous system cancer cholangiocarcinoma colorectal cancer colorectal carcinoma diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma hepatitis A hepatitis high grade glioma intrahepatic cholangiocarcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus melanoma mixed glioma pancreatic cancer pancreatic carcinoma pulmonary edema skin melanoma systemic lupus erythematosus type 2 diabetes mellitus
7378	uridine phosphorylase 1	UPP1 UDRPASE UPASE UPP	Stevens-Johnson syndrome allergic contact dermatitis breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy embryoma esophagus squamous cell carcinoma giardiasis large intestine cancer lung adenoma middle cerebral artery infarction placental insufficiency stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tuberculosis type 2 diabetes mellitus
7007	tectorin alpha	TECTA	Stickler syndrome X-linked nonsyndromic deafness 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 breast cancer herpes zoster obsolete autosomal recessive nonsyndromic deafness 105 sensorineural hearing loss trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
50999	transmembrane p24 trafficking protein 5	TMED5 CGI-100 p24g2 p24gamma2	T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adult T-cell leukemia/lymphoma breast cancer cancer central nervous system cancer chronic fatigue syndrome coronary thrombosis embryoma encephalitis encephalomyelitis exudative vitreoretinopathy 1 exudative vitreoretinopathy gliosarcoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma liver cancer melanoma mixed glioma multiple sclerosis myelitis myocardial infarction retinopathy of prematurity schizophrenia silent myocardial infarction skin melanoma
8870	immediate early response 3	IER3	T-cell non-Hodgkin lymphoma
10825	neuraminidase 3	NEU3	Tay-Sachs disease alternating hemiplegia of childhood amnestic disorder autonomic neuropathy cancer carcinoma central nervous system disease chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dissociative amnesia embryoma giant cell glioblastoma glioblastoma high grade glioma idiopathic interstitial pneumonia large intestine cancer lung cancer lung non-small cell carcinoma nervous system disease ovarian cancer ovarian carcinoma ovarian clear cell adenocarcinoma ovary adenocarcinoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pulmonary fibrosis renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma
6487	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	ST3GAL3 N-acetyllactosaminide alpha-2,3-sialyltransferase ST3Gal III	Unverricht-Lundborg syndrome West syndrome agnosia amyotrophic lateral sclerosis attention deficit hyperactivity disorder autosomal recessive intellectual developmental disorder 12 autosomal recessive intellectual developmental disorder bipolar disorder blepharospasm brain cancer breast cancer breast carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma choreatic disease congenital disorder of glycosylation depressive disorder developmental and epileptic encephalopathy 15 developmental coordination disorder diabetes mellitus dysthymic disorder dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy focal epilepsy focal hand dystonia hepatocellular carcinoma influenza intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia pancreatic adenocarcinoma partial motor epilepsy progressive muscular atrophy prostate cancer prostate carcinoma pterygium schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
3155	3-hydroxy-3-methylglutaryl-CoA lyase	HMGCL HL hydroxymethylglutaricaciduria hydroxymethylglutaryl-CoA lyase	Unverricht-Lundborg syndrome X-linked dilated cardiomyopathy acute pancreatitis amino acid metabolic disorder anemia blepharospasm brain disease cancer cardiac arrest congestive heart failure diarrhea dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy early myoclonic encephalopathy epilepsy focal hand dystonia hyperlysinemia hyperuricemia hypoglycemia hypoglycemic coma intellectual disability lactic acidosis learning disability leukopenia macrocytic anemia melanoma microcephaly mitochondrial metabolism disease mitochondrial myopathy obsolete infantile epileptic encephalopathy pancreatitis skin melanoma syndromic X-linked intellectual disability 94 thrombocytosis urea cycle disorder visual epilepsy
22901	arylsulfatase G	ARSG KIAA1001	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome type 3A Usher syndrome anxiety disorder astigmatism blepharospasm blindness cancer cataract cerebellar ataxia cerebellar disease congenital stationary night blindness 1A congenital stationary night blindness depressive disorder dysthymic disorder dystonia embryoma focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder night blindness obsolete melancholia peripheral retinal degeneration prostate cancer prostate carcinoma retinitis pigmentosa-deafness syndrome schizophrenia scotoma sensorineural hearing loss
122618	phospholipase D family member 4	PLD4	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatitis large intestine cancer retinitis pigmentosa-deafness syndrome rheumatoid arthritis scleroderma systemic lupus erythematosus systemic scleroderma
84317	coiled-coil domain containing 115	CCDC115 FLJ30131 MGC12981 ccp1	Wilson disease cancer congenital disorder of glycosylation type IIo congenital disorder of glycosylation gallbladder disease hemochromatosis iron metabolism disease liver disease male infertility measles neuroblastoma neurodegenerative disease prostate adenocarcinoma prostate cancer prostate carcinoma
51422	protein kinase AMP-activated non-catalytic subunit gamma 2	PRKAG2	Wolff-Parkinson-White syndrome glycogen storage disease hypertrophic cardiomyopathy 6 lethal congenital glycogen storage disease of heart neurodegenerative disease
53632	protein kinase AMP-activated non-catalytic subunit gamma 3	PRKAG3	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
8435	sterol O-acyltransferase 2	SOAT2 ACAT2 acyl-Coenzyme A: cholesterol acyltransferase 2	Wolman disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer celiac disease coronary artery disease end stage renal disease familial hyperlipidemia hepatocellular carcinoma lipid storage disease liver cancer lysosomal acid lipase deficiency nephrotic syndrome nutmeg liver steatotic liver disease

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