GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **9826 - 9850** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
56052	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 CDG1K HMAT1 HMT-1 Mat-1	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
27125	ALF transcription elongation factor 4	AFF4
3899	ALF transcription elongation factor 3	AFF3
2334	ALF transcription elongation factor 2	AFF2
84335	AKT1 substrate 1	AKT1S1
10000	AKT serine/threonine kinase 3	AKT3
208	AKT serine/threonine kinase 2	AKT2	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
207	AKT serine/threonine kinase 1	AKT1	Cowden syndrome 6 Parkinson's disease Proteus syndrome alcohol use disorder autosomal recessive polycystic kidney disease bipolar disorder brain ischemia breast cancer cancer chronic myeloid leukemia colon cancer colorectal cancer diabetic retinopathy esophageal cancer esophagus squamous cell carcinoma hepatocellular carcinoma hypertension idiopathic pulmonary fibrosis impotence in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paraplegia prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia type 2 diabetes mellitus ureteral obstruction urinary bladder cancer vulva cancer
254268	AKNA domain containing 1	AKNAD1
84883	AIF family member 2	AIFM2
113146	AHNAK nucleoprotein 2	AHNAK2
79026	AHNAK nucleoprotein	AHNAK
60509	AGBL carboxypeptidase 5	AGBL5
340351	AGBL carboxypeptidase 3	AGBL3
123624	AGBL carboxypeptidase 1	AGBL1
165	AE binding protein 1	AEBP1
11047	ADRM1 26S proteasome ubiquitin receptor	ADRM1
116969	ADP-ribosyltransferase 5	ART5 ARTC5	cholera
420	ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)	ART4 ARTC4 CD297 DOK1 NAD(+)--protein-arginine ADP-ribosyltransferase 4	carotid artery thrombosis carotid stenosis conjunctivitis
419	ADP-ribosyltransferase 3 (inactive)	ART3 ARTC3	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
417	ADP-ribosyltransferase 1	ART1 ART2 ARTC1 CD296	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
54936	ADP-ribosylserine hydrolase	ADPRS ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
113622	ADP-ribosylhydrolase like 1	ADPRHL1
141	ADP-ribosylarginine hydrolase	ADPRH ARH1 [Protein ADP-ribosylarginine] hydrolase	autosomal recessive hypercholesterolemia cancer cardiomyopathy cholera endomyocardial fibrosis familial hypercholesterolemia hypertrophic cardiomyopathy ovarian cancer ovarian carcinoma

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