GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3326 - 3350** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
56899	ankyrin repeat and sterile alpha motif domain containing 1B	ANKS1B
56898	3-hydroxybutyrate dehydrogenase 2	BDH2 FLJ13261 PRO20933 SDR15C1 UCPA-OR UNQ6308 short chain dehydrogenase/reductase family 15C, member 1	anaplastic astrocytoma breast cancer cancer childhood cerebral astrocytoma esophageal cancer esophageal carcinoma fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma juvenile pilocytic astrocytoma liver cancer lupus erythematosus malignant astrocytoma microcytic anemia nasopharynx carcinoma ovarian cancer ovarian carcinoma pilocytic astrocytoma protoplasmic astrocytoma subependymal giant cell astrocytoma systemic lupus erythematosus
56897	WRN helicase interacting protein 1	WRNIP1 CFAP93 FAP93 FLJ22526 WHIP bA420G6.2
56895	1-acylglycerol-3-phosphate O-acyltransferase 4	AGPAT4 1-acyl-sn-glycerol-3-phosphate acyltransferase delta LPAAT-delta LPAAT4 LPLAT4 dJ473J16.2 lysophosphatidic acid acyltransferase, delta lysophospholipid acyltransferase 4	bladder carcinoma urinary bladder cancer
56894	1-acylglycerol-3-phosphate O-acyltransferase 3	AGPAT3 1-acyl-sn-glycerol-3-phosphate acyltransferase gamma LPAAT-gamma LPAAT3 LPLAT3 lysophosphatidic acid acyltransferase gamma lysophospholipid acyltransferase 3	chronic obstructive pulmonary disease neurodegenerative disease
56893	ubiquilin 4	UBQLN4
56889	transmembrane 9 superfamily member 3	TM9SF3
56888	potassium channel modulatory factor 1	KCMF1
56886	UDP-glucose glycoprotein glucosyltransferase 1	UGGT1 HUGT1	Crigler-Najjar syndrome Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha 1-antitrypsin deficiency beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis embryoma epilepsy gallbladder disease hepatitis C hepatitis D leukopenia liver disease neonatal jaundice neutropenia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia visual epilepsy xeroderma pigmentosum group D
56884	follistatin like 5	FSTL5
56852	RAD18 E3 ubiquitin protein ligase	RAD18
56851	ER membrane protein complex subunit 7	EMC7
56850	GRIP1 associated protein 1	GRIPAP1
56848	sphingosine kinase 2	SPHK2	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 Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Kaposi's sarcoma Pick's disease Reye syndrome actinic keratosis acute lymphoblastic leukemia acute pancreatitis adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma alcoholic hepatitis alcoholic liver cirrhosis amnestic disorder anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bile duct adenocarcinoma bile duct carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cartilage disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease chikungunya childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma chondrosarcoma chronic fatigue syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma connective tissue disease coronary artery disease cystic fibrosis dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis essential hypertension fibrillary astrocytoma gallbladder disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma heart disease hematologic cancer hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia immune system disease influenza intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia malignant astrocytoma malignant pleural mesothelioma metabolic dysfunction-associated steatohepatitis middle cerebral artery infarction mixed glioma multiple myeloma multiple sclerosis myelitis neuroblastoma neurodegenerative disease obesity obsolete asthenopia obsolete ymphosarcoma osteoarthritis osteoglophonic dysplasia osteosarcoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis pilocytic astrocytoma pneumonia postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis pulmonary fibrosis pustulosis of palm and sole retinal disease retinitis retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma seborrheic keratosis skin disease skin squamous cell carcinoma steatotic liver disease subependymal giant cell astrocytoma synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia thyroid gland papillary carcinoma type 2 diabetes mellitus ureteral obstruction vascular disease viral infectious disease yellow fever
56834	G protein-coupled receptor 137	GPR137
56833	SLAM family member 8	SLAMF8
56829	zinc finger CCCH-type containing, antiviral 1	ZC3HAV1
56751	BarH like homeobox 1	BARHL1
56704	junctophilin 1	JPH1
56675	nuclear receptor interacting protein 3	NRIP3
56674	TMEM9 domain family member B	TMEM9B
56670	succinate receptor 1	SUCNR1
56667	mucin 13, cell surface associated	MUC13
56666	pannexin 2	PANX2
56660	potassium two pore domain channel subfamily K member 12	KCNK12

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