GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **2776 - 2800** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
79073	transmembrane protein 109	TMEM109
79071	ELOVL fatty acid elongase 6	ELOVL6 FLJ23378 LCE MGC5487	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
79070	protein O-glucosyltransferase 2	POGLUT2 EP58 MGC5302	bipolar disorder
79068	FTO alpha-ketoglutarate dependent dioxygenase	FTO
79065	autophagy related 9A	ATG9A
79058	ASPSCR1 tether for SLC2A4, UBX domain containing	ASPSCR1
79054	transient receptor potential cation channel subfamily M member 8	TRPM8
79053	ALG8 alpha-1,3-glucosyltransferase	ALG8 MGC2840 dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 anemia asphyxia neonatorum autosomal dominant polycystic kidney disease cataract cholestasis clubfoot congenital disorder of glycosylation Ih congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism cryptorchidism cystic kidney disease depressive disorder developmental and epileptic encephalopathy 36 diarrhea dysthymic disorder elephantiasis gastrointestinal system disease heart septal defect hypothyroidism intestinal disease lymphedema macrocytic anemia major depressive disorder melancholic depression myxedema neurotic disorder non-congenital cyst of kidney obsolete melancholia oligohydramnios patent ductus arteriosus placental insufficiency polycystic liver disease polyhydramnios protein-losing enteropathy thrombocytopenia
79048	SECIS binding protein 2	SECISBP2
79038	zinc finger FYVE-type containing 21	ZFYVE21
79035	nucleic acid binding protein 2	NABP2
79026	AHNAK nucleoprotein	AHNAK
79022	transmembrane protein 106C	TMEM106C
79020	chromosome 7 open reading frame 25	C7orf25
79019	centromere protein M	CENPM
79018	GID complex subunit 4 homolog	GID4
79012	CaM kinase like vesicle associated	CAMKV
79006	meteorin, glial cell differentiation regulator	METRN
79004	CUE domain containing 2	CUEDC2
78999	leucine rich repeat and fibronectin type III domain containing 4	LRFN4
78996	cell cycle regulator of NHEJ	CYREN
78995	homologous recombination factor with OB-fold	HROB
78994	proline rich 14	PRR14
78991	prenylcysteine oxidase 1 like	PCYOX1L
78990	OTU deubiquitinase, ubiquitin aldehyde binding 2	OTUB2

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