GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5176 - 5200** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
2645	glucokinase	GCK HK4 hexokinase 4	Chagas disease Fanconi anemia complementation group C Fanconi anemia Laron syndrome Marfan syndrome Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome adult-onset Still's disease agnosia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bronchus cancer bronchus carcinoma cancer cardiovascular system disease chronic fatigue syndrome congenital heart disease congenital ptosis coronary artery disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma encephalitis encephalomyelitis endocrine pancreas disease epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 3 generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease heart disease hepatocellular carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia hypoglycemic coma immune system disease insulinoma intellectual disability kidney disease learning disability leishmaniasis liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young type 3 maturity-onset diabetes of the young myelitis myotonic dystrophy type 1 myotonic dystrophy type 2 neonatal diabetes nephritis nephrosis neuropathy nutmeg liver obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic cancer pancreatic carcinoma peripheral nervous system disease permanent neonatal diabetes mellitus placental insufficiency polyneuropathy prediabetes syndrome progeria prostate cancer prostate carcinoma ptosis pyoureter retinal disease retinitis rheumatoid arthritis sensorineural hearing loss situs inversus steatotic liver disease syndromic X-linked intellectual disability 94 systemic lupus erythematosus transient neonatal diabetes mellitus trypanosomiasis tuberous sclerosis 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 urea cycle disorder visceral leishmaniasis visual epilepsy
26205	glucocorticoid modulatory element binding protein 2	GMEB2
10691	glucocorticoid modulatory element binding protein 1	GMEB1
113263	glucocorticoid induced 1	GLCCI1
2642	glucagon receptor	GCGR
9340	glucagon like peptide 2 receptor	GLP2R
2740	glucagon like peptide 1 receptor	GLP1R
2641	glucagon	GCG	Alzheimer's disease prediabetes syndrome
11146	glomulin, FKBP associated protein	GLMN
26301	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)	GBGT1 A3GALNT FS Forssman blood group Forssman glycolipid synthetase (FS) Forssman synthetase MGC44848 UDP-GalNAc	cancer celiac disease embryoma ovarian cancer ovarian carcinoma thrombophilia
342035	gliomedin	GLDN
2670	glial fibrillary acidic protein	GFAP
8521	glial cells missing transcription factor 1	GCM1
2668	glial cell derived neurotrophic factor	GDNF
8139	gigaxonin	GAN
51738	ghrelin and obestatin prepropeptide	GHRL	Prader-Willi syndrome cardiovascular system disease diabetic neuropathy end stage renal disease esophagus adenocarcinoma middle cerebral artery infarction morbid obesity multiple endocrine neoplasia obesity obstructive sleep apnea type 2 diabetes mellitus
93953	germ cell nuclear acidic peptidase	GCNA
10243	gephyrin	GPHN
2969	general transcription factor IIi	GTF2I
2976	general transcription factor IIIC subunit 2	GTF3C2
2975	general transcription factor IIIC subunit 1	GTF3C1
2965	general transcription factor IIH subunit 1	GTF2H1
2963	general transcription factor IIF subunit 2	GTF2F2
2962	general transcription factor IIF subunit 1	GTF2F1
2961	general transcription factor IIE subunit 2	GTF2E2

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