GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5051 - 5075** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
23163	golgi associated, gamma adaptin ear containing, ARF binding protein 3	GGA3
23164	myosin phosphatase Rho interacting protein	MPRIP
23165	nucleoporin 205	NUP205
23166	stabilin 1	STAB1
23167	EFR3 homolog A	EFR3A
23168	RTF1 homolog, Paf1/RNA polymerase II complex component	RTF1
23169	solute carrier family 35 member D1	SLC35D1 KIAA0260 UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter UGTREL7	cleft palate cryptorchidism dermatitis elephantiasis fibrochondrogenesis isolated cleft palate lymphedema mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia polyhydramnios schneckenbecken dysplasia
23171	glycerol-3-phosphate dehydrogenase 1 like	GPD1L KIAA0089	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
23172	abraxas 2, BRISC complex subunit	ABRAXAS2
23174	zinc finger CCHC-type containing 14	ZCCHC14
23175	lipin 1	LPIN1 KIAA0188 phosphatidate phosphatase LPIN1	46,XY sex reversal Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Pearson syndrome Richter's syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute kidney failure adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cervix uteri carcinoma in situ chronic kidney disease chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 diabetes mellitus diabetic ketoacidosis embryoma end stage renal disease essential hypertension familial periodic paralysis fibromyalgia gastroenteritis gestational diabetes glucose intolerance heart disease hepatoblastoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hyperinsulinism hypertension ileitis ileocolitis isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma middle cerebral artery infarction morbid obesity motor peripheral neuropathy myoglobinuria myopathy myositis neuropathy obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polycystic ovary syndrome polyneuropathy prediabetes syndrome prostate cancer prostate carcinoma retinitis pigmentosa 9 sarcomatoid carcinoma steatotic liver disease type 2 diabetes mellitus very long chain acyl-CoA dehydrogenase deficiency
23177	centrosomal protein 68	CEP68
23180	raftlin, lipid raft linker 1	RFTN1
23181	disco interacting protein 2 homolog A	DIP2A
23184	mesoderm development LRP chaperone	MESD
23185	La ribonucleoprotein 4B	LARP4B
23186	REST corepressor 1	RCOR1
23187	pleckstrin homology like domain family B member 1	PHLDB1
23189	KN motif and ankyrin repeat domains 1	KANK1
23190	UBX domain protein 4	UBXN4
23191	cytoplasmic FMR1 interacting protein 1	CYFIP1
23192	autophagy related 4B cysteine peptidase	ATG4B
23193	glucosidase II alpha subunit	GANAB G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
23194	F-box and leucine rich repeat protein 7	FBXL7
23195	midasin AAA ATPase 1	MDN1

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