GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6151 - 6175** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
54659	UDP glucuronosyltransferase family 1 member A3	UGT1A3 UGT1C	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis allergic asthma asthma beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis cryptococcosis diabetes mellitus differentiated thyroid gland carcinoma embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis gallbladder disease glycogen storage disease II hepatitis D influenza intrinsic asthma islet cell tumor leukopenia liver disease lung adenocarcinoma lung cancer neonatal jaundice neutropenia obesity pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
54664	transmembrane protein 106B	TMEM106B
54665	round spermatid basic protein 1	RSBN1
54674	leucine rich repeat neuronal 3	LRRN3
54675	cardiolipin synthase 1	CRLS1 CLS1 GCD10 GCD10 homolog (S. cerevisiae) dJ967N21.6	Coffin-Lowry syndrome adenosarcoma bilateral breast cancer breast cancer breast ductal carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer colitis combined oxidative phosphorylation deficiency 57 depressive disorder dysthymic disorder gastroenteritis hepatitis C hepatocellular carcinoma ileitis ileocolitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder mastitis melancholic depression microglandular adenosis nephroblastoma neurotic disorder obsolete melancholia paroxysmal nocturnal hemoglobinuria schizophrenia vascular dementia
54680	zinc finger HIT-type containing 6	ZNHIT6
54681	prolyl 4-hydroxylase, transmembrane	P4HTM
54682	MANSC domain containing 1	MANSC1
54704	pyruvate dehydrogenase phosphatase catalytic subunit 1	PDP1
54708	membrane associated ring-CH-type finger 5	MARCHF5
54716	solute carrier family 6 member 20	SLC6A20
54726	OTU deubiquitinase 4	OTUD4
54732	transmembrane p24 trafficking protein 9	TMED9 HSGP25L2G p24a2 p24alpha2	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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Unverricht-Lundborg syndrome adult T-cell leukemia/lymphoma alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 cancer central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy epilepsy frontotemporal dementia generalized anxiety disorder large intestine cancer lateral sclerosis malaria motor neuron disease nervous system disease neurodegenerative disease nonpapillary renal cell carcinoma obsolete T-cell lymphoblastic leukemia/lymphoma optic atrophy 1 optic atrophy papillary renal cell carcinoma phototoxic dermatitis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma status epilepticus tuberculosis visual epilepsy
54742	lymphocyte antigen 6 family member K	LY6K CT97 FLJ35226 HSJ001348 cancer/testis antigen 97	adult lymphoma bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system lymphoma childhood lymphoma diffuse large B-cell lymphoma duodenal ulcer embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma head and neck squamous cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma obsolete ymphosarcoma sarcomatoid carcinoma seminoma squamous cell carcinoma testicular cancer testis seminoma tongue squamous cell carcinoma urinary bladder cancer
54749	ependymin related 1	EPDR1
54756	interleukin 17 receptor D	IL17RD
54757	FAM20A golgi associated secretory pathway pseudokinase	FAM20A
54758	kelch domain containing 4	KLHDC4
54760	proprotein convertase subtilisin/kexin type 4	PCSK4
54768	HYDIN axonemal central pair apparatus protein	HYDIN
54776	protein phosphatase 1 regulatory subunit 12C	PPP1R12C
54777	cilia and flagella associated protein 46	CFAP46
54780	NSE4 homolog A, SMC5-SMC6 complex component	NSMCE4A
54790	tet methylcytosine dioxygenase 2	TET2
54795	transient receptor potential cation channel subfamily M member 4	TRPM4

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