GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6376 - 6400** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
55343	solute carrier family 35 member C1	SLC35C1 FLJ11320 FUCT1 GDP-fucose transporter 1	Laron syndrome achondroplasia anxiety disorder cellulitis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc echolalia generalized anxiety disorder hepatocellular carcinoma leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer microcephaly
55345	zinc finger GRF-type containing 1	ZGRF1
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial
55355	Holliday junction recognition protein	HJURP
55356	solute carrier family 22 member 15	SLC22A15
55357	TBC1 domain family member 2	TBC1D2
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A DKFZP761G1923 PI4KII PIK42A	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
55362	transmembrane protein 63B	TMEM63B
55365	transmembrane protein 176A	TMEM176A
55366	leucine rich repeat containing G protein-coupled receptor 4	LGR4
55367	p53-induced death domain protein 1	PIDD1 DKFZp434D229 MGC16925
55388	minichromosome maintenance 10 replication initiation factor	MCM10
55423	signal regulatory protein gamma	SIRPG
55425	GPALPP motifs containing 1	GPALPP1
55437	STE20 related adaptor beta	STRADB
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
55471	NADH:ubiquinone oxidoreductase complex assembly factor 7	NDUFAF7
55500	ethanolamine kinase 1	ETNK1 EKI EKI1	aggressive systemic mastocytosis atypical chronic myeloid leukemia, BCR-ABL1 negative cancer chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia disseminated eosinophilic collagen disease epilepsy heart conduction disease hypereosinophilic syndrome indolent systemic mastocytosis juvenile myelomonocytic leukemia mastocytosis microcephaly myeloid leukemia obsolete subacute myeloid leukemia seminoma systemic mastocytosis testicular cancer testicular germ cell cancer testis seminoma
55501	carbohydrate sulfotransferase 12	CHST12 C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	hypertension lupus erythematosus systemic lupus erythematosus
55503	transient receptor potential cation channel subfamily V member 6	TRPV6
55504	TNF receptor superfamily member 19	TNFRSF19
55506	macroH2A.2 histone	MACROH2A2
55508	solute carrier family 35 member E3	SLC35E3 BLOV1	cardiovascular system disease heart disease
55511	sarcoma antigen 1	SAGE1
55512	sphingomyelin phosphodiesterase 3	SMPD3 NSMASE2 neutral sphingomyelinase II	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 Ehlers-Danlos syndrome Guillain-Barre syndrome Kallmann syndrome Laron syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sheehan syndrome Zika fever achondroplasia acute myeloid leukemia acute pericementitis aggressive periodontitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma cancer central nervous system disease cerebral degeneration chronic kidney disease chronic obstructive pulmonary disease coronary artery disease embryoma essential thrombocythemia hepatocellular carcinoma hyperphosphatemia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency leprosy leukemia liver cancer lymphoid leukemia microcephaly myelodysplastic syndrome myeloid leukemia nervous system disease osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta panhypopituitarism periodontosis primary pulmonary hypertension pulmonary emphysema pulmonary hypertension schizophrenia thymus gland disease transient cerebral ischemia vertebrobasilar insufficiency

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