GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4476 - 4500** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
10446	leucine rich repeat neuronal 2	LRRN2
10449	acetyl-CoA acyltransferase 2	ACAA2 DSAEC mitochondrial 3-oxoacyl-Coenzyme A thiolase	adult respiratory distress syndrome arthritis arthropathy beta-ketothiolase deficiency hepatocellular carcinoma liver cancer newborn respiratory distress syndrome osteoarthritis
10450	peptidylprolyl isomerase E	PPIE
10451	vav guanine nucleotide exchange factor 3	VAV3
10452	translocase of outer mitochondrial membrane 40	TOMM40
10454	TGF-beta activated kinase 1 (MAP3K7) binding protein 1	TAB1
10455	enoyl-CoA delta isomerase 2	ECI2 ACBD2 DRS1 HCA88 Hepatocellular carcinoma-associated antigen 88 acyl-Coenzyme A binding domain containing 2	aplastic anemia paroxysmal nocturnal hemoglobinuria prostate cancer prostate carcinoma pure red-cell aplasia
10456	HCLS1 associated protein X-1	HAX1
10457	glycoprotein nmb	GPNMB HGFIN NMB glycoprotein NMB glycoprotein nmb-like protein glycoprotein nonmetastatic melanoma protein B hematopoietic growth factor inducible neurokinin-1 osteoactivin transmembrane glycoprotein	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 Gaucher's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sveinsson chorioretinal atrophy acute kidney failure acute myocardial infarction adenocarcinoma adenoma adult liposarcoma amyloidosis amyotrophic lateral sclerosis anxiety disorder arthritis arthropathy bladder carcinoma bone disease bone osteosarcoma brain cancer brain infarction brain ischemia breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood liposarcoma childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma connective tissue disease coronary thrombosis cystic fibrosis distal arthrogryposis embryoma endometriosis of uterus endometriosis follicular adenoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liposarcoma liver cancer liver cirrhosis lymphangioleiomyomatosis lysosomal storage disease melanoma microcystic adenoma microphthalmia mixed glioma monoclonal gammopathy of uncertain significance myocardial infarction neurodegenerative disease nonpapillary renal cell carcinoma open-angle glaucoma osteoarthritis osteoporosis osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma periodontal disease phobic disorder pigment dispersion syndrome pleomorphic liposarcoma primary localized cutaneous amyloidosis 3 progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma ureteral obstruction urinary bladder cancer
10458	BAR/IMD domain containing adaptor protein 2	BAIAP2
10460	transforming acidic coiled-coil containing protein 3	TACC3
10461	MER proto-oncogene, tyrosine kinase	MERTK
10462	C-type lectin domain containing 10A	CLEC10A CD301 HML HML2 macrophage lectin 2 (calcium dependent)	B-cell lymphoma Crohn's colitis Crohn's disease Ebola hemorrhagic fever acquired immunodeficiency syndrome acrodermatitis adenosquamous carcinoma adult lymphoma allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease asthma atopic dermatitis autosomal recessive distal hereditary motor neuronopathy 1 bipolar disorder breast cancer breast carcinoma cancer celiac disease central nervous system lymphoma centronuclear myopathy cervical adenocarcinoma cervical cancer cervix carcinoma childhood lymphoma cholesteatoma cholinergic urticaria congenital structural myopathy coronary artery disease dermatitis embryoma embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypereosinophilic syndrome inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma lateral sclerosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma melanoma motor neuron disease neurodegenerative disease obsolete malignant histiocytosis obsolete ymphosarcoma ovarian cancer ovarian carcinoma peripheral T-cell lymphoma polyp of middle ear progressive muscular atrophy prostate cancer prostate carcinoma rheumatoid arthritis schizophrenia skin melanoma squamous cell carcinoma teratocarcinoma tongue squamous cell carcinoma transient myeloproliferative syndrome tubular aggregate myopathy 1 ulcerative colitis viral infectious disease
10466	component of oligomeric golgi complex 5	COG5 GTC90	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 Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy
10468	follistatin	FST
10469	translocase of inner mitochondrial membrane 44	TIMM44
10475	tripartite motif containing 38	TRIM38
10479	solute carrier family 9 member A6	SLC9A6
10480	eukaryotic translation initiation factor 3 subunit M	EIF3M
10482	nuclear RNA export factor 1	NXF1
10483	SEC23 homolog B, COPII coat complex component	SEC23B CDA-II CDAII HEMPAS	congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia type III congenital dyserythropoietic anemia type Ib congenital dyserythropoietic anemia
10484	SEC23 homolog A, COPII coat complex component	SEC23A
10486	cyclase associated actin cytoskeleton regulatory protein 2	CAP2
10487	cyclase associated actin cytoskeleton regulatory protein 1	CAP1
10488	cAMP responsive element binding protein 3	CREB3

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