GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5676 - 5700** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
10095	actin related protein 2/3 complex subunit 1B	ARPC1B
10092	actin related protein 2/3 complex subunit 5	ARPC5
10090	uronyl 2-sulfotransferase	UST 2OST	Crohn's colitis Crohn's disease ankylosing spondylitis arthritis arthropathy atrial fibrillation attention deficit hyperactivity disorder cancer endometriosis of ovary endometriosis of uterus endometriosis inflammatory bowel disease 1 inflammatory bowel disease osteoarthritis ulcerative colitis
10089	potassium two pore domain channel subfamily K member 7	KCNK7
10086	HHLA1 neighbor of OC90	HHLA1
10085	EGF like repeats and discoidin domains 3	EDIL3
10084	polyglutamine binding protein 1	PQBP1
10082	glypican 6	GPC6 glypican proteoglycan 6	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 Pick's disease Reye syndrome Simpson-Golabi-Behmel syndrome type 1 atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect attention deficit hyperactivity disorder blepharophimosis breast cancer breast carcinoma cancer cardiovascular system disease cavernous hemangioma cerebral degeneration chorioangioma colorectal cancer colorectal carcinoma craniosynostosis cryptorchidism degenerative disc disease dissociative disorder embryoma enterocele familial retinoblastoma glomus tumor heart disease hemangioma histiocytoid hemangioma intellectual disability intramuscular hemangioma large intestine cancer learning disability lymphangioma melanoma neurotic disorder omodysplasia 1 omodysplasia omphalocele osteoporosis ovarian cancer ovarian carcinoma patent foramen ovale pterygium reflex sympathetic dystrophy retinoblastoma schizophrenia skin melanoma trilateral retinoblastoma umbilical hernia ventricular septal defect
10078	tumor suppressing subtransferable candidate 4	TSSC4
10076	protein tyrosine phosphatase receptor type U	PTPRU
10075	HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1	HUWE1
10073	snurportin 1	SNUPN
10072	dipeptidyl peptidase 3	DPP3
10071	mucin 12, cell surface associated	MUC12
10068	interleukin 18 binding protein	IL18BP
10066	secretory carrier membrane protein 2	SCAMP2
10062	nuclear receptor subfamily 1 group H member 3	NR1H3
10061	ATP binding cassette subfamily F member 2	ABCF2
10060	ATP binding cassette subfamily C member 9	ABCC9
10059	dynamin 1 like	DNM1L DRP1 DVLP DYMPLE HDYNIV VPS1
10058	ATP binding cassette subfamily B member 6 (LAN blood group)	ABCB6
10057	ATP binding cassette subfamily C member 5	ABCC5
10053	adaptor related protein complex 1 subunit mu 2	AP1M2
10051	structural maintenance of chromosomes 4	SMC4
10050	solute carrier family 17 member 4	SLC17A4

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