GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4301 - 4325** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
10072	dipeptidyl peptidase 3	DPP3
10073	snurportin 1	SNUPN
10075	HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1	HUWE1
10076	protein tyrosine phosphatase receptor type U	PTPRU
10078	tumor suppressing subtransferable candidate 4	TSSC4
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
10084	polyglutamine binding protein 1	PQBP1
10085	EGF like repeats and discoidin domains 3	EDIL3
10086	HHLA1 neighbor of OC90	HHLA1
10089	potassium two pore domain channel subfamily K member 7	KCNK7
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
10092	actin related protein 2/3 complex subunit 5	ARPC5
10095	actin related protein 2/3 complex subunit 1B	ARPC1B
10097	actin related protein 2	ACTR2
10098	tetraspanin 5	TSPAN5
10099	tetraspanin 3	TSPAN3
10100	tetraspanin 2	TSPAN2
10101	NUBP iron-sulfur cluster assembly factor 2, cytosolic	NUBP2
10103	tetraspanin 1	TSPAN1
10105	peptidylprolyl isomerase F	PPIF
10111	RAD50 double strand break repair protein	RAD50 RAD50-2 hRad50
10114	homeodomain interacting protein kinase 3	HIPK3
10117	enamelin	ENAM
10120	actin related protein 1B	ACTR1B
10121	actin related protein 1A	ACTR1A

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