GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8051 - 8075** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
93010	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	B3GNT7 beta3GnT7	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer
93035	PKHD1 like 1	PKHD1L1
93081	testis expressed 30	TEX30
93099	dermokine	DMKN
93109	transmembrane protein 44	TMEM44
93129	ORAI calcium release-activated calcium modulator 3	ORAI3
93134	zinc finger protein 561	ZNF561
93145	olfactomedin 2	OLFM2
93183	phosphatidylinositol glycan anchor biosynthesis class M	PIGM DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	Budd-Chiari syndrome epilepsy focal epilepsy paroxysmal nocturnal hemoglobinuria partial motor epilepsy portal hypertension portal vein thrombosis thrombophilia visual epilepsy
93185	immunoglobulin superfamily member 8	IGSF8
93210	post-GPI attachment to proteins phospholipase 3	PGAP3 CAB2 MGC9753 PER1 PP1498 post-GPI attachment to proteins 3	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 4 inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
93377	oligodendrocytic myelin paranodal and inner loop protein	OPALIN
93380	membrane magnesium transporter 1	MMGT1
93432	maltase-glucoamylase 2 (putative)	MGAM2
93487	mitogen-activated protein kinase 1 interacting protein 1 like	MAPK1IP1L
93589	calcium voltage-gated channel auxiliary subunit alpha2delta 4	CACNA2D4 alpha2delta-4	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness retinal cone dystrophy 4 spontaneous ocular nystagmus strabismus
93611	F-box protein 44	FBXO44 FBG3 FBX30 Fbx44 Fbxo6a MGC14140	polycystic ovary syndrome prostate cancer prostate carcinoma
93650	acid phosphatase 4	ACP4 testicular acid phosphatase
93659	chorionic gonadotropin subunit beta 5	CGB5
93661	capping actin protein of muscle Z-line subunit alpha 3	CAPZA3
93953	germ cell nuclear acidic peptidase	GCNA
93978	C-type lectin domain containing 6A	CLEC6A dectin-2 hDECTIN-2	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis
93986	forkhead box P2	FOXP2
94005	phosphatidylinositol glycan anchor biosynthesis class S	PIGS GPI transamidase component PIG-S GPI transamidase subunit PIG-S	breast cancer cancer congenital nystagmus developmental and epileptic encephalopathy 95 dissociated nystagmus embryoma epilepsy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gingival hypertrophy gingival overgrowth hepatocellular carcinoma liver cancer microcephaly omphalocele pathologic nystagmus spontaneous ocular nystagmus umbilical hernia visual epilepsy
94015	tweety family member 2	TTYH2

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