GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6976 - 7000** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
60482	solute carrier family 5 member 7	SLC5A7
60488	mitochondrial ribosomal protein S35	MRPS35
60493	FAST kinase domains 5	FASTKD5
60494	coiled-coil domain containing 81	CCDC81
60495	heparanase 2 (inactive)	HPSE2 HPA2 HPR2	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 Bloom syndrome Down syndrome Evans' syndrome Glanzmann's thrombasthenia Japanese encephalitis Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune thrombocytopenic purpura bladder carcinoma breast cancer cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chronic lymphocytic leukemia coronary artery disease coronary thrombosis cribriform carcinoma cryptorchidism dengue disease diabetic ketoacidosis dyskeratosis congenita essential hypertension essential thrombocythemia factor VIII deficiency gestational diabetes gestational trophoblastic neoplasm glaucoma granular cell carcinoma gray platelet syndrome head and neck squamous cell carcinoma hepatitis B hepatitis C hydronephrosis hypertension kidney failure kwashiorkor leiomyoma marasmus migraine multiple myeloma myelodysplastic syndrome myocardial infarction myofibroma nutmeg liver nutrition disease obsolete constipation obsolete type 1 diabetes mellitus 9 ocular hypertension platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma protein-energy malnutrition proteinuria qualitative platelet defect silent myocardial infarction squamous cell carcinoma tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus urethral obstruction urinary bladder cancer urinary tract obstruction urofacial syndrome uterine fibroid vesicoureteral reflux viral infectious disease yellow fever
60506	nyctalopin	NYX CLRP CSNB1A	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
60509	AGBL carboxypeptidase 5	AGBL5
60528	elaC ribonuclease Z 2	ELAC2
60529	ALX homeobox 4	ALX4
60559	signal peptidase complex subunit 3	SPCS3
60560	N-alpha-acetyltransferase 35, NatC auxiliary subunit	NAA35
60561	RAD50 interactor 1	RINT1
60625	DEAH-box helicase 35	DHX35
60676	pappalysin 2	PAPPA2
60681	FKBP prolyl isomerase 10	FKBP10
60682	small ArfGAP 1	SMAP1
63027	solute carrier family 22 member 23	SLC22A23
63035	BCL6 corepressor like 1	BCORL1
63827	brevican	BCAN BEHAB CSPG7 MGC13038 brevican proteoglycan chondroitin sulfate proteoglycan 7	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 bladder carcinoma central nervous system cancer cerebral degeneration giant cell glioblastoma glioblastoma gliosarcoma high grade glioma middle cerebral artery infarction mixed glioma retinitis pigmentosa urinary bladder cancer
63877	family with sequence similarity 204 member A	FAM204A
63891	ring finger protein 123	RNF123
63892	THADA armadillo repeat containing	THADA
63893	ubiquitin conjugating enzyme E2 O	UBE2O
63894	VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog	VIPAS39
63895	piezo type mechanosensitive ion channel component 2	PIEZO2

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