GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (10109) Glycans (5831) Glycoproteins (15837) Lectins (297) Pathways (2074)

Displaying entries **151 - 175** of **10109** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
26330	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	GAPDHS GAPD2 GAPDH-2	Alzheimer's disease
7337	ubiquitin protein ligase E3A	UBE3A	Angelman syndrome
5447	cytochrome p450 oxidoreductase	POR	Antley-Bixler syndrome with disordered steroidogenesis congenital adrenal hyperplasia cytochrome P450 oxidoreductase deficiency
2263	fibroblast growth factor receptor 2	FGFR2	Antley-Bixler syndrome without disordered steroidogenesis Antley-Bixler syndrome Beare-Stevenson cutis gyrata syndrome Crouzon syndrome Jackson-Weiss syndrome Pfeiffer syndrome Saethre-Chotzen syndrome acrocephalosyndactylia bent bone dysplasia syndrome 1 breast cancer colorectal adenocarcinoma craniosynostosis dysgerminoma female breast carcinoma hepatocellular carcinoma lacrimoauriculodentodigital syndrome 1 stomach cancer stomach carcinoma urinary bladder cancer
7994	lysine acetyltransferase 6A	KAT6A	Arboleda-Tham syndrome acute myeloid leukemia
5308	paired like homeodomain 2	PITX2	Arts syndrome Axenfeld-Rieger syndrome type 1 Axenfeld-Rieger syndrome anterior segment dysgenesis 4 ring dermoid of cornea
5631	phosphoribosyl pyrophosphate synthetase 1	PRPS1 CMTX5 DFNX1 PPRibP PRS I PRS-I ribose-phosphate diphosphokinase 1	Arts syndrome Charcot-Marie-Tooth disease X-linked recessive 5 X-linked deafness 1 gout phosphoribosylpyrophosphate synthetase superactivity retinitis pigmentosa
8604	solute carrier family 25 member 12	SLC25A12	Asperger syndrome autistic disorder developmental and epileptic encephalopathy 39
2296	forkhead box C1	FOXC1	Axenfeld-Rieger syndrome type 3 Axenfeld-Rieger syndrome anterior segment dysgenesis 3 glaucoma
6046	bromodomain containing 2	BRD2	B-cell lymphoma B-lymphoblastic leukemia/lymphoma juvenile myoclonic epilepsy photosensitivity disease
50615	interleukin 21 receptor	IL21R	B-cell lymphoma Behcet's disease Crohn's disease common variable immunodeficiency diffuse large B-cell lymphoma human immunodeficiency virus infectious disease immunodeficiency 56 multiple sclerosis systemic lupus erythematosus temporal arteritis
958	CD40 molecule	CD40	B-cell lymphoma Burkitt lymphoma Crohn's disease Graves' disease Kawasaki disease arthritis asthma diffuse large B-cell lymphoma end stage renal disease follicular lymphoma hyperimmunoglobulin syndrome immunodeficiency with hyper IgM type 3 melanoma multiple myeloma multiple sclerosis non-Hodgkin lymphoma pancreatic ductal carcinoma pemphigus plasma cell leukemia psoriasis rheumatoid arthritis systemic lupus erythematosus
695	Bruton tyrosine kinase	BTK	B-cell lymphoma Burkitt lymphoma X-linked agammaglobulinemia agammaglobulinemia central nervous system lymphoma isolated growth hormone deficiency type III mantle cell lymphoma
2146	enhancer of zeste 2 polycomb repressive complex 2 subunit	EZH2	B-cell lymphoma Weaver syndrome acute megakaryocytic leukemia acute myeloid leukemia cholangiocarcinoma chronic myelomonocytic leukemia colorectal adenocarcinoma colorectal cancer congestive heart failure glioblastoma hepatocellular carcinoma lung cancer myelodysplastic syndrome myelofibrosis oral squamous cell carcinoma osteosarcoma renal Wilms' tumor stomach cancer
9429	ATP binding cassette subfamily G member 2 (JR blood group)	ABCG2	B-cell lymphoma chronic myeloid leukemia gout multiple myeloma renal cell carcinoma toxic encephalopathy
2152	coagulation factor III, tissue factor	F3	B-lymphoblastic leukemia/lymphoma COVID-19 disseminated intravascular coagulation von Willebrand's disease
7157	tumor protein p53	TP53	B-lymphoblastic leukemia/lymphoma Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome acute myeloid leukemia basal cell carcinoma breast cancer choroid plexus papilloma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis endometrial adenocarcinoma esophagus squamous cell carcinoma gastric adenocarcinoma hematologic cancer hepatocellular carcinoma high grade glioma low tension glaucoma melanoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome nasal cavity cancer nasopharynx carcinoma oral squamous cell carcinoma osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm papillary thyroid carcinoma paranasal sinus benign neoplasm primary open angle glaucoma prostate cancer sarcoma squamous cell carcinoma stomach cancer
8644	aldo-keto reductase family 1 member C3	AKR1C3 3-alpha hydroxysteroid dehydrogenase, type II DDX HAKRB KIAA0119 PGFS dihydrodiol dehydrogenase X prostaglandin F synthase	B-lymphoblastic leukemia/lymphoma T-cell acute lymphoblastic leukemia leukemia
1577	cytochrome P450 family 3 subfamily A member 5	CYP3A5 CP35 P450PCN3 PCN3	B-lymphoblastic leukemia/lymphoma acute lymphoblastic leukemia chronic myeloid leukemia essential hypertension
10320	IKAROS family zinc finger 1	IKZF1	B-lymphoblastic leukemia/lymphoma acute lymphoblastic leukemia colorectal cancer common variable immunodeficiency 13
25	ABL proto-oncogene 1, non-receptor tyrosine kinase	ABL1	B-lymphoblastic leukemia/lymphoma acute myeloid leukemia chronic myeloid leukemia colorectal cancer esophagus adenocarcinoma oral squamous cell carcinoma
7035	tissue factor pathway inhibitor	TFPI	B-lymphoblastic leukemia/lymphoma disseminated intravascular coagulation factor VIII deficiency liver cirrhosis myocardial infarction osteonecrosis protein S deficiency pulmonary fibrosis toxic shock syndrome transient cerebral ischemia
8741	TNF superfamily member 13	TNFSF13	B-lymphoblastic leukemia/lymphoma
80816	ASXL transcriptional regulator 3	ASXL3	Bainbridge-Ropers syndrome
9401	RecQ like helicase 4	RECQL4	Baller-Gerold syndrome Rothmund-Thomson syndrome rapadilino syndrome

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