GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6126 - 6150** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
9168	thymosin beta 10	TMSB10
9162	diacylglycerol kinase iota	DGKI DGK-IOTA	acquired immunodeficiency syndrome alexia cancer dyslexia eclampsia giant cell glioblastoma glioblastoma high grade glioma human immunodeficiency virus infectious disease melanoma schizophrenia skin melanoma
9159	proprotein convertase subtilisin/kexin type 7	PCSK7
9156	exonuclease 1	EXO1
9154	solute carrier family 28 member 1	SLC28A1
9153	solute carrier family 28 member 2	SLC28A2
9152	solute carrier family 6 member 5	SLC6A5
9150	CTD phosphatase subunit 1	CTDP1
9147	nuclear export mediator factor	NEMF
9146	hepatocyte growth factor-regulated tyrosine kinase substrate	HGS
9144	synaptogyrin 2	SYNGR2
9140	autophagy related 12	ATG12
9134	cyclin E2	CCNE2
9131	apoptosis inducing factor mitochondria associated 1	AIFM1
9129	pre-mRNA processing factor 3	PRPF3
9128	pre-mRNA splicing tri-snRNP complex factor PRPF4	PRPF4
9127	purinergic receptor P2X 6	P2RX6
9126	structural maintenance of chromosomes 3	SMC3 BAM HCAP SMC3L1 bamacan bamacan proteoglycan	Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome 2 Cornelia de Lange syndrome 3 Cornelia de Lange syndrome Dubowitz syndrome Laron syndrome Marfan syndrome Meckel syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Peters anomaly Prader-Willi syndrome Roberts syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma allergic asthma anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis 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 atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome blepharitis blind hypotensive eye bone cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer carcinoma cataract 32 multiple types cataract central nervous system lymphoma childhood lymphoma choanal atresia chondrodysplasia-pseudohermaphroditism syndrome chronic interstitial cystitis chronic monocytic leukemia cleft palate cleidocranial dysplasia clubfoot colon carcinoma colorectal cancer cone-rod dystrophy congenital diaphragmatic hernia congenital nystagmus congenital ptosis cornea plana coronary artery disease craniosynostosis cribriform carcinoma cryptorchidism dissociated nystagmus embryoma epilepsy esophagitis fundus albipunctatus gastroesophageal reflux disease generalized anxiety disorder gingivitis glaucoma gonadal dysgenesis granular cell carcinoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hypertrichosis hypertropia hypospadias inguinal hernia intellectual disability interstitial cystitis intestinal benign neoplasm intestinal cancer intestinal volvulus intrinsic asthma isolated cleft palate kidney failure kwashiorkor large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia lymphoma marasmus mechanical strabismus megacolon microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly myeloid leukemia myopia neuropathy nutrition disease obsolete SC phocomelia syndrome obsolete ymphosarcoma ophthalmoplegia osteosarcoma patent foramen ovale pathologic nystagmus peptic esophagitis periodontitis peripheral nervous system disease placental insufficiency pneumonia prostate cancer prostate carcinoma protein-energy malnutrition prune belly syndrome ptosis pulmonary valve stenosis pyloric stenosis radioulnar synostosis retinitis pigmentosa sarcomatoid carcinoma sensorineural hearing loss situs inversus speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 thromboangiitis obliterans toxic megacolon trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma ventricular septal defect vesicoureteral reflux visual epilepsy
9124	PDZ and LIM domain 1	PDLIM1
9123	solute carrier family 16 member 3	SLC16A3
9119	keratin 75	KRT75
9118	internexin neuronal intermediate filament protein alpha	INA
9113	large tumor suppressor kinase 1	LATS1
9112	metastasis associated 1	MTA1
9111	N-myc and STAT interactor	NMI

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