GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5801 - 5825** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
50808	adenylate kinase 3	AK3
50809	heterochromatin protein 1 binding protein 3	HP1BP3
50810	HDGF like 3	HDGFL3
50814	NAD(P) dependent steroid dehydrogenase-like	NSDHL H105e3 SDR31E1 XAP104 short chain dehydrogenase/reductase family 31E, member 1	Bloch-Sulzberger syndrome CHILD syndrome CK syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia cancer chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
50831	taste 2 receptor member 3	TAS2R3
50832	taste 2 receptor member 4	TAS2R4
50833	taste 2 receptor member 16	TAS2R16
50834	taste 2 receptor member 1	TAS2R1
50835	taste 2 receptor member 9	TAS2R9
50836	taste 2 receptor member 8	TAS2R8
50837	taste 2 receptor member 7	TAS2R7
50838	taste 2 receptor member 13	TAS2R13
50839	taste 2 receptor member 10	TAS2R10
50840	taste 2 receptor member 14	TAS2R14
50848	F11 receptor	F11R
50856	C-type lectin domain family 4 member A	CLEC4A
50859	SPARC (osteonectin), cwcv and kazal like domains proteoglycan 3	SPOCK3
50862	ring finger protein 141	RNF141
50863	neurotrimin	NTM CEPU-1 HNT IGLON2 IgLON family member 2 NTRI neurotrimin	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
50937	cell adhesion associated, oncogene regulated	CDON
50939	interphotoreceptor matrix proteoglycan 2	IMPG2
50940	phosphodiesterase 11A	PDE11A Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A
50944	SH3 and multiple ankyrin repeat domains 1	SHANK1
50964	sclerostin	SOST
50999	transmembrane p24 trafficking protein 5	TMED5 CGI-100 p24g2 p24gamma2	T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adult T-cell leukemia/lymphoma breast cancer cancer central nervous system cancer chronic fatigue syndrome coronary thrombosis embryoma encephalitis encephalomyelitis exudative vitreoretinopathy 1 exudative vitreoretinopathy gliosarcoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma liver cancer melanoma mixed glioma multiple sclerosis myelitis myocardial infarction retinopathy of prematurity schizophrenia silent myocardial infarction skin melanoma

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