GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4151 - 4175** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
51061	thioredoxin domain containing 11	TXNDC11
51060	thioredoxin domain containing 12	TXNDC12
51058	zinc finger protein 691	ZNF691
51053	geminin DNA replication inhibitor	GMNN
51050	peptidase inhibitor 15	PI15
51046	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	ST8SIA3 ST8Sia III	acute myeloid leukemia basal ganglia disease cancer embryoma schizophrenia
51027	bolA family member 1	BOLA1
51014	transmembrane p24 trafficking protein 7	TMED7
51006	solute carrier family 35 member C2	SLC35C2 CGI-15 bA394O2.1
51005	amidohydrolase domain containing 2	AMDHD2 CGI-14 N-acetylglucosamine-6-phosphate deacetylase	colorectal cancer colorectal carcinoma large intestine cancer
51004	coenzyme Q6, monooxygenase	COQ6
51001	mitochondrial transcription termination factor 3	MTERF3
51000	solute carrier family 35 member B3	SLC35B3 3' phosphoadenosine 5' phosphosulfate transporter 2 CGI-19 PAPST2 dJ453H5.1	diabetes mellitus type 2 diabetes mellitus
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
50964	sclerostin	SOST
50944	SH3 and multiple ankyrin repeat domains 1	SHANK1
50940	phosphodiesterase 11A	PDE11A Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A
50939	interphotoreceptor matrix proteoglycan 2	IMPG2
50937	cell adhesion associated, oncogene regulated	CDON
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
50862	ring finger protein 141	RNF141
50859	SPARC (osteonectin), cwcv and kazal like domains proteoglycan 3	SPOCK3
50856	C-type lectin domain family 4 member A	CLEC4A
50848	F11 receptor	F11R
50840	taste 2 receptor member 14	TAS2R14

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