GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4751 - 4775** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
23516	solute carrier family 39 member 14	SLC39A14	hypermanganesemia with dystonia 2
23515	MORC family CW-type zinc finger 3	MORC3
23513	scribble planar cell polarity protein	SCRIB
23512	SUZ12 polycomb repressive complex 2 subunit	SUZ12
23511	nucleoporin 188	NUP188
23509	protein O-fucosyltransferase 1	POFUT1 FUT12 GDP-fucose protein O-fucosyltransferase 1 KIAA0180 O-FUT O-Fuc-T peptide-O-fucosyltransferase	Dowling-Degos disease acrodermatitis actinic keratosis acute myocardial infarction bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery anomaly coronary thrombosis dermatitis gallbladder disease hepatocellular carcinoma invasive ductal carcinoma large intestine cancer liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcephaly myeloproliferative neoplasm myocardial infarction reticulate acropigmentation of Kitamura schizophrenia seborrheic keratosis silent myocardial infarction skin disease
23507	leucine rich repeat containing 8 VRAC subunit B	LRRC8B
23506	BICRA like chromatin remodeling complex associated protein	BICRAL
23505	transmembrane protein 131	TMEM131
23504	RIMS binding protein 2	RIMBP2
23503	zinc finger FYVE-type containing 26	ZFYVE26
23500	dishevelled associated activator of morphogenesis 2	DAAM2
23499	microtubule actin crosslinking factor 1	MACF1
23495	TNF receptor superfamily member 13B	TNFRSF13B
23491	carboxylesterase 3	CES3
23483	TDP-glucose 4,6-dehydratase	TGDS SDR2E1 TDPGD short chain dehydrogenase/reductase family 2E, member 1	Alzheimer's disease Catel Manzke syndrome Laron syndrome Marfan syndrome achondroplasia 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 cleft lip cleft palate clubfoot cryptorchidism cystic lymphangioma dementia depressive disorder dextrocardia dysthymic disorder epilepsy hydrocephalus inguinal hernia isolated cleft palate major depressive disorder melancholic depression neurotic disorder obsolete melancholia omphalocele otitis media patent foramen ovale placental insufficiency scoliosis situs inversus temtamy preaxial brachydactyly syndrome tuberous sclerosis umbilical hernia ventricular septal defect visual epilepsy
23476	bromodomain containing 4	BRD4
23475	quinolinate phosphoribosyltransferase	QPRT QPRTase nicotinate-nucleotide pyrophosphorylase (carboxylating)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute myeloid leukemia adenoma adenosarcoma endemic goiter follicular adenoma gliosarcoma hepatitis C high grade glioma microcystic adenoma mixed glioma nephroblastoma neuroblastoma neurodegenerative disease papillary adenoma substernal goiter thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma
23473	calpain 7	CAPN7
23471	translocation associated membrane protein 1	TRAM1
23469	PHD finger protein 3	PHF3
23468	chromobox 5	CBX5
23467	neuronal pentraxin receptor	NPTXR
23461	ATP binding cassette subfamily A member 5	ABCA5
23460	ATP binding cassette subfamily A member 6	ABCA6

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