GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5201 - 5225** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
23424	tudor domain containing 7	TDRD7
23426	glutamate receptor interacting protein 1	GRIP1
23430	tryptase delta 1	TPSD1
23432	G protein-coupled receptor 161	GPR161
23435	TAR DNA binding protein	TARDBP
23436	chymotrypsin like elastase 3B	CELA3B
23443	solute carrier family 35 member A3	SLC35A3 UDP-N-acetylglucosamine transporter	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
23446	solute carrier family 44 member 1	SLC44A1
23450	splicing factor 3b subunit 3	SF3B3
23451	splicing factor 3b subunit 1	SF3B1
23452	angiopoietin like 2	ANGPTL2
23456	ATP binding cassette subfamily B member 10	ABCB10
23457	ATP binding cassette subfamily B member 9	ABCB9
23460	ATP binding cassette subfamily A member 6	ABCA6
23461	ATP binding cassette subfamily A member 5	ABCA5
23467	neuronal pentraxin receptor	NPTXR
23468	chromobox 5	CBX5
23469	PHD finger protein 3	PHF3
23471	translocation associated membrane protein 1	TRAM1
23473	calpain 7	CAPN7
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
23476	bromodomain containing 4	BRD4
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
23491	carboxylesterase 3	CES3
23495	TNF receptor superfamily member 13B	TNFRSF13B

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