GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8376 - 8400** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
126792	beta-1,3-galactosyltransferase 6	B3GALT6 beta-1,3-galactosyltransferase-6 beta3GalT6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease Hirschsprung's disease Laron syndrome Rothmund-Thomson syndrome achondroplasia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis 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 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease bone disease cartilage disease cherubism chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate clubfoot collagen disease collecting duct carcinoma connective tissue disease cutis laxa enophthalmos exostosis heart septal defect hepatocellular carcinoma intellectual disability isolated cleft palate isolated ectopia lentis learning disability liver cancer mal de Meleda mitral valve insufficiency mitral valve prolapse myopia nonpapillary renal cell carcinoma obsolete exophthalmos orbital disease osteogenesis imperfecta osteoporosis papillary renal cell carcinoma paraplegia patent foramen ovale periarthritis renal carcinoma renal cell carcinoma restrictive dermopathy sarcomatoid renal cell carcinoma scoliosis spinal cord disease spondyloepimetaphyseal dysplasia with joint laxity type 1 tendinitis ventricular septal defect
126820	dynein axonemal intermediate chain 3	DNAI3
126868	mab-21 like 3	MAB21L3
126969	solute carrier family 44 member 3	SLC44A3
127059	olfactory receptor family 2 subfamily M member 5	OR2M5
127062	olfactory receptor family 2 subfamily M member 3	OR2M3
127064	olfactory receptor family 2 subfamily T member 12	OR2T12
127066	olfactory receptor family 14 subfamily C member 36	OR14C36
127068	olfactory receptor family 2 subfamily T member 34	OR2T34
127069	olfactory receptor family 2 subfamily T member 10	OR2T10
127074	olfactory receptor family 2 subfamily T member 4	OR2T4
127077	olfactory receptor family 2 subfamily T member 11	OR2T11
127255	leucine rich repeats and IQ motif containing 3	LRRIQ3
127281	peroxiredoxin like 2B	PRXL2B MGC26818 prostamide/prostaglandin F synthase thioredoxin-type PGF synthase
127294	myomesin 3	MYOM3
127343	diencephalon/mesencephalon homeobox 1	DMBX1
127385	olfactory receptor family 10 subfamily J member 5	OR10J5
127396	zinc finger protein 684	ZNF684
127435	podocan	PODN
127550	alpha 1,3-galactosyltransferase 2	A3GALT2 IGB3S IGBS3S iGb3 synthase isoglobotriaosylceramide synthase
127579	DC-STAMP domain containing 2	DCST2
127602	dynein axonemal heavy chain 14	DNAH14
127623	olfactory receptor family 2 subfamily B member 11	OR2B11
127665	zinc finger protein 648	ZNF648
127707	kelch domain containing 7A	KLHDC7A

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