GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **9301 - 9325** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
284759	signal regulatory protein beta 2	SIRPB2
284996	ring finger protein 149	RNF149
285093	receptor transporter protein 5 (putative)	RTP5
285172	hyccin PI4KA lipid kinase complex subunit 2	HYCC2
285175	unc-80 homolog, NALCN channel complex subunit	UNC80
285190	RANBP2 like and GRIP domain containing 4	RGPD4
285195	solute carrier family 9 member A9	SLC9A9
285203	EGF domain specific O-linked N-acetylglucosamine transferase	EOGT AER61 AER61 glycosyltransferase FLJ33770	Adams-Oliver syndrome Clouston syndrome alopecia arteriovenous malformation autosomal recessive polycystic kidney disease cataract clubfoot communicating hydrocephalus epilepsy hydrocephalus hypertropia intellectual disability learning disability leukopenia mechanical strabismus microphthalmia obstructive hydrocephalus ophthalmoplegia periventricular leukomalacia polycystic kidney disease 4 portal hypertension primary pulmonary hypertension senile degeneration of brain strabismus tetralogy of Fallot thrombocytopenia visual epilepsy
285220	EPH receptor A6	EPHA6
285242	5-hydroxytryptamine receptor 3E	HTR3E
285313	immunoglobulin superfamily member 10	IGSF10
285362	sulfatase modifying factor 1	SUMF1 FGE UNQ3037	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
285368	proline rich transmembrane protein 3	PRRT3
285386	tumor protein p63 regulated 1	TPRG1
285489	docking protein 7	DOK7
285527	FRY like transcription coactivator	FRYL
285533	ring finger protein 175	RNF175
285550	family with sequence similarity 200 member B	FAM200B
285555	sperm tail PG-rich repeat containing 2	STPG2
285590	SH3 and PX domains 2B	SH3PXD2B
285605	DTW domain containing 2	DTWD2
285659	olfactory receptor family 2 subfamily V member 2	OR2V2
285704	repulsive guidance molecule BMP co-receptor b	RGMB DRAGON FLJ90406	allergic asthma asthma atrial fibrillation brain stem infarction breast cancer cancer cerebral artery occlusion cerebral infarction cerebrovascular disease colorectal cancer colorectal carcinoma embryoma hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatocellular carcinoma intrinsic asthma large intestine cancer liver cancer lung cancer lung non-small cell carcinoma middle cerebral artery infarction multiple sclerosis prostate cancer prostate carcinoma rheumatoid arthritis
285761	discoidin, CUB and LCCL domain containing 1	DCBLD1
285800	proline rich 18	PRR18

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