GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3076 - 3100** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
57727	nuclear receptor coactivator 5	NCOA5
57724	ectopic P-granules 5 autophagy tethering factor	EPG5
57722	immunoglobulin superfamily DCC subclass member 4	IGDCC4
57720	G protein-coupled receptor 107	GPR107
57718	protein phosphatase 4 regulatory subunit 4	PPP4R4
57717	protocadherin beta 16	PCDHB16
57715	semaphorin 4G	SEMA4G
57710	KIAA1614	KIAA1614
57709	solute carrier family 7 member 14	SLC7A14
57704	glucosylceramidase beta 2	GBA2 AD035 DKFZp762K054 KIAA1605 bile acid beta-glucosidase glucocerebrosidase 2 non-lysosomal glucosylceramidase	Charcot-Marie-Tooth disease type 5 Gaucher's disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood autonomic neuropathy cancer cataract central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration congenital nystagmus cystic fibrosis dementia dissociated nystagmus glaucoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis infertility intellectual disability learning disability male infertility nervous system disease paraplegia pathologic nystagmus scoliosis sensorineural hearing loss spontaneous ocular nystagmus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
57701	NCK associated protein 5 like	NCKAP5L
57700	FHF complex subunit HOOK interacting protein 2A	FHIP2A
57698	shootin 1	SHTN1
57697	FA complementation group M	FANCM
57696	DEAD-box helicase 55	DDX55
57695	ubiquitin specific peptidase 37	USP37
57692	MAGE family member E1	MAGEE1
57690	trinucleotide repeat containing adaptor 6C	TNRC6C
57688	zinc finger SWIM-type containing 6	ZSWIM6
57685	cache domain containing 1	CACHD1
57683	zinc finger DBF-type containing 2	ZDBF2
57680	chromodomain helicase DNA binding protein 8	CHD8
57678	glycerol-3-phosphate acyltransferase, mitochondrial	GPAM GPAT1 KIAA1560 MGC26846 glycerol-3-phosphate acyltransferase 1, mitochondrial	cancer embryoma familial nephrotic syndrome lipoid nephrosis melanoma metabolic dysfunction-associated steatotic liver disease nephrotic syndrome obesity overnutrition skin melanoma steatotic liver disease
57674	ring finger protein 213	RNF213 ALK lymphoma oligomerization partner on chromosome 17 ALO17 KIAA1554 NET57 mysterin
57673	BEN domain containing 3	BEND3

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