GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3601 - 3625** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
55423	signal regulatory protein gamma	SIRPG
55388	minichromosome maintenance 10 replication initiation factor	MCM10
55367	p53-induced death domain protein 1	PIDD1 DKFZp434D229 MGC16925
55366	leucine rich repeat containing G protein-coupled receptor 4	LGR4
55365	transmembrane protein 176A	TMEM176A
55362	transmembrane protein 63B	TMEM63B
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A DKFZP761G1923 PI4KII PIK42A	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
55357	TBC1 domain family member 2	TBC1D2
55356	solute carrier family 22 member 15	SLC22A15
55355	Holliday junction recognition protein	HJURP
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial
55345	zinc finger GRF-type containing 1	ZGRF1
55343	solute carrier family 35 member C1	SLC35C1 FLJ11320 FUCT1 GDP-fucose transporter 1	Laron syndrome achondroplasia anxiety disorder cellulitis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc echolalia generalized anxiety disorder hepatocellular carcinoma leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer microcephaly
55341	large 60S subunit nuclear export GTPase 1	LSG1 FLJ11301
55339	WD repeat domain 33	WDR33
55334	solute carrier family 39 member 9	SLC39A9
55331	alkaline ceramidase 3	ACER3 APHC FLJ11238 alkaline phytoceramidase	Cauda equina syndrome Laron syndrome achondroplasia acute myeloid leukemia cerebellar ataxia cerebellar disease cerebral degeneration dystonia hepatocellular carcinoma intellectual disability learning disability leukodystrophy liver cancer melanoma metabolic dysfunction-associated steatohepatitis neurogenic bladder neuropathy peripheral nervous system disease skin melanoma
55326	1-acylglycerol-3-phosphate O-acyltransferase 5	AGPAT5 1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon FLJ11210 LPAAT-e LPAAT-epsilon LPLAT5 lysophosphatidic acid acyltransferase, epsilon lysophospholipid acyltransferase 5
55324	ATP binding cassette subfamily F member 3	ABCF3
55323	La ribonucleoprotein 6, translational regulator	LARP6
55320	MIS18 binding protein 1	MIS18BP1
55315	solute carrier family 29 member 3	SLC29A3
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 FLJ11112 LCB2B hLCB2b	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
55301	oleoyl-ACP hydrolase	OLAH FLJ11106 S-acyl fatty acid synthase thioesterase, medium chain SAST oleoyl-acyl-carrier-protein hydrolase	migraine
55300	phosphatidylinositol 4-kinase type 2 beta	PI4K2B FLJ11105 PI4KIIB PIK42B	attention deficit hyperactivity disorder bipolar disorder childhood leukemia chronic myeloid leukemia disease of mental health leukemia psychotic disorder schizophrenia

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