GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5401 - 5425** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
26000	TBC1 domain family member 10B	TBC1D10B
26001	ring finger protein 167	RNF167
26002	monooxygenase DBH like 1	MOXD1
26003	golgi reassembly stacking protein 2	GORASP2
26005	C2 domain containing 3 centriole elongation regulator	C2CD3
26007	triokinase and FMN cyclase	TKFC DKFZP586B1621 FAD-AMP lyase (cyclizing) NET45	cataract diabetes mellitus diabetic ketoacidosis liver disease type 2 diabetes mellitus
26009	zinc finger ZZ-type containing 3	ZZZ3
26010	spermatogenesis associated serine rich 2 like	SPATS2L
26011	teneurin transmembrane protein 4	TENM4
26012	NMDA receptor synaptonuclear signaling and neuronal migration factor	NSMF
26013	L3MBTL histone methyl-lysine binding protein 1	L3MBTL1
26015	RNA polymerase II associated protein 1	RPAP1
26018	leucine rich repeats and immunoglobulin like domains 1	LRIG1
26019	UPF2 regulator of nonsense mediated mRNA decay	UPF2
26020	LDL receptor related protein 10	LRP10
26025	protocadherin gamma subfamily A, 12	PCDHGA12
26027	acyl-CoA thioesterase 11	ACOT11
26032	sushi domain containing 5	SUSD5
26033	attractin like 1	ATRNL1 ALP FLJ45344 KIAA0534	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Becker muscular dystrophy Bloom syndrome Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Laron syndrome Marfan syndrome Pick's disease Reye syndrome Sjogren's syndrome Wilson disease achondroplasia acromegaly acute myeloid leukemia adult hypophosphatasia allergic asthma amyotrophic lateral sclerosis ankylosing spondylitis asthma autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiovascular system disease cartilage disease cerebral degeneration cerebral palsy childhood osteosarcoma cholestasis choriocarcinoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer connective tissue disease craniosynostosis diabetes mellitus distal arthrogryposis distal myopathy embryonal cancer endomyocardial fibrosis esophagitis extrahepatic cholestasis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia familial hypocalciuric hypercalcemia 1 gallbladder disease gastroesophageal reflux disease germ cell and embryonal cancer germ cell cancer germinoma goiter heart disease hematopoietic system disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma hereditary elliptocytosis hypercalcemia hyperpituitarism hypogonadism hypophosphatasia infantile hypophosphatasia inflammatory liposarcoma iron metabolism disease isolated cleft palate keratoconjunctivitis sicca kidney failure large intestine cancer limb-girdle muscular dystrophy lipoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma muscular dystrophy myeloproliferative disorder with eosinophilia myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephrocalcinosis nephrolithiasis neurodegenerative disease non-Hodgkin lymphoma nonpapillary renal cell carcinoma nontoxic goiter obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete constipation obsolete ymphosarcoma oculopharyngeal muscular dystrophy osteoporosis osteosarcoma papillary renal cell carcinoma peptic esophagitis phosphorus metabolism disease placenta cancer pleomorphic lipoma primary biliary cholangitis primary hyperparathyroidism progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcomatoid renal cell carcinoma sclerosing liposarcoma situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy steatotic liver disease subcortical band heterotopia thyroid gland disease tuberous sclerosis type 2 diabetes mellitus uremia uric acid nephrolithiasis vitelliform macular dystrophy well-differentiated liposarcoma
26035	glucuronic acid epimerase	GLCE HSEPI KIAA0836 heparan sulfate epimerase	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions amyotrophic lateral sclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebrovascular disease embryoma essential hypertension frontotemporal dementia hypertension luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma nodular prostate progressive muscular atrophy prostate cancer prostate carcinoma prostate disease prostatic adenoma
26037	signal induced proliferation associated 1 like 1	SIPA1L1
26038	chromodomain helicase DNA binding protein 5	CHD5
26040	SET binding protein 1	SETBP1
26045	leucine rich repeat transmembrane neuronal 2	LRRTM2
26046	listerin E3 ubiquitin protein ligase 1	LTN1

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