GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6026 - 6050** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
51763	inositol polyphosphate-5-phosphatase K	INPP5K SKIP skeletal muscle and kidney enriched inositol phosphatase	Aicardi-Goutieres syndrome 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 Duchenne muscular dystrophy Gaucher's disease Laron syndrome Legg-Calve-Perthes disease Marinesco-Sjogren syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia agnosia anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bladder carcinoma breast cancer breast carcinoma cancer cardiovascular system disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral degeneration cerebrovascular disease congenital muscular dystrophy with cataracts and intellectual disability congenital muscular dystrophy congenital nystagmus coronary artery disease dementia depressive disorder developmental coordination disorder disease of mental health disease of metabolism dissociated nystagmus distal myopathy dysplastic nevus syndrome dysthymic disorder dystonia epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fragile X syndrome generalized anxiety disorder giant cell glioblastoma glioblastoma heart disease hepatocellular carcinoma high grade glioma hypertropia hypogonadism intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer major depressive disorder mechanical strabismus melancholic depression melanoma microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy neuropathy neurotic disorder 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 melancholia oculocerebrorenal syndrome oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease phobic disorder phototoxic dermatitis primary cerebellar degeneration psychotic disorder rippling muscle disease 2 scoliosis skin benign neoplasm skin cancer skin carcinoma skin melanoma spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus tauopathy urinary bladder cancer
51768	transmembrane 7 superfamily member 3	TM7SF3
51773	remodeling and spacing factor 1	RSF1
51780	lysine demethylase 3B	KDM3B
51802	acid sensing ion channel subunit family member 5	ASIC5
51804	SIX homeobox 4	SIX4
51805	coenzyme Q3, methyltransferase	COQ3
51806	calmodulin like 5	CALML5
51809	polypeptide N-acetylgalactosaminyltransferase 7	GALNT7 GALNAC-T7 polypeptide GalNAc transferase 7	arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma colorectal cancer colorectal carcinoma coronary artery disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma large intestine cancer laryngeal squamous cell carcinoma mixed glioma nasopharynx carcinoma
51816	adenosine deaminase 2	ADA2 ADGF
53335	BCL11 transcription factor A	BCL11A
53342	interleukin 17D	IL17D
53347	ubiquitin associated and SH3 domain containing A	UBASH3A
53349	zinc finger FYVE-type containing 1	ZFYVE1
53353	LDL receptor related protein 1B	LRP1B
53358	SHC adaptor protein 3	SHC3
53371	nucleoporin 54	NUP54
53373	two pore segment channel 1	TPCN1
53615	methyl-CpG binding domain protein 3	MBD3
53616	ADAM metallopeptidase domain 22	ADAM22
53630	beta-carotene oxygenase 1	BCO1
53632	protein kinase AMP-activated non-catalytic subunit gamma 3	PRKAG3	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
53637	sphingosine-1-phosphate receptor 5	S1PR5
53822	FXYD domain containing ion transport regulator 7	FXYD7
53827	FXYD domain containing ion transport regulator 5	FXYD5

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