GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **1776 - 1800** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9H496	Torsin-1A-interacting protein 2, isoform IFRG15	TOR1AIP2 IFRG15	Homo sapiens (human)	1
P52888	Thimet oligopeptidase	THOP1	Homo sapiens (human)	1
Q9Y6S9	Ribosomal protein S6 kinase-like 1	RPS6KL1	Homo sapiens (human)	1
P13716	Delta-aminolevulinic acid dehydratase	ALAD	Homo sapiens (human)	1
O14730	Serine/threonine-protein kinase RIO3	RIOK3 SUDD	Homo sapiens (human)	1
Q13442	28 kDa heat- and acid-stable phosphoprotein	PDAP1 HASPP28	Homo sapiens (human)	1
Q9Y577	E3 ubiquitin-protein ligase TRIM17	TRIM17 RBCC RNF16 TERF	Homo sapiens (human)	1
O95630	STAM-binding protein	STAMBP AMSH	Homo sapiens (human)	1
O75419	Cell division control protein 45 homolog	CDC45 CDC45L CDC45L2	Homo sapiens (human)	1
Q8TEA7	TBC domain-containing protein kinase-like protein	TBCK FERRY1 TBCKL	Homo sapiens (human)	1
O15228	Dihydroxyacetone phosphate acyltransferase	GNPAT DAPAT DHAPAT	Homo sapiens (human)	1	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 Pick's disease Reye syndrome Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
P48651	Phosphatidylserine synthase 1	PTDSS1 KIAA0024 PSSA	Homo sapiens (human)	1	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 Bell's palsy Hailey-Hailey disease Laron syndrome Lenz-Majewski hyperostotic dwarfism Pick's disease Reye syndrome Rothmund-Thomson syndrome achondroplasia aortic disease aortic valve disease 2 aortic valve stenosis autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant osteopetrosis 2 autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 7 cerebral degeneration choanal atresia communicating hydrocephalus cryptorchidism cutis laxa dental enamel hypoplasia facial nerve disease facial paralysis humeroradial synostosis hydrocephalus hypogonadism hypospadias inguinal hernia intellectual disability lateral meningocele syndrome learning disability mal de Meleda obstructive hydrocephalus osteopetrosis osteosclerosis placental insufficiency priapism restrictive dermopathy scoliosis senile degeneration of brain sensorineural hearing loss syndactyly tongue disease
Q9UGI9	5'-AMP-activated protein kinase subunit gamma-3	PRKAG3 AMPKG3	Homo sapiens (human)	1
P30305	M-phase inducer phosphatase 2	CDC25B CDC25HU2	Homo sapiens (human)	1
Q9Y592	Centrosomal protein of 83 kDa	CEP83 CCDC41	Homo sapiens (human)	1
Q5JVG8	Zinc finger protein 506	ZNF506	Homo sapiens (human)	1
P48163	NADP-dependent malic enzyme	ME1	Homo sapiens (human)	1	Fanconi anemia complementation group A Fanconi anemia adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral infarction cerebrovascular disease cholangiocarcinoma clear cell renal cell carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma epilepsy focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma kidney cancer kidney failure large cell carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma major depressive disorder malignant teratoma mature teratoma melancholic depression mixed glioma neurotic disorder obesity obsolete melancholia partial motor epilepsy renal carcinoma renal cell carcinoma squamous cell carcinoma teratoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uterine corpus sarcoma visual epilepsy
Q2TB90	Hexokinase HKDC1	HKDC1	Homo sapiens (human)	1	breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer colorectal cancer colorectal carcinoma cone-rod dystrophy corneal disease embryoma fundus albipunctatus gestational diabetes hepatitis hyperglycemia keratoconus large intestine cancer late-onset retinal degeneration lung benign neoplasm lung cancer lung carcinoma retinitis pigmentosa steatotic liver disease
Q92481	Transcription factor AP-2-beta	TFAP2B	Homo sapiens (human)	1
Q9NQR4	Omega-amidase NIT2	NIT2	Homo sapiens (human)	1
Q9Y3S2	Zinc finger protein 330	ZNF330 NOA36	Homo sapiens (human)	1
Q5VV41	Rho guanine nucleotide exchange factor 16	ARHGEF16 EPHEXIN4 NBR	Homo sapiens (human)	1
P51648	Aldehyde dehydrogenase family 3 member A2	ALDH3A2 ALDH10 FALDH	Homo sapiens (human)	1	Cogan syndrome Laron syndrome Senior-Loken syndrome Sjogren-Larsson syndrome X-linked adrenal hypoplasia congenita achondroplasia acquired hyperkeratosis acrodermatitis age related macular degeneration allergic asthma alternating hemiplegia of childhood angioedema asthma autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis central nervous system disease cerebral palsy cone-rod dystrophy corneal disease degeneration of macula and posterior pole dental enamel hypoplasia dermatitis diabetic ketoacidosis epilepsy ethylmalonic encephalopathy fundus albipunctatus granuloma annulare hepatitis B ichthyosis intellectual disability intrinsic asthma keratoconus keratosis follicularis learning disability lipid metabolism disorder localized scleroderma locked-in syndrome lung cancer lung non-small cell carcinoma macular degeneration microcephaly mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia myopia nephronophthisis nervous system disease normal pressure hydrocephalus obsolete asthenopia obsolete congenital ichthyosiform erythroderma obsolete type 1 diabetes mellitus 9 osteochondrodysplasia papilloma paraplegia pseudoxanthoma elasticum quadriplegia retinal disease retinitis pigmentosa retinitis scleroderma scoliosis spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy squamous cell papilloma squamous papillomatosis systemic scleroderma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus urticaria visual epilepsy
Q15796	Mothers against decapentaplegic homolog 2	SMAD2 MADH2 MADR2	Homo sapiens (human)	1
O75298	Reticulon-2	RTN2 NSPL1	Homo sapiens (human)	1

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