GlyCosmos Portal

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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 **122026 - 122050** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P46100	Transcriptional regulator ATRX	ATRX RAD54L XH2	Homo sapiens (human)	22	1
Q5VV63	Attractin-like protein 1	ATRNL1 KIAA0534	Homo sapiens (human)	8	0	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
O75882	Attractin	ATRN KIAA0548 MGCA	Homo sapiens (human)	31	122	3-methylglutaconic aciduria type 3 Barth syndrome allergic asthma anaplastic astrocytoma asthma cancer cardiomyopathy central nervous system cancer childhood cerebral astrocytoma endomyocardial fibrosis fibrillary astrocytoma gemistocytic astrocytoma gliosarcoma high grade glioma hypertrophic cardiomyopathy intrinsic asthma juvenile pilocytic astrocytoma leukodystrophy malignant astrocytoma mixed glioma obesity pilocytic astrocytoma protoplasmic astrocytoma restless legs syndrome skin benign neoplasm skin cancer squamous cell carcinoma subependymal giant cell astrocytoma tongue squamous cell carcinoma
Q8WXE1	ATR-interacting protein	ATRIP AGS1	Homo sapiens (human)	5	1
Q6UW56	All-trans retinoic acid-induced differentiation factor	ATRAID APR3 C2orf28	Homo sapiens (human)	6	8
M4C699	Avirulence protein ATR5	ATR5	Hyaloperonospora arabidopsidis Emoy2	1	0
A0A084R1M7	Cytochrome P450 monooxygenase ATR4	ATR4	Stachybotrys chlorohalonata IBT 40285	3	0
A0A084R1J1	Cytochrome P450 monooxygenase ATR3	ATR3	Stachybotrys chlorohalonata IBT 40285	2	0
A0A084R1M6	Cytochrome P450 monooxygenase ATR2	ATR2	Stachybotrys chlorohalonata IBT 40285	3	0
P13090	Aminotriazole resistance protein	ATR1 SNQ1	Saccharomyces cerevisiae S288C	1	0
Q13535	Serine/threonine-protein kinase ATR	ATR FRP1	Homo sapiens (human)	2	1
Q9SSS9	ATP synthase subunit delta, chloroplastic	ATPD	Arabidopsis thaliana (thale cress)	1	0
Q8N5M1	ATP synthase mitochondrial F1 complex assembly factor 2	ATPAF2 ATP12	Homo sapiens (human)	1	1
Q5TC12	ATP synthase mitochondrial F1 complex assembly factor 1	ATPAF1 ATP11	Homo sapiens (human)	0	1
Q8TF62	Probable phospholipid-transporting ATPase IM	ATP8B4 KIAA1939	Homo sapiens (human)	0	1
P98198	Phospholipid-transporting ATPase ID	ATP8B2 ATPID KIAA1137	Homo sapiens (human)	3	1
Q9NTI2	Phospholipid-transporting ATPase IB	ATP8A2 ATPIB	Homo sapiens (human)	0	1
Q9Y2Q0	Phospholipid-transporting ATPase IA	ATP8A1 ATPIA	Homo sapiens (human)	0	1
P35670	Copper-transporting ATPase 2	ATP7B PWD WC1 WND	Homo sapiens (human)	1	1
P49015	Copper-transporting ATPase 1 (Fragment)	ATP7A	Cricetulus griseus (Chinese hamster)	7	0
Q04656	Copper-transporting ATPase 1	ATP7A MC1 MNK	Homo sapiens (human)	3	2
Q9UI12	V-type proton ATPase subunit H	ATP6V1H	Homo sapiens (human)	0	1
O75348	V-type proton ATPase subunit G 1	ATP6V1G1 ATP6G ATP6G1 ATP6J	Homo sapiens (human)	0	1
P36543	V-type proton ATPase subunit E 1	ATP6V1E1 ATP6E ATP6E2	Homo sapiens (human)	1	1
P21283	V-type proton ATPase subunit C 1	ATP6V1C1 ATP6C ATP6D VATC	Homo sapiens (human)	0	1

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