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 **5351 - 5375** of **18496** in total

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UniProt ID	Protein Name ▼	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P0CG48	Polyubiquitin-C	UBC	Homo sapiens (human)	0	1
P0CG47	Polyubiquitin-B	UBB	Homo sapiens (human)	0	1
Q5K4E3	Polyserase-2	PRSS36	Homo sapiens (human)	9	0
Q8TCS8	Polyribonucleotide nucleotidyltransferase 1, mitochondrial	PNPT1 PNPASE	Homo sapiens (human)	2	1
O95758	Polypyrimidine tract-binding protein 3	PTBP3 ROD1	Homo sapiens (human)	0	1
Q9UKA9	Polypyrimidine tract-binding protein 2	PTBP2 NPTB PTB PTBLP	Homo sapiens (human)	1	2
P26599	Polypyrimidine tract-binding protein 1	PTBP1 PTB	Homo sapiens (human)	10	2
Q92562	Polyphosphoinositide phosphatase	FIG4 KIAA0274 SAC3	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Joubert syndrome Laron syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Papillon-Lefevre disease Yunis-Varon syndrome achondroplasia agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis type 11 amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease anxiety disorder atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal recessive distal hereditary motor neuronopathy 1 breast cancer breast carcinoma cardiomyopathy cataract communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cryptorchidism demyelinating disease demyelinating polyneuropathy depressive disorder distal arthrogryposis dysthymic disorder endomyocardial fibrosis enophthalmos epilepsy essential hypertension generalized anxiety disorder gingival recession gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 7 high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertension hypertrophic cardiomyopathy hypospadias laryngostenosis lateral sclerosis lissencephaly lysosomal storage disease major depressive disorder melancholic depression microcephaly mixed glioma motor neuron disease motor peripheral neuropathy neuroblastoma neurodegenerative disease neuropathy neurotic disorder obsolete exophthalmos obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive hydrocephalus orbital disease patent foramen ovale peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary pulmonary hypertension progressive muscular atrophy pyloric stenosis renal artery obstruction renovascular hypertension sclerocornea senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus status epilepticus subacute delirium syndactyly syndromic X-linked intellectual disability Najm type tetralogy of Fallot tuberous sclerosis ventricular septal defect
Q49A17	Polypeptide N-acetylgalactosaminyltransferase-like 6	GALNTL6 GALNT17	Homo sapiens (human)	2	0	nicotine dependence
Q9HCQ5	Polypeptide N-acetylgalactosaminyltransferase 9	GALNT9	Homo sapiens (human)	1	0	breast cancer breast carcinoma cancer neuroblastoma
Q8NCL4	Polypeptide N-acetylgalactosaminyltransferase 6	GALNT6	Homo sapiens (human)	8	1	adenocarcinoma adenoma breast cancer breast carcinoma cancer carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis granular cell carcinoma large intestine cancer lung adenocarcinoma lung cancer ovarian cancer ovarian carcinoma sarcomatoid carcinoma serous cystadenocarcinoma stomach cancer stomach carcinoma tubular adenocarcinoma uterine corpus cancer
Q68VJ5	Polypeptide N-acetylgalactosaminyltransferase 5 (Fragment)	GALNT5	Homo sapiens (human)	1	0
Q7Z7M9	Polypeptide N-acetylgalactosaminyltransferase 5	GALNT5	Homo sapiens (human)	65	4	breast cancer cancer embryoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma stomach cancer stomach carcinoma
Q8N4A0	Polypeptide N-acetylgalactosaminyltransferase 4	GALNT4	Homo sapiens (human)	2	2	acute chest syndrome arteriosclerotic cardiovascular disease atherosclerosis breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease large intestine cancer prostate cancer prostate carcinoma
Q14435	Polypeptide N-acetylgalactosaminyltransferase 3	GALNT3	Homo sapiens (human)	6	7	CHARGE syndrome X-linked dyskeratosis congenita adenocarcinoma adenoma angioid streaks arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive hypophosphatemic rickets bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cerebral infarction cerebrovascular disease chondrocalcinosis chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma dental enamel hypoplasia dental pulp calcification dentin dysplasia diabetes mellitus diabetic ketoacidosis disease of metabolism dyskeratosis congenita embryoma endometriosis of uterus endometriosis gallbladder cancer gallbladder carcinoma granular cell carcinoma hypercalcemia hyperostosis hyperphosphatemia hyperphosphatemic familial tumoral calcinosis hypotrichosis 1 hypotrichosis large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma microphthalmia musculoskeletal system disease nephrocalcinosis nodular prostate nutmeg liver obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma phosphorus metabolism disease prostate cancer prostate carcinoma prostatic adenoma pulp degeneration renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin disease skin melanoma squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma 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 type 2 diabetes mellitus viral infectious disease
Q10471	Polypeptide N-acetylgalactosaminyltransferase 2	GALNT2	Homo sapiens (human)	10	3	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 achondroplasia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus embryoma essential hypertension familial hyperlipidemia gastric adenocarcinoma gliosarcoma hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hypertension hypochondroplasia inflammatory bowel disease 1 inflammatory bowel disease liver cancer mixed glioma nutmeg liver obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma type 2 diabetes mellitus ulcerative colitis
Q6P9A2	Polypeptide N-acetylgalactosaminyltransferase 18	GALNT18 GALNTL4	Homo sapiens (human)	4	3	gastric adenocarcinoma rheumatoid arthritis
Q6IS24	Polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 WBSCR17	Homo sapiens (human)	3	0	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
Q8N428	Polypeptide N-acetylgalactosaminyltransferase 16	GALNT16 GALNTL1 KIAA1130	Homo sapiens (human)	3	1	breast cancer breast carcinoma idiopathic scoliosis
Q8N3T1	Polypeptide N-acetylgalactosaminyltransferase 15	GALNT15 GALNTL2	Homo sapiens (human)	2	0	colorectal cancer colorectal carcinoma large intestine cancer
Q96FL9	Polypeptide N-acetylgalactosaminyltransferase 14	GALNT14	Homo sapiens (human)	3	3	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
Q8IUC8	Polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 KIAA1918	Homo sapiens (human)	3	2	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
Q8IXK2	Polypeptide N-acetylgalactosaminyltransferase 12	GALNT12	Homo sapiens (human)	4	1	adenocarcinoma adenoma bilateral breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma islet cell tumor large intestine cancer microcystic adenoma papillary adenoma
Q8NCW6	Polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	Homo sapiens (human)	2	5	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
Q86SR1	Polypeptide N-acetylgalactosaminyltransferase 10	GALNT10	Homo sapiens (human)	9	2	hepatitis B hepatocellular carcinoma liver cancer schizophrenia

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