GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q16514	Transcription initiation factor TFIID subunit 12	TAF12 TAF15 TAF2J TAFII20	2	1
P05187	Alkaline phosphatase, placental type	ALPP PLAP	2	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 B-cell lymphoma Becker muscular dystrophy Bloom syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease 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 Q fever Reye syndrome Sjogren's syndrome Waardenburg syndrome type 1 Waardenburg syndrome Wilson disease X-linked lymphoproliferative syndrome 2 absence epilepsy achondroplasia acromegaly acute lymphoblastic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult cystic teratoma adult hypophosphatasia adult lymphoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis ankylosing spondylitis autoimmune pancreatitis 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 azoospermia bladder carcinoma bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease cartilage disease central nervous system lymphoma cerebral degeneration cerebral palsy cervical adenocarcinoma cervical cancer cervix carcinoma childhood absence epilepsy childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholestasis choriocarcinoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation connective tissue disease craniosynostosis cystic teratoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis distal myopathy dysplastic nevus syndrome embryoma embryonal cancer endemic goiter endometriosis of uterus endometriosis endomyocardial fibrosis esophagitis essential thrombocythemia exanthem extrahepatic cholestasis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypocalciuric hypercalcemia 1 fragile X syndrome gallbladder disease gastroesophageal reflux disease gastrointestinal system cancer germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glaucoma glioblastoma goiter heart disease hematologic cancer hematopoietic system disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypercalcemia hyperpituitarism hypogonadism hypophosphatasia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis infantile hypophosphatasia inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intrahepatic cholangiocarcinoma iron metabolism disease islet cell tumor isolated cleft palate keratoconjunctivitis sicca kidney failure large intestine cancer leukemia limb-girdle muscular dystrophy lipoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma malignant pleural mesothelioma malignant teratoma mature teratoma melanoma multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloproliferative disorder with eosinophilia myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nasopharynx carcinoma nephrocalcinosis nephrolithiasis neuroblastoma 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 obstructive lung disease oculopharyngeal muscular dystrophy osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis periodontitis 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 rhabdomyosarcoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma seminoma situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy steatotic liver disease stomach cancer stomach carcinoma subcortical band heterotopia substernal goiter teratoma testicular cancer testicular germ cell cancer testis seminoma thyroid gland disease trypanosomiasis tuberculosis tuberous sclerosis type 2 diabetes mellitus typhus ulcerative colitis uremia uric acid nephrolithiasis urinary bladder cancer uveal melanoma vitelliform macular dystrophy well-differentiated liposarcoma
Q5T7F0	Neuropilin	NRP1	2	0
Q8N1G4	Leucine-rich repeat-containing protein 47	LRRC47 KIAA1185	2	1
Q8NH55	Olfactory receptor 52E5	OR52E5	2	2
O14647	Chromodomain-helicase-DNA-binding protein 2	CHD2	2	1
Q8N135	Leucine-rich repeat LGI family member 4	LGI4 LGIL3	2	2
Q5TF21	Microtubule cross-linking factor 3	MTCL3 C6orf174 SOGA3	2	1
A0A5F9ZH80	Biotinidase	BTD	2	0
Q9BS91	UDP-sugar transporter protein SLC35A5	SLC35A5	2	1
Q9H069	Dynein regulatory complex subunit 3	DRC3 LRRC48	2	2
Q9UKI9	POU domain, class 2, transcription factor 3	POU2F3 OTF11 PLA1	2	1
Q9UEU0	Vesicle transport through interaction with t-SNAREs homolog 1B	VTI1B VTI1 VTI1L VTI1L1 VTI2	2	1
Q9H2X3	C-type lectin domain family 4 member M	CLEC4M CD209L CD209L1 CD299	2	0
Q9Y3P8	Signaling threshold-regulating transmembrane adapter 1	SIT1 SIT	2	1
A0A5F9ZI20	Lysosomal acid phosphatase	ACP2	2	0
Q6ZRI8	Rho GTPase-activating protein 36	ARHGAP36	2	1
Q9Y3I0	RNA-splicing ligase RtcB homolog	RTCB C22orf28	2	2
Q9NR48	Histone-lysine N-methyltransferase ASH1L	ASH1L KIAA1420 KMT2H	2	3
Q8IUK8	Cerebellin-2	CBLN2	2	0
Q96M60	Protein FAM227B	FAM227B C15orf33	2	1
Q9Y5Y2	Cytosolic Fe-S cluster assembly factor NUBP2	NUBP2	2	1
C9JF17	Apolipoprotein D (Fragment)	APOD	2	0
A0A1W2PRA6	MHC class I polypeptide-related sequence A	MICA	2	0
Q01664	Transcription factor AP-4	TFAP4 BHLHC41	2	1

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