GlyCosmos Portal

Displaying entries **3901 - 3925** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q6NUQ1	RAD50-interacting protein 1	RINT1	2	1
Q8N999	RNA ligase 1	RLIG1 C12orf29	0	1
Q9Y2D9	Zinc finger protein 652	ZNF652 KIAA0924	3	1
Q00325	Solute carrier family 25 member 3	SLC25A3 PHC	0	1
P49757	Protein numb homolog	NUMB C14orf41	0	1
Q9UBM7	7-dehydrocholesterol reductase	DHCR7 D7SR	0	1	3-methylglutaconic aciduria Behcet's disease Dandy-Walker syndrome Hailey-Hailey disease Laron syndrome Marfan syndrome Meckel syndrome Potter's syndrome Rapp-Hodgkin syndrome Rothmund-Thomson syndrome Smith-Lemli-Opitz syndrome X-linked ichthyosis achondroplasia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant polycystic kidney disease 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 bilateral optic nerve hypoplasia bilateral renal aplasia cardiovascular system disease choanal atresia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary artery disease cutis laxa dermatitis diabetes mellitus diabetic ketoacidosis fissured tongue glaucoma glycoproteinosis heart disease hepatitis C hepatocellular carcinoma hydrocephalus hypohidrotic ectodermal dysplasia hypospadias immune system disease intellectual disability interstitial nephritis large intestine cancer learning disability leukocyte adhesion deficiency 2 leukocyte adhesion deficiency lingual-facial-buccal dyskinesia liver cancer liver cirrhosis mal de Meleda microcephaly movement disease multiple sclerosis nutmeg liver obsolete type 1 diabetes mellitus 9 oligohydramnios osteomalacia periventricular nodular heterotopia photosensitive epilepsy photosensitivity disease placental insufficiency polycystic ovary syndrome polydactyly polyhydramnios pyelitis pyelonephritis restrictive dermopathy rheumatoid arthritis rickets scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability type 10 tongue disease tuberous sclerosis 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 ventricular septal defect
Q86Y22	Collagen alpha-1(XXIII) chain	COL23A1	0	1
Q10567	AP-1 complex subunit beta-1	AP1B1 ADTB1 BAM22 CLAPB2	0	1
Q658T7	Putative protein FAM90A2P	FAM90A2P	0	1
Q6XUX3	Dual serine/threonine and tyrosine protein kinase	DSTYK KIAA0472 RIP5 RIPK5 SGK496	1	1
Q9NSI2	Ribosome biogenesis protein SLX9 homolog	SLX9 C21orf70 FAM207A	1	1
Q96AP4	Zinc finger-containing ubiquitin peptidase 1	ZUP1 C6orf113 ZUFSP	0	1
P59046	NACHT, LRR and PYD domains-containing protein 12	NLRP12 NALP12 PYPAF7 RNO	0	1
Q9HD26	Golgi-associated PDZ and coiled-coil motif-containing protein	GOPC CAL FIG	0	1
Q96MT1	RING finger protein 145	RNF145	0	1
Q86X51	EZH inhibitory protein	EZHIP CXorf67	1	1
Q00872	Myosin-binding protein C, slow-type	MYBPC1 MYBPCS	0	1
P39656	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit	DDOST KIAA0115 OST48	0	1	Japanese encephalitis Laron syndrome achondroplasia animal phobia blood coagulation disease bone osteosarcoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma chronic kidney disease congenital disorder of glycosylation Ir congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dengue disease diabetes mellitus diabetic ketoacidosis epilepsy esophagitis esotropia gastroesophageal reflux disease glomerulonephritis glucose intolerance hepatitis C hypertropia hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia influenza kidney disease lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung benign neoplasm lung cancer lung carcinoma mechanical strabismus monocular esotropia nephritis nephrosis obsolete constipation obsolete inherited blood coagulation disease obsolete type 1 diabetes mellitus 9 ophthalmoplegia osteoporosis osteosarcoma peptic esophagitis periodontitis prediabetes syndrome prostate cancer prostate carcinoma pyoureter retinal disease retinitis sleeping sickness specific phobia speech disorder steatotic liver disease strabismus trypanosomiasis 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 vascular disease viral infectious disease visual epilepsy yellow fever
Q5XUX0	F-box only protein 31	FBXO31 FBX14 FBX31	0	1
P48201	ATP synthase F(0) complex subunit C3, mitochondrial	ATP5MC3 ATP5G3	0	1
Q7Z3T8	Zinc finger FYVE domain-containing protein 16	ZFYVE16 KIAA0305	4	1
Q5TCQ9	Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3	MAGI3 KIAA1634	0	1
Q7L8S5	OTU domain-containing protein 6A	OTUD6A DUBA2	1	1
Q8NE65	Zinc finger protein 738	ZNF738	0	1
Q96PQ1	Sialic acid-binding Ig-like lectin 12	SIGLEC12 SIGLECL1 SLG	11	1	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus

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