GlyCosmos Portal

Displaying entries **6126 - 6150** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P32189	Glycerol kinase	GK	1	1	Aland Island eye disease Becker muscular dystrophy Duchenne muscular dystrophy Kallmann syndrome Klinefelter syndrome Laron syndrome Patau syndrome Sheehan syndrome X-linked adrenal hypoplasia congenita achondroplasia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 chromosome Xp21 deletion syndrome cone-rod dystrophy congenital muscular dystrophy coronary artery disease diabetes mellitus distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypercholesterolemia fundus albipunctatus galactokinase deficiency galactosemia glycerol kinase deficiency hypertropia hypoglycemia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism intellectual disability isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency learning disability limb-girdle muscular dystrophy mechanical strabismus muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obesity 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 oculopharyngeal muscular dystrophy ophthalmoplegia osteoporosis panhypopituitarism placental insufficiency retinitis pigmentosa rippling muscle disease 2 strabismus tuberculosis type 2 diabetes mellitus
Q8WVZ7	E3 ubiquitin-protein ligase RNF133	RNF133	2	1
P47884	Olfactory receptor 1D4	OR1D4	2	1
Q8N111	Cell cycle exit and neuronal differentiation protein 1	CEND1 BM88	2	1
Q6QNY0	Biogenesis of lysosome-related organelles complex 1 subunit 3	BLOC1S3 BLOS3	0	1
Q96L92	Sorting nexin-27	SNX27 KIAA0488	0	1
Q9Y6G5	COMM domain-containing protein 10	COMMD10	0	1
O75689	Arf-GAP with dual PH domain-containing protein 1	ADAP1 CENTA1	0	1
Q96CW9	Netrin-G2	NTNG2 KIAA1857 LMNT2	5	1
P53814	Smoothelin	SMTN SMSMO	6	1
Q9NWV4	CXXC motif containing zinc binding protein	CZIB C1orf123	0	1
Q13506	NGFI-A-binding protein 1	NAB1	3	1
Q9H9T3	Elongator complex protein 3	ELP3	0	1
P43358	Melanoma-associated antigen 4	MAGEA4 MAGE4	0	1
Q9C0K3	Actin-related protein 3C	ACTR3C ARP11	1	1
O95500	Claudin-14	CLDN14	0	1
Q96E39	RNA binding motif protein, X-linked-like-1	RBMXL1	0	1
Q15475	Homeobox protein SIX1	SIX1	1	1
P08151	Zinc finger protein GLI1	GLI1 GLI	0	1
Q96AE4	Far upstream element-binding protein 1	FUBP1	9	1
P78347	General transcription factor II-I	GTF2I BAP135 WBSCR6	3	1
Q9Y3I1	F-box only protein 7	FBXO7 FBX7	2	1
Q8TD35	Protein LKAAEAR1	LKAAEAR1 C20orf201	0	1
Q9H2A9	Carbohydrate sulfotransferase 8	CHST8	8	1	allergic asthma asthma atopic dermatitis colorectal cancer colorectal carcinoma intrinsic asthma large intestine cancer parapsoriasis peeling skin syndrome psoriasis pustulosis of palm and sole scleroderma skin disease systemic scleroderma
P20815	Cytochrome P450 3A5	CYP3A5	1	1	Balkan nephropathy Cockayne syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia abdominal obesity-metabolic syndrome 1 acute biphenotypic leukemia acute chest syndrome acute intermittent porphyria acute leukemia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia adult medulloblastoma adult respiratory distress syndrome agnosia agranulocytosis alcohol dependence alcohol use disorder allergic asthma ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune lymphoproliferative syndrome bladder carcinoma bone disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cartilage disease central nervous system origin vertigo central sleep apnea cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia childhood medulloblastoma cholestasis chromophobe renal cell carcinoma chronic kidney disease chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma clonorchiasis collagen disease collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure connective tissue disease coronary artery disease diabetes mellitus diabetic ketoacidosis disease of mental health embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial nephrotic syndrome familial periodic paralysis follicular adenoma gastrointestinal system cancer glomerulonephritis heart disease hepatitis C hepatocellular carcinoma hypertension immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kidney failure large intestine cancer laryngeal squamous cell carcinoma leukemia leukopenia lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lupus nephritis lymphoblastic lymphoma lymphoid leukemia medulloblastoma medullomyoblastoma melanotic medulloblastoma membranous glomerulonephritis microcystic adenoma microphthalmia myasthenia gravis myelodysplastic syndrome myeloid leukemia myopathy nephritis nephrolithiasis nephrosclerosis nephrosis nephrotic syndrome neuroblastoma neuropathy neutropenia newborn respiratory distress syndrome nicotine dependence nodular prostate nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome oral submucous fibrosis ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma papillary adenoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy pre-eclampsia prostate cancer prostate carcinoma prostatic adenoma psychotic disorder pyoureter renal carcinoma renal cell carcinoma renal hypertension rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seminoma severe congenital neutropenia squamous cell carcinoma subacute delirium systemic lupus erythematosus testicular cancer testicular malignant germ cell cancer testis seminoma thrombophilia thrombosis tongue squamous cell carcinoma toxic encephalopathy tuberculosis type 2 diabetes mellitus ulcerative colitis uric acid nephrolithiasis urinary bladder cancer

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