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 **15676 - 15700** 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
P14406	Cytochrome c oxidase subunit 7A2, mitochondrial	COX7A2 COX7AL	Homo sapiens (human)	0	1
P14854	Cytochrome c oxidase subunit 6B1	COX6B1 COX6B	Homo sapiens (human)	0	1
P20674	Cytochrome c oxidase subunit 5A, mitochondrial	COX5A	Homo sapiens (human)	0	1
Q96KJ9	Cytochrome c oxidase subunit 4 isoform 2, mitochondrial	COX4I2 COX4L2	Homo sapiens (human)	1	1
P13073	Cytochrome c oxidase subunit 4 isoform 1, mitochondrial	COX4I1 COX4	Homo sapiens (human)	0	1
P00403	Cytochrome c oxidase subunit 2	MT-CO2 COII COX2 COXII MTCO2	Homo sapiens (human)	0	1
P00395	Cytochrome c oxidase subunit 1	MT-CO1 COI COXI MTCO1	Homo sapiens (human)	1	1
Q5RI15	Cytochrome c oxidase assembly protein COX20, mitochondrial	COX20 FAM36A	Homo sapiens (human)	0	1
Q96I36	Cytochrome c oxidase assembly protein COX14	COX14 C12orf62	Homo sapiens (human)	0	1
Q9Y6N1	Cytochrome c oxidase assembly protein COX11, mitochondrial	COX11	Homo sapiens (human)	1	1
Q96BR5	Cytochrome c oxidase assembly factor 7	COA7 C1orf163 RESA1 SELRC1	Homo sapiens (human)	0	1
Q5JTJ3	Cytochrome c oxidase assembly factor 6 homolog	COA6 C1orf31	Homo sapiens (human)	2	1
P99999	Cytochrome c	CYCS CYC	Homo sapiens (human)	0	1
O43169	Cytochrome b5 type B	CYB5B CYB5M OMB5	Homo sapiens (human)	0	1
P00167	Cytochrome b5	CYB5A CYB5	Homo sapiens (human)	0	1
P47985	Cytochrome b-c1 complex subunit Rieske, mitochondrial	UQCRFS1	Homo sapiens (human)	3	1
Q9UDW1	Cytochrome b-c1 complex subunit 9	UQCR10 UCRC	Homo sapiens (human)	0	1
O14949	Cytochrome b-c1 complex subunit 8	UQCRQ	Homo sapiens (human)	0	1
P14927	Cytochrome b-c1 complex subunit 7	UQCRB UQBP	Homo sapiens (human)	0	1
P22695	Cytochrome b-c1 complex subunit 2, mitochondrial	UQCRC2	Homo sapiens (human)	3	6
P31930	Cytochrome b-c1 complex subunit 1, mitochondrial	UQCRC1	Homo sapiens (human)	1	4
P04839	Cytochrome b-245 heavy chain	CYBB NOX2	Homo sapiens (human)	7	10
Q9HCS2	Cytochrome P450 4F12	CYP4F12	Homo sapiens (human)	1	1
P20815	Cytochrome P450 3A5	CYP3A5	Homo sapiens (human)	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
Q9HB55	Cytochrome P450 3A43	CYP3A43	Homo sapiens (human)	0	1

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