GlyCosmos Portal

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Displaying entries **9476 - 9500** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9HB21	Pleckstrin homology domain-containing family A member 1	PLEKHA1 TAPP1	Homo sapiens (human)	6	2
Q9HB20	Pleckstrin homology domain-containing family A member 3	PLEKHA3 FAPP1	Homo sapiens (human)	0	1
Q9HB15	Potassium channel subfamily K member 12	KCNK12	Homo sapiens (human)	1	0
Q9HB14	Potassium channel subfamily K member 13	KCNK13	Homo sapiens (human)	2	0
Q9HB09	Bcl-2-like protein 12	BCL2L12 BPR	Homo sapiens (human)	0	1
Q9HB07	MYG1 exonuclease	MYG1 C12orf10	Homo sapiens (human)	0	1
Q9HB03	Very long chain fatty acid elongase 3	ELOVL3 CIG30	Homo sapiens (human)	2	0	amnestic disorder atopic dermatitis dermatitis diabetes mellitus diabetic ketoacidosis ichthyosis prostate cancer prostate carcinoma retrograde amnesia type 2 diabetes mellitus
Q9HAZ2	Histone-lysine N-methyltransferase PRDM16	PRDM16 KIAA1675 MEL1 PFM13	Homo sapiens (human)	1	2
Q9HAY6	Beta,beta-carotene 15,15'-dioxygenase	BCO1 BCDO BCDO1 BCMO1	Homo sapiens (human)	1	1
Q9HAW9	UDP-glucuronosyltransferase 1A8	UGT1A8 GNT1 UGT1	Homo sapiens (human)	3	2	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leiomyoma leukopenia liver disease myofibroma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy xeroderma pigmentosum group D
Q9HAW8	UDP-glucuronosyltransferase 1A10	UGT1A10 GNT1 UGT1	Homo sapiens (human)	3	2	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hepatocellular carcinoma hereditary spherocytosis influenza intrahepatic cholangiocarcinoma kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver cancer liver disease lung benign neoplasm lung carcinoma lung small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
Q9HAW7	UDP-glucuronosyltransferase 1A7	UGT1A7 GNT1 UGT1	Homo sapiens (human)	4	3	Crigler-Najjar syndrome Crohn's colitis Crohn's disease Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 acute pancreatitis adult hepatocellular carcinoma agranulocytosis alcoholic pancreatitis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest childhood hepatocellular carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma hemoglobin H disease hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis inflammatory bowel disease 1 inflammatory bowel disease influenza kernicterus due to isoimmunization kernicterus large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer leukopenia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma tracheal disease type 2 diabetes mellitus ulcerative colitis urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
Q9HAW4	Claspin	CLSPN	Homo sapiens (human)	3	1
Q9HAW0	Transcription factor IIIB 50 kDa subunit	BRF2 BRFU	Homo sapiens (human)	3	1
Q9HAV7	GrpE protein homolog 1, mitochondrial	GRPEL1 GREPEL1	Homo sapiens (human)	0	1
Q9HAV5	Tumor necrosis factor receptor superfamily member 27	EDA2R TNFRSF27 XEDAR	Homo sapiens (human)	1	1
Q9HAV4	Exportin-5	XPO5 KIAA1291 RANBP21	Homo sapiens (human)	0	1
Q9HAV0	Guanine nucleotide-binding protein subunit beta-4	GNB4	Homo sapiens (human)	1	1
Q9HAU5	Regulator of nonsense transcripts 2	UPF2 KIAA1408 RENT2	Homo sapiens (human)	1	1
Q9HAU4	E3 ubiquitin-protein ligase SMURF2	SMURF2	Homo sapiens (human)	2	2
Q9HAU0	Pleckstrin homology domain-containing family A member 5	PLEKHA5 KIAA1686 PEPP2	Homo sapiens (human)	4	1
Q9HAT2	Sialate O-acetylesterase	SIAE YSG2	Homo sapiens (human)	7	47
Q9HAT1	Protein ERGIC-53-like	LMAN1L ERGL	Homo sapiens (human)	1	0
Q9HAS3	Solute carrier family 28 member 3	SLC28A3 CNT3	Homo sapiens (human)	3	2
Q9HAS0	Protein Njmu-R1	C17orf75	Homo sapiens (human)	0	1

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