GlyCosmos Portal

Displaying entries **17251 - 17275** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q07011	Tumor necrosis factor receptor superfamily member 9	TNFRSF9 CD137 ILA	2	0
Q9UNE0	Tumor necrosis factor receptor superfamily member EDAR	EDAR DL	2	1
Q15628	Tumor necrosis factor receptor type 1-associated DEATH domain protein	TRADD	2	1
P98066	Tumor necrosis factor-inducible gene 6 protein	TNFAIP6 TSG6	2	0
P55327	Tumor protein D52	TPD52	3	1
O43399	Tumor protein D54	TPD52L2	7	2
Q96J77	Tumor protein D55	TPD52L3	0	1
Q8NBR0	Tumor protein p53-inducible protein 13	TP53I13 DSCP1	9	3
Q6ZUI0	Tumor protein p63-regulated gene 1 protein	TPRG1 FAM79B	1	1
Q13454	Tumor suppressor candidate 3	TUSC3 N33	2	2	Peutz-Jeghers syndrome agnosia autosomal recessive intellectual developmental disorder 7 autosomal recessive intellectual developmental disorder bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration childhood osteosarcoma chondrosarcoma choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression microcephaly mixed glioma neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma partial motor epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tongue squamous cell carcinoma ulcerative colitis visual epilepsy von Hippel-Lindau disease
Q99816	Tumor susceptibility gene 101 protein	TSG101	0	1
C5IX07	Tumor-associated calcium signal transducer 2	TACSTD2	1	0
P09758	Tumor-associated calcium signal transducer 2	TACSTD2 GA733-1 M1S1 TROP2	7	34
Q12792	Twinfilin-1	TWF1 PTK9	0	1
Q6IBS0	Twinfilin-2	TWF2 PTK9L	2	1
Q15672	Twist-related protein 1	TWIST1 BHLHA38 TWIST	3	1
Q8WVJ9	Twist-related protein 2	TWIST2 BHLHA39 DERMO1	2	1
J3QS03	Twisted gastrulation BMP signaling modulator 1	TWSG1	1	0
Q9GZX9	Twisted gastrulation protein homolog 1	TWSG1 TSG	3	13
Q9ULQ1	Two pore channel protein 1	TPCN1 KIAA1169 TPC1	3	0
Q8NHX9	Two pore channel protein 2	TPCN2 TPC2	2	0
Q9Y274	Type 2 lactosamine alpha-2,3-sialyltransferase	ST3GAL6 SIAT10	7	16	cancer carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer multiple myeloma sarcomatoid carcinoma stomach cancer
A0A087WXB8	Type 2 lactosamine alpha-2,3-sialyltransferase	ST3GAL6	1	0
A0A0A8K8P7	Type I transmembrane receptor	PSK-1	2	0
P32019	Type II inositol 1,4,5-trisphosphate 5-phosphatase	INPP5B OCRL2	0	1	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis 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 congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema 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 progressive muscular atrophy rippling muscle disease 2

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