GlyCosmos Portal

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P10827	Thyroid hormone receptor alpha	THRA EAR7 ERBA1 NR1A1 THRA1 THRA2	0	1
Q9Y2W1	Thyroid hormone receptor-associated protein 3	THRAP3 BCLAF2 TRAP150	8	1
P07202	Thyroid peroxidase	TPO	4	1
Q15643	Thyroid receptor-interacting protein 11	TRIP11 CEV14	3	3
Q15654	Thyroid receptor-interacting protein 6	TRIP6 OIP1	3	1
P16473	Thyrotropin receptor	TSHR LGR3	6	2
P01222	Thyrotropin subunit beta	TSHB	1	7
P34981	Thyrotropin-releasing hormone receptor	TRHR	2	0
Q9UKU6	Thyrotropin-releasing hormone-degrading ectoenzyme	TRHDE	15	3
P05543	Thyroxine-binding globulin	SERPINA7 TBG	6	41
Q96MW7	Tigger transposable element-derived protein 1	TIGD1	1	1
Q4W5G0	Tigger transposable element-derived protein 2	TIGD2	0	1
Q8IY51	Tigger transposable element-derived protein 4	TIGD4	1	1
Q17RP2	Tigger transposable element-derived protein 6	TIGD6	1	7
Q07157	Tight junction protein ZO-1	TJP1 ZO1	15	7
Q9UDY2	Tight junction protein ZO-2	TJP2 X104 ZO2	3	3
O95049	Tight junction protein ZO-3	TJP3 ZO3	1	1
P04066	Tissue alpha-L-fucosidase	FUCA1	5	53	Laron syndrome Sjogren's syndrome achondroplasia acquired immunodeficiency syndrome angiokeratoma anhidrosis aspartylglucosaminuria autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypothyroidism craniosynostosis critical illness polyneuropathy diabetic cataract diabetic retinopathy embryoma enterocele epilepsy fucosidosis head and neck cancer human immunodeficiency virus infectious disease hypertrichosis hypohidrosis hypothyroidism immune system disease inflammatory and toxic neuropathy intellectual disability keratoconjunctivitis sicca large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy livedoid vasculitis lobular neoplasia locked-in syndrome lysosomal storage disease meningoencephalitis mucoepidermoid carcinoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myxedema neuropathy papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy quadriplegia recurrent corneal erosion scoliosis sensorineural hearing loss squamous cell carcinoma syndromic X-linked intellectual disability 94 thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma vascular skin disease visual epilepsy
P13726	Tissue factor	F3	2	9
A0A3B3IS67	Tissue factor pathway inhibitor	TFPI2	1	0
P10646	Tissue factor pathway inhibitor	TFPI LACI TFPI1	9	45
C9JKV3	Tissue factor pathway inhibitor (Fragment)	TFPI	1	0
P48307	Tissue factor pathway inhibitor 2	TFPI2	2	15
H7C4A3	Tissue factor pathway inhibitor 2 (Fragment)	TFPI2	1	0
A0A3B3IRW1	Tissue factor pathway inhibitor 2 (Fragment)	TFPI2	1	0

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