GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9UPY3	Endoribonuclease Dicer	DICER1 DICER HERNA KIAA0928	1	2
A0A7P0T885	Endoplasmin	HSP90B1	1	0
A0A7P0TAT8	Endoplasmin	HSP90B1	1	0
H0YIV0	Endoplasmin	HSP90B1	1	0
A0A7P0T917	Endoplasmin	HSP90B1	1	0
V9HWP2	Endoplasmin	HEL-S-125m HEL35 HSP90B1	1	0
A0A7P0T823	Endoplasmin	HSP90B1	1	0
P14625	Endoplasmin	HSP90B1 GRP94 HSPC4 TRA1	15	66
Q5CAQ5	Endoplasmin	TRA1	1	0
Q96GW1	Endoplasmin	HSP90B1	1	0
A0A7P0T8R3	Endoplasmin	HSP90B1	1	0
A0A7P0TAE1	Endoplasmin	HSP90B1	1	0
Q9Y282	Endoplasmic reticulum-Golgi intermediate compartment protein 3	ERGIC3 C20orf47 ERV46 SDBCAG84	5	3
Q96RQ1	Endoplasmic reticulum-Golgi intermediate compartment protein 2	ERGIC2 ERV41 PTX1	4	4
Q969X5	Endoplasmic reticulum-Golgi intermediate compartment protein 1	ERGIC1 ERGIC32 KIAA1181	2	4
Q9HD20	Endoplasmic reticulum transmembrane helix translocase	ATP13A1 ATP13A KIAA1825	4	2
Q9BS26	Endoplasmic reticulum resident protein 44	ERP44 KIAA0573 TXNDC4	9	6
P30040	Endoplasmic reticulum resident protein 29	ERP29 C12orf8 ERP28	1	8
Q96DN0	Endoplasmic reticulum resident protein 27	ERP27 C12orf46	1	0
Q92791	Endoplasmic reticulum protein SC65	P3H4 LEPREL4 NOL55 SC65	3	13
Q7Z2K6	Endoplasmic reticulum metallopeptidase 1	ERMP1 FXNA KIAA1815	3	16
Q14494	Endoplasmic reticulum membrane sensor NFE2L1	NFE2L1 HBZ17 NRF1 TCF11	5	1
Q9NPA0	Endoplasmic reticulum membrane protein complex subunit 7	EMC7 C11orf3 C15orf24	3	2
Q9UKM7	Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase	MAN1B1	17	4	Hailey-Hailey disease Rafiq syndrome Rothmund-Thomson syndrome agnosia alpha 1-antitrypsin deficiency autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bladder carcinoma bulimia nervosa cancer cerebral degeneration choreatic disease congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation cutis laxa depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease hepatocellular carcinoma hyperopia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver disease major depressive disorder mal de Meleda melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia oophoritis parametritis partial motor epilepsy pelvic inflammatory disease periventricular nodular heterotopia pyosalpinx restrictive dermopathy salpingitis stereotypic movement disorder syndactyly syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 urinary bladder cancer visual epilepsy
Q96DZ1	Endoplasmic reticulum lectin 1	ERLEC1 C2orf30 XTP3TPB	4	4	anorexia nervosa bronchus cancer bronchus carcinoma cancer cholestasis lung benign neoplasm lung cancer lung carcinoma spinal cord disease syringomyelia

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