GlyCosmos Portal

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9BXR3	Endogenous retrovirus group K member 6 Pol protein	ERVK-6 ERVK6	3	0
P63135	Endogenous retrovirus group K member 7 Pol protein	ERVK-7	1	1
Q902F8	Endogenous retrovirus group K member 8 Env polyprotein	ERVK-8	11	0
P62685	Endogenous retrovirus group K member 8 Gag polyprotein	ERVK-8	1	1
Q9UKH3	Endogenous retrovirus group K member 9 Env polyprotein	ERVK-9	11	0
B3KNS4	Endogenous retrovirus group K3 member 1	ERVK3-1	0	1
P60509	Endogenous retrovirus group PABLB member 1 Env polyprotein	ERVPABLB-1	11	0
B6SEH8	Endogenous retrovirus group V member 1 Env polyprotein	ERVV-1 ENVV1	2	1
B6SEH9	Endogenous retrovirus group V member 2 Env polyprotein	ERVV-2 ENVV2	1	0
P17813	Endoglin	ENG END	10	5
Q9ULC0	Endomucin	EMCN EMCN2 MUC14	17	7
Q8TAT5	Endonuclease 8-like 3	NEIL3	3	1	Fanconi anemia acute myocardial infarction basal cell carcinoma cancer coronary thrombosis differentiated thyroid gland carcinoma embryoma giant cell glioblastoma glioblastoma glomerulonephritis hepatocellular carcinoma kidney disease liver cancer myocardial infarction nephritis silent myocardial infarction
O94919	Endonuclease domain-containing 1 protein	ENDOD1 KIAA0830	0	1
Q99961	Endophilin-A2	SH3GL1 CNSA1 SH3D2B	3	1
Q99963	Endophilin-A3	SH3GL3 CNSA3 SH3D2C	1	1
Q9Y371	Endophilin-B1	SH3GLB1 KIAA0491	1	2
Q9NR46	Endophilin-B2	SH3GLB2 KIAA1848	0	1
Q9NZ08	Endoplasmic reticulum aminopeptidase 1	ERAP1 APPILS ARTS1 KIAA0525	8	32
Q6P179	Endoplasmic reticulum aminopeptidase 2	ERAP2 LRAP	10	43
P11021	Endoplasmic reticulum chaperone BiP	HSPA5 GRP78	12	2
Q9C0E8	Endoplasmic reticulum junction formation protein lunapark	LNPK KIAA1715 LNP	1	1
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
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
Q9NPA0	Endoplasmic reticulum membrane protein complex subunit 7	EMC7 C11orf3 C15orf24	3	2
Q14494	Endoplasmic reticulum membrane sensor NFE2L1	NFE2L1 HBZ17 NRF1 TCF11	5	1

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