GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **3601 - 3625** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9BXR3	Endogenous retrovirus group K member 6 Pol protein	ERVK-6 ERVK6	Homo sapiens (human)	3	0
P63135	Endogenous retrovirus group K member 7 Pol protein	ERVK-7	Homo sapiens (human)	1	1
Q902F8	Endogenous retrovirus group K member 8 Env polyprotein	ERVK-8	Homo sapiens (human)	11	0
P62685	Endogenous retrovirus group K member 8 Gag polyprotein	ERVK-8	Homo sapiens (human)	1	1
Q9UKH3	Endogenous retrovirus group K member 9 Env polyprotein	ERVK-9	Homo sapiens (human)	11	0
B3KNS4	Endogenous retrovirus group K3 member 1	ERVK3-1	Homo sapiens (human)	0	1
P60509	Endogenous retrovirus group PABLB member 1 Env polyprotein	ERVPABLB-1	Homo sapiens (human)	11	0
B6SEH8	Endogenous retrovirus group V member 1 Env polyprotein	ERVV-1 ENVV1	Homo sapiens (human)	2	1
B6SEH9	Endogenous retrovirus group V member 2 Env polyprotein	ERVV-2 ENVV2	Homo sapiens (human)	1	0
P17813	Endoglin	ENG END	Homo sapiens (human)	10	5
Q9ULC0	Endomucin	EMCN EMCN2 MUC14	Homo sapiens (human)	17	7
Q8TAT5	Endonuclease 8-like 3	NEIL3	Homo sapiens (human)	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	Homo sapiens (human)	0	1
Q99961	Endophilin-A2	SH3GL1 CNSA1 SH3D2B	Homo sapiens (human)	3	1
Q99963	Endophilin-A3	SH3GL3 CNSA3 SH3D2C	Homo sapiens (human)	1	1
Q9Y371	Endophilin-B1	SH3GLB1 KIAA0491	Homo sapiens (human)	1	2
Q9NR46	Endophilin-B2	SH3GLB2 KIAA1848	Homo sapiens (human)	0	1
Q9NZ08	Endoplasmic reticulum aminopeptidase 1	ERAP1 APPILS ARTS1 KIAA0525	Homo sapiens (human)	8	32
Q6P179	Endoplasmic reticulum aminopeptidase 2	ERAP2 LRAP	Homo sapiens (human)	10	43
P11021	Endoplasmic reticulum chaperone BiP	HSPA5 GRP78	Homo sapiens (human)	12	2
Q9C0E8	Endoplasmic reticulum junction formation protein lunapark	LNPK KIAA1715 LNP	Homo sapiens (human)	1	1
Q96DZ1	Endoplasmic reticulum lectin 1	ERLEC1 C2orf30 XTP3TPB	Homo sapiens (human)	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	Homo sapiens (human)	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	Homo sapiens (human)	3	2
Q14494	Endoplasmic reticulum membrane sensor NFE2L1	NFE2L1 HBZ17 NRF1 TCF11	Homo sapiens (human)	5	1

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