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 **17976 - 18000** 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
Q9Y3U8	Large ribosomal subunit protein eL36	RPL36	Homo sapiens (human)	0	1
Q9Y3X0	Coiled-coil domain-containing protein 9	CCDC9	Homo sapiens (human)	0	1
Q9Y3Y2	Chromatin target of PRMT1 protein	CHTOP C1orf77 FOP	Homo sapiens (human)	2	1
Q9Y3Z3	Deoxynucleoside triphosphate triphosphohydrolase SAMHD1	SAMHD1 MOP5	Homo sapiens (human)	4	1
Q9Y426	C2 domain-containing protein 2	C2CD2 C21orf25 C21orf258 TMEM24L	Homo sapiens (human)	0	1
Q9Y446	Plakophilin-3	PKP3	Homo sapiens (human)	0	1
Q9Y448	Small kinetochore-associated protein	KNSTRN C15orf23 SKAP TRAF4AF1	Homo sapiens (human)	1	2
Q9Y450	HBS1-like protein	HBS1L HBS1 KIAA1038	Homo sapiens (human)	3	1
Q9Y467	Sal-like protein 2	SALL2 KIAA0360 SAL2 ZNF795	Homo sapiens (human)	11	2
Q9Y468	Lethal(3)malignant brain tumor-like protein 1	L3MBTL1 KIAA0681 L3MBT L3MBTL	Homo sapiens (human)	1	1
Q9Y473	Zinc finger protein 175	ZNF175	Homo sapiens (human)	1	1
Q9Y484	WD repeat domain phosphoinositide-interacting protein 4	WDR45 WDRX1 WDRXI4 WIPI4	Homo sapiens (human)	0	1
Q9Y485	DmX-like protein 1	DMXL1 XL1	Homo sapiens (human)	4	2
Q9Y487	V-type proton ATPase 116 kDa subunit a 2	ATP6V0A2	Homo sapiens (human)	5	7	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease
Q9Y490	Talin-1	TLN1 KIAA1027 TLN	Homo sapiens (human)	4	1
Q9Y493	Zonadhesin	ZAN	Homo sapiens (human)	11	1
Q9Y496	Kinesin-like protein KIF3A	KIF3A KIF3	Homo sapiens (human)	2	1
Q9Y4A5	Transformation/transcription domain-associated protein	TRRAP PAF400	Homo sapiens (human)	7	3
Q9Y4A9	Olfactory receptor 10H1	OR10H1	Homo sapiens (human)	1	0
Q9Y4B4	Helicase ARIP4	RAD54L2 ARIP4 KIAA0809	Homo sapiens (human)	7	2
Q9Y4B5	Microtubule cross-linking factor 1	MTCL1 CCDC165 KIAA0802 SOGA2	Homo sapiens (human)	6	1
Q9Y4B6	DDB1- and CUL4-associated factor 1	DCAF1 KIAA0800 RIP VPRBP	Homo sapiens (human)	6	3
Q9Y4C0	Neurexin-3	NRXN3 C14orf60 KIAA0743	Homo sapiens (human)	7	0
Q9Y4C1	Lysine-specific demethylase 3A	KDM3A JHDM2A JMJD1 JMJD1A KIAA0742 TSGA	Homo sapiens (human)	1	2
Q9Y4C4	Malignant fibrous histiocytoma-amplified sequence 1	MFHAS1 MASL1	Homo sapiens (human)	2	2

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