GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96IZ7	Serine/Arginine-related protein 53	RSRC1 SRRP53	2	1
Q96IZ5	RNA-binding protein 41	RBM41	2	1
Q96IZ0	PRKC apoptosis WT1 regulator protein	PAWR PAR4	12	1
Q96IY4	Carboxypeptidase B2	CPB2	5	38
Q96IY1	Kinetochore-associated protein NSL1 homolog	NSL1 C1orf48	0	1
Q96IX9	Putative ankyrin repeat domain-containing protein 26-like 1	ANKRD36BP1 ANKRD26L1	0	1
Q96IX5	ATP synthase membrane subunit K, mitochondrial	ATP5MK ATP5MD DAPIT HCVFTP2 USMG5	0	1
Q96IV0	Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase	NGLY1 PNG1	1	1	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
Q96IU4	Putative protein-lysine deacylase ABHD14B	ABHD14B CIB	0	1
Q96IT1	Zinc finger protein 496	ZNF496 ZKSCAN17	0	1
Q96IR7	4-hydroxyphenylpyruvate dioxygenase-like protein	HPDL GLOXD1	1	1
Q96IQ9	Zinc finger protein 414	ZNF414	0	1
Q96IQ7	V-set and immunoglobulin domain-containing protein 2	VSIG2 CTH CTXL	2	0
Q96IK5	Germ cell-less protein-like 1	GMCL1 BTBD13 GCL SPATA29	0	1
Q96IK1	Biorientation of chromosomes in cell division protein 1	BOD1 FAM44B	1	1
Q96IJ6	Mannose-1-phosphate guanyltransferase alpha	GMPPA	1	2	Addison's disease Down syndrome Laron syndrome achalasia achondroplasia adrenal cortical hypofunction blindness coloboma epilepsy intellectual disability learning disability megaesophagus microcephaly nonepidermolytic palmoplantar keratoderma optic atrophy palmoplantar keratosis sensorineural hearing loss triple-A syndrome visual epilepsy
Q96IF1	LIM domain-containing protein ajuba	AJUBA JUB	0	1
Q96ID5	Immunoglobulin superfamily member 21	IGSF21	4	1
Q96IC2	RNA exonuclease 5	REXO5	0	1
Q96I99	Succinate--CoA ligase [GDP-forming] subunit beta, mitochondrial	SUCLG2	0	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cerebral degeneration endometriosis of ovary endometriosis methylmalonic acidemia prostate cancer prostate carcinoma
Q96I82	Kazal-type serine protease inhibitor domain-containing protein 1	KAZALD1	3	0
Q96I59	Asparaginyl-tRNA synthetase	NARS2	1	1
Q96I36	Cytochrome c oxidase assembly protein COX14	COX14 C12orf62	0	1
Q96I34	Protein phosphatase 1 regulatory subunit 16A	PPP1R16A MYPT3	1	1
Q96I25	Splicing factor 45	RBM17 SPF45	0	1

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