GlyCosmos Portal

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Displaying entries **12776 - 12800** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96J77	Tumor protein D55	TPD52L3	Homo sapiens (human)	0	1
Q96J66	ATP-binding cassette sub-family C member 11	ABCC11 MRP8	Homo sapiens (human)	2	0
Q96J65	ATP-binding cassette sub-family C member 12	ABCC12 MRP9	Homo sapiens (human)	4	0
Q96J42	Thioredoxin domain-containing protein 15	TXNDC15 C5orf14	Homo sapiens (human)	10	25
Q96J02	E3 ubiquitin-protein ligase Itchy homolog	ITCH	Homo sapiens (human)	0	1
Q96J01	THO complex subunit 3	THOC3	Homo sapiens (human)	1	1
Q96IZ7	Serine/Arginine-related protein 53	RSRC1 SRRP53	Homo sapiens (human)	2	1
Q96IZ5	RNA-binding protein 41	RBM41	Homo sapiens (human)	2	1
Q96IZ0	PRKC apoptosis WT1 regulator protein	PAWR PAR4	Homo sapiens (human)	12	1
Q96IY4	Carboxypeptidase B2	CPB2	Homo sapiens (human)	5	38
Q96IY1	Kinetochore-associated protein NSL1 homolog	NSL1 C1orf48	Homo sapiens (human)	0	1
Q96IX9	Putative ankyrin repeat domain-containing protein 26-like 1	ANKRD36BP1 ANKRD26L1	Homo sapiens (human)	0	1
Q96IX5	ATP synthase membrane subunit K, mitochondrial	ATP5MK ATP5MD DAPIT HCVFTP2 USMG5	Homo sapiens (human)	0	1
Q96IV0	Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase	NGLY1 PNG1	Homo sapiens (human)	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	Homo sapiens (human)	0	1
Q96IT1	Zinc finger protein 496	ZNF496 ZKSCAN17	Homo sapiens (human)	0	1
Q96IR7	4-hydroxyphenylpyruvate dioxygenase-like protein	HPDL GLOXD1	Homo sapiens (human)	1	1
Q96IQ9	Zinc finger protein 414	ZNF414	Homo sapiens (human)	0	1
Q96IQ7	V-set and immunoglobulin domain-containing protein 2	VSIG2 CTH CTXL	Homo sapiens (human)	2	0
Q96IK5	Germ cell-less protein-like 1	GMCL1 BTBD13 GCL SPATA29	Homo sapiens (human)	0	1
Q96IK1	Biorientation of chromosomes in cell division protein 1	BOD1 FAM44B	Homo sapiens (human)	1	1
Q96IJ6	Mannose-1-phosphate guanyltransferase alpha	GMPPA	Homo sapiens (human)	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	Homo sapiens (human)	0	1
Q96ID5	Immunoglobulin superfamily member 21	IGSF21	Homo sapiens (human)	4	1
Q96IC2	RNA exonuclease 5	REXO5	Homo sapiens (human)	0	1

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