GlyCosmos Portal

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GlyConnect	March 24, 2025
GlycoProtDB	December 4, 2018
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The O-GlcNAc Database	January 30, 2025
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Displaying entries **326 - 350** of **139028** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
O95831	Apoptosis-inducing factor 1, mitochondrial	AIF AIFM1 PDCD8	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease X-linked recessive 4 X-linked deafness 5 combined oxidative phosphorylation deficiency 6
P12036	Neurofilament heavy polypeptide	KIAA0845 NEFH NFH	Homo sapiens (human)	10	1	Charcot-Marie-Tooth disease axonal type 2CC amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis monoclonal gammopathy of uncertain significance
P04792	Heat shock protein beta-1	HSP27 HSP28 HSPB1	Homo sapiens (human)	7	1	Charcot-Marie-Tooth disease axonal type 2F autosomal dominant distal hereditary motor neuronopathy 3 pancreatic cancer sarcoma
Q9HDC5	Junctophilin-1	JP1 JPH1	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease axonal type 2K
Q9UJY1	Heat shock protein beta-8	CRYAC E2IG1 HSP22 HSPB8 PP1629	Homo sapiens (human)	3	1	Charcot-Marie-Tooth disease axonal type 2L autosomal dominant distal hereditary motor neuronopathy 2
P49588	Alanine--tRNA ligase, cytoplasmic	AARS AARS1	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease axonal type 2N developmental and epileptic encephalopathy 29 leukodystrophy trichothiodystrophy
Q14204	Cytoplasmic dynein 1 heavy chain 1	DHC1 DNCH1 DNCL DNECL DYHC DYNC1H1 KIAA0325	Homo sapiens (human)	8	2	Charcot-Marie-Tooth disease axonal type 2O autosomal dominant intellectual developmental disorder 13 spinal muscular atrophy with lower extremity predominant 1
Q9JHU4	Cytoplasmic dynein 1 heavy chain 1	Dhc1 Dnch1 Dnchc1 Dyhc Dync1h1	Mus musculus (house mouse)	4	3	Charcot-Marie-Tooth disease axonal type 2O
Q6UWE0	E3 ubiquitin-protein ligase LRSAM1	LRSAM1 TAL UNQ6496/PRO21356	Homo sapiens (human)	3	1	Charcot-Marie-Tooth disease axonal type 2P
P38935	DNA-binding protein SMUBP-2	IGHMBP2 SMBP2 SMUBP2	Homo sapiens (human)	2	0	Charcot-Marie-Tooth disease axonal type 2S autosomal recessive distal hereditary motor neuronopathy 1
P56192	Methionine--tRNA ligase, cytoplasmic	MARS MARS1	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease axonal type 2U hereditary spastic paraplegia 70 trichothiodystrophy
P54802	Alpha-N-acetylglucosaminidase	NAGLU UFHSD1	Homo sapiens (human)	7	70	Charcot-Marie-Tooth disease axonal type 2V mucopolysaccharidosis III mucopolysaccharidosis type IIIB
Q96JI7	Spatacsin	KIAA1840 SPG11	Homo sapiens (human)	2	2	Charcot-Marie-Tooth disease axonal type 2X amyotrophic lateral sclerosis type 5 hereditary spastic paraplegia 11
Q9Y6X9	ATPase MORC2	KIAA0852 MORC2 ZCWCC1	Homo sapiens (human)	7	1	Charcot-Marie-Tooth disease axonal type 2Z
Q92538	Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1	GBF1 KIAA0248	Homo sapiens (human)	5	1	Charcot-Marie-Tooth disease dominant intermediate A
P21576	Vacuolar protein sorting-associated protein 1	LAM1 SPO15 VPS1 YKR001C	Saccharomyces cerevisiae S288C	1	1	Charcot-Marie-Tooth disease dominant intermediate B centronuclear myopathy 1 developmental and epileptic encephalopathy hereditary spastic paraplegia lethal congenital contracture syndrome microcytic anemia
P50570	Dynamin-2	DNM2 DYN2	Homo sapiens (human)	4	2	Charcot-Marie-Tooth disease dominant intermediate B centronuclear myopathy 1 lethal congenital contracture syndrome
Q91WQ3	Tyrosine--tRNA ligase, cytoplasmic	Yars Yars1	Mus musculus (house mouse)	1	1	Charcot-Marie-Tooth disease dominant intermediate C
P54577	Tyrosine--tRNA ligase, cytoplasmic	YARS YARS1	Homo sapiens (human)	3	1	Charcot-Marie-Tooth disease dominant intermediate C
P25189	Myelin protein P0	MPZ	Homo sapiens (human)	1	15	Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease
Q27J81	Inverted formin-2	C14orf151 C14orf173 INF2	Homo sapiens (human)	4	2	Charcot-Marie-Tooth disease dominant intermediate E focal segmental glomerulosclerosis 5
Q9HAV0	Guanine nucleotide-binding protein subunit beta-4	GNB4	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease dominant intermediate F
P07196	Neurofilament light polypeptide	NEFL NF68 NFL	Homo sapiens (human)	24	1	Charcot-Marie-Tooth disease dominant intermediate G Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease amyotrophic lateral sclerosis invasive ductal carcinoma
Q15046	Lysine--tRNA ligase	KARS KARS1 KIAA0070	Homo sapiens (human)	2	1	Charcot-Marie-Tooth disease recessive intermediate B autosomal recessive nonsyndromic deafness 89
Q01453	Peripheral myelin protein 22	GAS3 PMP22	Homo sapiens (human)	1	0	Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease Guillain-Barre syndrome hereditary neuropathy with liability to pressure palsies

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