GlyCosmos Portal

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

Displaying entries **121626 - 121650** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
A0A1P8ANR5	ARF GAP-like zinc finger-containing protein ZIGA4	ZIGA4 AGD14 ARF-GAP domain 14	Arabidopsis thaliana (thale cress)	1
Q96MP5	Zinc finger SWIM domain-containing protein 3	ZSWIM3 C20orf164	Homo sapiens (human)	1
A0A1P8BCM2	Transducin/WD40 repeat-like superfamily protein	FY	Arabidopsis thaliana (thale cress)	1
Q96JN8	Neuralized-like protein 4	NEURL4 KIAA1787	Homo sapiens (human)	1
Q96S90	LysM and putative peptidoglycan-binding domain-containing protein 1	LYSMD1	Homo sapiens (human)	1
V5AYL6	DNA-directed RNA polymerase subunit beta	TCDM_05569	Trypanosoma cruzi Dm28c	1
Q9D8M7	PHD finger protein 10	Phf10 Baf45a	Mus musculus (house mouse)	1
Q9ULJ6	Zinc finger MIZ domain-containing protein 1	ZMIZ1 KIAA1224 RAI17 ZIMP10	Homo sapiens (human)	1
Q3V300	Kinesin-like protein KIF22	Kif22	Mus musculus (house mouse)	1
O15116	U6 snRNA-associated Sm-like protein LSm1	LSM1 CASM	Homo sapiens (human)	1
P55084	Trifunctional enzyme subunit beta, mitochondrial	HADHB	Homo sapiens (human)	1	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Norum disease Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia beta-ketothiolase deficiency breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease cholestasis choreaacanthocytosis clubfoot colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure critical illness polyneuropathy developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endomyocardial fibrosis epilepsy familial hyperlipidemia familial periodic paralysis fibromyalgia fundus albipunctatus heart disease hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hypercalcemia hypertrophic cardiomyopathy hypolipoproteinemia hypoparathyroidism inflammatory and toxic neuropathy intellectual disability lactic acidosis large intestine cancer learning disability melanoma meningoencephalitis mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse motor peripheral neuropathy myoglobinuria myopathy myositis nephrocalcinosis neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease phosphorus metabolism disease placental insufficiency polydactyly polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinitis pigmentosa sick sinus syndrome skin melanoma steatotic liver disease tricuspid valve insufficiency urea cycle disorder visual epilepsy
V5AV92	Proteasome regulatory non-ATPase subunit 2	TCDM_07100	Trypanosoma cruzi Dm28c	1
Q49AR2	UPF0489 protein C5orf22	C5orf22	Homo sapiens (human)	1
Q9BUE0	Mediator of RNA polymerase II transcription subunit 18	MED18	Homo sapiens (human)	1
A0A1I9LTD1	SAC3/GANP/Nin1/mts3/eIF-3 p25 family	SAC3B AtSAC3B yeast Sac3 homolog B	Arabidopsis thaliana (thale cress)	1
Q9H496	Torsin-1A-interacting protein 2, isoform IFRG15	TOR1AIP2 IFRG15	Homo sapiens (human)	1
P52888	Thimet oligopeptidase	THOP1	Homo sapiens (human)	1
Q9Y6S9	Ribosomal protein S6 kinase-like 1	RPS6KL1	Homo sapiens (human)	1
Q4DBV1	Transmembrane protein	Tc00.1047053510357.130	Trypanosoma cruzi strain CL Brener	1
P61211	ADP-ribosylation factor-like protein 1	Arl1	Mus musculus (house mouse)	1
P13716	Delta-aminolevulinic acid dehydratase	ALAD	Homo sapiens (human)	1
V5B773	UV excision repair protein RAD23	TCDM_02094	Trypanosoma cruzi Dm28c	1
A0A140LJ98	Arginyltransferase 1 (Fragment)	Ate1	Mus musculus (house mouse)	1
Q4DQV3	Uncharacterized protein	Tc00.1047053511911.102	Trypanosoma cruzi strain CL Brener	1
E9Q1T9	Exportin-2	Cse1l	Mus musculus (house mouse)	1

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