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 **3126 - 3150** 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
Q3U8A7	Acid ceramidase	Asah1	Mus musculus (house mouse)	2	0
A0A383ZFX3	Acid ceramidase	ASAH1	Balaenoptera acutorostrata scammoni	4	0
A0A1B0GVG2	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GW68	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A0P6JG37	Acid ceramidase	ASAH1	Heterocephalus glaber (naked mole-rat)	4	0
Q3TWT5	Acid ceramidase	Asah1	Mus musculus (house mouse)	2	0
A0A1B0GTZ5	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
Q60HH4	Acid ceramidase	ASAH1	Macaca fascicularis (crab-eating macaque)	6	0
Q3U646	Acid ceramidase	Asah1	Mus musculus (house mouse)	2	0
Q13510	Acid ceramidase	ASAH1 ASAH	Homo sapiens (human)	8	123	Albright's hereditary osteodystrophy 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 Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
Q78P93	Acid ceramidase	Asah1	Mus musculus (house mouse)	2	0
Q6P7S1	Acid ceramidase	Asah1	Rattus norvegicus (Norway rat)	4	6
A0A1B0GUH5	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
A0A1B0GTM3	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
E7EMM4	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
Q92389	Acid extracellular protease	AXP1 AXP	Yarrowia lipolytica CLIB122	3	0
P08091	Acid phosphatase	pho1	Schizosaccharomyces pombe 972h-	9	0
Q8X176	Acid phosphatase	phoA	Aspergillus fumigatus Af293	12	0
P30887	Acid phosphatase	PHO2	Yarrowia lipolytica CLIB122	7	0
P34724	Acid phosphatase	phoA	Aspergillus niger	6	0
Q12546	Acid phosphatase	aphA	Aspergillus ficuum	13	0
P27061	Acid phosphatase 1	APS1 APS-1(1)	Solanum lycopersicum (tomato)	1	0
P52291	Acid phosphatase PHO1	PHO1	Komagataella pastoris	6	0
P35842	Acid phosphatase PHO11	PHO11	Saccharomyces cerevisiae S288C	10	0
P38693	Acid phosphatase PHO12	PHO12	Saccharomyces cerevisiae S288C	10	0

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