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 **14001 - 14025** 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
P16036	Solute carrier family 25 member 3	Slc25a3 Phc	Rattus norvegicus (Norway rat)	1	1
V5BAL2	EamA domain-containing protein	TCDM_00776	Trypanosoma cruzi Dm28c	0	1
P59541	Taste receptor type 2 member 30	TAS2R30 TAS2R47	Homo sapiens (human)	2	1
B0I1T2	Unconventional myosin-Ig	MYO1G HA2	Homo sapiens (human)	1	1
Q8CE64	Zinc finger protein 276	Znf276 Zfp276	Mus musculus (house mouse)	0	1
A6NEL2	Ankyrin repeat domain-containing protein SOWAHB	SOWAHB ANKRD56	Homo sapiens (human)	3	1
Q80WE1	Fragile X messenger ribonucleoprotein 1	Fmr1	Rattus norvegicus (Norway rat)	0	1
Q8R404	MICOS complex subunit MIC13	Micos13 Mic13 Qil1	Mus musculus (house mouse)	0	1
O75419	Cell division control protein 45 homolog	CDC45 CDC45L CDC45L2	Homo sapiens (human)	0	1
P84244	Histone H3.3	H3-3a H3-3b H3.3a H3.3b H3f3a H3f3b	Mus musculus (house mouse)	0	1
Q8TEA7	TBC domain-containing protein kinase-like protein	TBCK FERRY1 TBCKL	Homo sapiens (human)	0	1
O15228	Dihydroxyacetone phosphate acyltransferase	GNPAT DAPAT DHAPAT	Homo sapiens (human)	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 Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
P48651	Phosphatidylserine synthase 1	PTDSS1 KIAA0024 PSSA	Homo sapiens (human)	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 Bell's palsy Hailey-Hailey disease Laron syndrome Lenz-Majewski hyperostotic dwarfism Pick's disease Reye syndrome Rothmund-Thomson syndrome achondroplasia aortic disease aortic valve disease 2 aortic valve stenosis autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant osteopetrosis 2 autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 7 cerebral degeneration choanal atresia communicating hydrocephalus cryptorchidism cutis laxa dental enamel hypoplasia facial nerve disease facial paralysis humeroradial synostosis hydrocephalus hypogonadism hypospadias inguinal hernia intellectual disability lateral meningocele syndrome learning disability mal de Meleda obstructive hydrocephalus osteopetrosis osteosclerosis placental insufficiency priapism restrictive dermopathy scoliosis senile degeneration of brain sensorineural hearing loss syndactyly tongue disease
Q9UGI9	5'-AMP-activated protein kinase subunit gamma-3	PRKAG3 AMPKG3	Homo sapiens (human)	0	1
Q92585	Mastermind-like protein 1	MAML1 KIAA0200	Homo sapiens (human)	11	1
Q7TT45	Ras-related GTP-binding protein D	Rragd Ragd	Mus musculus (house mouse)	2	1
D3Z5K8	SH3 and multiple ankyrin repeat domains 2	Shank2	Mus musculus (house mouse)	0	1
Q80Z38	SH3 and multiple ankyrin repeat domains protein 2	Shank2 Cortbp1 Kiaa1022	Mus musculus (house mouse)	14	1
A1KXC4	Immunoglobulin mu Fc receptor	Fcmr Faim3 Toso	Mus musculus (house mouse)	0	1
Q9H3U7	SPARC-related modular calcium-binding protein 2	SMOC2 SMAP2	Homo sapiens (human)	3	1
K2MUS2	Proteasome subunit alpha type	MOQ_005330	Trypanosoma cruzi marinkellei	0	1
P45953	Very long-chain specific acyl-CoA dehydrogenase, mitochondrial	Acadvl	Rattus norvegicus (Norway rat)	1	1
Q6ZUA9	Maestro heat-like repeat family member 5	MROH5	Homo sapiens (human)	1	1
P30305	M-phase inducer phosphatase 2	CDC25B CDC25HU2	Homo sapiens (human)	0	1
Q4DZF5	Threonine dehydratase-like, putative	Tc00.1047053506825.70	Trypanosoma cruzi strain CL Brener	0	1

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