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 **15551 - 15575** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q9NQ36	Signal peptide, CUB and EGF-like domain-containing protein 2	SCUBE2 CEGP1	Homo sapiens (human)	4	3
P14784	Interleukin-2 receptor subunit beta	IL2RB IL15RB	Homo sapiens (human)	4	5
A0A7I2V3X6	Angiotensin-converting enzyme	ACE2	Homo sapiens (human)	4	0
O75311	Glycine receptor subunit alpha-3	GLRA3	Homo sapiens (human)	4	1
Q6NT32	Carboxylesterase 5A	CES5A CES7	Homo sapiens (human)	4	0
Q9UN74	Protocadherin alpha-4	PCDHA4	Homo sapiens (human)	4	0
Q15075	Early endosome antigen 1	EEA1 ZFYVE2	Homo sapiens (human)	4	2
Q9Y2B1	Ribitol-5-phosphate xylosyltransferase 1	RXYLT1 TMEM5	Homo sapiens (human)	4	2	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
P20848	Alpha-1-antitrypsin-related protein	SERPINA2 ARGS ATR PIL SERPINA2P	Homo sapiens (human)	4	0
P01031	Complement C5	C5 CPAMD4	Homo sapiens (human)	4	27
Q6NYC8	Phostensin	PPP1R18 HKMT1098 KIAA1949	Homo sapiens (human)	4	2
O43173	Alpha-N-acetylneuraminate alpha-2,8-sialyltransferase ST8SIA3	ST8SIA3 SIAT8C	Homo sapiens (human)	4	0	acute myeloid leukemia basal ganglia disease cancer embryoma schizophrenia
Q66K74	Microtubule-associated protein 1S	MAP1S BPY2IP1 C19orf5 MAP8 VCY2IP1	Homo sapiens (human)	4	3
P02549	Spectrin alpha chain, erythrocytic 1	SPTA1 SPTA	Homo sapiens (human)	4	1
Q9P2Y4	Zinc finger protein 219	ZNF219	Homo sapiens (human)	4	1
P09529	Inhibin beta B chain	INHBB	Homo sapiens (human)	4	2
Q9H845	Complex I assembly factor ACAD9, mitochondrial	ACAD9	Homo sapiens (human)	4	2
Q63HK5	Teashirt homolog 3	TSHZ3 KIAA1474 TSH3 ZNF537	Homo sapiens (human)	4	1
Q8N0V4	Leucine-rich repeat LGI family member 2	LGI2 KIAA1916 LGIL2	Homo sapiens (human)	4	0
P61204	ADP-ribosylation factor 3	ARF3	Homo sapiens (human)	4	2
P46821	Microtubule-associated protein 1B	MAP1B	Homo sapiens (human)	4	1
Q15116	Programmed cell death protein 1	PDCD1 PD1	Homo sapiens (human)	4	0
Q8WWK9	Cytoskeleton-associated protein 2	CKAP2 LB1 TMAP	Homo sapiens (human)	4	2
Q86T13	C-type lectin domain family 14 member A	CLEC14A C14orf27 EGFR5	Homo sapiens (human)	4	8	IgA glomerulonephritis breast cancer cancer embryoma lung adenocarcinoma lung cancer melanoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma skin melanoma thymic carcinoma thymoma
P06729	T-cell surface antigen CD2	CD2 SRBC	Homo sapiens (human)	4	19

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