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 **16376 - 16400** 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
Q14DG7	Transmembrane protein 132B	TMEM132B KIAA1786 KIAA1906	Homo sapiens (human)	5	1
Q695T7	Sodium-dependent neutral amino acid transporter B(0)AT1	SLC6A19 B0AT1	Homo sapiens (human)	5	0
O75022	Leukocyte immunoglobulin-like receptor subfamily B member 3	LILRB3 ILT5 LIR3	Homo sapiens (human)	5	1
O15054	Lysine-specific demethylase 6B	KDM6B JMJD3 KIAA0346	Homo sapiens (human)	5	1
P29017	T-cell surface glycoprotein CD1c	CD1C	Homo sapiens (human)	5	0
Q15375	Ephrin type-A receptor 7	EPHA7 EHK3 HEK11	Homo sapiens (human)	5	2
Q9Y2U8	Inner nuclear membrane protein Man1	LEMD3 MAN1	Homo sapiens (human)	5	7
O95721	Synaptosomal-associated protein 29	SNAP29	Homo sapiens (human)	5	2
Q8WU66	Thrombospondin-type laminin G domain and EAR repeat-containing protein	TSPEAR C21orf29	Homo sapiens (human)	5	0
Q02952	A-kinase anchor protein 12	AKAP12 AKAP250	Homo sapiens (human)	5	1
P10809	60 kDa heat shock protein, mitochondrial	HSPD1 HSP60	Homo sapiens (human)	5	6
Q04671	P protein	OCA2 D15S12 P	Homo sapiens (human)	5	1
Q96E93	Killer cell lectin-like receptor subfamily G member 1	KLRG1 CLEC15A MAFA MAFAL	Homo sapiens (human)	5	1
P35232	Prohibitin 1	PHB1 PHB	Homo sapiens (human)	5	3
P38435	Vitamin K-dependent gamma-carboxylase	GGCX GC	Homo sapiens (human)	5	7
Q9H5K3	Protein O-mannose kinase	POMK SGK196	Homo sapiens (human)	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia 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 bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia 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 ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
O75147	Obscurin-like protein 1	OBSL1 KIAA0657	Homo sapiens (human)	5	1
Q9NUL3	Double-stranded RNA-binding protein Staufen homolog 2	STAU2	Homo sapiens (human)	5	2
Q969V6	Myocardin-related transcription factor A	MRTFA KIAA1438 MAL MKL1	Homo sapiens (human)	5	2
Q5SSJ5	Heterochromatin protein 1-binding protein 3	HP1BP3	Homo sapiens (human)	5	1
Q4G0M1	Erythroferrone	ERFE C1QTNF15 CTRP15 FAM132B	Homo sapiens (human)	5	2
Q9Y662	Heparan sulfate glucosamine 3-O-sulfotransferase 3B1	HS3ST3B1 3OST3B1 HS3ST3B	Homo sapiens (human)	5	1	bladder carcinoma breast cancer endometriosis of ovary endometriosis of uterus endometriosis hepatitis B lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma urinary bladder cancer
P21453	Sphingosine 1-phosphate receptor 1	S1PR1 CHEDG1 EDG1	Homo sapiens (human)	5	4
P24071	Immunoglobulin alpha Fc receptor	FCAR CD89	Homo sapiens (human)	5	0
Q9NYB5	Solute carrier organic anion transporter family member 1C1	SLCO1C1 OATP14 OATP1C1 OATPF SLC21A14	Homo sapiens (human)	5	1

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