GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NPG1	Frizzled-3	FZD3	4	2
Q14332	Frizzled-2	FZD2	8	4
Q9ULW2	Frizzled-10	FZD10	3	0
Q9UP38	Frizzled-1	FZD1	4	3
Q01543	Friend leukemia integration 1 transcription factor	FLI1	14	2
Q5NUL3	Free fatty acid receptor 4	FFAR4 GPR120 GPR129 O3FAR1 PGR4	1	0
O14843	Free fatty acid receptor 3	FFAR3 GPR41	1	0
O15552	Free fatty acid receptor 2	FFAR2 FFA2 GPCR43 GPR43	2	0
O14842	Free fatty acid receptor 1	FFAR1 GPR40	1	0
Q06787	Fragile X messenger ribonucleoprotein 1	FMR1	1	2
P78423	Fractalkine	CX3CL1 FKN NTT SCYD1	13	12
Q86VR8	Four-jointed box protein 1	FJX1	1	0
Q13643	Four and a half LIM domains protein 3	FHL3 SLIM2	1	1
Q14192	Four and a half LIM domains protein 2	FHL2 DRAL SLIM3	0	1
Q13642	Four and a half LIM domains protein 1	FHL1 SLIM1	2	2
P15408	Fos-related antigen 2	FOSL2 FRA2	7	2
P15407	Fos-related antigen 1	FOSL1 FRA1	0	1
Q8NBK3	Formylglycine-generating enzyme	SUMF1	2	12	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
Q8IVF7	Formin-like protein 3	FMNL3 FHOD3 FRL2 KIAA2014 WBP3	3	1
Q96PY5	Formin-like protein 2	FMNL2 FHOD2 KIAA1902	4	1
O95466	Formin-like protein 1	FMNL1 C17orf1 C17orf1B FMNL FRL1	1	1
Q8N3X1	Formin-binding protein 4	FNBP4 FBP30 KIAA1014	18	2
Q96RU3	Formin-binding protein 1	FNBP1 FBP17 KIAA0554	2	1
Q9NZ56	Formin-2	FMN2	0	1
Q68DA7	Formin-1	FMN1 FMN LD	1	2

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