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 **14276 - 14300** 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
Q9NPG1	Frizzled-3	FZD3	Homo sapiens (human)	4	2
Q14332	Frizzled-2	FZD2	Homo sapiens (human)	8	4
Q9ULW2	Frizzled-10	FZD10	Homo sapiens (human)	3	0
Q9UP38	Frizzled-1	FZD1	Homo sapiens (human)	4	3
Q01543	Friend leukemia integration 1 transcription factor	FLI1	Homo sapiens (human)	14	2
Q5NUL3	Free fatty acid receptor 4	FFAR4 GPR120 GPR129 O3FAR1 PGR4	Homo sapiens (human)	1	0
O14843	Free fatty acid receptor 3	FFAR3 GPR41	Homo sapiens (human)	1	0
O15552	Free fatty acid receptor 2	FFAR2 FFA2 GPCR43 GPR43	Homo sapiens (human)	2	0
O14842	Free fatty acid receptor 1	FFAR1 GPR40	Homo sapiens (human)	1	0
Q06787	Fragile X messenger ribonucleoprotein 1	FMR1	Homo sapiens (human)	1	2
P78423	Fractalkine	CX3CL1 FKN NTT SCYD1	Homo sapiens (human)	13	12
Q86VR8	Four-jointed box protein 1	FJX1	Homo sapiens (human)	1	0
Q13643	Four and a half LIM domains protein 3	FHL3 SLIM2	Homo sapiens (human)	1	1
Q14192	Four and a half LIM domains protein 2	FHL2 DRAL SLIM3	Homo sapiens (human)	0	1
Q13642	Four and a half LIM domains protein 1	FHL1 SLIM1	Homo sapiens (human)	2	2
P15408	Fos-related antigen 2	FOSL2 FRA2	Homo sapiens (human)	7	2
P15407	Fos-related antigen 1	FOSL1 FRA1	Homo sapiens (human)	0	1
Q8NBK3	Formylglycine-generating enzyme	SUMF1	Homo sapiens (human)	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	Homo sapiens (human)	3	1
Q96PY5	Formin-like protein 2	FMNL2 FHOD2 KIAA1902	Homo sapiens (human)	4	1
O95466	Formin-like protein 1	FMNL1 C17orf1 C17orf1B FMNL FRL1	Homo sapiens (human)	1	1
Q8N3X1	Formin-binding protein 4	FNBP4 FBP30 KIAA1014	Homo sapiens (human)	18	2
Q96RU3	Formin-binding protein 1	FNBP1 FBP17 KIAA0554	Homo sapiens (human)	2	1
Q9NZ56	Formin-2	FMN2	Homo sapiens (human)	0	1
Q68DA7	Formin-1	FMN1 FMN LD	Homo sapiens (human)	1	2

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