FKRP

Last Update:2016-05-20

FKRP encodes glycosyltransferase-like protein and is considered as a causative gene of limb-girdle muscular dystrophy. FKRP has homology to glycosyltransferase-like protein Fukutin (considered as a causative gene of Fukuyama congenital muscular dystrophy), and thus named as fukutin-related protein (FKRP). The gene-knockout mice exhibit glycan structure alteration of α−dystroglycan. FKRP synthesizes the Rbo5P structure (Rbo5P-Rbo5P-3GalNAcb1-3GlcNAcb1-4(phospho-6)Man-Ser/Thr), the second of the tandem repeats of ribitol 5-phosphate (Rbo5P) in the O-mannose glycan structure of α−dystroglycan. The substrate sugar nucleotide, cytidine diphosphate ribitol (CDP-Rbo) is synthesized by isoprenoid synthase domain-containing protein (ISPD), which is also known as a causative gene of muscular dystrophy.

Keyword: Limb-Girdle muscular dystrophy ,  glycosyltransferase ,  ribitol 5-phosphate (Rbo5P) ,  α−dystroglycan

CDP-Rbo
JCGG-STR033528 JCGG-STR033529

Glycosyltransferase-like


GGDB Symbol FKRP    Alias
DesignationhFKRP
OrganismHomo sapiens
GeneID 79147
HGNC FKRP (17997)
mRNA NM_024301
map19q13.33
Protein NP_077277
EC#    
CAZy
GlyCosmos Glycogenes FKRP
OMIM 606596
Disease name Congenital muscular dystrophy type 1C ,  LGMD2I ,  Limb-girdle muscular dystrophy 2I ,  MDC1C
GDGDB CON00381    CON00382   
Human Protein Atlas ENSG00000181027
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Orthologous Gene

Acceptor Substrates (Reference)

Acceptor Substrates (KEM-C)

Expression

RNA Expression from Human Protein Atlas
This RNA expression data uses "HPA data" from the Human Protein Atlas. Tissue RNA Expression

data available from v22.proteinatlas.org

Expression (Reference)

Gene Ontology

This page does not indicate all of the enzymatic reaction, and expression of "FKRP".