Mus musculus Protein: Mfrp
Summary
InnateDB Protein IDBP-541899.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Mfrp
Protein Name membrane-type frizzled-related protein
Synonyms
Species Mus musculus
Ensembl Protein ENSMUSP00000124456
InnateDB Gene IDBG-155695 (Mfrp)
Protein Structure
UniProt Annotation
Function May play a role in eye development.
Subcellular Localization Apical cell membrane {ECO:0000269PubMed:17122143}; Single-pass type II membrane protein {ECO:0000269PubMed:17122143}.
Disease Associations Note=Defects in Mfrp are the cause of retinal degeneration 6 (RD6). RD6 is an autosomal recessive degeneration of the photoreceptors causing dysfunction of both rods and cones.
Tissue Specificity Expressed in retinal pigment epithelium and ciliary epithelium of the eye. {ECO:0000269PubMed:12140190, ECO:0000269PubMed:17122143}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID MGI:2385957
InterPro IPR000859 CUB domain
IPR002172 Low-density lipoprotein (LDL) receptor class A repeat
IPR020067 Frizzled domain
PFAM PF00431
PF00057
PF01392
PRINTS PR00261
PIRSF
SMART SM00042
SM00192
SM00063
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8K480
PhosphoSite PhosphoSite-Q8K480
TrEMBL
UniProt Splice Variant
Entrez Gene 259172
UniGene Mm.227110
RefSeq NP_001177243
MGI ID
MGI Symbol Mfrp
OMIM
CCDS CCDS52776
HPRD
IMGT
EMBL AF469650 AK053629
GenPept AAM89216 BAC35452