FRZB Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description frizzled-related protein|The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility. [provided by RefSeq, Apr 2010] (NCBI Entrez Gene Database, 2487)
External Link http://www.ncbi.nlm.nih.gov/gene/2487
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Genes

26 interacting proteins for FRZB from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
BBS10 Bardet-Biedl syndrome 10
EHF ets homologous factor
ELF5 E74-like factor 5 (ets domain transcription factor)
PNO1 partner of NOB1 homolog (S. cerevisiae)
POLA2 polymerase (DNA directed), alpha 2, accessory subunit
RBX1 ring-box 1, E3 ubiquitin protein ligase
SMAD1 SMAD family member 1
WNT1 wingless-type MMTV integration site family, member 1
WNT10A wingless-type MMTV integration site family, member 10A
WNT10B wingless-type MMTV integration site family, member 10B
WNT11 wingless-type MMTV integration site family, member 11
WNT16 wingless-type MMTV integration site family, member 16
WNT2 wingless-type MMTV integration site family member 2
WNT2B wingless-type MMTV integration site family, member 2B
WNT3 wingless-type MMTV integration site family, member 3
WNT3A wingless-type MMTV integration site family, member 3A
WNT4 wingless-type MMTV integration site family, member 4
WNT5A wingless-type MMTV integration site family, member 5A
WNT5B wingless-type MMTV integration site family, member 5B
WNT6 wingless-type MMTV integration site family, member 6
WNT7A wingless-type MMTV integration site family, member 7A
WNT7B wingless-type MMTV integration site family, member 7B
WNT8A wingless-type MMTV integration site family, member 8A
WNT8B wingless-type MMTV integration site family, member 8B
WNT9A wingless-type MMTV integration site family, member 9A
WNT9B wingless-type MMTV integration site family, member 9B