Publication for BBS9 and WDPCP

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
hsa	BBS9	Bardet-Biedl syndrome 9	27241			[link]
hsa	WDPCP	WD repeat containing planar cell polarity effector	51057

Pubmed ID	Priority	Text
24257694	0.97	BBS9, BBS10, TRIM32, BBS12, MKS1, WDPCP, TMEM216, AHI1, and CCDC28B.
28761321	0.97	BBS9 on chromosome 7p14, BBS10 on chromosome 12q21.2, BBS11 (TRIM32) on chromosome 9q33.1, BBS12 on chromosome 4q27, BBS13 (MKS1) on chromosome 17q23, BBS14 (CEP290) on chromosome 12q21.3, BBS15 (C2ORF86) on chromosome 2p15, BBS16 on chromosome 1q43, BBS17 (LZTFL1) on chromosome 3p21.31, BBS18 (BBIP1) on chromosome 10q25.2, BBS19 (IFT27) on chromosome 22q12, BBS20 (IFT172) on chromosome 2p23.3, and BBS21 (C8ORF37) on chromosome 8q22.1.
28143435	0.93	BBS9, BBS10, BBS11 (TRIM32), BBS12, MKS1, CEP290, C2ORF86, SDCCAG8, LZTFL1, BBIP1, IFT27, which account for 70-80% of BBS cases.
29156830	0.93	BBS9 / (PTHB1, 7p14), BBS10 (12q21.2), BBS11/ TRIM32(9q33.1), BBS12 (4q27), BBS13 /MKS1 (17q23), BBS14 / CEP290 (12q21.3), BBS15/C2ORF86 (2p15), BBS16/ SDCCAG8(1q43), BBS17 / LZTFL1 (3p21.31), BBS18/ BBIP1/ BBIP10 (10q25.2) and BBS19 / IFT27(22q12.3).
29263957	0.83	BBS9 (PTHB1) on chr7p14.3, BBS4 on chr15q24.1, BBS7 on chr4q27, BBS5 on chr2q31.1, MKS1 on chr17q22, BBS8 (TTC8) on chr14q31.3, SDCCAG8 on chr1q43-q44, LZTFL1 on chr3p21.31, WDPCP on chr2p15, BBS4 on chr15q24.1, BBS12 on chr4q27, TMEM67 on chr8q22.1, CEP290 on chr12q21.32, TRIM32 on chr9q33.1, BBIP1 on chr10q25.2, chr22q12.3 on IFT27, and IFT172 on chr2p23.3.
23548655	0.54	BBS9, BBS10, BBS11 (TRIM32), BBS12, MKS1, CEP290, C2ORF86, SDCCAG8, and LZTFL1) have been implicated in causing BBS so far.