SDCCAG8 gene. This protein localizes to the centrioles. Mutations in SDCCAG8 have been found to cause nephronophthisis-related ciliopathies. SDCCAG8 has...
4 KB (480 words) - 17:48, 11 October 2022
P31431 14425 SDCBP HGNC:10662 O00560 14426 SDCBP2 HGNC:15756 Q9H190 14427 SDCCAG8 HGNC:10671 Q86SQ7 14428 SDE2 HGNC:26643 Q6IQ49 14429 SDF2 HGNC:10675 Q99470...
282 KB (17 words) - 18:42, 6 October 2024
RSPH9, LRRC50 Senior–Løken syndrome 266900 NPHP1, NPHP4, IQCB1, CEP290, SDCCAG8 Eye Sensenbrenner syndrome (cranioectodermal dysplasia) 218330 IFT122 Short...
35 KB (2,499 words) - 18:40, 12 July 2024
BBS10, TRIM32 (BBS11), BBS12, MKS1 (BBS13), CEP290 (BBS14), WDPCP (BBS15), SDCCAG8 (BBS16), LZTFL1 (BBS17), BBIP1 (BBS18), IFT27 (BBS19), IFT72 (BBS20), and...
18 KB (2,184 words) - 17:44, 17 April 2024
Type OMIM Genes SLSN1 266900 NPHP1 SLSN3 606995 unknown SLSN4 606996 NPHP4 SLSN5 609254 NPHP5/IQCB1 SLSN6 610189 NPHP6/CEP290 SLSN7 613615 SDCCAG8...
5 KB (374 words) - 18:43, 5 November 2023