RPGRIP1L
RPGRIP1-like
Sinónimos:
CORS3, FTM, JBTS7, MKS5, NPHP8
Especie:
Human RPGRIP1L (23322), Mouse Rpgrip1l (244585), Rat Rpgrip1l (307724), dog RPGRIP1L (487278), domestic guinea pig Rpgrip1l (100715832), Zebrafish rpgrip1l (557688), Horse RPGRIP1L (100050527), Domestic Rabbit RPGRIP1L (100354520), naked mole-rat Rpgrip1l (101699328), sheep RPGRIP1L (101115055) ...Más
ID UniProtKB:
ID del gen:
- Human(23322) Summary: The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
- Mouse(244585) Rpgrip1-like
- Rat(307724) Rpgrip1-like
- dog(487278) RPGRIP1-like
- domestic guinea pig(100715832) RPGRIP1-like
- Zebrafish(557688) RPGRIP1-like
- Horse(100050527) RPGRIP1-like
- Domestic Rabbit(100354520) RPGRIP1-like
- naked mole-rat(101699328) RPGRIP1-like
- sheep(101115055) RPGRIP1-like
- chicken(425392) RPGRIP1-like
- cow(518659) RPGRIP1-like
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