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UnknownThe mitotic arrest deficient protein MAD2B interacts with the small GTPase RAN throughout the cell cycle.
Not available
S-EPMC2737141 | biostudies-literature
UnknownThe mitotic arrest deficient protein MAD2B interacts with the clathrin light chain A during mitosis.
Not available
S-EPMC2994903 | biostudies-literature
ProteomicsAffinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina - GST
Mutations in WHRN lead to Usher syndrome type 2d (USH2d) or to non-syndromic hearing impairment (DFNB31). The WHRN-encoded gene product whirlin directly interacts with the intracellular regions of the other two Usher syndrome type 2 (USH2)-associated proteins, usherin and ADGRV1. Together with PDZD...
ORGANISM(S): Danio rerio (Zebrafish) (Brachydanio rerio) 
2023-12-28 | PXD034247 | Pride
Complexes Cilia Gst Zebrafish 
UnknownMissense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa.
Not available
S-EPMC5574394 | biostudies-literature
UnknownUsherin defects lead to early-onset retinal dysfunction in zebrafish.
Not available
S-EPMC6054812 | biostudies-literature
UnknownZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature.
Not available
S-EPMC3683717 | biostudies-literature
UnknownThe Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.
Not available
S-EPMC4617701 | biostudies-literature
UnknownActive transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain.
Not available
S-EPMC3854969 | biostudies-literature
UnknownNINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish.
Not available
S-EPMC4617706 | biostudies-literature
UnknownKIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.
Not available
S-EPMC4699358 | biostudies-literature
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