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ENSDARP00000060652 | Si:ch211-57i17.5. (199 aa) | ||||
ush2a | Usher syndrome 2A (autosomal recessive, mild). (5236 aa) | ||||
TMC1 | Transmembrane channel-like protein 1; Probable ion channel required for the normal function of hair cells (By similarity). Component of the hair cell's mechanotransduction (MET) machinery ; Belongs to the TMC family. (990 aa) | ||||
whrna | Whirlin a. (939 aa) | ||||
whrnb | Whirlin b. (946 aa) | ||||
rp2 | Protein XRP2; Acts as a GTPase-activating protein (GAP) involved in trafficking between the Golgi and the ciliary membrane (By similarity). Acts as a GTPase-activating protein (GAP) for tubulin in concert with tubulin-specific chaperone C, but does not enhance tubulin heterodimerization (By similarity). In the retina, required for maintenance of rod and cone photoreceptor cells. May have a role in normal retinal localization of the transducins GNB1 and GNAT1, and the rhodopsin kinase GRK1. (376 aa) | ||||
pdzd7a | PDZ domain-containing 7a. (954 aa) | ||||
adgrv1 | Adhesion G-protein coupled receptor V1; Receptor that may have an important role in the development of the sensory nervous system. (6198 aa) |