BBS4
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Template:Short description Template:Infobox gene Bardet–Biedl syndrome 4 is a protein that in humans is encoded by the BBS4 gene.[1][2][3]
This gene encodes a protein which contains tetratricopeptide repeats (TPR), similar to O-linked N-acetylglucosamine transferase. Mutations in this gene have been observed in patients with Bardet–Biedl syndrome type 4. The encoded protein may play a role in pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation.[3]
Interactions
BBS4 has been shown to interact with DCTN1.[4]
References
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Further reading
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