4WBE, 4WBP407653872ENSG00000135387ENSMUSG00000027184Q14444Q60865NM_005898NM_203364NM_001111289NM_001111290NM_001111291NM_001111292NM_016739NP_005889NP_976240NP_001104759NP_001104760NP_001104761NP_001104762NP_058019Caprin-1 is a protein that in humans is encoded by the CAPRIN1 gene.

[11] In 2022, loss-of-function mutations of the CAPRIN1 gene were shown to result in an autosomal-dominant disorder.

Patients having the newly-discovered disorder suffer from language impairment, speech delay, intellectual disability, ADHD and autism spectrum disorder.

[12] Somatically, they have respiratory problems, limb/skeletal anomalies, developmental delay, feeding difficulties, seizures and ophthalmologic problems.

This article on a gene on human chromosome 11 is a stub.