Protein Domain : LisH domain-containing protein ARMC9 IPR040369

Type  Family
Description  Proteins in this family are mostly from animals. The only characterized protein is LisH domain-containing protein ARMC9, which is localized to the basal body of a cilium and is upregulated during ciliogenesis. Mutations in the ARMC9 gene cause Joubert Syndrome, a recessive neurodevelopmental disorder characterized by hypotonia, ataxia, abnormal eye movements, and variable cognitive impairment [ ].
Short Name  ARMC9

0 Child Features

0 Gene Families

0 Genes

2 Ontology Annotations

0 Parent Features

0 Publications

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