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INVS gene: integrated information on diseases, variants, publications, expression, function, pathways and interactions, from 193 sources on GeneCards.

Inversin is a protein that in humans is encoded by the INVS gene. [5][6] This gene encodes a protein containing multiple ankyrin domains and two IQ calmodulin-binding domains. The encoded protein …

Learn about the INVS gene, its role in epidermal differentiation and skin barrier formation, and its potential association with skin disorders. Explore its function, expression, and related research.

INVS refers to the Inversin 1 gene, also known as nephrocystin 2, which encodes a cytoplasmic protein involved in renal tubular development, left–right axis determination, and interacts with N-cadherin.

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Jul 6, 2026 · Title: A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway. Observational study of gene-disease association.

Clinical resource with information about Infantile nephronophthisis and its clinical features, INVS, available genetic tests from US and labs around the world and links to practice guidelines and …