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Results for "WHRN": 1 gene, 2 gene sets

Name

WHRN Gene

whirlin

This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]

WHRN Gene Set

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the WHRN gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.

Whrn homodimer complex Gene Set

From CORUM Protein Complexes

proteins in the Whrn homodimer complex protein complex from the CORUM Protein Complexes dataset.