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Data · dataset · 2025

Female-specific cone changes from Arr3-deficiency

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Heterozygous variants in ARR3, encoding cone arrestin, have been identified to cause high myopia with a unique X-linked female limited inheritance but the potential mechanism for the unusual anti-X-linked pattern is still unclear.

Description

Arr3 expression profiles showed that Arr3, with significant expression in retina since P14, was almost co-stained with Opsin red/green in cones including some partially co-stained with both Opsin red/green and Opsin blue.

And then Arr3 knock-in mice and Arr3 knock-out rats were generated. Retinal single-cell RNA sequencing was perform to reveal the changes of cone sub-clusters and the differentially expressed genes (DEGs) to explain the mechanism of ARR3-eoHM.

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Inferred from text
RNA sequencing 75% · Sequencing 75% · Single-cell RNA sequencing 75%
Provenance · 1 source records, 12 field assertions
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ScienceDB10.57760/sciencedb.2789012 d agoJSON v1
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