LRRN1

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For Research Use Only. Not For Clinical Use.


Background

LRRN1 (Leucine Rich Repeat Neuronal 1) is a Protein Coding gene. Diseases associated with LRRN1 include Corneal Dystrophy, Posterior Polymorphous, 1 and Autism Spectrum Disorder. An important paralog of this gene is LRRN3.
Predicted location

Membrane

Single cell type specificity

Cell type enriched (Oligodendrocyte precursor cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enhanced (AF22, CAPAN-2, HAP1, NTERA-2, SuSa)

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