Varaico: Literature-Extracted Genetic Variants

Gene:SIM1
Variant:p.E62K
Back to variants list

SIM1

NM_005068.3:p.E62K

Associated Papers

Novel SIM1 Variants Expanding the Spectrum of SIM1-Related Obesity.

Mohammed I et al.

International Journal of Molecular Sciences, 2026

Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome.

Cheon CK

Annals of Pediatric Endocrinology & Metabolism, 2016

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.

Bonnefond A et al.

The Journal of Clinical Investigation, 2013

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."