Skip to search formSkip to main contentSkip to account menu

SYNJ1 wt Allele

Known as: INPP5G, KIAA0910, Synaptojanin 1 wt Allele 
Human SYNJ1 wild-type allele is located in the vicinity of 21q22.2 and is approximately 99 kb in length. This allele, which encodes synaptojanin-1… 
National Institutes of Health

Related topics

Related topics

6 relations
21q22.2DephosphorylationEndocytosisHydrolysis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population
Highly Cited
2014
Highly Cited
2014
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family
SYNJ1 has been recently identified by two independent groups as the gene defective in a novel form of autosomal recessive, early… 
2014
2014
Clinical progression of SYNJ1-related early onset atypical parkinsonism: 3-year follow up of the original Italian family
During the past few years, several Mendelian forms of human parkinsonism have been identified [1]. As regards autosomal recessive… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)