RecName: Full=Spatacsin; AltName: Full=Colorectal carcinoma-associated - Protein

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Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia. [Nutrients. 2022]
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia.
Regensburger M, Krumm L, Schmidt MA, Schmid A, Spatz IT, Marterstock DC, Kopp C, Kohl Z, Doerfler A, Karrasch T, et al. Nutrients. 2022 Nov 13; 14(22). Epub 2022 Nov 13.
"Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers. [J Neurol. 2022]
"Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers.
Rattay TW, Schöls L, Zeltner L, Rohrschneider WK, Ernemann U, Lindig T. J Neurol. 2022 Nov; 269(11):6148-6151. Epub 2022 May 25.
Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study. [J Neurol Sci. 2022]
Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study.
Alfaidi N, Sobahy T, Ali Q, Al Said Y, Karim G, Khan H, Kurdi K, Cupler E. J Neurol Sci. 2022 Mar 15; 434:120144. Epub 2022 Jan 13.

RefSeq genomic sequence
See the genomic reference sequence for the SPG11 gene (NG_008885.1).
RefSeq protein isoforms
See 13 reference sequence protein isoforms for the SPG11 gene.

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Transcript/Protein Information [PANTHER Classification System]
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Protein