RecName: Full=ADP-ribosylation factor-like protein 6-interacting prote - Protein

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Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia. [Clin Genet. 2021]
Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia.
Cao Y, Manning M, Pope K, He W, Vetrini F, Siskind C, Rosenfeld JA, Yang Y, Xiao R. Clin Genet. 2021 Mar; 99(3):477-480. Epub 2020 Nov 13.
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia. [BMC Med Genet. 2019]
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia.
Wakil SM, Alhissi S, Al Dossari H, Alqahtani A, Shibin S, Melaiki BT, Finsterer J, Al-Hashem A, Bohlega S, Alazami AM. BMC Med Genet. 2019 Jul 4; 20(1):119. Epub 2019 Jul 4.
A new case of infantile-onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family. [Eur J Neurol. 2019]
A new case of infantile-onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family.
Chukhrova AL, Akimova IA, Shchagina OA, Kadnikova VA, Ryzhkova OP, Polyakov AV. Eur J Neurol. 2019 May; 26(5):e61-e62.

RefSeq genomic sequence
See the genomic reference sequence for the ARL6IP1 gene (NG_042860.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the ARL6IP1 gene.

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Q15041 [Domain Mapping of Disease Mut...]
Q15041
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
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reagents [ExactAntigen/Labome]
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Protein