ADP-ribosylation factor-like protein 6-interacting protein 1 isoform 1 - 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 mRNA
See reference mRNA sequence for the ARL6IP1 gene (NM_015161.3).
RefSeq protein isoforms
See the other reference sequence protein isoform for the ARL6IP1 gene (NP_001300787.1).

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NP_055976 [Domain Mapping of Disease Mut...]
NP_055976
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

Invertebrate sample from Beaufort Sea
Invertebrate sample from Beaufort Sea

biosample

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Protein