receptor expression-enhancing protein 2 isoform 2 [Homo sapiens]

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A Nepalese family with an REEP2 mutation: clinical and genetic study. [J Hum Genet. 2021]
A Nepalese family with an REEP2 mutation: clinical and genetic study.
Nan H, Takaki R, Hata T, Koh K, Takiyama Y. J Hum Genet. 2021 Jul; 66(7):749-752. Epub 2021 Feb 1.
De novo REEP2 missense mutation in pure hereditary spastic paraplegia. [Ann Clin Transl Neurol. 2017]
De novo REEP2 missense mutation in pure hereditary spastic paraplegia.
Roda RH, Schindler AB, Blackstone C. Ann Clin Transl Neurol. 2017 May; 4(5):347-350. Epub 2017 Apr 11.
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. [Am J Hum Genet. 2014]
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.
Esteves T, Durr A, Mundwiller E, Loureiro JL, Boutry M, Gonzalez MA, Gauthier J, El-Hachimi KH, Depienne C, Muriel MP, et al. Am J Hum Genet. 2014 Feb 6; 94(2):268-77. Epub 2014 Jan 2.

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SNP
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NP_057690 [Domain Mapping of Disease Mut...]
NP_057690
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
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome

receptor expression-enhancing protein 2 isoform 2 [Homo sapiens]
receptor expression-enhancing protein 2 isoform 2 [Homo sapiens]
gi|42476206|ref|NP_057690.2|

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