E3 ubiquitin-protein ligase RNF170 isoform a [Homo sapiens]

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RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement. [Eur J Neurol. 2022]
RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement.
Van Daele SH, Moisse M, Race V, Van Eesbeeck A, Keldermans L, Vermeer S, Van Esch H, Claeys KG, Van Damme P. Eur J Neurol. 2022 Jan; 29(1):345-349. Epub 2021 Sep 17.
RNF170-Related Hereditary Spastic Paraplegia: Confirmation by a Novel Mutation. [Mov Disord. 2021]
RNF170-Related Hereditary Spastic Paraplegia: Confirmation by a Novel Mutation.
de Sainte Agathe JM, Mercier S, Mahé JY, Péréon Y, Buratti J, Tissier L, Kol B, Said SA, Leguern É, Banneau G, et al. Mov Disord. 2021 Mar; 36(3):771-774. Epub 2020 Nov 9.
Mutation in RNF170 causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimic. [J Neurol Neurosurg Psychiatry....]
Mutation in RNF170 causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimic.
Cortese A, Callegari I, Currò R, Vegezzi E, Colnaghi S, Versino M, Alfonsi E, Cosentino G, Valente E, Gana S, et al. J Neurol Neurosurg Psychiatry. 2020 Nov; 91(11):1237-1238. Epub 2020 Sep 17.

RefSeq mRNA
See reference mRNA sequence for the RNF170 gene (NM_001160223.2).
RefSeq protein isoforms
See 33 reference sequence protein isoforms for the RNF170 gene.

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NP_001153695 [Domain Mapping of Disease Mut...]
NP_001153695
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
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GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

calpain-3b [Oryzias melastigma]
calpain-3b [Oryzias melastigma]
gi|1910594924|ref|XP_036066336.1|

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