SIAH1 short protein [Homo sapiens]

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Siah1 in cancer and nervous system diseases (Review). [Oncol Rep. 2022]
Siah1 in cancer and nervous system diseases (Review).
Zhang H, Wang J, Ge Y, Ye M, Jin X. Oncol Rep. 2022 Feb; 47(2). Epub 2021 Dec 27.
miR-129-5p Ameliorates Ischemic Brain Injury by Binding to SIAH1 and Activating the mTOR Signaling Pathway. [J Mol Neurosci. 2021]
miR-129-5p Ameliorates Ischemic Brain Injury by Binding to SIAH1 and Activating the mTOR Signaling Pathway.
Lei Y, Jin X, Sun M, Ji Z. J Mol Neurosci. 2021 Sep; 71(9):1761-1771. Epub 2021 Aug 5.
De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features. [J Med Genet. 2021]
De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features.
Buratti J, Ji L, Keren B, Lee Y, Booke S, Erdin S, Kim SY, Palculict TB, Meiner V, Chae JH, et al. J Med Genet. 2021 Mar; 58(3):205-212. Epub 2020 May 19.

RefSeq protein isoforms
See 6 reference sequence protein isoforms for the SIAH1 gene.

Nucleotide
Nucleotide sequence from coding region
Taxonomy
Taxonomy sequences associated with protein record
BioSystems
BioSystems
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PubMed (Weighted)
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Related Structures (List)
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Dryad Digital Repository [Dryad Digital Repository]
Dryad Digital Repository
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Evolutionary Trace of Functional Site [Evolutionary Trace of Functio...]
Evolutionary Trace of Functional Site

seven in absentia homolog [Homo sapiens]
seven in absentia homolog [Homo sapiens]
gi|3041825|gb|AAC12950.1|

Protein
Myelin tomacula
Myelin tomacula

MedGen

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Protein