pre-mRNA-processing factor 17 [Mus musculus]

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Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly. [Neuron. 2021]
Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly.
Chai G, Webb A, Li C, Antaki D, Lee S, Breuss MW, Lang N, Stanley V, Anzenberg P, Yang X, et al. Neuron. 2021 Jan 20; 109(2):241-256.e9. Epub 2020 Nov 20.
Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations. [Bioinformatics. 2019]
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations.
Tang H, Finn RD, Thomas PD. Bioinformatics. 2019 Feb 1; 35(3):518-520.

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Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

pre-mRNA-processing factor 17 [Mus musculus]
pre-mRNA-processing factor 17 [Mus musculus]
gi|198278501|ref|NP_082155.1|

Protein
Hypophosphatemia
Hypophosphatemia
A condition of an abnormally low level of PHOSPHATES in the blood.<br/>Year introduced: 1994

MeSH
Protein Tyrosine Phosphatase, Non-Receptor Type 22
Protein Tyrosine Phosphatase, Non-Receptor Type 22
A subtype of non-receptor protein tyrosine phosphatases that is characterized by the presence of an N-terminal catalytic domain and a C-terminal PROLINE-rich domain. The phosp...<br/>Year introduced: 2008(1999)

MeSH

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Protein