Homo sapiens proline-serine-threonine phosphatase interacting protein - Nucleotide

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PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review. [Genes (Basel). 2023]
PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review.
Mejbri M, Renella R, Candotti F, Jaques C, Holzinger D, Hofer M, Theodoropoulou K. Genes (Basel). 2023 Aug 19; 14(8). Epub 2023 Aug 19.
Rare missense variants in the SH3 domain of PSTPIP1 are associated with hidradenitis suppurativa. [HGG Adv. 2023]
Rare missense variants in the SH3 domain of PSTPIP1 are associated with hidradenitis suppurativa.
Morales-Heil DJ, Cao L, Sweeney C, Malara A, Brown F, Milam P, Anadkat M, Kaffenberger J, Kaffenberger B, Nagele P, et al. HGG Adv. 2023 Apr 13; 4(2):100187. Epub 2023 Mar 13.
Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype. [Rheumatology (Oxford). 2023]
Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.
Özkılınç Önen M, Onat UI, Uğurlu S, Timuçin AC, Öz Arslan D, Everest E, Özdoğan H, Tahir Turanlı E. Rheumatology (Oxford). 2023 Sep 1; 62(9):3188-3196.

RefSeq alternative splicing
See 29 reference mRNA sequence splice variants for the PSTPIP1 gene.
RefSeq protein product
See the reference protein sequence for proline-serine-threonine phosphatase-interacting protein 1 isoform 2 (NP_001308064.1).

Protein
Protein sequence from Nucleotide coding region
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OMIM
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Nucleotide