serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A al - Protein

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PPP2R1A neurodevelopmental disorder is associated with congenital heart defects. [Am J Med Genet A. 2022]
PPP2R1A neurodevelopmental disorder is associated with congenital heart defects.
Baker EK, Solivio B, Pode-Shakked B, Cross LA, Sullivan B, Raas-Rothschild A, Chorin O, Barel O, Bar-Yosef O, Husami A, et al. Am J Med Genet A. 2022 Nov; 188(11):3262-3277. Epub 2022 Aug 15.
PPP2R1A-Related Neurodevelopmental Disorder. [GeneReviews(®). 1993]
PPP2R1A-Related Neurodevelopmental Disorder.
Douzgou S, Janssens V, Houge G. GeneReviews(®). 1993-2024. 2022 May 12
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction. [Genet Med. 2021]
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction.
Lenaerts L, Reynhout S, Verbinnen I, Laumonnier F, Toutain A, Bonnet-Brilhault F, Hoorne Y, Joss S, Chassevent AK, Smith-Hicks C, et al. Genet Med. 2021 Feb; 23(2):352-362. Epub 2020 Oct 27.

RefSeq genomic sequence
See the genomic reference sequence for the PPP2R1A gene (NG_047068.2).
RefSeq mRNA
See reference mRNA sequence for the PPP2R1A gene (NM_001363656.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the PPP2R1A gene (NP_055040.2).

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource

FYN-binding protein 1 isoform X2 [Homo sapiens]
FYN-binding protein 1 isoform X2 [Homo sapiens]
gi|2217355448|ref|XP_047273028.1|

Protein
medium tumor antigen-associated 61-kD protein, partial [Homo sapiens]
medium tumor antigen-associated 61-kD protein, partial [Homo sapiens]
gi|178663|gb|AAA35531.1|

Protein
txid28119[Organism] (1)
SRA
OR13C3[gene] (67)
ClinVar
ORF1a polyprotein [Allamanda chlorotic virus A]
ORF1a polyprotein [Allamanda chlorotic virus A]
gi|2664215573|gb|WVH15858.1|

Protein

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