phosphatidylserine decarboxylase proenzyme, mitochondrial isoform d [H - Protein

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Conditional targeting of phosphatidylserine decarboxylase to lipid droplets. [Biol Open. 2021]
Conditional targeting of phosphatidylserine decarboxylase to lipid droplets.
Kumar S, Chitraju C, Farese RV Jr, Walther TC, Burd CG. Biol Open. 2021 Mar 3; 10(3). Epub 2021 Mar 3.
The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in thePISD gene. [Genet Med. 2019]
The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in thePISD gene.
Peter VG, Quinodoz M, Pinto-Basto J, Sousa SB, Di Gioia SA, Soares G, Ferraz Leal G, Silva ED, Pescini Gobert R, Miyake N, et al. Genet Med. 2019 Dec; 21(12):2734-2743. Epub 2019 Jul 2.
PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes. [Life Sci Alliance. 2019]
PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes.
Zhao T, Goedhart CM, Sam PN, Sabouny R, Lingrell S, Cornish AJ, Lamont RE, Bernier FP, Sinasac D, Parboosingh JS, et al. Life Sci Alliance. 2019 Apr; 2(2). Epub 2019 Mar 11.

RefSeq genomic sequence
See the genomic reference sequence for the PISD gene (NG_050741.1).
RefSeq mRNA
See reference mRNA sequence for the PISD gene (NM_001326416.2).
RefSeq protein isoforms
See 13 reference sequence protein isoforms for the PISD gene.

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Taxonomy Links for Protein (Select 973583883) (1)
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Nucleotide Links for Protein (Select 2217321145) (2)
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Related DataSets for GEO Profiles (Select 50532713) (1)
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Confluent and sub-confluent umbilical vein endothelial cell cultures
Confluent and sub-confluent umbilical vein endothelial cell cultures
Accession: GDS3177

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Taxonomy Links for Protein (Select 767992635) (1)
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