RecName: Full=Mesoderm posterior protein 2; AltName: Full=Class C basi - Protein

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MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation. [J Mol Med (Berl). 2020]
MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation.
Zhang E, Yang J, Liu Y, Hong N, Xie H, Fu Q, Li F, Chen S, Yu Y, Sun K. J Mol Med (Berl). 2020 Jul; 98(7):1035-1048. Epub 2020 Jun 22.
Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome. [Am J Hum Genet. 2008]
Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome.
Cornier AS, Staehling-Hampton K, Delventhal KM, Saga Y, Caubet JF, Sasaki N, Ellard S, Young E, Ramirez N, Carlo SE, et al. Am J Hum Genet. 2008 Jun; 82(6):1334-41. Epub 2008 May 15.
Phenotype characterization and natural history of spondylothoracic dysplasia syndrome: a series of 27 new cases. [Am J Med Genet A. 2004]
Phenotype characterization and natural history of spondylothoracic dysplasia syndrome: a series of 27 new cases.
Cornier AS, Ramírez N, Arroyo S, Acevedo J, García L, Carlo S, Korf B. Am J Med Genet A. 2004 Jul 15; 128A(2):120-6.

RefSeq genomic sequence
See the genomic reference sequence for the MESP2 gene (NG_008608.2).
RefSeq protein
See the reference protein sequence for mesoderm posterior protein 2 (NP_001035047.1).

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Q0VG99 [Domain Mapping of Disease Mut...]
Q0VG99
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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