Rattus norvegicus FRAS1 related extracellular matrix 2 (Frem2), mRNA

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Loss-of-function mutations in FREM2 disrupt eye morphogenesis. [Exp Eye Res. 2019]
Loss-of-function mutations in FREM2 disrupt eye morphogenesis.
Zhang X, Wang D, Dongye M, Zhu Y, Chen C, Wang R, Long E, Liu Z, Wu X, Lin D, et al. Exp Eye Res. 2019 Apr; 181:302-312. Epub 2019 Feb 22.
A homozygous mutation p.Arg2167Trp in FREM2 causes isolated cryptophthalmos. [Hum Mol Genet. 2018]
A homozygous mutation p.Arg2167Trp in FREM2 causes isolated cryptophthalmos.
Yu Q, Lin B, Xie S, Gao S, Li W, Liu Y, Wang H, Huang D, Xie Z. Hum Mol Genet. 2018 Jul 1; 27(13):2357-2366.
Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology. [Dev Biol. 2016]
Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.
Palmer K, Fairfield H, Borgeia S, Curtain M, Hassan MG, Dionne L, Yong Karst S, Coombs H, Bronson RT, Reinholdt LG, et al. Dev Biol. 2016 Jul 15; 415(2):216-227. Epub 2015 Jul 31.

RefSeq protein product
See the reference protein sequence for FRAS1-related extracellular matrix protein 2 precursor (NP_001232907.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide