wingless-type MMTV integration site 9B [Mus musculus]

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Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome. [Clin Genet. 2016]
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Waschk DE, Tewes AC, Römer T, Hucke J, Kapczuk K, Schippert C, Hillemanns P, Wieacker P, Ledig S. Clin Genet. 2016 May; 89(5):590-6. Epub 2016 Jan 20.
Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain. [Birth Defects Res A Clin Mol T...]
Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain.
Juriloff DM, Harris MJ, Mager DL, Gagnier L. Birth Defects Res A Clin Mol Teratol. 2014 Oct; 100(10):772-88. Epub 2014 Sep 25.
Molecular cloning and characterization of mouse Wnt14b, clustered with mouse Wnt3 in mouse chromosome 11. [Int J Mol Med. 2002]
Molecular cloning and characterization of mouse Wnt14b, clustered with mouse Wnt3 in mouse chromosome 11.
Kirikoshi H, Katoh M. Int J Mol Med. 2002 Feb; 9(2):135-9.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the Wnt9b gene.

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Gene
Mcm8 minichromosome maintenance 8 homologous recombination repair factor [Mus mu...
Mcm8 minichromosome maintenance 8 homologous recombination repair factor [Mus musculus]
Gene ID:66634

Gene
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