coiled-coil domain-containing protein 32 isoform X1 [Mus musculus]

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Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies. [Hum Mol Genet. 2020]
Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies.
Harel T, Griffin JN, Arbogast T, Monroe TO, Palombo F, Martinelli M, Seri M, Pippucci T, Elpeleg O, Katsanis N. Hum Mol Genet. 2020 Jun 3; 29(9):1489-1497.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. [Brief Bioinform. 2011]
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD. Brief Bioinform. 2011 Sep; 12(5):449-62. Epub 2011 Aug 27.
A high-resolution anatomical atlas of the transcriptome in the mouse embryo. [PLoS Biol. 2011]
A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Diez-Roux G, Banfi S, Sultan M, Geffers L, Anand S, Rozado D, Magen A, Canidio E, Pagani M, Peluso I, et al. PLoS Biol. 2011 Jan 18; 9(1):e1000582. Epub 2011 Jan 18.

RefSeq mRNA
See reference mRNA sequence for the Ccdc32 gene (XM_011239574.1).
RefSeq protein isoforms
See the other reference sequence protein isoform for the Ccdc32 gene (NP_955014.2).

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coiled-coil domain-containing protein 32 isoform X1 [Mus musculus]
coiled-coil domain-containing protein 32 isoform X1 [Mus musculus]
gi|755499758|ref|XP_011237876.1|

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