Gene Expression Literature Summary

• Symbol: Mmaa
• Name: methylmalonic aciduria (cobalamin deficiency) type A
• ID: MGI:1923805

2 matching records from 2 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.

Age	E10.5	E11.5	E12.5	A
In situ RNA (section)	2	1	2	1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.

Mmaa  methylmalonic aciduria (cobalamin deficiency) type A   (Synonyms: 2810018E08Rik)
Results	Reference
2	J:112701 Bailey PJ, Klos JM, Andersson E, Karlen M, Kallstrom M, Ponjavic J, Muhr J, Lenhard B, Sandelin A, Ericson J, A global genomic transcriptional code associated with CNS-expressed genes. Exp Cell Res. 2006 Oct 1;312(16):3108-19
4	J:190313 Moreno-Garcia MA, Rosenblatt DS, Jerome-Majewska LA, The methylmalonic aciduria related genes, Mmaa, Mmab, and Mut, are broadly expressed in placental and embryonic tissues during mouse organogenesis. Mol Genet Metab. 2012 Nov;107(3):368-74