Gene Expression Literature Summary

• Symbol: Cecr2
• Name: CECR2, histone acetyl-lysine reader
• ID: MGI:1923799

8 matching records from 8 references.

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

Age	E8	E8.5	E9	E9.5	E10.5	E11.5	E12.5	E13.5	E14.5	E16.5	E18.5	E19.5	P
Immunohistochemistry (section)											1
In situ RNA (section)									1
In situ reporter (knock in)	1		1	2	1	1	1	1	1	1	4	1	2
Western blot											1		1
RT-PCR		1	2										1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Cecr2  CECR2, histone acetyl-lysine reader   (Synonyms: 2610101O16Rik, 2810409N01Rik, cat eye syndrome chromosome region, candidate 2, Gtl4, mKIAA1740)
Results	Reference
7	J:167834 Dawe CE, Kooistra MK, Fairbridge NA, Pisio AC, McDermid HE, Role of chromatin remodeling gene Cecr2 in neurulation and inner ear development. Dev Dyn. 2011 Feb;240(2):372-83
5*	J:302095 Dicipulo R, Norton KA, Fairbridge NA, Kibalnyk Y, Fox SC, Hornberger LK, McDermid HE, Cecr2 mutant mice as a model for human cat eye syndrome. Sci Rep. 2021 Feb 4;11(1):3111
1*	J:153498 Diez-Roux G, Banfi S, Sultan M, Geffers L, Anand S, Rozado D, Magen A, Canidio E, Pagani M, Peluso I, Lin-Marq N, Koch M, Bilio M, Cantiello I, Verde R, De Masi C, Bianchi SA, Cicchini J, Perroud E, Mehmeti S, Dagand E, Schrinner S, Nurnberger A, SchmidtK, Metz K, Zwingmann C, Brieske N, Springer C, Hernandez AM, Herzog S, Grabbe F, Sieverding C, Fischer B, Schrader K, Brockmeyer M, Dettmer S, Helbig C, Alunni V, Battaini MA, Mura C, Henrichsen CN, Garcia-Lopez R, Echevarria D, Puelles E, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582
2*	J:163648 Fairbridge NA, Dawe CE, Niri FH, Kooistra MK, King-Jones K, McDermid HE, Cecr2 mutations causing exencephaly trigger misregulation of mesenchymal/ectodermal transcription factors. Birth Defects Res A Clin Mol Teratol. 2010 Aug;88(8):619-25
1	J:242825 Fong KS, Hufnagel RB, Khadka VS, Corley MJ, Maunakea AK, Fogelgren B, Ahmed ZM, Lozanoff S, A mutation in the tuft mouse disrupts TET1 activity and alters the expression of genes that are crucial for neural tube closure. Dis Model Mech. 2016 May 01;9(5):585-96
1*	J:177709 Kooistra MK, Leduc RY, Dawe CE, Fairbridge NA, Rasmussen J, Man JH, Bujold M, Juriloff D, King-Jones K, McDermid HE, Strain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes. Physiol Genomics. 2012 Jan 18;44(1):35-46
5*	J:306124 Norton KA, Niri F, Weatherill CB, Williams CE, Duong K, McDermid HE, Implantation failure and embryo loss contribute to subfertility in female mice mutant for chromatin remodeler Cecr2. Biol Reprod. 2021 Apr 1;104(4):835-849
3*	J:197015 Thompson PJ, Norton KA, Niri FH, Dawe CE, McDermid HE, CECR2 is involved in spermatogenesis and forms a complex with SNF2H in the testis. J Mol Biol. 2012 Feb 3;415(5):793-806