Gene Expression Literature Summary

• Symbol: Trp53inp2
• Name: transformation related protein 53 inducible nuclear protein 2
• ID: MGI:1915978

7 matching records from 7 references.

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

Age	E9.5	E10.5	E11	E11.5	E12.5	E13.5	E14.5	E17.5	P
In situ RNA (section)		1		1	1	1	3		1
In situ RNA (whole mount)	1	2	1	1	1	1	1
RT-PCR								1	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

Trp53inp2  transformation related protein 53 inducible nuclear protein 2   (Synonyms: 1110029F20Rik, Tp53inp2)
Results	Reference
1*	J:313619 Bedogni F, Hevner RF, Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development. Front Mol Neurosci. 2021;14:686034
1	J:383028 Bennetts JS, Fowles LF, Butterfield NC, Berkman JL, Teasdale RD, Simpson F, Wicking C, Identification and analysis of novel genes expressed in the mouse embryonic facial primordia. Front Biosci. 2006 Sep 1;11:2631-46
11*	J:118344 Bennetts JS, Rendtorff ND, Simpson F, Tranebjaerg L, Wicking C, The coding region of TP53INP2, a gene expressed in the developing nervous system, is not altered in a family with autosomal recessive non-progressive infantile ataxia on chromosome 20q11-q13. Dev Dyn. 2007 Mar;236(3):843-52
2*	J:276249 Crerar H, Scott-Solomon E, Bodkin-Clarke C, Andreassi C, Hazbon M, Logie E, Cano-Jaimez M, Gaspari M, Kuruvilla R, Riccio A, Regulation of NGF Signaling by an Axonal Untranslated mRNA. Neuron. 2019 May 8;102(3):553-563.e8
1*	J:282838 Fan J, Campioli E, Sottas C, Zirkin B, Papadopoulos V, Amhr2-Cre-Mediated Global Tspo Knockout. J Endocr Soc. 2020 Feb 1;4(2):bvaa001
1*	J:138815 Kawaguchi A, Ikawa T, Kasukawa T, Ueda HR, Kurimoto K, Saitou M, Matsuzaki F, Single-cell gene profiling defines differential progenitor subclasses in mammalian neurogenesis. Development. 2008 Sep;135(18):3113-24
1*	J:367387 Zhang B, Pan X, Chi D, Wang Y, Ruan W, Ma J, Duan X, Huang Y, Arhgap29 Deficiency Directly Leads to Systemic and Craniofacial Skeletal Abnormalities. Int J Mol Sci. 2025 May 13;26(10)