Gene Expression Literature Summary

• Symbol: Hnrnpa2b1
• Name: heterogeneous nuclear ribonucleoprotein A2/B1
• ID: MGI:104819

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	E0.5	E3.5	E12.5	E13.5	E15	E19	P
In situ RNA (section)			1	1
Immunohistochemistry (whole mount)	1
Western blot				1	1	1	4
RT-PCR	1	1					4
cDNA clones			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

Hnrnpa2b1  heterogeneous nuclear ribonucleoprotein A2/B1   (Synonyms: 9130414A06Rik, Hnrpa2, Hnrpa2b1)
Results	Reference
3	J:311486 Chalupnikova K, Solc P, Sulimenko V, Sedlacek R, Svoboda P, An oocyte-specific ELAVL2 isoform is a translational repressor ablated from meiotically competent antral oocytes. Cell Cycle. 2014;13(7):1187-200
1	J:23142 Ferreira J, Carmo-Fonseca M, The biogenesis of the coiled body during early mouse development. Development. 1995 Feb;121(2):601-12
2	J:249066 Gompers AL, Su-Feher L, Ellegood J, Copping NA, Riyadh MA, Stradleigh TW, Pride MC, Schaffler MD, Wade AA, Catta-Preta R, Zdilar I, Louis S, Kaushik G, Mannion BJ, Plajzer-Frick I, Afzal V, Visel A, Pennacchio LA, Dickel DE, Lerch JP, Crawley JN, Zarbalis KS, Silverman JL, Nord AS, Germline Chd8 haploinsufficiency alters brain development in mouse. Nat Neurosci. 2017 Aug;20(8):1062-1073
3	J:286293 Li M, Zhuang Y, Batra R, Thomas JD, Li M, Nutter CA, Scotti MM, Carter HA, Wang ZJ, Huang XS, Pu CQ, Swanson MS, Xie W, HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy. Proc Natl Acad Sci U S A. 2020 Mar 10;117(10):5472-5477
2*	J:238260 Liu TY, Chen YC, Jong YJ, Tsai HJ, Lee CC, Chang YS, Chang JG, Chang YF, Muscle developmental defects in heterogeneous nuclear Ribonucleoprotein A1 knockout mice. Open Biol. 2017 Jan;7(1)
3*	J:93141 Mattar P, Britz O, Johannes C, Nieto M, Ma L, Rebeyka A, Klenin N, Polleux F, Guillemot F, Schuurmans C, A screen for downstream effectors of Neurogenin2 in the embryonic neocortex. Dev Biol. 2004 Sep 15;273(2):373-89
2	J:323057 Verdile V, Svetoni F, La Rosa P, Ferrante G, Cesari E, Sette C, Paronetto MP, EWS splicing regulation contributes to balancing Foxp1 isoforms required for neuronal differentiation. Nucleic Acids Res. 2022 Apr 8;50(6):3362-3378
1	J:339368 Yao F, Huang S, Liu J, Tan C, Xu M, Wang D, Huang M, Zhu Y, Huang X, He S, Deletion of ARGLU1 causes global defects in alternative splicing in vivo and mouse cortical malformations primarily via apoptosis. Cell Death Dis. 2023 Aug 23;14(8):543