Sequence Detail

ID/Version

P97822 Q3TX26 Q8C2L4 Q8BPF8 Q9CZD2 E9Q5H9 Q8C7Q8 Q3TH89 (UniProt | EBI)

Last sequence update: 2000-05-01
Last annotation update: 2024-11-27

Sequence description from provider

RecName: Full=Acidic leucine-rich nuclear phosphoprotein 32 family member E;AltName: Full=Cerebellar postnatal development protein 1;AltName: Full=LANP-like protein; Short=LANP-L;

Provider

SWISS-PROT

Sequence

Polypeptide 260 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Anp32e	acidic nuclear phosphoprotein 32 family member E	21	97	3	33

Sequence references in MGI

J:70333 Radrizzani M, et al., Differential expression of CPD1 during postnatal development in the mouse cerebellum. Brain Res. 2001 Jul 13;907(1-2):162-74
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:105399 Costanzo RV, et al., Anp32e/Cpd1 regulates protein phosphatase 2A activity at synapses during synaptogenesis. Eur J Neurosci. 2006 Jan;23(2):309-24
J:165128 Kular RK, et al., Cpd-1 null mice display a subtle neurological phenotype. PLoS One. 2010;5(9)
J:166683 Reilly PT, et al., Generation and characterization of the Anp32e-deficient mouse. PLoS One. 2010;5(10):e13597
J:200622 Wong P, et al., Targeted ANP32E mutant mice do not demonstrate obvious movement defects. PLoS One. 2013;8(5):e63815
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89