Sequence Detail

ID/Version

O70299 (UniProt | EBI)

Last sequence update: 1998-08-01
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Putative nucleotidyltransferase MAB21L1; EC=2.7.7.- {ECO:0000305};AltName: Full=Protein mab-21-like 1;

Provider

SWISS-PROT

Sequence

Polypeptide 359 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	Mab21l1	mab-21-like 1	13	113	3	4

Sequence references in MGI

J:52199 Mariani M, et al., Mab21, the mouse homolog of a C. elegans cell-fate specification gene, participates in cerebellar, midbrain and eye development. Mech Dev. 1998 Dec;79(1-2):131-5
J:58808 Mariani M, et al., Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development. Hum Mol Genet. 1999 Dec;8(13):2397-406
J:74595 Wong RL, et al., Depletion of Mab21l1 and Mab21l2 messages in mouse embryo arrests axial turning, and impairs notochord and neural tube differentiation. Teratology. 2002 Feb;65(2):70-7
J:82312 Yamada R, et al., Cell-autonomous involvement of Mab21l1 is essential for lens placode development. Development. 2003 May;130(9):1759-70
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:256266 Nguyen D, et al., Involvement of the Mab21l1 gene in calvarial osteogenesis. Differentiation. 2017 Nov - Dec;98:70-78