Sequence Detail

ID/Version

Q9D4I2 B2RQ44 F8WHB9 (UniProt | EBI)

Last sequence update: 2017-12-20
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Meiosis inhibitor protein 1;AltName: Full=Meiosis defective protein 1;

Provider

SWISS-PROT

Sequence

Polypeptide 1268 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	Mei1	meiotic double-stranded break formation protein 1	13	102	2	6

Sequence references in MGI

J:74632 Libby BJ, et al., The mouse meiotic mutation mei1 disrupts chromosome synapsis with sexually dimorphic consequences for meiotic progression. Dev Biol. 2002 Feb 15;242(2):174-87
J:87802 Libby BJ, et al., Positional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice. Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15706-11
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:103876 Reinholdt LG, et al., Mei1 is epistatic to Dmc1 during mouse meiosis. Chromosoma. 2005 Jul;114(2):127-34
J:269282 Nguyen NMP, et al., Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles. Am J Hum Genet. 2018 Nov 1;103(5):740-751