Sequence Detail

ID/Version

Q8C4X7 Q6DI98 A0A0R4J0Q0 E9Q5J6 (UniProt | EBI)

Last sequence update: 2018-12-05
Last annotation update: 2024-03-27

Sequence description from provider

RecName: Full=Major intrinsically disordered NOTCH2-binding receptor 1-like homolog {ECO:0000305};AltName: Full=Major intrinsically disordered NOTCH2-associated receptor 2 {ECO:0000303|PubMed:32954300};AltName: Full=Membrane integral NOTCH2-associated rec

Provider

SWISS-PROT

Sequence

Polypeptide 193 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	Minar2	membrane integral NOTCH2 associated receptor 2	9	100	2	6

Sequence references in MGI

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:298983 Ho RX, et al., Loss of MINAR2 impairs motor function and causes Parkinson's disease-like symptoms in mice. Brain Commun. 2020;2(1):fcaa047
J:326355 Bademci G, et al., Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice. Proc Natl Acad Sci U S A. 2022 Jun 28;119(26):e2204084119