Sequence Detail

ID/Version

Q9QUS6 (UniProt | EBI)

Last sequence update: 2010-04-20
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Probable E3 ubiquitin-protein ligase MID2; EC=2.3.2.27;AltName: Full=Midline defect 2;AltName: Full=Midline-2;AltName: Full=RING-type E3 ubiquitin transferase MID2 {ECO:0000305};AltName: Full=Tripartite motif-containing protein 1;

Provider

SWISS-PROT

Sequence

Polypeptide 705 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	Mid2	midline 2	31	105	3	6

Sequence references in MGI

J:56619 Buchner G, et al., MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development. Hum Mol Genet. 1999 Aug;8(8):1397-407
J:60299 Perry J, et al., FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules. Genomics. 1999 Dec 15;62(3):385-94