MID1 Products

Description

Defects in the Midline-1 (MID1) gene are the cause of Opitz syndrome, an X-linked recessive disorder characterized by developmental defects. MID1 is a microtubule-associated protein (MAP) with E3 ubiquitin ligase activity. MID1 has been shown to target protein phosphatases 2A (PP2Ac) on microtubules for degradation. MID1 association with PP2A has been proposed to regulate microtubule stabilization for cellular processes such as cell division and migration.

Bioinformatics

Entrez	4281 Human
Uniprot	AAH53626 Human NM_000381 Human NM_033290 Human NP_000372.1 Human NP_001092094 Human O15344 Human
Product By Gene ID	4281
Alternate Names	EC 6.3.2.- FLJ57031 FLJ58683 FLJ76288 FXYGBBB1 Midin midline 1 (Opitz/BBB syndrome) RNF59MIDIN TRIM18mouse, homolog of

Research Areas for MID1

Find related products by research area and learn more about each of the different research areas below.

Lipid and Metabolism
Zinc Finger

Related MID1 Blog Posts

Check out the latest blog posts on MID1.

Beta Tubulin III and neurogenesis Beta tubulin III, also known as Tuj-1, is a class III member of the beta tubulin protein family. Beta tubulins are one of two structural components that form our microtubule network. While general tubulins play a role in a wide range of cellular pr...    Read more.

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