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- Table of Contents
1 Q&As
Facts about E3 ubiquitin-protein ligase Midline-1.
Human | |
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Gene Name: | MID1 |
Uniprot: | O15344 |
Entrez: | 4281 |
Belongs to: |
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TRIM/RBCC family |
EC 6.3.2.-; FLJ57031; FLJ58683; FLJ76288; FXYGBBB1; Midin; midline 1 (Opitz/BBB syndrome); RNF59MIDIN; TRIM18mouse, homolog of
Mass (kDA):
75.251 kDA
Human | |
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Location: | Xp22.2 |
Sequence: | X; NC_000023.11 (10445310..10833683, complement) |
In the fetus, highest expression found in kidney, followed by brain and lung. Expressed at low levels in fetal liver. In the adult, most abundant in heart, placenta and brain.
Cytoplasm. Cytoplasm, cytoskeleton. Cytoplasm, cytoskeleton, spindle. Microtubule-associated. It is associated with microtubules throughout the cell cycle, co-localizing with cytoplasmic fibers in interphase and with the mitotic spindle and midbodies during mitosis and cytokinesis.
PMID: 9354791 by Quaderi N.A., et al. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.
PMID: 9425238 by Perry J., et al. The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome.