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- Table of Contents
Facts about Probable E3 ubiquitin-protein ligase MID2.
Human | |
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Gene Name: | MID2 |
Uniprot: | Q9UJV3 |
Entrez: | 11043 |
Belongs to: |
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TRIM/RBCC family |
EC 6.3.2.-; FLJ37715; FLJ41813; FXY2midin-2; midin 2; Midin-2; midline 2; Midline defect 2; Midline-2; RING finger protein 60; RNF60midline-2; TRIM1probable E3 ubiquitin-protein ligase MID2; tripartite motif protein 1; Tripartite motif-containing protein 1
Mass (kDA):
83.21 kDA
Human | |
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Location: | Xq22.3 |
Sequence: | X; NC_000023.11 (107820453..107931637) |
Low level in fetal kidney and lung, and in adult prostate, ovary and small intestine.
Cytoplasm. Cytoplasm, cytoskeleton. Microtubule-associated.
PMID: 10644436 by 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.
PMID: 10400986 by Buchner G., et al. MID2, a homologue of the Opitz syndrome gene MID1: similarities in a sub-cellular localization and differences in expression during development.