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MID1, midline 1

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MID1, midline 1

  • The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]

  • Gene Synonyms (BBBG1, FXY, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY, E3 ubiquitin-protein ligase Midline-1, Opitz/BBB syndrome, RING finger protein 59, RING finger protein Midline-1, RING-type E3 ubiquitin transferase Midline-1, midline 1 RING finger protein, putative transcription factor XPRF, tripartite motif protein TRIM18, tripartite motif-containing protein 18, zinc finger on X and Y, mouse, homolog of,)
  • NCBI Gene ID: 4281
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A087X255
    UNIPROT ID#>>O15344
    UNIPROT ID#>>A0A024RBV4
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

midline 1 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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