| Entrez gene ID | | 54252 |
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| Official gene symbol | | Mid1 |
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| Full name | | midline 1 |
|
| Aliases | | Fxy,Midline1 |
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| Gene summary | | human homolog forms homodimers which associate with microtubules in the cytoplasm and mutations in gene are associated with Opitz syndrome [RGD] |
|
| Location | | Chromosome: 0 Locus: Xq21 |
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| Gene position | | 44751949 - 44879998 Map Viewer |
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| Gene orientation | | minus |
|
| Gene size | | 128050 bp |
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| Gene sequence |
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