| Entrez gene ID | | 6898 |
| Official gene symbol | | TAT |
| Full name | | tyrosine aminotransferase |
| Aliases | | ,-, |
| Gene summary | | This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq] |
| Location | | Chromosome: 16 Locus: 16q22.1 |
| Gene position | | 71610998 - 71600754 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 10245 bp |
| Gene sequence |
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