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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.
Novel DUF738 containing protein (2610110G12Rik) , acetyltransferase mec-17 homolog , alpha-TAT , alpha-tubulin N-acetyltransferase , tyrosine aminotransferase , tyrosine aminotransferase-like , L-tyrosine:2-oxoglutarate aminotransferase , tyrosine aminotransferase, cytosolic , tyrosine transaminase
GENE ID | SPECIES |
---|---|
73242 | Mus musculus |
361789 | Rattus norvegicus |
415884 | Gallus gallus |
448486 | Xenopus (Silurana) tropicalis |
454227 | Pan troglodytes |
479665 | Canis lupus familiaris |
561410 | Danio rerio |
708005 | Macaca mulatta |
9681609 | Micromonas pusilla CCMP1545 |
100020832 | Monodelphis domestica |
100068116 | Equus caballus |
100077699 | Ornithorhynchus anatinus |
100410667 | Callithrix jacchus |
100446283 | Pongo abelii |
100483605 | Ailuropoda melanoleuca |
100549583 | Meleagris gallopavo |
100583147 | Nomascus leucogenys |
786491 | Bos taurus |
6898 | Homo sapiens |
234724 | Mus musculus |
24813 | Rattus norvegicus |
533481 | Bos taurus |
817022 | Arabidopsis thaliana |