TAT

GENE INFORMATION

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Gene name

TAT

Synonyms

Description

Tyrosine aminotransferase (HGNC Symbol)

Entrez 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, Jul 2008]

Chromosome

16

Cytoband

q22.2

Chromosome location (bp)

71565660 - 71577130

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000198650 (version 78.38)

Entrez gene

6898

UniProt

P17735 (UniProt - Evidence at protein level)

neXtProt

NX_P17735

Antibodypedia

TAT antibodies
 

PROTEIN VIEW

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TAT-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

TAT-001 ENSP00000348234
ENST00000355962
P17735
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