QuickView for FTCD (gene)

Gene Symbol:

FTCD Homo sapiens

Full name:

formimidoyltransferase cyclodeaminase

Synonyms:

LCHC1, formimidoyltransferase-cyclodeaminase, formiminotransferase-cyclodeaminase

Genomic Location:

Chr 21: 46380604-46399909

Description:

The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.

The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Danio rerio ,  Gallus gallus ,  Pan troglodytes ,  Bos taurus ,  Canis lupus familiaris

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

PXR_Q2

Cytogenetic Map:

21q22.3

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