QuickView for TMEM126A (gene)

Gene Symbol:

TMEM126A Homo sapiens

Full name:

transmembrane protein 126A

Synonyms:

OPA7, transmembrane protein 126A

Genomic Location:

Chr 11: 85036693-85045235

Description:

The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene.

The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms 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:

SRF_Q6 ,  SRF_Q5_01

Cytogenetic Map:

11q14.1

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