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Article

Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Jan 1992

Ramesh V, Cheng S V, Kozak C A, Herron B J, Shih V E, Taylor B A, Gusella J F

Abstract excerpt

Ornithine aminotransferase (OAT), a mitochondrial matrix enzyme, is deficient in patients with gyrate atrophy of the choroid and retina. In human, the OAT structural gene maps to Chromosome (Chr) 10q26 and several OAT-related sequences, some of which are known to be processed pseudogenes, which map to Xp11.3-11.21. Here, we report chromosomal localization in the mouse of the OAT gene and related sequences....

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Source

Identifiers

PMID: 1349842
DOI: 10.1007/BF00355836

Genes

OAT

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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