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Gene Review:

AFG3L1P - AFG3-like AAA ATPase 1, pseudogene

Homo sapiens

Synonyms: AFG3, AFG3L1

Shah, Z.H. et al., Kremmidiotis, G. et al.

Kremmidiotis, Gardner, Settasatian, Savoia, Sutherland, Callen,

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Disease relevance of AFG3L1

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein [1].

High impact information on AFG3L1

Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus [2].
AFG3L1 is located on chromosome 16q24, very close to the telomere [2].

References

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein. Kremmidiotis, G., Gardner, A.E., Settasatian, C., Savoia, A., Sutherland, G.R., Callen, D.F. Genomics (2001) [Pubmed]
Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus. Shah, Z.H., Migliosi, V., Miller, S.C., Wang, A., Friedman, T.B., Jacobs, H.T. Genomics (1998) [Pubmed]

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