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Gene Review

IMMP2L  -  IMP2 inner mitochondrial membrane...

Homo sapiens

Synonyms: IMMP2L-IT1, IMP2, IMP2-LIKE, IMP2-like protein, Mitochondrial inner membrane protease subunit 2
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Psychiatry related information on IMMP2L


High impact information on IMMP2L


Biological context of IMMP2L

  • In the present study we sought to identify genetic variation in IMMP2L, which, through alteration of protein function or level of expression might contribute to the manifestation of GTS [2].


  1. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome. Petek, E., Windpassinger, C., Vincent, J.B., Cheung, J., Boright, A.P., Scherer, S.W., Kroisel, P.M., Wagner, K. Am. J. Hum. Genet. (2001) [Pubmed]
  2. Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome. Petek, E., Schwarzbraun, T., Noor, A., Patel, M., Nakabayashi, K., Choufani, S., Windpassinger, C., Stamenkovic, M., Robertson, M.M., Aschauer, H.N., Gurling, H.M., Kroisel, P.M., Wagner, K., Scherer, S.W., Vincent, J.B. Mol. Genet. Genomics (2007) [Pubmed]
  3. Association between 7q31 markers and Tourette syndrome. Díaz-Anzaldúa, A., Joober, R., Rivière, J.B., Dion, Y., Lespérance, P., Chouinard, S., Richer, F., Rouleau, G.A. Am. J. Med. Genet. A (2004) [Pubmed]
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