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Gene Review

SNTG2  -  syntrophin, gamma 2

Homo sapiens

Synonyms: G2SYN, Gamma-2-syntrophin, SYN5, Syntrophin-5
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High impact information on SNTG2

  • Use of a monochromosomal somatic cell hybrid panel and metaphase-FISH mapping demonstrated that the insertion originated from 2p25 and contained a segment of the SNTG2 gene that lacked an open reading frame [1].
  • Analyses of segregation data associated with markers genotyped in three B73/Mo17-derived mapping populations (F(2), Syn5, and IBM) demonstrate that allele frequencies were significantly altered during the development of the IBM IRILs [2].


  1. An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism. Bowl, M.R., Nesbit, M.A., Harding, B., Levy, E., Jefferson, A., Volpi, E., Rizzoti, K., Lovell-Badge, R., Schlessinger, D., Whyte, M.P., Thakker, R.V. J. Clin. Invest. (2005) [Pubmed]
  2. Genetic dissection of intermated recombinant inbred lines using a new genetic map of maize. Fu, Y., Wen, T.J., Ronin, Y.I., Chen, H.D., Guo, L., Mester, D.I., Yang, Y., Lee, M., Korol, A.B., Ashlock, D.A., Schnable, P.S. Genetics (2006) [Pubmed]
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