Health Conditions Related to Genetic Changes
Gordon Holmes syndrome
At least eight RNF216 gene mutations have been found to cause Gordon Holmes syndrome, a rare condition characterized by reduced production of hormones that direct sexual development (hypogonadotropic hypogonadism) and difficulty coordinating movements (cerebellar ataxia). Many people with Gordon Holmes syndrome caused by RNF216 gene mutations experience a decline in intellectual function (dementia). These mutations impair the ability of the RNF216 protein to tag unneeded proteins to be broken down. Impaired breakdown of Arc disrupts normal synaptic connections and plasticity, which likely contributes to dementia in people with Gordon Holmes syndrome. It is unclear how a lack of RNF216 protein function causes hypogonadotropic hypogonadism or cerebellar ataxia.
More About This Health ConditionOther Names for This Gene
- CAHH
- E3 ubiquitin-protein ligase RNF216 isoform a
- E3 ubiquitin-protein ligase RNF216 isoform b
- RING-type E3 ubiquitin transferase RNF216
- triad domain-containing protein 3
- TRIAD3
- U7I1
- UBCE7IP1
- ubiquitin-conjugating enzyme 7-interacting protein 1
- ZIN
- zinc finger protein inhibiting NF-kappa-B
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
References
- Alqwaifly M, Bohlega S. Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation. Neurol Int. 2016 Jun 15;8(2):6444. doi: 10.4081/ni.2016.6444. eCollection 2016 Jun 15. Citation on PubMed or Free article on PubMed Central
- Chuang TH, Ulevitch RJ. Triad3A, an E3 ubiquitin-protein ligase regulating Toll-like receptors. Nat Immunol. 2004 May;5(5):495-502. doi: 10.1038/ni1066. Epub 2004 Apr 25. Erratum In: Nat Immunol. 2004 Sep;5(9):968. Citation on PubMed
- Husain N, Yuan Q, Yen YC, Pletnikova O, Sally DQ, Worley P, Bichler Z, Shawn Je H. TRIAD3/RNF216 mutations associated with Gordon Holmes syndrome lead to synaptic and cognitive impairments via Arc misregulation. Aging Cell. 2017 Apr;16(2):281-292. doi: 10.1111/acel.12551. Epub 2016 Dec 20. Citation on PubMed or Free article on PubMed Central
- Mabb AM, Je HS, Wall MJ, Robinson CG, Larsen RS, Qiang Y, Correa SA, Ehlers MD. Triad3A regulates synaptic strength by ubiquitination of Arc. Neuron. 2014 Jun 18;82(6):1299-316. doi: 10.1016/j.neuron.2014.05.016. Citation on PubMed or Free article on PubMed Central
- Margolin DH, Kousi M, Chan YM, Lim ET, Schmahmann JD, Hadjivassiliou M, Hall JE, Adam I, Dwyer A, Plummer L, Aldrin SV, O'Rourke J, Kirby A, Lage K, Milunsky A, Milunsky JM, Chan J, Hedley-Whyte ET, Daly MJ, Katsanis N, Seminara SB. Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitination. N Engl J Med. 2013 May 23;368(21):1992-2003. doi: 10.1056/NEJMoa1215993. Epub 2013 May 8. Citation on PubMed or Free article on PubMed Central
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