Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome

Tadashi Kaname, Kumiko Yanagi, Yasutsugu Chinen, Yoshio Makita, Nobuhiko Okamoto, Hiroki Maehara, Ichiro Owan, Fuminori Kanaya, Yoshiaki Kubota, Yuichi Oike, Toshiyuki Yamamoto, Kenji Kurosawa, Yoshimitsu Fukushima, Axel Bohring, John M. Opitz, Ko Ichiro Yoshiura, Norio Niikawa, Kenji Naritomi

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Abstract

The C syndrome is characterized by trigonocephaly and associated anomalies, such as unusual facies, psychomotor retardation, redundant skin, joint and limb abnormalities, and visceral anomalies. In an individual with the C syndrome who harbors a balanced chromosomal translocation, t(3;18)(q13.13;q12.1), we discovered that the TACTILE gene for CD96, a member of the immunoglobulin superfamily, was disrupted at the 3q13.3 breakpoint. In mutation analysis of nine karyotypically normal patients given diagnoses of the C or C-like syndrome, we identified a missense mutation (839CrT, T280M) in exon 6 of the CD96 gene in one patient with the C-like syndrome. The missense mutation was not found among 420 unaffected Japanese individuals. Cells with mutated CD96 protein (T280M) lost adhesion and growth activities in vitro. These findings indicate that CD96 mutations may cause a form of the C syndrome by interfering with cell adhesion and growth.

Original languageEnglish
Pages (from-to)835-841
Number of pages7
JournalAmerican Journal of Human Genetics
Volume81
Issue number4
DOIs
Publication statusPublished - 2007

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Immunoglobulins
Mutation
Missense Mutation
Craniosynostoses
Genetic Translocation
Growth
Cell Adhesion
Genes
Exons
Extremities
Joints
Opitz trigonocephaly syndrome
Skin
Proteins

ASJC Scopus subject areas

  • Genetics

Cite this

Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome. / Kaname, Tadashi; Yanagi, Kumiko; Chinen, Yasutsugu; Makita, Yoshio; Okamoto, Nobuhiko; Maehara, Hiroki; Owan, Ichiro; Kanaya, Fuminori; Kubota, Yoshiaki; Oike, Yuichi; Yamamoto, Toshiyuki; Kurosawa, Kenji; Fukushima, Yoshimitsu; Bohring, Axel; Opitz, John M.; Yoshiura, Ko Ichiro; Niikawa, Norio; Naritomi, Kenji.

In: American Journal of Human Genetics, Vol. 81, No. 4, 2007, p. 835-841.

Research output: Contribution to journalArticle

Kaname, T, Yanagi, K, Chinen, Y, Makita, Y, Okamoto, N, Maehara, H, Owan, I, Kanaya, F, Kubota, Y, Oike, Y, Yamamoto, T, Kurosawa, K, Fukushima, Y, Bohring, A, Opitz, JM, Yoshiura, KI, Niikawa, N & Naritomi, K 2007, 'Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome', American Journal of Human Genetics, vol. 81, no. 4, pp. 835-841. https://doi.org/10.1086/522014
Kaname, Tadashi ; Yanagi, Kumiko ; Chinen, Yasutsugu ; Makita, Yoshio ; Okamoto, Nobuhiko ; Maehara, Hiroki ; Owan, Ichiro ; Kanaya, Fuminori ; Kubota, Yoshiaki ; Oike, Yuichi ; Yamamoto, Toshiyuki ; Kurosawa, Kenji ; Fukushima, Yoshimitsu ; Bohring, Axel ; Opitz, John M. ; Yoshiura, Ko Ichiro ; Niikawa, Norio ; Naritomi, Kenji. / Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome. In: American Journal of Human Genetics. 2007 ; Vol. 81, No. 4. pp. 835-841.
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