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. Author manuscript; available in PMC: 2013 Jun 28.
Published in final edited form as: Hum Genet. 2011 Aug 13;131(2):301–310. doi: 10.1007/s00439-011-1078-6

Table 2.

Clinical characteristics of affected individuals with missense variants in GAS1

Individual GAS1 variant
Inheritance Other HPE-associated genes Relevant clinical data Reference
Position Change
10042 c.16C > G p.Leu6Val Paternal SHH, SIX3, ZIC2 and TGIF are normal Lobar HPE, hypotelorism, single nostril, cleft lip/palate. Father is phenotypically unaffected, mother described as having clear “microforms” of HPE This study
9490 c.133C > G p.Arg45Gly Paternal de novo ZIC2: c.994_1005dup, p. Cys335_Pro338dup; SHH, SIX3, TGIF are normal Semilobar HPE, developmental delay, agenesis of the corpus callosum, microcephaly and spasticity This study
Patient 1 c.599C > G p.Thr200Arg NA SHH, SIX3, ZIC2 and TGIF are normal Semilobar HPE, developmental delay, hypoplastic midface, upslanting palpebral fissures, proptosis, depressed nasal bridge, absent collumella, and bilateral cleft lip and palate Ribeiro et al. (2010)
1024 c.660C > G p.Asn220Lys Paternal ZIC2: c.709_711dup; p.His239dup (polymorphism); SHH, SIX3 and TGIF are normal Hypoplastic corpus callosum, diabetes insipidus, craniosynostosis of metopic suture, pyriform apeture stenosis, midline cleft lip with complete premaxillary agenesis This study
Patient 7 c.736G > T p.Ala246Ser NA No data available No data available Ribeiro et al. (2010)
Patient 2 c.775G > A p.Gly259Arg NA Normal karyotype, SHH, SIX3, TGIF, ZIC2 and GLI2 are normal Hypotelorism, with proptosis, hypoplastic midface, depressed nasal bridge, absent collumella with notching of the tip, bilateral cleft lip and palate Ribeiro et al. (2010)
Patient 3 c.808G > T p.Asp270Tyr NA Paternally inherited SHH: c.653T > C, p.Leu218Pro; SIX3, ZIC2, TGIF and GLI2 are normal Microcephaly, hypotelorism, hypoplastic midface, depressed nasal bridge and nasal bones, right cleft lip and palate, no brain structural anomalies Ribeiro et al. (2010)
Patient 4 c.863A > G p.Asp288Gly de novo de novo SHH: c.1088G > A, p.Cys363Tyr Microcephaly, hypotelorism, midface hypoplasia, hypoplastic nasal bones, depressed nasal bridge, midline cleft lip and palate Ribeiro et al. (2010)
6386 c.928C > T p.Pro310Ser Paternal SHH, SIX3, ZIC2 and TGIF are normal Semilobar HPE, absent pituitary and olfactory bulbs, microcephaly, hypotelorism, midface hypoplasia, depressed nasal bridge and hypoplastic septum, midline cleft lip with intact palate, micropenis This study
4953 c.958G > T p.Gly320Cys Mother is normal; father is unavailable ZIC2: c.709_711dup; p.His239dup (polymorphism); SHH, SIX3 and TGIF: are normal HPE, no further clinical data available This study