Abstract
Inherited defects of skull ossification often manifest as symmetric parietal foramina (PFM; MIM 168500). We previously identified mutations of MSX2 in non-syndromic PFM and demonstrated genetic heterogeneity. Deletions of 11p11-p12 (proximal 11p deletion syndrome, P11pDS; MIM 601224) are characterized by multiple exostoses, attributable to haploinsufficiency of EXT2 and PFM. Here we identify ALX4, which encodes a paired-related homeodomain transcription factor, as the PFM disease gene in P11pDS.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Base Sequence
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Craniofacial Abnormalities / genetics*
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DNA Mutational Analysis
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DNA-Binding Proteins*
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Exons / genetics
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Genes, Homeobox / genetics*
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Homeodomain Proteins / genetics
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Humans
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Mice
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Molecular Sequence Data
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Mutation / genetics*
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Osteogenesis / genetics*
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Phenotype
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Physical Chromosome Mapping
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Proteins / genetics*
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Skull / abnormalities*
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Skull / embryology
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Transcription Factors / genetics
Substances
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ALX4 protein, human
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DNA-Binding Proteins
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Homeodomain Proteins
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Proteins
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Transcription Factors
Associated data
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GENBANK/AF294629
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GENBANK/AJ279074
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GENBANK/AJ279075
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GENBANK/AJ279076
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GENBANK/AJ279077
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GENBANK/AJ404888