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Title:
Partial deletion of GLRB and GRIA2 in a patient with intellectual disability | European Journal of Human Genetics
Description:
We report about the partial de novo loss of GLRB and GRIA2 in an individual with intellectual disability (ID). No additional mutations were found in either gene. GLRB itself does not seem to be a good candidate as it causes autosomal recessive hyperekplexia and no symptoms were found in the patient. Mutations of GRIA2 have not been described as cause of ID to date. Nonetheless, it is a very attractive candidate because it encodes a subunit of a glutamate receptor, which is highly expressed in postsynaptic structures and has an important role in signal transduction across synapses. Although we were able to isolate a fragment of a fusion transcript of both genes from the patient
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gria, article, glrb, nature, patient, google, scholar, deletion, cas, receptor, genet, information, found, fusion, data, patients, mutations, genes, human, intellectual, gene, glutamate, transcript, blood, open, supplementary, content, disability, ampa, exon, hum, cookies, european, autosomal, brain, receptors, parents, chromosome, privacy, journal, genetics, partial, novo, recessive, figure, mutation, hackmann, hyperekplexia, subunit, frame,
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nature portfolio α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid permissions reprints privacy policy nature 2006 nature advertising social media array-cgh data revealed author information authors open reading frame middle synonymous amino-acid exchange pafah1b3-clk2 fusion gene author correspondence human protein-encoding transcriptomes glutamate receptor subunits remains open potential dominant-negative effect array-cgh data nonsyndromic intellectual disability x-linked mental retardation permissions array data represent ampa receptor trafficking encode glutamate receptors glutamate receptor human genetics frame shift mutation fosmid-specific fish-signal dominant-negative properties intellectual disability molecular life sciences occurred de novo de novo loss explore content similar content privacy european economic area derivative fusion protein fusion transcript derived eva-maria gerlach journals search log variable neurodevelopmental phenotypes glutamate receptors supplementary table s1 fusion gene green vertical lines aberrant gria3 transcripts severe speech delay
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headline:Partial deletion of GLRB and GRIA2 in a patient with intellectual disability
description:We report about the partial de novo loss of GLRB and GRIA2 in an individual with intellectual disability (ID). No additional mutations were found in either gene. GLRB itself does not seem to be a good candidate as it causes autosomal recessive hyperekplexia and no symptoms were found in the patient. Mutations of GRIA2 have not been described as cause of ID to date. Nonetheless, it is a very attractive candidate because it encodes a subunit of a glutamate receptor, which is highly expressed in postsynaptic structures and has an important role in signal transduction across synapses. Although we were able to isolate a fragment of a fusion transcript of both genes from the patient's blood, we were not able to isolate a transcript with an open reading frame throughout the entire length. The reading frame could be restored by differential splicing, which might take place in brain tissue but not in blood. We assume that either haploinsufficiency of GRIA2 or a GLRB/GRIA2 fusion gene leading to a protein with dominant-negative properties is causing the phenotype of the patient.
datePublished:2012-06-06T00:00:00Z
dateModified:2012-06-06T00:00:00Z
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Disease genetics
Mutation
Psychiatric disorders
GLRB
GRIA2
intellectual disability
fusion gene
glutamate receptor
Biomedicine
general
Human Genetics
Bioinformatics
Gene Expression
Cytogenetics
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headline:Partial deletion of GLRB and GRIA2 in a patient with intellectual disability
description:We report about the partial de novo loss of GLRB and GRIA2 in an individual with intellectual disability (ID). No additional mutations were found in either gene. GLRB itself does not seem to be a good candidate as it causes autosomal recessive hyperekplexia and no symptoms were found in the patient. Mutations of GRIA2 have not been described as cause of ID to date. Nonetheless, it is a very attractive candidate because it encodes a subunit of a glutamate receptor, which is highly expressed in postsynaptic structures and has an important role in signal transduction across synapses. Although we were able to isolate a fragment of a fusion transcript of both genes from the patient's blood, we were not able to isolate a transcript with an open reading frame throughout the entire length. The reading frame could be restored by differential splicing, which might take place in brain tissue but not in blood. We assume that either haploinsufficiency of GRIA2 or a GLRB/GRIA2 fusion gene leading to a protein with dominant-negative properties is causing the phenotype of the patient.
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dateModified:2012-06-06T00:00:00Z
pageStart:112
pageEnd:114
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Disease genetics
Mutation
Psychiatric disorders
GLRB
GRIA2
intellectual disability
fusion gene
glutamate receptor
Biomedicine
general
Human Genetics
Bioinformatics
Gene Expression
Cytogenetics
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