About: De novo mutation

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A de novo mutation is any mutation/alteration in the genome of any organism (humans, animals, plant, microbes, etc.) that wasn't present or transmitted by their parents. This type of mutation (like any other) occurs spontaneously during the process of DNA replication during cell division in a fetus whose close, biological relatives don't have the mutation. Often, these kind of mutations have very little to no effect on the affected organism, but in rare cases they have a notable and/or serious effect on overall health, physical appearance, etc.

Attributes	Values
rdfs:label	De novo mutation (en) Mutation de novo (fr)
rdfs:comment	A de novo mutation is any mutation/alteration in the genome of any organism (humans, animals, plant, microbes, etc.) that wasn't present or transmitted by their parents. This type of mutation (like any other) occurs spontaneously during the process of DNA replication during cell division in a fetus whose close, biological relatives don't have the mutation. Often, these kind of mutations have very little to no effect on the affected organism, but in rare cases they have a notable and/or serious effect on overall health, physical appearance, etc. (en) En médecine et en génétique, une mutation de novo (néomutation ou néo-mutation) est une mutation du gène apparaissant chez un individu alors qu'aucun des parents ne la possède dans son patrimoine génétique. La mutation est donc survenue dans les gamètes d'un des deux parents, ou, plus rarement ce peut être une mutation post-zygotique, c'est-à-dire une mutation de l'œuf fécondé. (fr)
dcterms:subject	Mutated genes Mutation
Wikipage page ID	3370507 (xsd:integer)
Wikipage revision ID	1092293087 (xsd:integer)
Link from a Wikipage to another Wikipage	Mutated genes DNA replication Cancer syndromes Cell division Family 1p36 deletion syndrome Mutation Cri-du-chat syndrome dbr:University_of_Utah_Health
sameAs	De novo mutation De novo mutation De novo mutation
dbp:wikiPageUsesTemplate	dbt:Reflist
has abstract	A de novo mutation is any mutation/alteration in the genome of any organism (humans, animals, plant, microbes, etc.) that wasn't present or transmitted by their parents. This type of mutation (like any other) occurs spontaneously during the process of DNA replication during cell division in a fetus whose close, biological relatives don't have the mutation. Often, these kind of mutations have very little to no effect on the affected organism, but in rare cases they have a notable and/or serious effect on overall health, physical appearance, etc. (en) En médecine et en génétique, une mutation de novo (néomutation ou néo-mutation) est une mutation du gène apparaissant chez un individu alors qu'aucun des parents ne la possède dans son patrimoine génétique. La mutation est donc survenue dans les gamètes d'un des deux parents, ou, plus rarement ce peut être une mutation post-zygotique, c'est-à-dire une mutation de l'œuf fécondé. (fr)
prov:wasDerivedFrom	wikipedia-en:De_novo_mutation?oldid=1092293087&ns=0
page length (characters) of wiki page	1913 (xsd:nonNegativeInteger)
foaf:isPrimaryTopicOf	wikipedia-en:De_novo_mutation
is Link from a Wikipage to another Wikipage of	Progeria Neotenic complex syndrome Mendelian error Birt–Hogg–Dubé syndrome Huntington's disease Czech dysplasia, metatarsal type Inbreeding depression 13q deletion syndrome Cri du chat syndrome Genocopy dbr:Neurofibromin_1 Nicolaides–Baraitser syndrome Otocephaly 17q12 microdeletion syndrome Glossary of genetics Glossary of genetics (0–L) Marsili syndrome Androgen insensitivity syndrome Bohring–Opitz syndrome Calvarial doughnut lesions-bone fragility syndrome Hallermann–Streiff syndrome Treacher Collins syndrome GABRB3 DNM Lamb-Shaffer syndrome Alternating hemiplegia Alternating hemiplegia of childhood Facioscapulohumeral muscular dystrophy Familial hemiplegic migraine Osimertinib Osteogenesis imperfecta Chromosomal deletion syndrome Familial multiple cafe-au-lait spots KCNH1 Kabuki syndrome Lennox–Gastaut syndrome List of Latin phrases (D) 1p36 deletion syndrome Hemiplegic migraine Bainbridge–Ropers syndrome Hypohidrotic ectodermal dysplasia with immune deficiency Histone H4 Snijders Blok-Campeau syndrome Coding region Coffin–Siris syndrome Ectrodactyly Autosomal dominant cerebellar ataxia, deafness, and narcolepsy Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome CHAMP1-associated intellectual disability syndrome Spinal muscular atrophy Intellectual disability Wolfram-like syndrome X-linked severe combined immunodeficiency Mitochondrial membrane protein-associated neurodegeneration Muscular dystrophy Neurogenetics Oculopharyngodistal myopathy Olivopontocerebellar atrophy-deafness syndrome PASLI disease POLD1 Severe intellectual disability-progressive spastic diplegia syndrome Pai syndrome SCN1A
is Wikipage disambiguates of	DNM
is foaf:primaryTopic of	wikipedia-en:De_novo_mutation

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