General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations. Issue 1 (11th October 2012)
- Record Type:
- Journal Article
- Title:
- General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations. Issue 1 (11th October 2012)
- Main Title:
- General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations
- Authors:
- Keydar, Ifat
Ben‐Asher, Edna
Feldmesser, Ester
Nativ, Noam
Oshimoto, Arisa
Restrepo, Diego
Matsunami, Hiroaki
Chien, Ming‐Shan
Pinto, Jayant M.
Gilad, Yoav
Olender, Tsviya
Lancet, Doron - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Genetic variations in olfactory receptors likely contribute to the diversity of odorant‐specific sensitivity phenotypes. Our working hypothesis is that genetic variations in auxiliary olfactory genes, including those mediating transduction and sensory neuronal development, may constitute the genetic basis for general olfactory sensitivity (GOS) and congenital general anosmia (CGA). We thus performed a systematic exploration for auxiliary olfactory genes and their documented variation. This included a literature survey, seeking relevant functional in vitro studies, mouse gene knockouts and human disorders with olfactory phenotypes, as well as data mining in published transcriptome and proteome data for genes expressed in olfactory tissues. In addition, we performed next‐generation transcriptome sequencing (RNA‐seq) of human olfactory epithelium and mouse olfactory epithelium and bulb, so as to identify sensory‐enriched transcripts. Employing a global score system based on attributes of the 11 data sources utilized, we identified a list of 1, 680 candidate auxiliary olfactory genes, of which 450 are shortlisted as having higher probability of a functional role. For the top‐scoring 136 genes, we identified genomic variants (probably damaging single nucleotide polymorphisms, indels, and copy number deletions) gleaned from public variation repositories. This database of genes and their variants should assist in<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Genetic variations in olfactory receptors likely contribute to the diversity of odorant‐specific sensitivity phenotypes. Our working hypothesis is that genetic variations in auxiliary olfactory genes, including those mediating transduction and sensory neuronal development, may constitute the genetic basis for general olfactory sensitivity (GOS) and congenital general anosmia (CGA). We thus performed a systematic exploration for auxiliary olfactory genes and their documented variation. This included a literature survey, seeking relevant functional in vitro studies, mouse gene knockouts and human disorders with olfactory phenotypes, as well as data mining in published transcriptome and proteome data for genes expressed in olfactory tissues. In addition, we performed next‐generation transcriptome sequencing (RNA‐seq) of human olfactory epithelium and mouse olfactory epithelium and bulb, so as to identify sensory‐enriched transcripts. Employing a global score system based on attributes of the 11 data sources utilized, we identified a list of 1, 680 candidate auxiliary olfactory genes, of which 450 are shortlisted as having higher probability of a functional role. For the top‐scoring 136 genes, we identified genomic variants (probably damaging single nucleotide polymorphisms, indels, and copy number deletions) gleaned from public variation repositories. This database of genes and their variants should assist in rationalizing the great interindividual variation in human overall olfactory sensitivity (http://genome.weizmann.ac.il/GOSdb).</p> </abstract> … (more)
- Is Part Of:
- Human mutation. Volume 34:Issue 1(2013:Jan.)
- Journal:
- Human mutation
- Issue:
- Volume 34:Issue 1(2013:Jan.)
- Issue Display:
- Volume 34, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 34
- Issue:
- 1
- Issue Sort Value:
- 2013-0034-0001-0000
- Page Start:
- 32
- Page End:
- 41
- Publication Date:
- 2012-10-11
- Subjects:
- Human chromosome abnormalities -- Periodicals
Mutation (Biology) -- Periodicals
616.04205 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/humu.22212 ↗
- Languages:
- English
- ISSNs:
- 1059-7794
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.217000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3424.xml