euL1db: the European database of L1HS retrotransposon insertions in humans
2015
Retrotransposonsaccount for almost half of our genome. They are
mobile genetics elements—also known as
jumping genes—but only the L1HS subfamily of
Long Interspersed Nuclear Elements(LINEs) has retained the ability to jump autonomously in modern humans. Their mobilization in germline—but also some somatic tissues—contributes to
human geneticdiversity and to diseases, such as cancer. Here, we present euL1db, the European database of L1HS
retrotransposon
insertionsin humans (available at http://euL1db.unice.fr). euL1db provides a curated and comprehensive summary of L1HS
insertionpolymorphisms identified in healthy or pathological human samples and published in peer-reviewed journals. A key feature of euL1db is its sample-wise organization. Hence L1HS
insertionpolymorphisms are connected to samples, individuals, families and clinical conditions. The current version of euL1db centralizes results obtained in 32 studies. It contains >900 samples, >140 000 sample-wise
insertionsand almost 9000 distinct merged
insertions. euL1db will help understanding the link between L1
retrotransposon
insertionpolymorphisms and phenotype or disease.
Keywords:
-
Correction
-
Source
-
Cite
-
Save
43
References
45
Citations
NaN
KQI