2018
DOI: 10.5897/ajb2018.16464
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Applications of genomic copy number variations on livestock: A review

Abstract: Genomic copy number variations (CNVs) have significantly modified genomic regions during inversions, translocations, duplications and deletions that keep shaping phenotypic variation through changes in gene dosage, regulation and transcript structure. The objective of this review was to discuss the current application of CNVs on domestication, adaptations, productions, coat colour, morphology and diseases of livestock, and also address implication of CNV on genotyping selections, limitation and in the future, … Show more

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Cited by 4 publications
(2 citation statements)
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“…However, only a few genes have previously been reported to have mechanism indirectly related to total solid. The gene IRAG1 is found in the membrane of the endoplasmic reticulum, functioning in intracellular calcium modulation, body growth, and adaptation to the arid environment (Widmann et al, 2013;Oberheim Bush and Nedergaard, 2017;Goshu et al, 2018). The gene ADM is found to be involved in several pathways including vasodilation, hormone regulation, angiogenesis, and antimicrobial activity (Schönauer et al, 2017).…”
Section: Candidate Genes For Tsymentioning
confidence: 99%
“…However, only a few genes have previously been reported to have mechanism indirectly related to total solid. The gene IRAG1 is found in the membrane of the endoplasmic reticulum, functioning in intracellular calcium modulation, body growth, and adaptation to the arid environment (Widmann et al, 2013;Oberheim Bush and Nedergaard, 2017;Goshu et al, 2018). The gene ADM is found to be involved in several pathways including vasodilation, hormone regulation, angiogenesis, and antimicrobial activity (Schönauer et al, 2017).…”
Section: Candidate Genes For Tsymentioning
confidence: 99%
“…Copy number variation (CNV) is a type of structural variation that includes large-scale duplications, insertions and deletions which create imbalances in gene dosage and are described as the deletion or duplication of a genome copy number [1] that can have great functional and evolutionary impact [2]. For instance, CNVs play a key role in generating the required variation in a population [3].…”
Section: Introductionmentioning
confidence: 99%