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exon shuffling can drive the functional diversification of gene families over evolutionary time, the temporal and/or tissue specific alternative splicing of a gene can give rise to functional diversification of a single gene during the development of an organism. Although no alternative splicing of TACC3 has been clearly documented, both temporal and tissue specific splicing is observed in the TACC1 and TACC2 genes. In the case of TACC2, an additional large (5 kb) exon accounts for the main difference between the major splice variants of the vertebrate TACC2 genes [3]. The alternative splicing of this exon suggests a major functional difference between the two TACC2 isoforms, TACC2s and TACC2l [3], as well as a significant difference between TACC2 and its closest TACC family relative, TACC1. However, the function of this region of the TACC2l isoform is current unknown."}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T6306","span":{"begin":8,"end":12},"obj":"SO_EXT:0000147"},{"id":"T6307","span":{"begin":67,"end":71},"obj":"SO_EXT:0000704"},{"id":"T6308","span":{"begin":125,"end":131},"obj":"UBERON:0000479"},{"id":"T6309","span":{"begin":141,"end":161},"obj":"GO:0000380"},{"id":"T6310","span":{"begin":167,"end":171},"obj":"SO_EXT:0000704"},{"id":"T6311","span":{"begin":228,"end":232},"obj":"SO_EXT:0000704"},{"id":"T6312","span":{"begin":244,"end":258},"obj":"_FRAGMENT"},{"id":"T6313","span":{"begin":262,"end":270},"obj":"GO:0044767"},{"id":"T6314","span":{"begin":262,"end":270},"obj":"NCBITaxon:1"},{"id":"T6315","span":{"begin":284,"end":304},"obj":"GO:0000380"},{"id":"T6316","span":{"begin":308,"end":313},"obj":"PR_EXT:000016008"},{"id":"T6317","span":{"begin":361,"end":367},"obj":"UBERON:0000479"},{"id":"T6318","span":{"begin":377,"end":385},"obj":"GO:0008380"},{"id":"T6319","span":{"begin":405,"end":410},"obj":"PR_EXT:000016006"},{"id":"T6320","span":{"begin":415,"end":420},"obj":"PR_EXT:000016007"},{"id":"T6321","span":{"begin":421,"end":426},"obj":"SO_EXT:0000704"},{"id":"T6322","span":{"begin":443,"end":448},"obj":"PR_EXT:000016007"},{"id":"T6323","span":{"begin":474,"end":475},"obj":"CHEBI_SO_EXT:base"},{"id":"T6324","span":{"begin":477,"end":481},"obj":"SO_EXT:0000147"},{"id":"T6325","span":{"begin":533,"end":539},"obj":"GO:0008380"},{"id":"T6326","span":{"begin":533,"end":548},"obj":"SO_EXT:alternative_splice_variant"},{"id":"T6327","span":{"begin":556,"end":566},"obj":"NCBITaxon:7742"},{"id":"T6328","span":{"begin":567,"end":572},"obj":"PR_EXT:000016007"},{"id":"T6329","span":{"begin":573,"end":578},"obj":"SO_EXT:0000704"},{"id":"T6330","span":{"begin":588,"end":608},"obj":"GO:0000380"},{"id":"T6331","span":{"begin":617,"end":621},"obj":"SO_EXT:0000147"},{"id":"T6332","span":{"begin":677,"end":682},"obj":"PR_EXT:000016007"},{"id":"T6333","span":{"begin":683,"end":691},"obj":"SO_EXT:0001060"},{"id":"T6334","span":{"begin":760,"end":765},"obj":"PR_EXT:000016007"},{"id":"T6335","span":{"begin":804,"end":809},"obj":"PR_EXT:000016006"},{"id":"T6336","span":{"begin":862,"end":869},"obj":"SO_EXT:0001060"}],"relations":[{"id":"R4062","pred":"_lexicallyChainedTo","subj":"T6313","obj":"T6312"}],"text":"Whereas exon shuffling can drive the functional diversification of gene families over evolutionary time, the temporal and/or tissue specific alternative splicing of a gene can give rise to functional diversification of a single gene during the development of an organism. Although no alternative splicing of TACC3 has been clearly documented, both temporal and tissue specific splicing is observed in the TACC1 and TACC2 genes. In the case of TACC2, an additional large (5 kb) exon accounts for the main difference between the major splice variants of the vertebrate TACC2 genes [3]. The alternative splicing of this exon suggests a major functional difference between the two TACC2 isoforms, TACC2s and TACC2l [3], as well as a significant difference between TACC2 and its closest TACC family relative, TACC1. However, the function of this region of the TACC2l isoform is current unknown."}

{"project":"craft-ca-core-dev","denotations":[{"id":"T6242","span":{"begin":8,"end":12},"obj":"SO:0000147"},{"id":"T6243","span":{"begin":67,"end":71},"obj":"SO:0000704"},{"id":"T6244","span":{"begin":125,"end":131},"obj":"UBERON:0000479"},{"id":"T6245","span":{"begin":141,"end":161},"obj":"GO:0000380"},{"id":"T6246","span":{"begin":167,"end":171},"obj":"SO:0000704"},{"id":"T6247","span":{"begin":228,"end":232},"obj":"SO:0000704"},{"id":"T6248","span":{"begin":244,"end":258},"obj":"_FRAGMENT"},{"id":"T6249","span":{"begin":262,"end":270},"obj":"GO:0044767"},{"id":"T6250","span":{"begin":262,"end":270},"obj":"NCBITaxon:1"},{"id":"T6251","span":{"begin":284,"end":304},"obj":"GO:0000380"},{"id":"T6252","span":{"begin":308,"end":313},"obj":"PR:000016008"},{"id":"T6253","span":{"begin":361,"end":367},"obj":"UBERON:0000479"},{"id":"T6254","span":{"begin":377,"end":385},"obj":"GO:0008380"},{"id":"T6255","span":{"begin":405,"end":410},"obj":"PR:000016006"},{"id":"T6256","span":{"begin":415,"end":420},"obj":"PR:000016007"},{"id":"T6257","span":{"begin":421,"end":426},"obj":"SO:0000704"},{"id":"T6258","span":{"begin":443,"end":448},"obj":"PR:000016007"},{"id":"T6259","span":{"begin":477,"end":481},"obj":"SO:0000147"},{"id":"T6260","span":{"begin":533,"end":539},"obj":"GO:0008380"},{"id":"T6261","span":{"begin":556,"end":566},"obj":"NCBITaxon:7742"},{"id":"T6262","span":{"begin":567,"end":572},"obj":"PR:000016007"},{"id":"T6263","span":{"begin":573,"end":578},"obj":"SO:0000704"},{"id":"T6264","span":{"begin":588,"end":608},"obj":"GO:0000380"},{"id":"T6265","span":{"begin":617,"end":621},"obj":"SO:0000147"},{"id":"T6266","span":{"begin":677,"end":682},"obj":"PR:000016007"},{"id":"T6267","span":{"begin":683,"end":691},"obj":"SO:0001060"},{"id":"T6268","span":{"begin":760,"end":765},"obj":"PR:000016007"},{"id":"T6269","span":{"begin":804,"end":809},"obj":"PR:000016006"},{"id":"T6270","span":{"begin":862,"end":869},"obj":"SO:0001060"}],"relations":[{"id":"R4060","pred":"_lexicallyChainedTo","subj":"T6249","obj":"T6248"}],"text":"Whereas exon shuffling can drive the functional diversification of gene families over evolutionary time, the temporal and/or tissue specific alternative splicing of a gene can give rise to functional diversification of a single gene during the development of an organism. Although no alternative splicing of TACC3 has been clearly documented, both temporal and tissue specific splicing is observed in the TACC1 and TACC2 genes. In the case of TACC2, an additional large (5 kb) exon accounts for the main difference between the major splice variants of the vertebrate TACC2 genes [3]. The alternative splicing of this exon suggests a major functional difference between the two TACC2 isoforms, TACC2s and TACC2l [3], as well as a significant difference between TACC2 and its closest TACC family relative, TACC1. However, the function of this region of the TACC2l isoform is current unknown."}

{"project":"2_test","denotations":[{"id":"15207008-12620397-9666013","span":{"begin":580,"end":581},"obj":"12620397"},{"id":"15207008-12620397-9666014","span":{"begin":712,"end":713},"obj":"12620397"}],"text":"Whereas exon shuffling can drive the functional diversification of gene families over evolutionary time, the temporal and/or tissue specific alternative splicing of a gene can give rise to functional diversification of a single gene during the development of an organism. Although no alternative splicing of TACC3 has been clearly documented, both temporal and tissue specific splicing is observed in the TACC1 and TACC2 genes. In the case of TACC2, an additional large (5 kb) exon accounts for the main difference between the major splice variants of the vertebrate TACC2 genes [3]. The alternative splicing of this exon suggests a major functional difference between the two TACC2 isoforms, TACC2s and TACC2l [3], as well as a significant difference between TACC2 and its closest TACC family relative, TACC1. However, the function of this region of the TACC2l isoform is current unknown."}