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History Report on CCDS ID 37566 Interpretation | Date | Source | Comment | Data |
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CCDS: Made public |
11/28/2007 |
NCBI |
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CCDS Release: 4 |
CCDS: Retained |
12/22/2010 |
NCBI |
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CCDS Release: 7 |
CCDS: Public note |
01/19/2011 |
NCBI |
This CCDS representation lacks publicly available full-length transcript support in mouse. However, it is supported by the full-length human transcript AF163762.1, by partial mouse EST alignments including BB840099.1, and by the full-length sequence described for this mouse protein in PMID:15355968. Other mouse full-length transcript variants are available for this gene, including BC082773.1, AK042525.1 and BC056427.1, but it should be noted that all of these include an alternative splice acceptor site in exon 6, which results in a premature termination codon that likely leads to nonsense-mediated mRNA decay (NMD). The exon combination represented in this CCDS is therefore more likely to be protein-coding. |
CCDS version: 37566.1 |
CCDS: Retained |
06/21/2012 |
NCBI |
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CCDS Release: 10 |
CCDS: Retained |
07/24/2013 |
NCBI |
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CCDS Release: 13 |
CCDS: Retained |
02/25/2014 |
NCBI |
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CCDS Release: 16 |
CCDS: Retained |
07/07/2015 |
NCBI |
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CCDS Release: 19 |
CCDS: Review status |
10/03/2016 |
NCBI |
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by RefSeq, Havana and CCDS collaboration |
CCDS: Retained |
11/07/2016 |
NCBI |
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CCDS Release: 21 |
CCDS: Retained |
10/02/2019 |
NCBI |
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CCDS Release: 23 |
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