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History Report on CCDS ID 47925 Interpretation | Date | Source | Comment | Data |
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CCDS: Made public |
09/02/2009 |
NCBI |
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CCDS Release: 6 |
CCDS: Public note |
08/09/2010 |
NCBI |
The coding region has been updated to shorten the N-terminus to one that is supported by the reference genome allele (GRCh37 assembly). The previous representation used a polymorphic start codon that exists as ACG in the reference genome allele versus ATG in the alternate allele (also known as the T allele). This corresponds to the reference SNP rs2294008. Some individuals contain the reference genome allele, while others contain the T allele. Data in PMIDs 18488030, 19554573, 19582881 and 19648920 indicate that the T allele may be a risk allele for gastric and bladder cancers. It is also associated with decreased promoter activity (PMIDs 18488030 and 19648920). The current update results in a protein that is 9 aa shorter at the N-terminus. |
CCDS version: 47925.1 |
CCDS: Partial match |
03/30/2011 |
NCBI |
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CCDS Release: 8 |
CCDS: Partial match |
08/11/2011 |
NCBI |
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CCDS Release: 9 |
CCDS: Reinstated |
09/19/2012 |
NCBI |
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CCDS Release: 11 |
CCDS: Updated |
09/19/2012 |
NCBI |
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CCDS Release: 11 |
CCDS: Retained |
03/21/2013 |
NCBI |
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CCDS Release: 12 |
CCDS: Retained |
08/30/2013 |
NCBI |
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CCDS Release: 14 |
CCDS: Retained |
11/21/2013 |
NCBI |
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CCDS Release: 15 |
CCDS: Retained |
06/20/2014 |
NCBI |
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CCDS Release: 17 |
CCDS: Retained |
04/03/2015 |
NCBI |
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CCDS Release: 18 |
CCDS: Retained |
08/11/2016 |
NCBI |
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CCDS Release: 20 |
CCDS: Review status |
10/03/2016 |
NCBI |
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by RefSeq, Havana and CCDS collaboration |
CCDS: Retained |
05/16/2018 |
NCBI |
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CCDS Release: 22 |
CCDS: Retained |
08/10/2022 |
NCBI |
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CCDS Release: 24 |
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