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Report for CCDS12688.2 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
12688.2 |
Public |
Homo sapiens |
19 |
DACT3 |
24 |
110 |
108 |
![CCDS History](IMG/ccds-History.jpg) ![](/corehtml/transparent.gif) ![NCBI Gene:147906](IMG/ccds-Gene.jpg) ![](/corehtml/transparent.gif) ![Re-query CCDS DB by CCDS ID:12688.2](IMG/ccds-Cquery.jpg) ![](/corehtml/transparent.gif) ![Re-query CCDS DB by GeneID:147906](IMG/ccds-Gquery.jpg) ![](/corehtml/transparent.gif) ![See the combined annotation on chromosome 19 in Sequence Viewer](IMG/ccds-SeqViewer.jpg) ![](/corehtml/transparent.gif) |
Public Note for CCDS 12688.1 |
The coding region has been updated to extend the N-terminus to one that is more supported by available homology data. There are no full-length transcripts representing the splice pattern of this update in human, but it is supported by human ESTs that tile across the gene, by the mouse ortholog NM_001081655.1 (CCDS39788.1), and by experimental data in PMID:18538736. |
Public since: CCDS release 1, NCBI annotation release 35.1, Ensembl annotation release 23
Review status: Reviewed (by RefSeq, Havana and CCDS collaboration) Sequence IDs included in CCDS 12688.2
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
---|
![Original member](IMG/ccds-Check.jpg) |
![Current member](IMG/ccds-Check.jpg) |
EBI |
ENST00000391916.7 |
ENSP00000375783.2 |
MANE Select |
Accepted |
alive |
![Link to Ensembl Transcript Viewer:ENST00000391916.7](IMG/ccds-Nucleotide.jpg) ![Link to Ensembl Protein Viewer:ENSP00000375783.2](IMG/ccds-Protein.jpg) ![](/corehtml/transparent.gif) ![Re-query CCDS DB by Nucleotide ID:ENST00000391916](IMG/ccds-Nquery.jpg) ![Re-query CCDS DB by Protein ID:ENSP00000375783](IMG/ccds-Pquery.jpg) ![](/corehtml/transparent.gif) |
![Original member](IMG/ccds-Check.jpg) |
![Current member](IMG/ccds-Check.jpg) |
NCBI |
NM_145056.3 |
NP_659493.2 |
MANE Select |
Accepted |
alive |
![Link to Nucleotide Sequence:NM_145056.3](IMG/ccds-Nucleotide.jpg) ![Link to Protein Sequence:NP_659493.2](IMG/ccds-Protein.jpg) ![](/corehtml/transparent.gif) ![Re-query CCDS DB by Nucleotide ID:NM_145056](IMG/ccds-Nquery.jpg) ![Re-query CCDS DB by Protein ID:NP_659493](IMG/ccds-Pquery.jpg) ![](/corehtml/transparent.gif) ![Link to BLAST:NP_659493.2](IMG/ccds-BLAST.jpg) ![](/corehtml/transparent.gif) |
RefSeq |
Length |
Related UniProtKB/SwissProt |
Length |
Identity |
Gaps |
Mismatches |
NP_659493.2 |
629 |
Q96B18 |
629 |
100% |
0 |
0 |
Chromosomal Locations for CCDS 12688.2
Assembly GRCh38.p14 (GCF_000001405.40)
CCDS Sequence Data |
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Blue highlighting indicates alternating exons. | Red highlighting indicates amino acids encoded across a splice junction. | | Mouse over the nucleotide or protein sequence below and click on the highlighted codon or residue to select the pair. |
Nucleotide Sequence (1890 nt): ATGATCCGGGCCTTCTCGTTCCCGGTGAGCCCTGAGCGGGGCCGGCTGCGGGGCTGGCTGGAGGGTAGCC TGGCCGGGCTCTGCGAGTTACATTGGCTCCGGGAGAGGCAGGAGTACCGCGTGCAGCAGGCGCTGCGGCT GGCCCAGCCCGGAATGGGGGGCGCCGAGGCCGAGGACGAGGAGGACGCCGATGAGGATGAAGATGCGGCG GCGGCGCGCCGGGCCGCAGCGGCCCTGGAGGAGCAGCTGGAGGCCCTGCCTGGTCTCGTCTGGGACCTGG GACAGCAGCTGGGAGACCTGAGCCTGGAGTCTGGGGGCCTGGAACAGGAGAGCGGGCGTAGCTCGGGCTT CTATGAAGATCCCAGCTCTACAGGAGGTCCAGATTCACCACCCTCAACCTTCTGTGGGGACAGTGGCTTC TCTGGATCCAGCTCCTATGGTCGCCTGGGTCCCTCTGAGCCCCGGGGCATCTATGCCAGTGAGAGGCCCA AGTCCCTAGGAGACGCCAGTCCCAGCGCTCCGGAGGTGGTGGGCGCGCGGGCAGCGGTGCCGCGGTCCTT CTCAGCGCCCTACCCGACGGCAGGGGGGTCCGCCGGCCCGGAGGCCTGCTCCTCGGCGGAGCGGCGGGCC CGCGCCGGGCCCTTTCTGACGCCCAGCCCCCTGCACGCCGTGGCGATGCGCAGCCCGCGGCCCTGCGGCC GCCCTCCCACCGACTCGCCCGACGCGGGGGGCGCAGGGCGGCCCCTGGACGGCTACATCTCGGCGCTCCT GCGCAGGCGCCGCCGCCGGGGGGCGGGCCAGCCCCGGACCAGTCCCGGGGGCGCGGACGGCGGCCCGCGG CGCCAGAACAGCGTGCGCCAGCGGCCGCCCGACGCGTCTCCGTCCCCCGGCAGCGCGCGACCCGCGCGGG AGCCCTCGTTGGAGCGCGTCGGGGGCCACCCCACCAGCCCTGCCGCCTTGAGCCGCGCCTGGGCGTCGTC GTGGGAGTCGGAGGCGGCACCCGAGCCCGCTGCGCCGCCCGCCGCCCCCTCACCCCCCGACAGCCCGGCT GAGGGCCGCTTGGTGAAGGCGCAGTACATCCCGGGCGCGCAGGCGGCCACCCGAGGCCTCCCTGGCCGCG CCGCCCGCCGCAAACCGCCGCCACTGACCCGCGGCCGCAGCGTGGAGCAGTCACCACCCCGGGAGCGTCC CCGGGCCGCCGGCCGCCGTGGACGCATGGCCGAGGCTTCGGGCCGCCGCGGCTCGCCCAGGGCCCGCAAG GCCTCGCGCTCCCAGTCTGAGACCAGCCTGCTGGGCCGCGCCTCCGCGGTCCCTTCGGGGCCCCCTAAGT ACCCCACGGCGGAGCGGGAAGAGCCTCGGCCTCCACGGCCACGCCGCGGCCCAGCGCCCACGCTGGCGGC CCAGGCCGCAGGGTCCTGCCGTCGCTGGCGCTCCACTGCGGAGATCGACGCTGCCGATGGGCGCCGCGTG CGGCCCCGAGCCCCTGCGGCGCGTGTTCCCGGCCCCGGCCCGTCCCCGTCAGCTCCCCAGCGTCGTCTGC TTTACGGCTGCGCGGGCAGCGACTCCGAGTGCTCGGCTGGGCGCCTGGGGCCCCTGGGACGCCGGGGGCC TGCGGGAGGCGTCGGCGGGGGTTACGGGGAGAGCGAATCGAGCGCCAGCGAGGGAGAATCGCCTGCCTTC AGCTCTGCCTCCAGCGACTCAGACGGCAGCGGTGGCCTCGTGTGGCCGCAGCAGCTGGTGGCGGCCACCG CGGCCTCTGGGGGTGGAGCAGGTGCAGGGGCGCCCGCAGGCCCCGCCAAAGTCTTCGTGAAAATCAAAGC TTCCCACGCGCTCAAGAAAAAGATACTGCGTTTCCGTTCGGGTTCTCTCAAGGTCATGACTACAGTGTGA
Translation (629 aa): MIRAFSFPVSPERGRLRGWLEGSLAGLCELHWLRERQEYRVQQALRLAQPGMGGAEAEDEEDADEDEDAA AARRAAAALEEQLEALPGLVWDLGQQLGDLSLESGGLEQESGRSSGFYEDPSSTGGPDSPPSTFCGDSGF SGSSSYGRLGPSEPRGIYASERPKSLGDASPSAPEVVGARAAVPRSFSAPYPTAGGSAGPEACSSAERRA RAGPFLTPSPLHAVAMRSPRPCGRPPTDSPDAGGAGRPLDGYISALLRRRRRRGAGQPRTSPGGADGGPR RQNSVRQRPPDASPSPGSARPAREPSLERVGGHPTSPAALSRAWASSWESEAAPEPAAPPAAPSPPDSPA EGRLVKAQYIPGAQAATRGLPGRAARRKPPPLTRGRSVEQSPPRERPRAAGRRGRMAEASGRRGSPRARK ASRSQSETSLLGRASAVPSGPPKYPTAEREEPRPPRPRRGPAPTLAAQAAGSCRRWRSTAEIDAADGRRV RPRAPAARVPGPGPSPSAPQRRLLYGCAGSDSECSAGRLGPLGRRGPAGGVGGGYGESESSASEGESPAF SSASSDSDGSGGLVWPQQLVAATAASGGGAGAGAPAGPAKVFVKIKASHALKKKILRFRSGSLKVMTTV
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