DHX16
From Wikipedia, the free encyclopedia
DEAH (Asp-Glu-Ala-His) box polypeptide 16
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Identifiers | ||||||||||||||
Symbol(s) | DHX16; DBP2; DDX16; PRO2014; PRP8 | |||||||||||||
External IDs | OMIM: 603405 MGI: 1916442 HomoloGene: 2658 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 8449 | 69192 | ||||||||||||
Ensembl | ENSG00000204560 | ENSMUSG00000024422 | ||||||||||||
Uniprot | O60231 | n/a | ||||||||||||
Refseq | NM_003587 (mRNA) NP_003578 (protein) |
NM_026987 (mRNA) NP_081263 (protein) |
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Location | Chr 6: 30.73 - 30.75 Mb | Chr 17: 35.49 - 35.5 Mb | ||||||||||||
Pubmed search | [1] | [2] |
DEAH (Asp-Glu-Ala-His) box polypeptide 16, also known as DHX16, is a human gene.[1]
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked.[1]
[edit] References
[edit] Further reading
- Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.". Cell 127 (3): 635-48. doi: . PMID 17081983.
- Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.". Cell 125 (4): 801-14. doi: . PMID 16713569.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi: . PMID 15489334.
- Beausoleil SA, Jedrychowski M, Schwartz D, et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins.". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130-5. doi: . PMID 15302935.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi: . PMID 12477932.
- Nakayama M, Kikuno R, Ohara O (2003). "Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs.". Genome Res. 12 (11): 1773-84. doi: . PMID 12421765.
- Nagase T, Ishikawa K, Miyajima N, et al. (1998). "Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.". DNA Res. 5 (1): 31-9. PMID 9628581.
- Imamura O, Saiki K, Tani T, et al. (1998). "Cloning and characterization of a human DEAH-box RNA helicase, a functional homolog of fission yeast Cdc28/Prp8.". Nucleic Acids Res. 26 (9): 2063-8. PMID 9547260.