SMARCAD1
From Wikipedia, the free encyclopedia
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
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Identifiers | ||||||||||||||
Symbol(s) | SMARCAD1; ETL1; DKFZp762K2015; KIAA1122 | |||||||||||||
External IDs | MGI: 95453 HomoloGene: 5301 | |||||||||||||
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Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 56916 | 13990 | ||||||||||||
Ensembl | ENSG00000163104 | ENSMUSG00000029920 | ||||||||||||
Uniprot | Q9H4L7 | Q3UGK6 | ||||||||||||
Refseq | NM_020159 (mRNA) NP_064544 (protein) |
NM_007958 (mRNA) NP_031984 (protein) |
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Location | Chr 4: 95.35 - 95.43 Mb | Chr 6: 64.97 - 65.05 Mb | ||||||||||||
Pubmed search | [1] | [2] |
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1, also known as SMARCAD1, is a human gene.[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.
- 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.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi: . PMID 14702039.
- 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.
- Adra CN, Donato JL, Badovinac R, et al. (2001). "SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases.". Genomics 69 (2): 162-73. doi: . PMID 11031099.
- Hirosawa M, Nagase T, Ishikawa K, et al. (2000). "Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain.". DNA Res. 6 (5): 329-36. PMID 10574461.
- Soininen R, Schoor M, Henseling U, et al. (1993). "The mouse Enhancer trap locus 1 (Etl-1): a novel mammalian gene related to Drosophila and yeast transcriptional regulator genes.". Mech. Dev. 39 (1-2): 111-23. PMID 1489724.