- DENND1A
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DENN/MADD domain containing 1A Identifiers Symbols DENND1A; FAM31A; FLJ38464; KIAA1608; RP11-230L22.3 External IDs OMIM: 613633 MGI: 2442794 HomoloGene: 17141 GeneCards: DENND1A Gene Gene Ontology Molecular function • guanyl-nucleotide exchange factor activity
• SH3 domain bindingCellular component • plasma membrane
• cell junction
• dendrite
• clathrin coated vesicle membrane
• cytoplasmic vesicle
• presynaptic membrane
• neuronal cell body
• synapseBiological process • synaptic vesicle endocytosis Sources: Amigo / QuickGO RNA expression pattern More reference expression data Orthologs Species Human Mouse Entrez 57706 227801 Ensembl ENSG00000119522 ENSMUSG00000035392 UniProt Q8TEH3 A0MCI0 RefSeq (mRNA) NM_020946.1 NM_146122.3 RefSeq (protein) NP_065997.1 NP_666234.3 Location (UCSC) Chr 9:
126.14 – 126.69 MbChr 2:
37.65 – 38.14 MbPubMed search [1] [2] DENN domain-containing protein 1A is a protein that in humans is encoded by the DENND1A gene.[1][2]
References
- ^ Nagase T, Kikuno R, Nakayama M, Hirosawa M, Ohara O (Dec 2000). "Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res 7 (4): 273–81. doi:10.1093/dnares/7.4.271. PMID 10997877.
- ^ "Entrez Gene: DENND1A DENN/MADD domain containing 1A". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57706.
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:10.1016/j.cell.2006.09.026. 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:10.1101/gr.2596504. PMC 528928. PMID 15489334. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=528928.
- Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9". Nature 429 (6990): 369–74. doi:10.1038/nature02465. PMC 2734081. PMID 15164053. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2734081.
- 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:10.1038/ng1285. 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:10.1073/pnas.242603899. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Categories:- Human proteins
- Chromosome 9 gene stubs
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