CENTA2

From Wikipedia, the free encyclopedia

Centaurin, alpha 2

Identifiers

CENTA2; HSA272195; cent-b

External IDs

OMIM: 608635 MGI: 2663075 HomoloGene: 10179

Gene ontology
Molecular Function:	• GTPase activator activity • phosphatidylinositol-4,5-bisphosphate binding • phosphatidylinositol-3,4,5-triphosphate binding • zinc ion binding • protein binding, bridging • phosphatidylinositol-3,4-bisphosphate binding • inositol 1,3,4,5 tetrakisphosphate binding • metal ion binding
Cellular Component:	• cytoplasm • mitochondrial envelope • plasma membrane
Biological Process:	• heart development • regulation of GTPase activity

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_018404 (mRNA)
NP_060874 (protein)

NM_172133 (mRNA)
NP_742145 (protein)

Location

Chr 17: 26.27 - 26.31 Mb

Chr 11: 79.97 - 80 Mb

Pubmed search

[1]

[2]

Centaurin, alpha 2, also known as CENTA2, is a human gene.^[1]

[edit] References

^ Entrez Gene: CENTA2 centaurin, alpha 2.

[edit] Further reading

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. PMID 8125298.
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. PMID 9373149.
Jenne DE, Tinschert S, Stegmann E, et al. (2000). "A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions.". Genomics 66 (1): 93-7. doi:10.1006/geno.2000.6179. PMID 10843809.
Whitley P, Gibbard AM, Koumanov F, et al. (2003). "Identification of centaurin-alpha2: a phosphatidylinositide-binding protein present in fat, heart and skeletal muscle.". Eur. J. Cell Biol. 81 (4): 222-30. PMID 12018390.
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. PMID 12477932.
Hanck T, Stricker R, Sedehizade F, Reiser G (2004). "Identification of gene structure and subcellular localization of human centaurin alpha 2, and p42IP4, a family of two highly homologous, Ins 1,3,4,5-P4-/PtdIns 3,4,5-P3-binding, adapter proteins.". J. Neurochem. 88 (2): 326-36. PMID 14690521.
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. PMID 15489334.
Venturin M, Bentivegna A, Moroni R, et al. (2005). "Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval.". Ann. Hum. Genet. 69 (Pt 5): 508-16. doi:10.1111/j.1529-8817.2005.00203.x. PMID 16138909.
Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.". Nat. Genet. 39 (8): 963-5. doi:10.1038/ng2083. PMID 17632510.