FAM127A

RTL8C

Identifiers

RTL8C, CXX1, MAR8C, MART8C, Mar8, Mart8, FAM127A, family with sequence similarity 127 member A, SIRH5, retrotransposon Gag like 8C

External IDs

MGI: 1920115 HomoloGene: 124163 GeneCards: RTL8C

Gene ontology
Molecular function	• protein binding
Cellular component	• membrane • plasma membrane
Biological process	• biological process
Sources:Amigo / QuickGO

Orthologs

Species

Human

Mouse


8933


72865


ENSG00000134590


ENSMUSG00000051851


O15255


Q9D6I0

RefSeq (mRNA)


NM_003928 NM_001078171


NM_028375

RefSeq (protein)


NP_001071639


NP_082651

Location (UCSC)

Chr X: 135.03 – 135.03 Mb

Chr X: 53.61 – 53.61 Mb

PubMed search

^[1]

^[2]

View/Edit Human

View/Edit Mouse

CAAX box protein 1 is a protein that in humans is encoded by the FAM127A gene.^[3]^[4]^[5]^[6]

References

↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Frattini A, Faranda S, Zucchi I, Vezzoni P (Jan 1998). "A low-copy repeat in Xq26 represents a novel putatively prenylated protein gene (CXX1) and its pseudogenes (DXS9914, DXS9915, and DXS9916)". Genomics. 46 (1): 167–9. PMID 9403077. doi:10.1006/geno.1997.5006.
↑ Brandt J, Schrauth S, Veith AM, Froschauer A, Haneke T, Schultheis C, Gessler M, Leimeister C, Volff JN (Apr 2005). "Transposable elements as a source of genetic innovation: expression and evolution of a family of retrotransposon-derived neogenes in mammals". Gene. 345 (1): 101–11. PMID 15716091. doi:10.1016/j.gene.2004.11.022.
↑ Brandt J, Veith AM, Volff JN (Aug 2005). "A family of neofunctionalized Ty3/gypsy retrotransposon genes in mammalian genomes". Cytogenet Genome Res. 110 (1-4): 307–17. PMID 16093683. doi:10.1159/000084963.
↑ "Entrez Gene: FAM127A family with sequence similarity 127, member A".

Further reading

Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction.". Anal. Biochem. 236 (1): 107–13. PMID 8619474. doi:10.1006/abio.1996.0138.
Yu W, Andersson B, Worley KC, et al. (1997). "Large-scale concatenation cDNA sequencing.". Genome Res. 7 (4): 353–8. PMC 139146 . PMID 9110174. doi:10.1101/gr.7.4.353.
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. PMC 139241 . PMID 12477932. doi:10.1073/pnas.242603899.
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. PMC 528928 . PMID 15489334. doi:10.1101/gr.2596504.
Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature. 434 (7031): 325–37. PMC 2665286 . PMID 15772651. doi:10.1038/nature03440.
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. PMID 16713569. doi:10.1016/j.cell.2006.03.032.

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