FAM13A1

From Wikipedia, the free encyclopedia


Family with sequence similarity 13, member A1
Identifiers
Symbol(s) FAM13A1; FLJ34562; MGC105131
External IDs MGI1889842 HomoloGene8922
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 10144 58909
Ensembl ENSG00000138640 ENSMUSG00000037709
Uniprot O94988 Q05DP6
Refseq NM_001015045 (mRNA)
NP_001015045 (protein)
NM_153574 (mRNA)
NP_705802 (protein)
Location Chr 4: 89.87 - 90.2 Mb Chr 6: 58.86 - 58.95 Mb
Pubmed search [1] [2]

Family with sequence similarity 13, member A1, also known as FAM13A1, is a human gene.[1]


[edit] References

[edit] Further reading

  • Beausoleil SA, Villén J, Gerber SA, et al. (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization.". Nat. Biotechnol. 24 (10): 1285-92. doi:10.1038/nbt1240. PMID 16964243. 
  • 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:10.1073/pnas.0404720101. PMID 15302935. 
  • Cohen M, Reichenstein M, Everts-van der Wind A, et al. (2005). "Cloning and characterization of FAM13A1--a gene near a milk protein QTL on BTA6: evidence for population-wide linkage disequilibrium in Israeli Holsteins.". Genomics 84 (2): 374-83. doi:10.1016/j.ygeno.2004.03.005. PMID 15234000. 
  • 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. PMID 12477932. 
  • Nagase T, Ishikawa K, Suyama M, et al. (1999). "Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.". DNA Res. 5 (6): 355-64. PMID 10048485. 
  • Ranta S, Lehesjoki AE, de Fatima Bonaldo M, et al. (1997). "High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.". Genome Res. 7 (9): 887-96. PMID 9314494.