Family with sequence similarity 13, member A1

FAM13A

Identifiers

FAM13A, ARHGAP48, FAM13A1, Family with sequence similarity 13, member A1, family with sequence similarity 13 member A

External IDs

HomoloGene: 8922 GeneCards: FAM13A

Genetically Related Diseases

chronic obstructive pulmonary disease, interstitial lung disease^[1]

Gene ontology
Molecular function	• GTPase activator activity
Cellular component	• cytosol
Biological process	• positive regulation of GTPase activity • regulation of small GTPase mediated signal transduction • signal transduction
Sources:Amigo / QuickGO

RNA expression pattern

More reference expression data

Orthologs

Species

Human

Mouse


10144


n/a


ENSG00000138640


n/a


O94988 Q6P521


n/a

RefSeq (mRNA)


NM_001015045 NM_001265578 NM_001265579 NM_001265580 NM_014883


n/a

RefSeq (protein)


NP_001015045.1 NP_001252507.1 NP_001252508.1 NP_001252509.1 NP_055698.2


n/a

Location (UCSC)

Chr 4: 88.73 – 89.11 Mb

n/a

PubMed search

^[2]

n/a

View/Edit Human

Protein FAM13A is a protein that in humans is encoded by the FAM13A gene.^[3]

References

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. PMC 514446. 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. PMC 139241. 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. doi:10.1093/dnares/5.6.355. 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. doi:10.1101/gr.7.9.887. PMID 9314494.

External links

FAM13A human gene location in the UCSC Genome Browser.
FAM13A human gene details in the UCSC Genome Browser.

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