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FAM13A
Identifiers
Aliases	FAM13A, ARHGAP48, FAM13A1, Family with sequence similarity 13, member A1, family with sequence similarity 13 member A
External IDs	OMIM: 613299; MGI: 1889842; HomoloGene: 8922; GeneCards: FAM13A; OMA:FAM13A - orthologs
Gene location (Human) Chr. Chromosome 4 (human) Band 4q22.1 Start 88,725,955 bp End 89,111,398 bp
Gene location (Mouse) Chr. Chromosome 6 (mouse) Band 6|6 B3 Start 58,909,075 bp End 59,001,534 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in secondary oocyte jejunal mucosa retinal pigment epithelium bronchial epithelial cell Epithelium of choroid plexus parietal pleura parotid gland hair follicle renal medulla duodenum Top expressed in retinal pigment epithelium cumulus cell brown adipose tissue lobe of cerebellum cerebellar vermis ciliary body intercostal muscle mammary gland otolith organ utricle More reference expression data BioGPS More reference expression data
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
Orthologs Species Human Mouse Entrez 10144 58909 Ensembl ENSG00000138640 ENSMUSG00000037709 UniProt O94988 Q6P521 Q8BGI4 RefSeq (mRNA) NM_001015045 NM_001265578 NM_001265579 NM_001265580 NM_014883 NM_153574 RefSeq (protein) NP_001015045 NP_001252507 NP_001252508 NP_001252509 NP_055698 NP_705802 Location (UCSC) Chr 4: 88.73 – 89.11 Mb Chr 6: 58.91 – 59 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Protein FAM13A is a protein that in humans is encoded by the FAM13A gene.

References

1. ^ GRCh38: Ensembl release 89: ENSG00000138640 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000037709 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "Entrez Gene: FAM13A1 family with sequence similarity 13, member A1".

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. S2CID 14294292.
• 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. Bibcode:2004PNAS..10112130B. 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. Bibcode:2002PNAS...9916899M. 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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