ITFG3

FAM234A

Identifiers

FAM234A, C16orf9, gs19, ITFG3, family with sequence similarity 234 member A

External IDs

MGI: 2146854 HomoloGene: 12932 GeneCards: FAM234A

Gene location (Human)

Chr.	Chromosome 16 (human)^[1]

Band	No data available	Start	234,546 bp^[1]
Band	No data available	End	268,971 bp^[1]

Gene location (Mouse)

Chr.	Chromosome 17 (mouse)^[2]

Band	No data available	Start	26,211,822 bp^[2]
Band	No data available	End	26,244,223 bp^[2]

Gene ontology
Molecular function	• molecular function
Cellular component	• membrane • cell surface • extracellular exosome • integral component of membrane
Biological process	• biological process
Sources:Amigo / QuickGO

Orthologs

Species

Human

Mouse


83986


106581


ENSG00000167930


ENSMUSG00000024187


Q9H0X4


Q8C0Z1

RefSeq (mRNA)


NM_001284497 NM_032039


NM_001206335 NM_207217

RefSeq (protein)


NP_001271426 NP_114428


NP_001193264 NP_997100

Location (UCSC)

Chr 16: 0.23 – 0.27 Mb

Chr 17: 26.21 – 26.24 Mb

PubMed search

^[3]

^[4]

View/Edit Human

View/Edit Mouse

Protein ITFG3 is a protein that in humans is encoded by the ITFG3 gene.^[5]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000167930 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024187 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ "Entrez Gene: ITFG3 integrin alpha FG-GAP repeat containing 3".

Further reading

Flint J, Thomas K, Micklem G, et al. (1997). "The relationship between chromosome structure and function at a human telomeric region.". Nat. Genet. 15 (3): 252–7. PMID 9054936. doi:10.1038/ng0397-252.
Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination.". Genome Res. 10 (11): 1788–95. PMC 310948 . PMID 11076863. doi:10.1101/gr.143000.
Daniels RJ, Peden JF, Lloyd C, et al. (2001). "Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.". Hum. Mol. Genet. 10 (4): 339–52. PMID 11157797. doi:10.1093/hmg/10.4.339.
Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422–35. PMC 311072 . PMID 11230166. doi:10.1101/gr.GR1547R.
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.
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. PMID 14702039. doi:10.1038/ng1285.
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.
Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline.". Genome Res. 14 (10B): 2136–44. PMC 528930 . PMID 15489336. doi:10.1101/gr.2576704.
Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006.". Nucleic Acids Res. 34 (Database issue): D415–8. PMC 1347501 . PMID 16381901. doi:10.1093/nar/gkj139.

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