C11orf49

C11orf49
Identifiers
AliasesC11orf49, chromosome 11 open reading frame 49
External IDsMGI: 1915079 HomoloGene: 11471 GeneCards: C11orf49
Gene location (Human)
Chr.Chromosome 11 (human)[1]
Band11p11.2Start46,936,689 bp[1]
End47,164,385 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

79096

228356

Ensembl

ENSG00000149179

ENSMUSG00000040591

UniProt

Q9H6J7

Q8BHR8

RefSeq (mRNA)

NM_001003676
NM_001003677
NM_001003678
NM_001278222
NM_024113

NM_175123
NM_001311144

RefSeq (protein)

NP_001003676
NP_001003677
NP_001003678
NP_001265151
NP_077018

NP_001298073
NP_780332

Location (UCSC)Chr 11: 46.94 – 47.16 MbChr 2: 91.28 – 91.44 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

UPF0705 protein C11orf49 is a protein that in humans is encoded by the C11orf49 gene.[5]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000149179 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000040591 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ "Entrez Gene: C11orf49 chromosome 11 open reading frame 49".

Further reading

  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
  • Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.
  • Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
  • Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
  • Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
  • 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. doi:10.1016/j.cell.2006.03.032. PMID 16713569.


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