C5orf22 - significado y definición. Qué es C5orf22
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Qué (quién) es C5orf22 - definición


C5orf22         
  • '''C5orf22 gene diagram.''' Human C5orf22 is located on chromosome 5 (5p13.3) at base pair 31,532,275 to 31,555,053. Transcript variant 1 (depicted above) encodes 9 exons.1 Promoter prediction is from Genomatix.<ref name=":2"/> The GXP# for the promoter is GXP_55076. Pro1, is the assigned promoter for all transcript variants. This promoter lies directly upstream from the 5’ UTR and spans 1,081 base pairs. Promoter is labeled in green. Exons (Ex) are denoted in dark blue. Illustration was created using Domain Illustrator.21  
  • '''UPF0489 C5orf22 rate of evolution.''' Estimated time of divergence from human C5orf22 (millions of years ago; MYA) versus % corrected divergence of orthologous protein (m; total # of AA changes/100 residues). Slopes for fibrinogen alpha, C5orf22, and cytochrome C are 0.24, 0.09, and 0.03, respectively. Orthologs are monkey (''Callithrix jacchus''), mouse (''Mus musculus''), bird (''Merops nubicus''), frog (''Xenopus laevis''), and fish (''Danio rerio''). Data points for C5orf22 are displayed in blue. Data points for cytochrome C are shown in red. Data points for fibrinogen alpha are indicated in yellow. All data was collected from NCBI BLASTP.
  • '''C5orf22 protein structure contains 2 globular domains and 3 disordered regions.'''
  • '''Annotated human chromosome 5.''' Retrieved from NCBI Gene.<ref name=":1" />
  • website=www.mirdb.org}}</ref> PolyA signal: Polyadenylation regulatory signal.
PROTEIN-CODING GENE IN THE SPECIES HOMO SAPIENS
Chromosome 5 open reading frame 22 (c5orf22) is a protein-coding gene of poorly characterized function in Homo sapiens. The primary alias is unknown protein family 0489 (UPF0489).