C16orf96, or chromosome 16 open reading frame 96, is a protein in humans that is encoded by C16orf96 that is found on the 16th chromosome.[5] In Homo sapiens, the protein is 1141 amino acids in length[6]

C16orf96
Identifiers
AliasesC16orf96, chromosome 16 open reading frame 96
External IDsMGI: 1926059; HomoloGene: 53527; GeneCards: C16orf96; OMA:C16orf96 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145011
NM_001387219

NM_001252142
NM_030192

RefSeq (protein)

NP_001138483

NP_084468

Location (UCSC)Chr 16: 4.56 – 4.6 MbChr 16: 4.65 – 4.69 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein

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The structure of human C16orf96 protein with important regions labeled. The dark grey lines within the proline rich region and the domain of unknown function are nuclear import and export signals, respectively.

Characteristics

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The molecular weight of the processed C16orf96 protein in humans is 125kdal with an isoelectric point of 6.58[7] About 9% of the amino acid makeup of C16orf96 is proline, which is significantly higher than an average human gene.[8]

Post Translational Modification

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Human C16orf96 has a large amount of predicted phosphorylation sites on serines throughout the protein.[9] C16orf96 also has been found in primates and mammals to have both a nuclear import and export signal[10]

Domains

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This gene contains some known domains, such as: an RNA recognition motif, a Merozoite surface protein (MSP-1), a pentapeptide repeat MXKDX, and a domain of unknown function (DUF1387). These domains could give a hint of what the function of this gene is.[6]

Structure

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Secondary Structure

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The majority of the secondary structure of C16orf96 is alpa-helices with coils being the second most abundant structure.[11]

Tertiary Structure

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At this time there is no known tertiary structure for C16orf96.

Cellular Localization

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The C16orf96 protein is predicted to be localized in the nucleus 82% of the time and 4.5% of the time in the cytosol and 4.5% of the time in the mitochondria.[12]

Expression

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Expression of C16orf96 when different hypoxia-inducible factors are reduced

C16orf96 expression is generally low in cells. in situ hybridization experiments suggest that C16orf96 RNA is only expressed in the testis while the EST profile for C16orf96 shows gene expression is low in testis and skin only.[13][14] Expression of the C16orf96 gene is modulated by the depletion of both hypoxia induced factor 1/2α (HIF1/2α). When only one of the factors is depleted expression does not change suggesting that there is redundancy with these two HIF.[15]

Homology

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Strict orthologs of this gene exist only in mammals. However, a portion of DUF1387 is found in more distant species back to reptiles.[16] No orthologs of this gene can be found in plants, fungi, or bacteria. Suggesting that this gene is relatively new and evolves quickly.

Function

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The function of C16orf96 is currently unknown. Studies have cited this gene among many other genes as a possible candidate that has an effect on childhood obesity.[17]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000205832Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022518Ensembl, 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. ^ Martin J, Han C, Gordon LA, Terry A, Prabhakar S, She X, et al. (December 2004). "The sequence and analysis of duplication-rich human chromosome 16". Nature. 432 (7020): 988–94. Bibcode:2004Natur.432..988M. doi:10.1038/nature03187. PMID 15616553.
  6. ^ a b NCBI Protein NP_001138483
  7. ^ GeneCards C16orf96
  8. ^ Biology Workbench: SAPS Tool[permanent dead link]
  9. ^ NetPhos 2.0
  10. ^ NetNES 1.1
  11. ^ Biology Workbench: PELE Tool
  12. ^ "PSORT II Server". Archived from the original on 2021-07-09. Retrieved 2015-04-30.
  13. ^ The Human Protein Atlas of C16orf96
  14. ^ EST profile Hs.684212
  15. ^ GeoProfiles ID:40057343
  16. ^ NCBI BLAST
  17. ^ Comuzzie AG, Cole SA, Laston SL, Voruganti VS, Haack K, Gibbs RA, et al. (2012). "Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population". PLOS ONE. 7 (12): e51954. Bibcode:2012PLoSO...751954C. doi:10.1371/journal.pone.0051954. PMC 3522587. PMID 23251661.]
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