Uncharacterized protein C15orf32 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Uncharacterized protein C15orf32" in English language version.

refsWebsite

Global rank English rank

24nih.gov

4^th place

10doi.org

2^nd place

3dtu.dk

low place

8,755^th place

2harvard.edu

18^th place

17^th place

2web.archive.org

1^st place

2semanticscholar.org

11^th place

8^th place

1ensembl.org

1,626^th place

1,007^th place

1genecards.org

low place

1biologicalpsychiatryjournal.com

low place

1biogem.org

low place

1phosphosite.org

low place

1ebi.ac.uk

5,849^th place

7,886^th place

1umich.edu

459^th place

360^th place

1su.se

low place

1genomatix.de

low place

1oreganno.org

low place

1albany.edu

7,412^th place

4,821^st place

1targetscan.org

low place

1sigmaaldrich.com

924^th place

2,352^nd place

1genscript.com

low place

1abcepta.com

low place

1thebiogrid.org

low place

1expasy.org

7,021^st place

7,383^rd place

abcepta.com

"SUMOplot™ Analysis Program | Abcepta". www.abcepta.com. Retrieved 2020-05-03.

albany.edu

unafold.rna.albany.edu

"RNA Folding Form | mfold.rit.albany.edu". unafold.rna.albany.edu. Retrieved 2020-05-03.

biogem.org

"CFSSP: Chou & Fasman Secondary Structure Prediction Server". www.biogem.org. Retrieved 2020-05-03.

biologicalpsychiatryjournal.com

Heath AC, Whitfield JB, Martin NG, Pergadia ML, Goate AM, Lind PA, et al. (September 2011). "A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications". Biological Psychiatry. 70 (6): 513–8. doi:10.1016/j.biopsych.2011.02.028. PMC 3210694. PMID 21529783.

doi.org

Lee MT, Chen CH, Lee CS, Chen CC, Chong MY, Ouyang WC, et al. (May 2011). "Genome-wide association study of bipolar I disorder in the Han Chinese population". Molecular Psychiatry. 16 (5): 548–56. doi:10.1038/mp.2010.43. PMID 20386566.
McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, et al. (2012-05-31). "Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26". PLOS ONE. 7 (5): e38172. Bibcode:2012PLoSO...738172M. doi:10.1371/journal.pone.0038172. PMC 3364966. PMID 22693595.
Heath AC, Whitfield JB, Martin NG, Pergadia ML, Goate AM, Lind PA, et al. (September 2011). "A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications". Biological Psychiatry. 70 (6): 513–8. doi:10.1016/j.biopsych.2011.02.028. PMC 3210694. PMID 21529783.
Lv H, Zhang M, Shang Z, Li J, Zhang S, Lian D, Zhang R (January 2017). "Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia". Oncotarget. 8 (5): 7891–7899. doi:10.18632/oncotarget.13631. PMC 5352368. PMID 27903959.
Fouz N, Amid A, Hashim YZ (August 2014). "Gene expression analysis in MCF-7 breast cancer cells treated with recombinant bromelain". Applied Biochemistry and Biotechnology. 173 (7): 1618–39. doi:10.1007/s12010-014-0947-6. PMID 24928548. S2CID 207356247.
Nicoloso MS, Sun H, Spizzo R, Kim H, Wickramasinghe P, Shimizu M, et al. (April 2010). "Single-nucleotide polymorphisms inside microRNA target sites influence tumor susceptibility". Cancer Research. 70 (7): 2789–98. doi:10.1158/0008-5472.CAN-09-3541. PMC 2853025. PMID 20332227.
Rubicz R, Yolken R, Alaedini A, Drigalenko E, Charlesworth JC, Carless MA, et al. (July 2014). "Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens". Genetic Epidemiology. 38 (5): 439–46. doi:10.1002/gepi.21817. PMC 4171053. PMID 24962563.
Wilk JB, Walter RE, Laramie JM, Gottlieb DJ, O'Connor GT (September 2007). "Framingham Heart Study genome-wide association: results for pulmonary function measures". BMC Medical Genetics. 8 Suppl 1 (1): S8. doi:10.1186/1471-2350-8-S1-S8. PMC 1995616. PMID 17903307.
Chernus J, Roosenboom J, Ford M, Lee MK, Emanuele B, Anderton J, et al. (May 2018). "GWAS reveals loci associated with velopharyngeal dysfunction". Scientific Reports. 8 (1): 8470. Bibcode:2018NatSR...8.8470C. doi:10.1038/s41598-018-26880-w. PMC 5981322. PMID 29855589.
Kamien B, Harraway J, Lundie B, Smallhorne L, Gibbs V, Heath A, Fullerton JM (March 2014). "Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy". American Journal of Medical Genetics. Part A. 164A (3): 782–8. doi:10.1002/ajmg.a.36345. PMID 24357335. S2CID 27921887.

dtu.dk

services.healthtech.dtu.dk

"DeepLoc - 1.0". DTU Health Tech.
"NetPhos 3.1: Generic phosphorylation sites in eukaryotic proteins". healthtech.dtu.dk. Retrieved 2020-05-03.
"NetOGlyc - 4.0". DTU Health Tech.

ebi.ac.uk

"SAPS < Sequence Statistics < EMBL-EBI". www.ebi.ac.uk. Retrieved 2020-05-03.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000183643 – Ensembl, May 2017

expasy.org

web.expasy.org

"UniProtKB/SwissProt variant VAR_050884". web.expasy.org. Retrieved 2020-03-02.

genecards.org

"C15orf32 Gene - GeneCards | C15orf32 RNA Gene". www.genecards.org. Retrieved 2020-03-02.

genomatix.de

"Genomatix - NGS Data Analysis & Personalized Medicine". www.genomatix.de. Archived from the original on 2001-02-24. Retrieved 2020-05-03.

genscript.com

"PSORT II server - GenScript". www.genscript.com. Retrieved 2020-05-03.

harvard.edu

ui.adsabs.harvard.edu

McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, et al. (2012-05-31). "Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26". PLOS ONE. 7 (5): e38172. Bibcode:2012PLoSO...738172M. doi:10.1371/journal.pone.0038172. PMC 3364966. PMID 22693595.
Chernus J, Roosenboom J, Ford M, Lee MK, Emanuele B, Anderton J, et al. (May 2018). "GWAS reveals loci associated with velopharyngeal dysfunction". Scientific Reports. 8 (1): 8470. Bibcode:2018NatSR...8.8470C. doi:10.1038/s41598-018-26880-w. PMC 5981322. PMID 29855589.

nih.gov

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, et al. (2012-05-31). "Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26". PLOS ONE. 7 (5): e38172. Bibcode:2012PLoSO...738172M. doi:10.1371/journal.pone.0038172. PMC 3364966. PMID 22693595.
Heath AC, Whitfield JB, Martin NG, Pergadia ML, Goate AM, Lind PA, et al. (September 2011). "A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications". Biological Psychiatry. 70 (6): 513–8. doi:10.1016/j.biopsych.2011.02.028. PMC 3210694. PMID 21529783.
Lv H, Zhang M, Shang Z, Li J, Zhang S, Lian D, Zhang R (January 2017). "Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia". Oncotarget. 8 (5): 7891–7899. doi:10.18632/oncotarget.13631. PMC 5352368. PMID 27903959.
"Homo sapiens chromosome 15 putative open reading frame 32 (C15orf32), transcript variant 2, long non-coding RNA". 2019-10-06. {{cite journal}}: Cite journal requires |journal= (help)
"Homo sapiens chromosome 15 putative open reading frame 32 (C15orf32), transcript variant 1, long non-coding RNA". 2019-10-06. {{cite journal}}: Cite journal requires |journal= (help)
"C15orf32 Gene Expression - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2020-05-03.
"GDS4089 / ILMN_1773848". www.ncbi.nlm.nih.gov. Retrieved 2020-05-03.
"GDS4065 / 1553482_at". www.ncbi.nlm.nih.gov. Retrieved 2020-05-03.
Nicoloso MS, Sun H, Spizzo R, Kim H, Wickramasinghe P, Shimizu M, et al. (April 2010). "Single-nucleotide polymorphisms inside microRNA target sites influence tumor susceptibility". Cancer Research. 70 (7): 2789–98. doi:10.1158/0008-5472.CAN-09-3541. PMC 2853025. PMID 20332227.
Rubicz R, Yolken R, Alaedini A, Drigalenko E, Charlesworth JC, Carless MA, et al. (July 2014). "Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens". Genetic Epidemiology. 38 (5): 439–46. doi:10.1002/gepi.21817. PMC 4171053. PMID 24962563.
Wilk JB, Walter RE, Laramie JM, Gottlieb DJ, O'Connor GT (September 2007). "Framingham Heart Study genome-wide association: results for pulmonary function measures". BMC Medical Genetics. 8 Suppl 1 (1): S8. doi:10.1186/1471-2350-8-S1-S8. PMC 1995616. PMID 17903307.
Chernus J, Roosenboom J, Ford M, Lee MK, Emanuele B, Anderton J, et al. (May 2018). "GWAS reveals loci associated with velopharyngeal dysfunction". Scientific Reports. 8 (1): 8470. Bibcode:2018NatSR...8.8470C. doi:10.1038/s41598-018-26880-w. PMC 5981322. PMID 29855589.
"HomoloGene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2020-03-02.

pubmed.ncbi.nlm.nih.gov

Lee MT, Chen CH, Lee CS, Chen CC, Chong MY, Ouyang WC, et al. (May 2011). "Genome-wide association study of bipolar I disorder in the Han Chinese population". Molecular Psychiatry. 16 (5): 548–56. doi:10.1038/mp.2010.43. PMID 20386566.
McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, et al. (2012-05-31). "Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26". PLOS ONE. 7 (5): e38172. Bibcode:2012PLoSO...738172M. doi:10.1371/journal.pone.0038172. PMC 3364966. PMID 22693595.
Heath AC, Whitfield JB, Martin NG, Pergadia ML, Goate AM, Lind PA, et al. (September 2011). "A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications". Biological Psychiatry. 70 (6): 513–8. doi:10.1016/j.biopsych.2011.02.028. PMC 3210694. PMID 21529783.
Lv H, Zhang M, Shang Z, Li J, Zhang S, Lian D, Zhang R (January 2017). "Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia". Oncotarget. 8 (5): 7891–7899. doi:10.18632/oncotarget.13631. PMC 5352368. PMID 27903959.
Fouz N, Amid A, Hashim YZ (August 2014). "Gene expression analysis in MCF-7 breast cancer cells treated with recombinant bromelain". Applied Biochemistry and Biotechnology. 173 (7): 1618–39. doi:10.1007/s12010-014-0947-6. PMID 24928548. S2CID 207356247.
Nicoloso MS, Sun H, Spizzo R, Kim H, Wickramasinghe P, Shimizu M, et al. (April 2010). "Single-nucleotide polymorphisms inside microRNA target sites influence tumor susceptibility". Cancer Research. 70 (7): 2789–98. doi:10.1158/0008-5472.CAN-09-3541. PMC 2853025. PMID 20332227.
Rubicz R, Yolken R, Alaedini A, Drigalenko E, Charlesworth JC, Carless MA, et al. (July 2014). "Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens". Genetic Epidemiology. 38 (5): 439–46. doi:10.1002/gepi.21817. PMC 4171053. PMID 24962563.
Wilk JB, Walter RE, Laramie JM, Gottlieb DJ, O'Connor GT (September 2007). "Framingham Heart Study genome-wide association: results for pulmonary function measures". BMC Medical Genetics. 8 Suppl 1 (1): S8. doi:10.1186/1471-2350-8-S1-S8. PMC 1995616. PMID 17903307.
Chernus J, Roosenboom J, Ford M, Lee MK, Emanuele B, Anderton J, et al. (May 2018). "GWAS reveals loci associated with velopharyngeal dysfunction". Scientific Reports. 8 (1): 8470. Bibcode:2018NatSR...8.8470C. doi:10.1038/s41598-018-26880-w. PMC 5981322. PMID 29855589.
Kamien B, Harraway J, Lundie B, Smallhorne L, Gibbs V, Heath A, Fullerton JM (March 2014). "Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy". American Journal of Medical Genetics. Part A. 164A (3): 782–8. doi:10.1002/ajmg.a.36345. PMID 24357335. S2CID 27921887.

oreganno.org

"ORegAnno Temporary Homepage". www.oreganno.org. Archived from the original on 2021-03-21. Retrieved 2020-05-03.

phosphosite.org

"C15orf32 (human)". www.phosphosite.org. Retrieved 2020-03-02.

semanticscholar.org

api.semanticscholar.org

Fouz N, Amid A, Hashim YZ (August 2014). "Gene expression analysis in MCF-7 breast cancer cells treated with recombinant bromelain". Applied Biochemistry and Biotechnology. 173 (7): 1618–39. doi:10.1007/s12010-014-0947-6. PMID 24928548. S2CID 207356247.
Kamien B, Harraway J, Lundie B, Smallhorne L, Gibbs V, Heath A, Fullerton JM (March 2014). "Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy". American Journal of Medical Genetics. Part A. 164A (3): 782–8. doi:10.1002/ajmg.a.36345. PMID 24357335. S2CID 27921887.

sigmaaldrich.com

"Anti-C15orf32 antibody produced in rabbit HPA041883". Immunohistochemistry. Retrieved 2020-05-03.

su.se

phobius.sbc.su.se

"Phobius". phobius.sbc.su.se. Retrieved 2020-05-03.

targetscan.org

"TargetScanHuman 7.2". www.targetscan.org. Retrieved 2020-05-03.

thebiogrid.org

"C15orf32 Result Summary | BioGRID". thebiogrid.org. Retrieved 2020-05-03.

umich.edu

zhanglab.ccmb.med.umich.edu

"I-TASSER server for protein structure and function prediction". zhanglab.ccmb.med.umich.edu. Retrieved 2020-05-03.

web.archive.org

"Genomatix - NGS Data Analysis & Personalized Medicine". www.genomatix.de. Archived from the original on 2001-02-24. Retrieved 2020-05-03.
"ORegAnno Temporary Homepage". www.oreganno.org. Archived from the original on 2021-03-21. Retrieved 2020-05-03.