HORMAD2: Difference between revisions
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* {{cite journal | vauthors = Imielinski M, Baldassano RN, Griffiths A, Russell RK, Annese V, Dubinsky M, Kugathasan S, Bradfield JP, Walters TD, Sleiman P, Kim CE, Muise A, Wang K, Glessner JT, Saeed S, Zhang H, Frackelton EC, Hou C, Flory JH, Otieno G, Chiavacci RM, Grundmeier R, Castro M, Latiano A, Dallapiccola B, Stempak J, Abrams DJ, Taylor K, McGovern D, Silber G, Wrobel I, Quiros A, Barrett JC, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmuda MM, Bitton A, Dassopoulos T, Datta LW, Green T, Griffiths AM, Kistner EO, Murtha MT, Regueiro MD, Rotter JI, Schumm LP, Steinhart AH, Targan SR, Xavier RJ, Libioulle C, Sandor C, Lathrop M, Belaiche J, Dewit O, Gut I, Heath S, Laukens D, Mni M, Rutgeerts P, Van Gossum A, Zelenika D, Franchimont D, Hugot JP, de Vos M, Vermeire S, Louis E, Cardon LR, Anderson CA, Drummond H, Nimmo E, Ahmad T, Prescott NJ, Onnie CM, Fisher SA, Marchini J, Ghori J, Bumpstead S, Gwillam R, Tremelling M, Delukas P, Mansfield J, Jewell D, Satsangi J, Mathew CG, Parkes M, Georges M, Daly MJ, Heyman MB, Ferry GD, Kirschner B, Lee J, Essers J, Grand R, Stephens M, Levine A, Piccoli D, Van Limbergen J, Cucchiara S, Monos DS, Guthery SL, Denson L, Wilson DC, Grant SF, Daly M, Silverberg MS, Satsangi J, Hakonarson H | display-authors = 6 | title = Common variants at five new loci associated with early-onset inflammatory bowel disease | journal = Nature Genetics | volume = 41 | issue = 12 | pages = 1335–40 | date = December 2009 | pmid = 19915574 | pmc = 3267927 | doi = 10.1038/ng.489 }} | * {{cite journal | vauthors = Imielinski M, Baldassano RN, Griffiths A, Russell RK, Annese V, Dubinsky M, Kugathasan S, Bradfield JP, Walters TD, Sleiman P, Kim CE, Muise A, Wang K, Glessner JT, Saeed S, Zhang H, Frackelton EC, Hou C, Flory JH, Otieno G, Chiavacci RM, Grundmeier R, Castro M, Latiano A, Dallapiccola B, Stempak J, Abrams DJ, Taylor K, McGovern D, Silber G, Wrobel I, Quiros A, Barrett JC, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmuda MM, Bitton A, Dassopoulos T, Datta LW, Green T, Griffiths AM, Kistner EO, Murtha MT, Regueiro MD, Rotter JI, Schumm LP, Steinhart AH, Targan SR, Xavier RJ, Libioulle C, Sandor C, Lathrop M, Belaiche J, Dewit O, Gut I, Heath S, Laukens D, Mni M, Rutgeerts P, Van Gossum A, Zelenika D, Franchimont D, Hugot JP, de Vos M, Vermeire S, Louis E, Cardon LR, Anderson CA, Drummond H, Nimmo E, Ahmad T, Prescott NJ, Onnie CM, Fisher SA, Marchini J, Ghori J, Bumpstead S, Gwillam R, Tremelling M, Delukas P, Mansfield J, Jewell D, Satsangi J, Mathew CG, Parkes M, Georges M, Daly MJ, Heyman MB, Ferry GD, Kirschner B, Lee J, Essers J, Grand R, Stephens M, Levine A, Piccoli D, Van Limbergen J, Cucchiara S, Monos DS, Guthery SL, Denson L, Wilson DC, Grant SF, Daly M, Silverberg MS, Satsangi J, Hakonarson H | display-authors = 6 | title = Common variants at five new loci associated with early-onset inflammatory bowel disease | journal = Nature Genetics | volume = 41 | issue = 12 | pages = 1335–40 | date = December 2009 | pmid = 19915574 | pmc = 3267927 | doi = 10.1038/ng.489 }} | ||
* {{cite journal | vauthors = Amre DK, Mack DR, Morgan K, Israel D, Deslandres C, Seidman EG, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Xhu Z, Grimard G, Levy E | display-authors = 6 | title = Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children | journal = Human Genetics | volume = 128 | issue = 2 | pages = 131–5 | date = August 2010 | pmid = 20473688 | doi = 10.1007/s00439-010-0835-2 }} | * {{cite journal | vauthors = Amre DK, Mack DR, Morgan K, Israel D, Deslandres C, Seidman EG, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Xhu Z, Grimard G, Levy E | display-authors = 6 | title = Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children | journal = Human Genetics | volume = 128 | issue = 2 | pages = 131–5 | date = August 2010 | pmid = 20473688 | doi = 10.1007/s00439-010-0835-2 }} | ||
* {{cite journal | vauthors = Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, Sanna-Cherchi S, Men CJ, Julian BA, Wyatt RJ, Novak J, He JC, Wang H, Lv J, Zhu L, Wang W, Wang Z, Yasuno K, Gunel M, Mane S, Umlauf S, Tikhonova I, Beerman I, Savoldi S, Magistroni R, Ghiggeri GM, Bodria M, Lugani F, Ravani P, Ponticelli C, Allegri L, Boscutti G, Frasca G, Amore A, Peruzzi L, Coppo R, Izzi C, Viola BF, Prati E, Salvadori M, Mignani R, Gesualdo L, Bertinetto F, Mesiano P, Amoroso A, Scolari F, Chen N, Zhang H, Lifton RP | display-authors = 6 | title = Genome-wide association study identifies susceptibility loci for IgA nephropathy | journal = Nature Genetics | volume = 43 | issue = 4 | pages = 321–7 | date = March 2011 | pmid = 21399633 | pmc = 3412515 | doi = 10.1038/ng.787 }} | * {{cite journal | vauthors = Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, Sanna-Cherchi S, Men CJ, Julian BA, Wyatt RJ, Novak J, He JC, Wang H, Lv J, Zhu L, Wang W, Wang Z, Yasuno K, Gunel M, Mane S, Umlauf S, Tikhonova I, Beerman I, Savoldi S, Magistroni R, Ghiggeri GM, Bodria M, Lugani F, Ravani P, Ponticelli C, Allegri L, Boscutti G, Frasca G, Amore A, Peruzzi L, Coppo R, Izzi C, Viola BF, Prati E, Salvadori M, Mignani R, Gesualdo L, Bertinetto F, Mesiano P, Amoroso A, Scolari F, Chen N, Zhang H, Lifton RP | display-authors = 6 | title = Genome-wide association study identifies susceptibility loci for IgA nephropathy | journal = Nature Genetics | volume = 43 | issue = 4 | pages = 321–7 | date = March 2011 | pmid = 21399633 | pmc = 3412515 | doi = 10.1038/ng.787 | url = https://iris.unito.it/bitstream/2318/83966/2/copertinagaravi2011nihms-379264.pdf }} | ||
{{refend}} | {{refend}} | ||
{{gene-22-stub}} | {{gene-22-stub}} | ||
Latest revision as of 12:31, 9 January 2019
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| External IDs | GeneCards: [1] | ||||||
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| Species | Human | Mouse | |||||
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| Location (UCSC) | n/a | n/a | |||||
| PubMed search | n/a | n/a | |||||
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HORMA domain containing 2 is a protein that in humans is encoded by the HORMAD2 gene.[1]
References
- ↑ "Entrez Gene: HORMA domain containing 2". Retrieved 2011-10-22.
Further reading
- Imielinski M, Baldassano RN, Griffiths A, Russell RK, Annese V, Dubinsky M, et al. (December 2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease". Nature Genetics. 41 (12): 1335–40. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.
- Amre DK, Mack DR, Morgan K, Israel D, Deslandres C, Seidman EG, et al. (August 2010). "Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children". Human Genetics. 128 (2): 131–5. doi:10.1007/s00439-010-0835-2. PMID 20473688.
- Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, et al. (March 2011). "Genome-wide association study identifies susceptibility loci for IgA nephropathy" (PDF). Nature Genetics. 43 (4): 321–7. doi:10.1038/ng.787. PMC 3412515. PMID 21399633.
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