Citations for
1NPAP1, POM121
The imprinted NPAP1 gene in the Prader-Willi syndrome region belongs to a POM121-related family of retrogenes.
Neumann LC, Feiner N, Meyer A, Buiting K, Horsthemke B.
Genome Biol Evol 6(2):344-51. doi: 10.1093/gbe/evu019. 2014
2NPAP1, POM121
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein.
Neumann LC, Markaki Y, Mladenov E, Hoffmann D, Buiting K, Horsthemke B.
Hum Mol Genet 21(18):4038-48. doi: 10.1093/hmg/dds228. 2012
3POM121, SUN1
POM121 and Sun1 play a role in early steps of interphase NPC assembly.
Talamas JA, Hetzer MW.
J Cell Biol 194(1):27-37. Epub 2011 Jul 4. 2011
4POM121
Localization of Pom121 to the inner nuclear membrane is required for an early step of interphase nuclear pore complex assembly.
Funakoshi T, Clever M, Watanabe A, Imamoto N.
Mol Biol Cell 22(7):1058-69. Epub 2011 Feb 2. 2011
5POM121
A dominant-negative form of POM121 binds chromatin and disrupts the two separate modes of nuclear pore assembly.
Shaulov L, Gruber R, Cohen I, Harel A.
J Cell Sci 124(Pt 22):3822-34. Epub 2011 Nov 18. 2011
6NUP155, NUP160, POM121
Pom121 links two essential subcomplexes of the nuclear pore complex core to the membrane.
Mitchell JM, Mansfeld J, Capitanio J, Kutay U, Wozniak RW.
J Cell Biol 191(3):505-21. Epub 2010 Oct 25. 2010
7POM121
NLS-mediated NPC functions of the nucleoporin Pom121.
Yavuz S, Santarella-Mellwig R, Koch B, Jaedicke A, Mattaj IW, Antonin W.
FEBS Lett 584(15):3292-8. Epub 2010 Jul 14. 2010
8AHCTF1, NDC1, POM121
Capture of AT-rich chromatin by ELYS recruits POM121 and NDC1 to initiate nuclear pore assembly.
Rasala BA, Ramos C, Harel A, Forbes DJ.
Mol Biol Cell 19(9):3982-96. doi: 10.1091/mbc.E08-01-0012. Epub 2008 Jul 2. 2008
9POM121
Two distinct human POM121 genes: requirement for the formation of nuclear pore complexes.
Funakoshi T, Maeshima K, Yahata K, Sugano S, Imamoto F, Imamoto N.
FEBS Lett 581(25):4910-6. Epub 2007 Sep 21. 2007
10ABL2, AKAP8, ANKRD13D, AP3D1, ARFGAP3, ARMCX6, ASUN, BAT2L, BCl2L13, BNIP3L, BPTF, BRD7, BZW1, BZW2, C12orf43, C19orf26, C1orf105, C2orf49, C6orf81, CA10, CAD, CARHSP1, CBX4, CCDC55, CCDC61, CCNK, CDC42BPB, CDC42EP3, CDC42EP4, CDS2, CENPN, CLK1, COPA, CSDA, CTPS2, DBN1, DCP1A, DECR2, DPF2, DPM1, EIF2AK1, EPB41L4A, EPN1, FAM91A1, FOSL2, FOXK1, GDF5OS, GFOD2, GIGYF2, GPATCH8, GTPBP1, HES7, HNRNPUL1, KIF1C, LPIN2, LRCH4, MAN2C1, MAST1, MED13, MED24, MED26, MINK1, MISP, MYO10, NKTR, OSBP, PAM, PCDH7, PEX14, PHF16, PHRF1, PLCB4, PLXNC1, POM121, POM121L2, PPHLN1, PRICKLE3, PRX, PUM2, RABGGTB, RBEL1, RIMS1, RIMS2, RPL14, RRP1B, RRP8, SAFB, SCAMP3, SCMH1, SCYL1, SENP6, SERBP1, SFRS13A, SFRS17A, SIPA1L1, SLC26A6, SLIRP, SLMAP, SNTA1, SORBS3, SPICE1, SSFA2, STAM, SUB1, TFIP11, TLN2, TMC6, TMEM104, TMEM106B, TMEM22, TOM1, UHRF1, UTP14A, WDR43, ZNF324, ZNF648
Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.
Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M.
Cell. 127(3):635-48. 2006
11POM121
Nuclear pore complex assembly and maintenance in POM121- and gp210-deficient cells.
Stavru F, Nautrup-Pedersen G, Cordes VC, Görlich D.
J Cell Biol 173(4):477-83. Epub 2006 May 15. 2006
12GTF2I, NCF1, POM121, EIF4H, MLXIPL, WBS
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
DeSilva U, Elnitski L, Idol JR, Doyle JL, Gan W, Thomas JW, Schwartz S, Dietrich NL, Beckstrom-Sternberg SM, McDowell JC, Blakesley RW, Bouffard GG, Thomas PJ, Touchman JW, Miller W, Green ED.
Genome Res 12(1):3-15. 2002
13FKBP6, POM121, WBS
A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23.
Peoples R, Franke Y, Wang YK, Perez-Jurado L, Paperna T, Cisco M, Francke U.
Am J Hum Genet 66(1):47-68. 2000