Primary ovarian insufficiency (Homo sapiens)

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SLX4 COX10FANCLCCDC150NUP43CENPELHX8SOHLH2PPM1BANTXR1ZP3CYP17A1HSD17B1ZAR1MLH1ELAVL2SHOC1MGME1STARCCDC185PRORPPREPLBMP6FANCAMST1RFMR1XPNPEP2 STRA8MCMDC2NLRP11RFWD3HMMRSWI5PRDM1ALOX12EIF2B1SPATA33MEIOSINH1-8C1orf146POF1BKASH5HROBHELQFANCCLGR4ARLIG4XRCC4FANCISGO2DAZL322039201414202020391439392020272011202020203914520391414513939391420142025202162014420939391420CYP19A139BMP1539MCM939ESR214RCBTB139CAV114AIRE39PSMC3IPSPIDR3939SOHLH1EIF4ENIF13914PCCB14BMPR1A39SOX8PGRMC11439FIGLA39DIAPH239DMC139SIL114FSHR39MSH539BLMMSH439LAMC139NBN1239BMPR1B39NOBOX39LMNA39ATG9AGNAS39AMH3914KHDRBS139WRN39ESR139GALT39HARS239MND114EIF2B2AMHR21439TGFBR342GDF939NANOS3AARS23939ERAL139BMPR2ATG739MCM839NR5A13939HSD17B439RAD5116EXO116FANCM39ERCC639POLR3H39HAX114RECQL439CLPP39WT114TP63PMM23939LARS239MEIOBWDR623939TWNK39BRCA239FOXL239BNC139C14ORF3939EIF2B514SYCE1SALL439XRCC21439ATM39PCCANUP1071439CPEB139MRPS2239NOTCH239DCAF17HFM139POLG39SYCP2L3914STAG339POLR2C14EIF2B454


Description

Primary Ovarian Insufficiency pathway

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Bibliography

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  1. Liu H, Wei X, Sha Y, Liu W, Gao H, Lin J, Li Y, Tang Y, Wang Y, Wang Y, Su Z; ''Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention''; doi: 10.1186/s13048-020-00716-6, 2020 PubMed Europe PMC Scholia
  2. Eskenazi S, Bachelot A, Hugon-Rodin J, Plu-Bureau G, Gompel A, Catteau-Jonard S, Molina-Gomes D, Dewailly D, Dodé C, Christin-Maitre S, Touraine P; ''Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency''; doi: 10.1210/jendso/bvab032. PMID: 34095689, 2021 PubMed Europe PMC Scholia
  3. Massad-Costa AM, da Silva ID, Affonso R, Soares JM Jr, Nunes MG, de Lima GR, Baracat EC; ''Gene analysis in patients with premature ovarian failure or gonadal dysgenesis: a preliminary study. Maturitas''; doi: 10.1016/j.maturitas.2007.04.005, 2007 PubMed Europe PMC Scholia
  4. Lili Cao #, Xinmiao He #, Jiayi Ren, Canxin Wen, Ting Guo, Fan Yang 9 10, Yingying Qin, Zi-Jiang Chen, Shidou Zhao, Yajuan Yang; ''Novel compound heterozygous variants in FANCI cause premature ovarian insufficiency''; DOI: 10.1007/s00439-024-02650-9, 2024 PubMed Europe PMC Scholia
  5. França MM, Funari MFA, Lerario AM, Santos MG, Nishi MY, Domenice S, Moraes DR, Costalonga EF, Maciel GAR, Maciel-Guerra AT, Guerra-Junior G, Mendonca BB; ''Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency''; doi: 10.1371/journal.pone.0240795, 2020 PubMed Europe PMC Scholia
  6. Bachelot A, Bouilly J, Liu Y, Rebourcet D, Leux C, Kuttenn F, Touraine P, Binart N; ''Sequence variation analysis of the prolactin receptor C-terminal region in women with premature ovarian failure''; doi: 10.1016/j.fertnstert.2010.06.040, 2010 PubMed Europe PMC Scholia
  7. Czyzyk A, Filipowicz D, Podfigurna A, Ptas P, Piestrzynska M, Smolarczyk R, Genazzani AR, Meczekalski B; ''Brain-derived neurotrophic factor (BDNF) plasma concentration in patients diagnosed with premature ovarian insufficiency (POI)''; doi: 10.1080/09513590.2017.1290073, 2017 PubMed Europe PMC Scholia
  8. Zhang C, Shen J, Kong S, Zhang M, Zhang Q, Zhou J, Zhen X, Kang N, Jiang Y, Ding L, Sun H, Yan G; ''MicroRNA-181a promotes follicular granulosa cell apoptosis via sphingosine-1-phosphate receptor 1 expression downregulation†''; doi: 10.1093/biolre/ioz135, 2019 PubMed Europe PMC Scholia
  9. Huhtaniemi I, Hovatta O, La Marca A, Livera G, Monniaux D, Persani L, Heddar A, Jarzabek K, Laisk-Podar T, Salumets A, Tapanainen JS, Veitia RA, Visser JA, Wieacker P, Wolczynski S, Misrahi M; ''Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency''; DOI: 10.1016/j.tem.2018.03.010, 2018 PubMed Europe PMC Scholia
  10. Thanatsis N, Kaponis A, Koika V, Georgopoulos NA, Decavalas GO; ''Reduced Foxo3a, FoxL2, and p27 mRNA expression in human ovarian tissue in premature ovarian insufficiency''; doi: 10.1007/s42000-019-00134-4, 2019 PubMed Europe PMC Scholia
  11. Qin Y, Jiao X, Dalgleish R, Vujovic S, Li J, Simpson JL, Al-Azzawi F, Chen ZJ; ''Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure''; doi: 10.1016/j.fertnstert.2014.01.001, 2014 PubMed Europe PMC Scholia
  12. Pyun JA, Cha DH, Kwack K; ''LAMC1 gene is associated with premature ovarian failure''; doi: 10.1016/j.maturitas.2012.01.011, 2012 PubMed Europe PMC Scholia
  13. Dang Y, Zhao S, Qin Y, Han T, Li W, Chen ZJ; ''MicroRNA-22-3p is down-regulated in the plasma of Han Chinese patients with premature ovarian failure''; doi: 10.1016/j.fertnstert.2014.12.106, 2015 PubMed Europe PMC Scholia
  14. Heddar A, Ogur C, Da Costa S, Braham I, Billaud-Rist L, Findikli N, Beneteau C, Reynaud R, Mahmoud K, Legrand S, Marchand M, Cedrin-Durnerin I, Cantalloube A, Peigne M, Bretault M, Dagher-Hayeck B, Perol S, Droumaguet, Cavkaytar S, Nicolas-Bonne C, lloumi H, Khrouf M, Rougier-LeMasle C, Fradin M, Le Boette E, Luigi P, Guerrot AM, Ginglinger E, Zampa A, Fauconnier A, Auger N, Paris F, Brischoux-Boucher E, Cabrol C, Brun A, Guyon L, Berard M, Riviere A, Gruchy N, Odent S, Gilbert-Dussardier B, Isidor B, Piard J, Lambert L, Hamamah S, Guedj AM, Brac de la Perriere A, Fernandez H, Raffin-Sanson ML, Polak M, Letur H, Epelboin S, Plu-Bureau G, Wołczyński S, Hieronimus S, Aittomaki K, Catteau-Jonard S, Misrahi M.; ''Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine''; doi: 10.1016/j.ebiom.2022.104246, 2022 PubMed Europe PMC Scholia
  15. Nelson LM, Kimzey LM, Merriam GR, Fleisher TA; ''Increased peripheral T lymphocyte activation in patients with karyotypically normal spontaneous premature ovarian failure''; doi: 10.1016/s0015-0282(16)54356-8, 1991 PubMed Europe PMC Scholia
  16. Luo W, Guo T, Li G, Liu R, Zhao S, Song M, Zhang L, Wang S, Chen ZJ, Qin Y; ''Variants in Homologous Recombination Genes EXO1 and RAD51 Related with Premature Ovarian Insufficiency.''; doi: 10.1210/clinem/dgaa505, 2020 PubMed Europe PMC Scholia
  17. Zhou Y, Qin Y, Qin Y, Xu B, Guo T, Ke H, Chen M, Zhang L, Han F, Li Y, Chen M, Behrens A, Wang Y, Xu Z, Chen ZJ, Gao F; ''Wdr62 is involved in female meiotic initiation via activating JNK signaling and associated with POI in humans''; doi: 10.1371/journal.pgen.1007463, 2018 PubMed Europe PMC Scholia
  18. Pan H, Chen B, Wang J, Wang X, Hu P, Wu S, Liu Y, Xu Z, Zhang W, Wang B, Cao Y; ''The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency. Menopause''; doi: 10.1097/GME.0000000000000659, 2016 PubMed Europe PMC Scholia
  19. Caburet S, Todeschini AL, Petrillo C, Martini E, Farran ND, Legois B, Livera G, Younis JS, Shalev S, Veitia RA; ''A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks''; doi: 10.1016/j.ebiom.2019.03.075, 2019 PubMed Europe PMC Scholia
  20. Ke H, Tang S, Guo T, Hou D, Jiao X, Li S, Luo W, Xu B, Zhao S, Li G, Zhang X, Xu S, Wang L, Wu Y, Wang J, Zhang F, Qin Y, Jin L, Chen ZJ; ''Landscape of pathogenic mutations in premature ovarian insufficiency''; doi: 10.1038/s41591-022-02194-3, 2023 PubMed Europe PMC Scholia
  21. Karlberg S, Tiitinen A, Alfthan H, Lipsanen-Nyman M; ''Premature ovarian insufficiency and early depletion of the ovarian reserve in the monogenic Mulibrey nanism disorder''; doi: 10.1093/humrep/dey103, 2018 PubMed Europe PMC Scholia
  22. Pyun JA, Kim S, Kwack K; ''Epistasis between polymorphisms in ACVR2B and ADAMTS19 is associated with premature ovarian failure''; doi: 10.1097/GME.0000000000000285, 2015 PubMed Europe PMC Scholia
  23. Wang B, Suo P, Chen B, Wei Z, Yang L, Zhou S, Wang J, Cao Y, Ma X; '' Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women''; doi: 10.1093/humrep/der001, 2011 PubMed Europe PMC Scholia
  24. Qin CR, Yao JL, Zhu WJ, Wu WQ, Xie JS; ''FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure''; doi: 10.1186/1477-7827-9-158, 2011 PubMed Europe PMC Scholia
  25. Heddar A, Ogur C, Da Costa S, Braham I, Billaud-Rist L, Findikli N, Beneteau C, Reynaud R, Mahmoud K, Legrand S, Marchand M, Cedrin-Durnerin I, Cantalloube A, Peigne M, Bretault M, Dagher-Hayeck B, Perol S, Droumaguet C, Cavkaytar S, Nicolas-Bonne C, Elloumi H, Khrouf M, Rougier-LeMasle C, Fradin M, Le Boette E, Luigi P, Guerrot AM, Ginglinger E, Zampa A, Fauconnier A, Auger N, Paris F, Brischoux-Boucher E, Cabrol C, Brun A, Guyon L, Berard M, Riviere A, Gruchy N, Odent S, Gilbert-Dussardier B, Isidor B, Piard J, Lambert L, Hamamah S, Guedj AM, Brac de la Perriere A, Fernandez H, Raffin-Sanson ML, Polak M, Letur H, Epelboin S, Plu-Bureau G, Wołczyński S, Hieronimus S, Aittomaki K, Catteau-Jonard S, Misrahi M.; ''''; ,
  26. Rzepka-Górska I, Tarnowski B, Chudecka-Głaz A, Górski B, Zielińska D, Tołoczko-Grabarek A; ''Premature menopause in patients with BRCA1 gene mutation''; doi: 10.1007/s10549-006-9220-1, 2006 PubMed Europe PMC Scholia
  27. Qi Y, Wang Y, Li W, Zhuang S, Li S, Xu K, Qin Y, Guo T; ''Pathogenic bi-allelic variants of meiotic ZMM complex gene SPO16 in premature ovarian insufficiency''; doi: 10.1111/cge.14380, 2023 PubMed Europe PMC Scholia
  28. Wang B, Mu Y, Ni F, Zhou S, Wang J, Cao Y, Ma X; ''Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure''; doi: 10.1016/j.rbmo.2010.01.008, 2010 PubMed Europe PMC Scholia
  29. Yang Y, Guo T, Liu R, Ke H, Xu W, Zhao S, Qin Y; ''FANCL gene mutations in premature ovarian insufficiency''; doi: 10.1002/humu.23997, 2020 PubMed Europe PMC Scholia
  30. Kang H, Lee SK, Kim MH, Choi H, Lee SH, Kwack K; ''Acyl-CoA synthetase long-chain family member 6 is associated with premature ovarian failure''; doi: 10.1016/j.fertnstert.2008.03.035, 2009 PubMed Europe PMC Scholia
  31. Pyun JA, Kim S, Cha DH, Kwack K; ''Epistasis between polymorphisms in TSHB and ADAMTS16 is associated with premature ovarian failure''; doi: 10.1097/GME.0000000000000172, 2014 PubMed Europe PMC Scholia
  32. Faridi R, Rehman AU, Morell RJ, Friedman PL, Demain L, Zahra S, Khan AA, Tohlob D, Assir MZ, Beaman G, Khan SN, Newman WG, Riazuddin S, Friedman TB; ''Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome''; doi: 10.1111/cge.12867, 2017 PubMed Europe PMC Scholia
  33. Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A, Ciccone R, Giorda R, Toniolo D, Maraschio P, Zuffardi O; ''A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea''; doi: 10.1016/j.ejmg.2008.06.010, 2008 PubMed Europe PMC Scholia
  34. Espeche LD, Chiauzzi V, Ferder I, Arrar M, Solari AP, Bruque CD, Delea M, Belli S, Fernández CS, Buzzalino ND, Charreau EH, Dain LB; ''Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency''; doi: 10.3390/genes8080194, 2017 PubMed Europe PMC Scholia
  35. Ma X, Chen Y, Zhao X, Chen J, Shen C, Yang S; ''Association study of TGFBR2 and miR-518 gene polymorphisms with age at natural menopause, premature ovarian failure, and early menopause among Chinese Han women''; doi: 10.1097/MD.0000000000000093, 2014 PubMed Europe PMC Scholia
  36. Rehnitz J, Messmer B, Bender U, Nguyen XP, Germeyer A, Hinderhofer K, Strowitzki T, Capp E; ''Activation of AKT/mammalian target of rapamycin signaling in the peripheral blood of women with premature ovarian insufficiency and its correlation with FMR1 expression''; doi: 10.1186/s12958-022-00919-0, 2022 PubMed Europe PMC Scholia
  37. Arif S, Underhill JA, Donaldson P, Conway GS, Peakman M; ''Human leukocyte antigen-DQB1* genotypes encoding aspartate at position 57 are associated with 3beta-hydroxysteroid dehydrogenase autoimmunity in premature ovarian failure''; doi: 10.1210/jcem.84.3.5556, 1999 PubMed Europe PMC Scholia
  38. Bouazzi L, Sproll P, Eid W, Biason-Lauber A; ''The transcriptional regulator CBX2 and ovarian function: A whole genome and whole transcriptome approach''; doi: 10.1038/s41598-019-53370-4, 2019 PubMed Europe PMC Scholia
  39. França MM, Mendonca BB; ''Genetics of ovarian insufficiency and defects of folliculogenesis''; doi: 10.1016/j.beem.2021.101594, 2022 PubMed Europe PMC Scholia
  40. Guo Z, Yu Q; ''Role of mTOR Signaling in Female Reproduction''; doi: 10.3389/fendo.2019.00692, 2019 PubMed Europe PMC Scholia
  41. Dang Y, Wang X, Hao Y, Zhang X, Zhao S, Ma J, Qin Y, Chen ZJ; ''MicroRNA-379-5p is associate with biochemical premature ovarian insufficiency through PARP1 and XRCC6''; doi: 10.1038/s41419-017-0163-8, 2018 PubMed Europe PMC Scholia
  42. Qin CR, Chen SL, Yao JL, Li T, Wu WQ; ''Haplotype and mutation analysis of the TGFBR3 gene in Chinese women with idiopathic premature ovarian failure''; doi: 10.3109/09513590.2011.583954, 2012 PubMed Europe PMC Scholia
  43. Thanatsis N, Kaponis A, Koika V, Georgopoulos NA, Decavalas GO; ''Reduced Foxo3a, FoxL2, and p27 mRNA expression in human ovarian tissue in premature ovarian insufficiency''; doi: 10.1007/s42000-019-00134-4, 2019 PubMed Europe PMC Scholia
  44. Mansouri MR, Schuster J, Badhai J, Stattin EL, Lösel R, Wehling M, Carlsson B, Hovatta O, Karlström PO, Golovleva I, Toniolo D, Bione S, Peluso J, Dahl N; ''Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure''; doi: 10.1093/hmg/ddn274, 2008 PubMed Europe PMC Scholia
  45. Bouilly J, Roucher-Boulez F, Gompel A, Bry-Gauillard H, Azibi K, Beldjord C, Dodé C, Bouligand J, Mantel AG, Hécart AC, Delemer B, Young J, Binart N; ''New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression''; doi: 10.1210/jc.2014-2761, 2015 PubMed Europe PMC Scholia
  46. Bai X, Wang S; ''Signaling pathway intervention in premature ovarian failure''; doi: 10.3389/fmed.2022.999440, 2022 PubMed Europe PMC Scholia
  47. Li B, Hu X, Yang Y, Zhu M, Zhang J, Wang Y, Pei X, Zhou H, Wu J; ''GAS5/miR-21 Axis as a Potential Target to Rescue ZCL-082-Induced Autophagy of Female Germline Stem Cells In Vitro''; doi: 10.1016/j.omtn.2019.06.012, 2019 PubMed Europe PMC Scholia
  48. Sun S, Chen H, Zheng X, Ma C, Yue R; ''Analysis on the level of IL-6, IL-21, AMH in patients with auto-immunity premature ovarian failure and study of correlation''; doi: 10.3892/etm.2018.6592, 2018 PubMed Europe PMC Scholia
  49. Watkins WJ, Umbers AJ, Woad KJ, Harris SE, Winship IM, Gersak K, Shelling AN; ''Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure''; doi: 10.1016/j.fertnstert.2006.03.054, 2006 PubMed Europe PMC Scholia
  50. Laissue P, Lakhal B, Benayoun BA, Dipietromaria A, Braham R, Elghezal H, Philibert P, Saâd A, Sultan C, Fellous M, Veitia RA; ''Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2''; doi: 10.1136/jmg.2008.065086, 2009 PubMed Europe PMC Scholia
  51. Dov Tiosano, Jason A Mears, David A Buchner; ''Mitochondrial Dysfunction in Primary Ovarian Insufficiency''; https://doi.org/10.1210/en.2019-00441, 2019 PubMed Europe PMC Scholia
  52. Xu B, Li Z, Li S, Ke H, Zhang Q, Qin Y, Guo T; ''Pathogenic variants in TSC2 might cause premature ovarian insufficiency through activated mTOR induced hyperactivation of primordial follicles''; doi: 10.1016/j.fertnstert.2022.08.853, 2022 PubMed Europe PMC Scholia
  53. Shao T, Ke H, Liu R, Zhao S, Qin Y; ''Variation analysis of theTMEM150B gene in Chinese women with premature ovarian insufficiency''; doi: 10.1016/j.rbmo.2018.12.009, 2019 PubMed Europe PMC Scholia
  54. Heddar A, Ogur C, Da Costa S, Braham I, Billaud-Rist L, Findikli N, Beneteau C, Reynaud R, Mahmoud K, Legrand S, Marchand M, Cedrin-Durnerin I, Cantalloube A, Peigne M, Bretault M, Dagher-Hayeck B, Perol S, Droumaguet C, Cavkaytar S, Nicolas-Bonne C, Elloumi H, Khrouf M, Rougier-LeMasle C, Fradin M, Le Boette E, Luigi P, Guerrot AM, Ginglinger E, Zampa A, Fauconnier A, Auger N, Paris F, Brischoux-Boucher E, Cabrol C, Brun A, Guyon L, Berard M, Riviere A, Gruchy N, Odent S, Gilbert-Dussardier B, Isidor B, Piard J, Lambert L, Hamamah S, Guedj AM, Brac de la Perriere A, Fernandez H, Raffin-Sanson ML, Polak M, Letur H, Epelboin S, Plu-Bureau G, Wołczyński S, Hieronimus S, Aittomaki K, Catteau-Jonard S, Misrahi M; ''Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine''; doi: 10.1016/j.ebiom.2022.104246, 2022 PubMed Europe PMC Scholia

History

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134143view11:50, 4 July 2024VanessaSousa
129430view11:21, 19 April 2024VanessaSousa
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External references

DataNodes

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NameTypeDatabase referenceComment
AARS2 GeneProductENSG00000124608 (Ensembl)
AIRE GeneProductENSG00000160224 (Ensembl)
ALOX12GeneProductENSG00000108839 (Ensembl)
AMHGeneProductENSG00000104899 (Ensembl)
AMHR2 GeneProductENSG00000135409 (Ensembl)
ANTXR1GeneProductENSG00000169604 (Ensembl)
ARGeneProductENSG00000169083 (Ensembl)
ATG7 GeneProductENSG00000197548 (Ensembl)
ATG9A GeneProductENSG00000198925 (Ensembl)
ATM GeneProductENSG00000149311 (Ensembl)
BLMGeneProductENSG00000197299 (Ensembl)
BMP15 GeneProductENSG00000130385 (Ensembl)
BMP6GeneProductENSG00000153162 (Ensembl)
BMPR1A GeneProductENSG00000107779 (Ensembl)
BMPR1B GeneProductENSG00000138696 (Ensembl)
BMPR2 GeneProductENSG00000204217 (Ensembl)
BNC1 GeneProductENSG00000169594 (Ensembl)
BRCA2 GeneProductENSG00000139618 (Ensembl)
C14ORF39 GeneProductENSG00000179008 (Ensembl)
C1orf146GeneProductENSG00000203910 (Ensembl)
CAV1GeneProductENSG00000105974 (Ensembl)
CCDC150 GeneProductENSG0000014439 (Ensembl)
CCDC185 GeneProductENSG00000178395 (Ensembl)
CENPE GeneProductENSG00000138778 (Ensembl)
CLPP GeneProductENSG00000125656 (Ensembl)
COX10GeneProductENSG00000006695 (Ensembl)
CPEB1 GeneProductENSG00000214575 (Ensembl)
CYP17A1GeneProductENSG00000148795 (Ensembl)
CYP19A1 GeneProductENSG00000137869 (Ensembl)
DAZLGeneProductENSG00000092345 (Ensembl)
DCAF17GeneProductENSG00000115827 (Ensembl)
DIAPH2 GeneProductENSG00000147202 (Ensembl)
DMC1 GeneProductENSG00000100206 (Ensembl)
EIF2B1GeneProductENSG00000111361 (Ensembl)
EIF2B2 GeneProductENSG00000119718 (Ensembl)
EIF2B4 GeneProductENSG00000115211 (Ensembl)
EIF2B5 GeneProductENSG00000145191 (Ensembl)
EIF4ENIF1 GeneProductENSG00000184708 (Ensembl)
ELAVL2 GeneProductENSG00000107105 (Ensembl)
ERAL1 GeneProductENSG00000132591 (Ensembl)
ERCC6 GeneProductENSG00000225830 (Ensembl)
ESR1 GeneProductENSG00000091831 (Ensembl)
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EXO1GeneProductENSG00000174371 (Ensembl)
FANCAGeneProductENSG00000187741 (Ensembl)
FANCCGeneProductENSG00000158169 (Ensembl)
FANCIGeneProductENSG00000140525 (Ensembl)
FANCL GeneProductENSG00000115392 (Ensembl)
FANCM GeneProductENSG00000187790 (Ensembl)
FIGLA GeneProductENSG00000183733 (Ensembl)
FMR1GeneProductENSG00000102081 (Ensembl)
FOXL2 GeneProductENSG00000183770 (Ensembl)
FSHR GeneProductENSG00000170820 (Ensembl)
GALT GeneProductENSG00000213930 (Ensembl)
GDF9 GeneProductENSG00000164404 (Ensembl)
GNAS GeneProductENSG00000087460 (Ensembl)
H1-8 GeneProductENSG00000178804 (Ensembl)
HARS2 GeneProductENSG00000112855 (Ensembl)
HAX1 GeneProductENSG00000143575 (Ensembl)
HELQGeneProductENSG00000163312 (Ensembl)
HFM1 GeneProductENSG00000162669 (Ensembl)
HMMRGeneProductENSG00000072571 (Ensembl)
HROBGeneProductENSG00000125319 (Ensembl)
HSD17B1 GeneProductENSG00000108786 (Ensembl)
HSD17B4 GeneProductENSG00000133835 (Ensembl)
KASH5 GeneProductENSG00000161609 (Ensembl)
KHDRBS1 GeneProductENSG00000121774 (Ensembl)
LAMC1 GeneProductENSG00000135862 (Ensembl)
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LGR4 GeneProductENSG00000205213 (Ensembl)
LHX8GeneProductENSG00000162624 (Ensembl)
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LMNA GeneProductENSG00000160789 (Ensembl)
MCM8 GeneProductENSG00000125885 (Ensembl)
MCM9 GeneProductENSG00000111877 (Ensembl)
MCMDC2GeneProductENSG00000178460 (Ensembl)
MEIOB GeneProductENSG00000162039 (Ensembl)
MEIOSIN GeneProductENSG00000237452 (Ensembl)
MGME1 GeneProductENSG00000125871 (Ensembl)
MLH1GeneProductENSG00000076242 (Ensembl)
MND1 GeneProductENSG00000121211 (Ensembl)
MRPS22 GeneProductENSG00000175110 (Ensembl)
MSH4 GeneProductENSG00000057468 (Ensembl)
MSH5 GeneProductENSG00000204410 (Ensembl)
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NANOS3 GeneProductENSG00000187556 (Ensembl)
NBN GeneProductENSG00000104320 (Ensembl)
NLRP11 GeneProductENSG00000179873 (Ensembl)
NOBOX GeneProductENSG00000106410 (Ensembl)
NOTCH2 GeneProductENSG00000134250 (Ensembl)
NR5A1 GeneProductENSG00000136931 (Ensembl)
NUP107 GeneProductENSG00000111581 (Ensembl)
NUP43 GeneProductENSG00000120253 (Ensembl)
PCCA GeneProductENSG00000175198 (Ensembl)
PCCB GeneProductENSG00000114054 (Ensembl)
PGRMC1 GeneProductENSG00000101856 (Ensembl)
PMM2 GeneProductENSG00000140650 (Ensembl)
POF1BGeneProductENSG00000124429 (Ensembl)
POLG GeneProductENSG00000140521 (Ensembl)
POLR2C GeneProductENSG00000102978 (Ensembl)
POLR3H GeneProductENSG00000100413 (Ensembl)
PPM1B GeneProductENSG00000138032 (Ensembl)
PRDM1 GeneProductENSG00000057657 (Ensembl)
PREPLGeneProductENSG00000138078 (Ensembl)
PRORPGeneProductENSG00000100890 (Ensembl)
PSMC3IP GeneProductENSG00000131470 (Ensembl)
RAD51GeneProductENSG00000051180 (Ensembl)
RCBTB1 GeneProductENSG00000136144 (Ensembl)
RECQL4 GeneProductENSG00000160957 (Ensembl)
RFWD3 GeneProductENSG00000168411 (Ensembl)
SALL4 GeneProductENSG00000101115 (Ensembl)
SGO2 GeneProductENSG00000163535 (Ensembl)
SHOC1 GeneProductENSG00000165181 (Ensembl)
SIL1 GeneProductENSG00000120725 (Ensembl)
SLX4 GeneProductENSG00000188827 (Ensembl)
SOHLH1 GeneProductENSG00000165643 (Ensembl)
SOHLH2GeneProductENSG00000120669 (Ensembl)
SOX8 GeneProductENSG00000005513 (Ensembl)
SPATA33GeneProductENSG00000167523 (Ensembl)
SPIDR GeneProductENSG00000164808 (Ensembl)
STAG3GeneProductENSG00000066923 (Ensembl)
STAR GeneProductENSG00000147465 (Ensembl)
STRA8 GeneProductENSG00000146857 (Ensembl)
SWI5 GeneProductENSG00000175854 (Ensembl)
SYCE1 GeneProductENSG00000171772 (Ensembl)
SYCP2L GeneProductENSG00000153157 (Ensembl)
TGFBR3 GeneProductENSG00000069702 (Ensembl)
TP63 GeneProductENSG00000073282 (Ensembl)
TWNK GeneProductENSG00000107815 (Ensembl)
WDR62 GeneProductENSG00000075702 (Ensembl)
WRN GeneProductENSG00000165392 (Ensembl)
WT1 GeneProductENSG00000184937 (Ensembl)
XPNPEP2  GeneProductENSG00000122121 (Ensembl)
XRCC2GeneProductENSG00000196584 (Ensembl)
XRCC4 GeneProductENSG00000152422 (Ensembl)
ZAR1 GeneProductENSG00000182223 (Ensembl)
ZP3 GeneProductENSG00000188372 (Ensembl)

Annotated Interactions

No annotated interactions

Retrieved from "https://classic.wikipathways.org/index.php/Pathway:WP5461"
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