ALOX12 c.136-69G>A

Variant ID: 17-6900076-G-A

NM_000697.2(ALOX12):c.136-69G>A

This variant was identified in 16 publications

View GRCh38 version.




Publications:


A case of midbrain germinoma: A literature review for radiographic and clinical features.

Neuro-Oncology Advances
Miyake, Yohei Y; Tateishi, Kensuke K; Oshima, Akito A; Hongo, Takeshi T; Satomi, Kaishi K; Ichimura, Koichi K; Kato, Ayumi A; Iwashita, Hiromichi H; Utsunomiya, Daisuke D; Yamamoto, Tetsuya T
Publication Date: 2023

Variant appearance in text: rs2073438
PubMed Link: 37215953
Variant Present in the following documents:
  • vdad043_suppl_supplementary_tables.xlsx, sheet 1
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs2073438
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Interactions of Colorectal Cancer, Dietary Fats, and Polymorphisms of Arachidonate Lipoxygenase and Cyclooxygenase Genes: A Literature Review.

Frontiers In Oncology
Gholamalizadeh, Maryam M; Majidi, Nazanin N; Tajaddod, Shirin S; Abdollahi, Sepideh S; Poorhosseini, Seyed Mohammad SM; Ahmadzadeh, Mina M; Naimi Joubani, Mohammad M; Mirzaei Dahka, Samaneh S; Shafaei, Hanieh H; Hajiesmaeil, Mogge M; Alizadeh, Atiyeh A; Doaei, Saeid S; Houshiar-Rad, Anahita A
Publication Date: 2022

Variant appearance in text: rs2073438
PubMed Link: 35928873
Variant Present in the following documents:
  • Main text
  • fonc-12-865208.pdf
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Plasma Concentration of 12-Hydroxyeicosatetraenoic Acid, Single Nucleotide Polymorphisms of 12-Lipooxygenase Gene and Vaso-Occlusion in Sickle Cell Disease.

Frontiers In Genome Editing
Duru, Augustine Nwakuche AN; Ocheni, Sunday S; Ibegbulam, Obike O; Okpala, Iheanyi I
Publication Date: 2021

Variant appearance in text: rs2073438
PubMed Link: 34713264
Variant Present in the following documents:
  • Main text
  • fgeed-03-722190.pdf
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs2073438
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: ALOX12: 136-69G>A; rs2073438
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2073438
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs2073438
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



A novel locus in the oxidative stress-related gene ALOX12 moderates the association between PTSD and thickness of the prefrontal cortex.

Psychoneuroendocrinology
Miller, Mark W MW; Wolf, Erika J EJ; Sadeh, Naomi N; Logue, Mark M; Spielberg, Jeffrey M JM; Hayes, Jasmeet P JP; Sperbeck, Emily E; Schichman, Steven A SA; Stone, Angie A; Carter, Weleetka C WC; Humphries, Donald E DE; Milberg, William W; McGlinchey, Regina R
Publication Date: 2015-12

Variant appearance in text: rs2073438
PubMed Link: 26372769
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mammalian lipoxygenases and their biological relevance.

Biochimica Et Biophysica Acta
Kuhn, Hartmut H; Banthiya, Swathi S; van Leyen, Klaus K
Publication Date: 2015-04

Variant appearance in text: rs2073438
PubMed Link: 25316652
Variant Present in the following documents:
  • Main text
View BVdb publication page



Impact of genetic polymorphisms on adenoma recurrence and toxicity in a COX2 inhibitor (celecoxib) trial: results from a pilot study.

Pharmacogenetics And Genomics
Kraus, Sarah S; Hummler, Simone S; Toriola, Adetunji T AT; Poole, Elizabeth M EM; Scherer, Dominique D; Kotzmann, Jana J; Makar, Karen W KW; Kazanov, Dina D; Galazan, Lior L; Naumov, Inna I; Coghill, Anna E AE; Duggan, David D; Gigic, Biljana B; Arber, Nadir N; Ulrich, Cornelia M CM
Publication Date: 2013-08

Variant appearance in text: rs2073438
PubMed Link: 23778325
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in the lipoxygenase pathway and risk of colorectal neoplasia.

Genes, Chromosomes & Cancer
Kleinstein, Sarah E SE; Heath, Laura L; Makar, Karen W KW; Poole, Elizabeth M EM; Seufert, Brenna L BL; Slattery, Martha L ML; Xiao, Liren L; Duggan, David J DJ; Hsu, Li L; Curtin, Karen K; Koepl, Lisel L; Muehling, Jill J; Taverna, Darin D; Caan, Bette J BJ; Carlson, Christopher S CS; Potter, John D JD; Ulrich, Cornelia M CM
Publication Date: 2013-05

Variant appearance in text: rs2073438
PubMed Link: 23404351
Variant Present in the following documents:
  • Main text
View BVdb publication page



Different genes interact with particulate matter and tobacco smoke exposure in affecting lung function decline in the general population.

Plos One
Curjuric, Ivan I; Imboden, Medea M; Nadif, Rachel R; Kumar, Ashish A; Schindler, Christian C; Haun, Margot M; Kronenberg, Florian F; Künzli, Nino N; Phuleria, Harish H; Postma, Dirkje S DS; Russi, Erich W EW; Rochat, Thierry T; Demenais, Florence F; Probst-Hensch, Nicole M NM
Publication Date: 2012

Variant appearance in text: rs2073438
PubMed Link: 22792237
Variant Present in the following documents:
  • Main text
  • pone.0040175.pdf
View BVdb publication page



ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families.

International Journal Of Obesity (2005)
Xiao, W-J WJ; He, J-W JW; Zhang, H H; Hu, W-W WW; Gu, J-M JM; Yue, H H; Gao, G G; Yu, J-B JB; Wang, C C; Ke, Y-H YH; Fu, W-Z WZ; Zhang, Z-L ZL
Publication Date: 2011-03

Variant appearance in text: rs2073438
PubMed Link: 20697415
Variant Present in the following documents:
  • Main text
  • ijo2010157a.pdf
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ALOX12 gene is associated with the onset of natural menopause in white women.

Menopause (New York, N.Y.)
Liu, Pengyuan P; Lu, Yan Y; Recker, Robert R RR; Deng, Hong-Wen HW; Dvornyk, Volodymyr V
Publication Date: 2010

Variant appearance in text: rs2073438
PubMed Link: 20061896
Variant Present in the following documents:
  • Main text
View BVdb publication page



Robust and comprehensive analysis of 20 osteoporosis candidate genes by very high-density single-nucleotide polymorphism screen among 405 white nuclear families identified significant association and gene-gene interaction.

Journal Of Bone And Mineral Research : The Official Journal Of The American Society For Bone And Mineral Research
Xiong, Dong-Hai DH; Shen, Hui H; Zhao, Lan-Juan LJ; Xiao, Peng P; Yang, Tie-Lin TL; Guo, Yan Y; Wang, Wei W; Guo, Yan-Fang YF; Liu, Yong-Jun YJ; Recker, Robert R RR; Deng, Hong-Wen HW
Publication Date: 2006-11

Variant appearance in text: rs2073438
PubMed Link: 17002564
Variant Present in the following documents:
  • Main text
View BVdb publication page