PRM1 c.102G>T ;(p.R34S)

Variant ID: 16-11374994-C-A

NM_002761.2(PRM1):c.102G>T;(p.R34S)

This variant was identified in 13 publications

View GRCh38 version.




Publications:


SMAP is a pipeline for sample matching in proteogenomics.

Nature Communications
Li, Ling L; Niu, Mingming M; Erickson, Alyssa A; Luo, Jie J; Rowbotham, Kincaid K; Guo, Kai K; Huang, He H; Li, Yuxin Y; Jiang, Yi Y; Hur, Junguk J; Liu, Chunyu C; Peng, Junmin J; Wang, Xusheng X
Publication Date: 2022-02-08

Variant appearance in text: PRM1: R34S
PubMed Link: 35136070
Variant Present in the following documents:
  • 41467_2022_28411_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



The expression, function, and utilization of Protamine1: a literature review.

Translational Cancer Research
Ren, Shengnan S; Chen, Xuebo X; Tian, Xiaofeng X; Yang, Dingquan D; Dong, Yongli Y; Chen, Fangfang F; Fang, Xuedong X
Publication Date: 2021-11

Variant appearance in text: PRM1: 102G>T
PubMed Link: 35116345
Variant Present in the following documents:
  • Main text
  • tcr-10-11-4947.pdf
View BVdb publication page



Evaluation of the association between polymorphisms of PRM1 and PRM2 and the risk of male infertility: a systematic review, meta-analysis, and meta-regression.

Scientific Reports
Nemati, Houshang H; Sadeghi, Masoud M; Nazeri, Mehri M; Mohammadi, Mohana M
Publication Date: 2020-10-14

Variant appearance in text: rs35576928
PubMed Link: 33057064
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_74233.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: PRM1: R34S; rs35576928
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page



Analysis of PRM1 and PRM2 Polymorphisms in Iranian Infertile Men with Idiopathic Teratozoospermia.

International Journal Of Fertility & Sterility
Dehghanpour, Fatemeh F; Fesahat, Farzaneh F; Miresmaeili, Seyed Mohsen SM; Zare Mehrjardi, Ehsan E; Honarju, Ahmad A; Talebi, Ali Reza AR
Publication Date: 2019-04

Variant appearance in text: PRM1: 102G>T; rs35576928
PubMed Link: 30644249
Variant Present in the following documents:
  • Main text
  • Int-J-Fertil-Steril-13-77.pdf
View BVdb publication page



Polymorphisms in protamine 1 and 2 genes in asthenozoospermic men: A case-control study.

International Journal Of Reproductive Biomedicine
Nabi, Ali A; Khalili, Mohammad Ali MA; Moshrefi, Mojgan M; Sheikhha, Mohammad Hasan MH; Zare Mehrjardi, Ehsan E; Ashrafzadeh, Hamid Reza HR
Publication Date: 2018-06

Variant appearance in text: rs35576928
PubMed Link: 30123866
Variant Present in the following documents:
  • Main text
  • ijrb-16-379.pdf
View BVdb publication page



Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.

Nature Communications
Schrader, A A; Crispatzu, G G; Oberbeck, S S; Mayer, P P; Pützer, S S; von Jan, J J; Vasyutina, E E; Warner, K K; Weit, N N; Pflug, N N; Braun, T T; Andersson, E I EI; Yadav, B B; Riabinska, A A; Maurer, B B; Ventura Ferreira, M S MS; Beier, F F; Altmüller, J J; Lanasa, M M; Herling, C D CD; Haferlach, T T; Stilgenbauer, S S; Hopfinger, G G; Peifer, M M; Brümmendorf, T H TH; Nürnberg, P P; Elenitoba-Johnson, K S J KSJ; Zha, S S; Hallek, M M; Moriggl, R R; Reinhardt, H C HC; Stern, M-H MH; Mustjoki, S S; Newrzela, S S; Frommolt, P P; Herling, M M
Publication Date: 2018-02-15

Variant appearance in text: PRM1: R34S; rs35576928
PubMed Link: 29449575
Variant Present in the following documents:
  • 41467_2017_2688_MOESM14_ESM.xls, sheet 3
View BVdb publication page



Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population.

Oncotarget
Jiang, Weijun W; Zhu, Peiran P; Zhang, Jing J; Wu, Qiuyue Q; Li, Weiwei W; Liu, Shuaimei S; Ni, Mengxia M; Yu, Maomao M; Cao, Jin J; Li, Yi Y; Cui, Yingxia Y; Xia, Xinyi X
Publication Date: 2017-09-22

Variant appearance in text: rs35576928
PubMed Link: 28977892
Variant Present in the following documents:
  • Main text
  • oncotarget-08-61637.pdf
View BVdb publication page



Polymorphisms in Protamine 1 and Protamine 2 predict the risk of male infertility: a meta-analysis.

Scientific Reports
Jiang, Weijun W; Sun, Hui H; Zhang, Jing J; Zhou, Qing Q; Wu, Qiuyue Q; Li, Tianfu T; Zhang, Cui C; Li, Weiwei W; Zhang, Mingchao M; Xia, Xinyi X
Publication Date: 2015-10-16

Variant appearance in text: PRM1: Arg34Ser; rs35576928
PubMed Link: 26472740
Variant Present in the following documents:
  • Main text
  • srep15300.pdf
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: PRM1: R34S; rs35576928
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives.

Asian Journal Of Andrology
Kläver, Ruth R; Gromoll, Jörg J
Publication Date: 2014

Variant appearance in text: rs35576928
PubMed Link: 24923457
Variant Present in the following documents:
  • AJA-16-669.pdf
View BVdb publication page



An SNP in protamine 1: a possible genetic cause of male infertility?

Journal Of Medical Genetics
Iguchi, N N; Yang, S S; Lamb, D J DJ; Hecht, N B NB
Publication Date: 2006-04

Variant appearance in text: PRM1: R34S
PubMed Link: 16199539
Variant Present in the following documents:
  • Main text
View BVdb publication page