OR10G4 c.436G>A ;(p.G146S)

Variant ID: 11-123886717-G-A

NM_001004462.1(OR10G4):c.436G>A;(p.G146S)

This variant was identified in 12 publications

View GRCh38 version.




Publications:


Integrative proteomic characterization of adenocarcinoma of esophagogastric junction.

Nature Communications
Li, Shengli S; Yuan, Li L; Xu, Zhi-Yuan ZY; Xu, Jing-Li JL; Chen, Gui-Ping GP; Guan, Xiaoqing X; Pan, Guang-Zhao GZ; Hu, Can C; Dong, Jinyun J; Du, Yi-An YA; Yang, Li-Tao LT; Ni, Mao-Wei MW; Jiang, Rui-Bin RB; Zhu, Xiu X; Lv, Hang H; Xu, Han-Dong HD; Zhang, Sheng-Jie SJ; Qin, Jiang-Jiang JJ; Cheng, Xiang-Dong XD
Publication Date: 2023-02-11

Variant appearance in text: OR10G4: 436G>A; G146S; rs503223
PubMed Link: 36774361
Variant Present in the following documents:
  • 41467_2023_36462_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



An explainable model of host genetic interactions linked to COVID-19 severity.

Communications Biology
Onoja, Anthony A; Picchiotti, Nicola N; Fallerini, Chiara C; Baldassarri, Margherita M; Fava, Francesca F; , ; Colombo, Francesca F; Chiaromonte, Francesca F; Renieri, Alessandra A; Furini, Simone S; Raimondi, Francesco F
Publication Date: 2022-10-26

Variant appearance in text: OR10G4: G146S; rs503223
PubMed Link: 36289370
Variant Present in the following documents:
  • 42003_2022_4073_MOESM4_ESM.xlsx, sheet 1
  • 42003_2022_4073_MOESM4_ESM.xlsx, sheet 12
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: OR10G4: G146S; rs503223
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: OR10G4: 436G>A; G146S; rs503223
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Establishment and Characterization of a Novel Human Ocular Adnexal Sebaceous Carcinoma Cell Line.

Translational Vision Science & Technology
Rong, Andrew J AJ; Gallo, Ryan A RA; Zhang, Michelle G MG; Doddapaneni, Ravi R; Griswold, Anthony J AJ; Lee, John Y JY; Kurtenbach, Stefan S; Dubovy, Sander R SR; Tse, David T DT; Pelaez, Daniel D
Publication Date: 2021-05-03

Variant appearance in text: OR10G4: G146S; rs503223
PubMed Link: 34043754
Variant Present in the following documents:
  • tvst-10-6-34_s002.xlsx, sheet 1
  • tvst-10-6-34_s001.xlsx, sheet 1
View BVdb publication page



The mutational landscape of human olfactory G protein-coupled receptors.

Bmc Biology
Jimenez, Ramón Cierco RC; Casajuana-Martin, Nil N; García-Recio, Adrián A; Alcántara, Lidia L; Pardo, Leonardo L; Campillo, Mercedes M; Gonzalez, Angel A
Publication Date: 2021-02-05

Variant appearance in text: OR10G4: 436G>A; Gly146Ser; rs503223
PubMed Link: 33546694
Variant Present in the following documents:
  • 12915_2021_962_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Discovery of a molecular glue promoting CDK12-DDB1 interaction to trigger cyclin K degradation.

Elife
Lv, Lu L; Chen, Peihao P; Cao, Longzhi L; Li, Yamei Y; Zeng, Zhi Z; Cui, Yue Y; Wu, Qingcui Q; Li, Jiaojiao J; Wang, Jian-Hua JH; Dong, Meng-Qiu MQ; Qi, Xiangbing X; Han, Ting T
Publication Date: 2020-08-17

Variant appearance in text: OR10G4: G146S
PubMed Link: 32804079
Variant Present in the following documents:
  • elife-59994-fig2-data2.xlsx, sheet 3
View BVdb publication page



Tumor mutation burden and recurrent tumors in hereditary lung cancer.

Cancer Medicine
Hsu, Yi-Chiung YC; Chang, Ya-Hsuan YH; Chang, Gee-Chen GC; Ho, Bing-Ching BC; Yuan, Shin-Sheng SS; Li, Yu-Cheng YC; Zeng, Jhih-Wun JW; Yu, Sung-Liang SL; Li, Ker-Chau KC; Yang, Pan-Chyr PC; Chen, Hsuan-Yu HY
Publication Date: 2019-05

Variant appearance in text: OR10G4: G146S; rs503223
PubMed Link: 30941903
Variant Present in the following documents:
  • CAM4-8-2179-s001.xlsx, sheet 2
View BVdb publication page



Genomic Evaluation of Multiparametric Magnetic Resonance Imaging-visible and -nonvisible Lesions in Clinically Localised Prostate Cancer.

European Urology Oncology
Parry, Marina A MA; Srivastava, Shambhavi S; Ali, Adnan A; Cannistraci, Alessio A; Antonello, Jenny J; Barros-Silva, João Diogo JD; Ubertini, Valentina V; Ramani, Vijay V; Lau, Maurice M; Shanks, Jonathan J; Nonaka, Daisuke D; Oliveira, Pedro P; Hambrock, Thomas T; Leong, Hui Sun HS; Dhomen, Nathalie N; Miller, Crispin C; Brady, Ged G; Dive, Caroline C; Clarke, Noel W NW; Marais, Richard R; Baena, Esther E
Publication Date: 2019-02

Variant appearance in text: OR10G4: G146S; rs503223
PubMed Link: 30929837
Variant Present in the following documents:
  • mmc6.xlsx, sheet 6
  • mmc7.xlsx, sheet 2
View BVdb publication page



Genetic variants affecting equivalent protein family positions reflect human diversity.

Scientific Reports
Raimondi, Francesco F; Betts, Matthew J MJ; Lu, Qianhao Q; Inoue, Asuka A; Gutkind, J Silvio JS; Russell, Robert B RB
Publication Date: 2017-10-06

Variant appearance in text: OR10G4: G146S
PubMed Link: 28986545
Variant Present in the following documents:
  • 41598_2017_12971_MOESM2_ESM.xlsx, sheet 13
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs503223
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



The missense of smell: functional variability in the human odorant receptor repertoire.

Nature Neuroscience
Mainland, Joel D JD; Keller, Andreas A; Li, Yun R YR; Zhou, Ting T; Trimmer, Casey C; Snyder, Lindsey L LL; Moberly, Andrew H AH; Adipietro, Kaylin A KA; Liu, Wen Ling L WL; Zhuang, Hanyi H; Zhan, Senmiao S; Lee, Somin S SS; Lin, Abigail A; Matsunami, Hiroaki H
Publication Date: 2014-01

Variant appearance in text: OR10G4: G146S
PubMed Link: 24316890
Variant Present in the following documents:
  • NIHMS560003-supplement-1.pdf
View BVdb publication page