STK36 c.3008G>A ;(p.G1003D)

Variant ID: 2-219562675-G-A

NM_015690.4(STK36):c.3008G>A;(p.G1003D)

This variant was identified in 33 publications

View GRCh38 version.




Publications:


Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: STK36: G1003D
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: STK36: G1003D
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM4_ESM.xlsx, sheet 2
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: STK36: G1003D
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



Integrated molecular profiling of patient-derived ovarian cancer models identifies clinically relevant signatures and tumor vulnerabilities.

International Journal Of Cancer
Lupia, Michela M; Melocchi, Valentina V; Bizzaro, Francesca F; Lo Riso, Pietro P; Dama, Elisa E; Baronio, Micol M; Ranghiero, Alberto A; Barberis, Massimo M; Bernard, Loris L; Bertalot, Giovanni G; Giavazzi, Raffaella R; Testa, Giuseppe G; Bianchi, Fabrizio F; Cavallaro, Ugo U
Publication Date: 2022-07-15

Variant appearance in text: STK36: Gly1003Asp; rs1863704
PubMed Link: 35218560
Variant Present in the following documents:
  • IJC-151-240-s001.xlsx, sheet 7
View BVdb publication page



Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Molecular & Cellular Proteomics : Mcp
Schmitt, Marisa M; Sinnberg, Tobias T; Bratl, Katrin K; Zittlau, Katharina K; Garbe, Claus C; Macek, Boris B; Nalpas, Nicolas C NC
Publication Date: 2021-10-19

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 34673281
Variant Present in the following documents:
  • mmc2.xlsx, sheet 11
  • mmc2.xlsx, sheet 3
  • mmc2.xlsx, sheet 9
View BVdb publication page



Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Molecular & Cellular Proteomics : Mcp
Schmitt, Marisa M; Sinnberg, Tobias T; Bratl, Katrin K; Zittlau, Katharina K; Garbe, Claus C; Macek, Boris B; Nalpas, Nicolas C NC
Publication Date: 2021

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 34673281
Variant Present in the following documents:
  • mmc2.xlsx, sheet 11
  • mmc2.xlsx, sheet 3
  • mmc2.xlsx, sheet 9
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: STK36: 3008G>A; G1003D; rs1863704
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: STK36: 3008G>A; Gly1003Asp; rs1863704
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Plos One
Sebate, Boiketlo B; Cuttler, Katelyn K; Cloete, Ruben R; Britz, Marcell M; Christoffels, Alan A; Williams, Monique M; Carr, Jonathan J; Bardien, Soraya S
Publication Date: 2021

Variant appearance in text: STK36: 3008G>A; G1003D; rs1863704
PubMed Link: 33770142
Variant Present in the following documents:
  • pone.0249324.s003.xlsx, sheet 1
  • pone.0249324.s003.xlsx, sheet 2
  • pone.0249324.s003.xlsx, sheet 3
View BVdb publication page



Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08

Variant appearance in text: STK36: 3008G>A; G1003D; rs1863704
PubMed Link: 33420045
Variant Present in the following documents:
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 4
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune profile, clinical outcome and sensitivity to targeted therapies.

Ebiomedicine
Toulmonde, Maud M; Lucchesi, Carlo C; Verbeke, Stéphanie S; Crombe, Amandine A; Adam, Julien J; Geneste, Damien D; Chaire, Vanessa V; Laroche-Clary, Audrey A; Perret, Raul R; Bertucci, François F; Bertolo, Frederic F; Bianchini, Laurence L; Dadone-Montaudie, Bérengère B; Hembrough, Todd T; Sweet, Steve S; Kim, Yeoun Jin YJ; Cecchi, Fabiola F; Le Loarer, François F; Italiano, Antoine A
Publication Date: 2020-12

Variant appearance in text: STK36: 3008G>A; G1003D; rs1863704
PubMed Link: 33254023
Variant Present in the following documents:
  • mmc5.xlsx, sheet 1
View BVdb publication page



Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.

Communications Biology
Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF
Publication Date: 2020-04-20

Variant appearance in text: rs1863704
PubMed Link: 32313182
Variant Present in the following documents:
  • 42003_2020_885_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



YAP1 mediates survival of ALK-rearranged lung cancer cells treated with alectinib via pro-apoptotic protein regulation.

Nature Communications
Tsuji, Takahiro T; Ozasa, Hiroaki H; Aoki, Wataru W; Aburaya, Shunsuke S; Yamamoto Funazo, Tomoko T; Furugaki, Koh K; Yoshimura, Yasushi Y; Yamazoe, Masatoshi M; Ajimizu, Hitomi H; Yasuda, Yuto Y; Nomizo, Takashi T; Yoshida, Hironori H; Sakamori, Yuichi Y; Wake, Hiroaki H; Ueda, Mitsuyoshi M; Kim, Young Hak YH; Hirai, Toyohiro T
Publication Date: 2020-01-03

Variant appearance in text: STK36: G1003D
PubMed Link: 31900393
Variant Present in the following documents:
  • 41467_2019_13771_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



The role of myoglobin in epithelial cancers: Insights from transcriptomics.

International Journal Of Molecular Medicine
Bicker, Anne A; Nauth, Theresa T; Gerst, Daniela D; Aboouf, Mostafa Ahmed MA; Fandrey, Joachim J; Kristiansen, Glen G; Gorr, Thomas Alexander TA; Hankeln, Thomas T
Publication Date: 2020-02

Variant appearance in text: STK36: 3008G>A; Gly1003Asp
PubMed Link: 31894249
Variant Present in the following documents:
  • Supplementary_Data2.xlsx, sheet 7
  • Supplementary_Data2.xlsx, sheet 6
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: STK36: 3008G>A; Gly1003Asp; rs1863704
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
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: STK36: G1003D; rs1863704
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
View BVdb publication page



DNA methylation loss promotes immune evasion of tumours with high mutation and copy number load.

Nature Communications
Jung, Hyunchul H; Kim, Hong Sook HS; Kim, Jeong Yeon JY; Sun, Jong-Mu JM; Ahn, Jin Seok JS; Ahn, Myung-Ju MJ; Park, Keunchil K; Esteller, Manel M; Lee, Se-Hoon SH; Choi, Jung Kyoon JK
Publication Date: 2019-09-19

Variant appearance in text: STK36: G1003D
PubMed Link: 31537801
Variant Present in the following documents:
  • 41467_2019_12159_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page



A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Scientific Reports
Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW
Publication Date: 2019-03-20

Variant appearance in text: rs1863704
PubMed Link: 30894629
Variant Present in the following documents:
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 9
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 4
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 3
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 12
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 13
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 6
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 10
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 11
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 7
View BVdb publication page



Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: STK36: 3008G>A; Gly1003Asp; rs1863704
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Tobacco habituated and non-habituated subjects exhibit different mutational spectrums in head and neck squamous cell carcinoma.

3 Biotech
Rawal, Rakesh M RM; Joshi, Madhvi N MN; Bhargava, Poonam P; Shaikh, Inayat I; Pandit, Aanal S AS; Patel, Riddhi P RP; Patel, Shanaya S; Kothari, Kiran K; Shah, Manoj M; Saxena, Akshay A; Bagatharia, Snehal B SB
Publication Date: 2015-10

Variant appearance in text: STK36: G1003D
PubMed Link: 28324520
Variant Present in the following documents:
  • 13205_2014_267_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.

The Journal Of Pathology
Maguire, Sarah L SL; Peck, Barrie B; Wai, Patty T PT; Campbell, James J; Barker, Holly H; Gulati, Aditi A; Daley, Frances F; Vyse, Simon S; Huang, Paul P; Lord, Christopher J CJ; Farnie, Gillian G; Brennan, Keith K; Natrajan, Rachael R
Publication Date: 2016-11

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 27512948
Variant Present in the following documents:
  • PATH-240-315-s015.xlsx, sheet 1
View BVdb publication page



PredictSNP2: A Unified Platform for Accurately Evaluating SNP Effects by Exploiting the Different Characteristics of Variants in Distinct Genomic Regions.

Plos Computational Biology
Bendl, Jaroslav J; Musil, Miloš M; Štourač, Jan J; Zendulka, Jaroslav J; Damborský, Jiří J; Brezovský, Jan J
Publication Date: 2016-05

Variant appearance in text: STK36: G1003D
PubMed Link: 27224906
Variant Present in the following documents:
  • pcbi.1004962.s005.xlsx, sheet 3
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: rs1863704
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 2
  • mmc3.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Scientific Reports
Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R
Publication Date: 2015-03-16

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 25773295
Variant Present in the following documents:
  • srep09124-s3.xls, sheet 1
View BVdb publication page



Genetic studies of body mass index yield new insights for obesity biology.

Nature
Locke, Adam E AE; Kahali, Bratati B; Berndt, Sonja I SI; Justice, Anne E AE; Pers, Tune H TH; Day, Felix R FR; Powell, Corey C; Vedantam, Sailaja S; Buchkovich, Martin L ML; Yang, Jian J; Croteau-Chonka, Damien C DC; Esko, Tonu T; Fall, Tove T; Ferreira, Teresa T; Gustafsson, Stefan S; Kutalik, Zoltán Z; Luan, Jian'an J; Mägi, Reedik R; Randall, Joshua C JC; Winkler, Thomas W TW; Wood, Andrew R AR; Workalemahu, Tsegaselassie T; Faul, Jessica D JD; Smith, Jennifer A JA; Zhao, Jing Hua JH; Zhao, Wei W; Chen, Jin J; Fehrmann, Rudolf R; Hedman, Åsa K ÅK; Karjalainen, Juha J; Schmidt, Ellen M EM; Absher, Devin D; Amin, Najaf N; Anderson, Denise D; Beekman, Marian M; Bolton, Jennifer L JL; Bragg-Gresham, Jennifer L JL; Buyske, Steven S; Demirkan, Ayse A; Deng, Guohong G; Ehret, Georg B GB; Feenstra, Bjarke B; Feitosa, Mary F MF; Fischer, Krista K; Goel, Anuj A; Gong, Jian J; Jackson, Anne U AU; Kanoni, Stavroula S; Kleber, Marcus E ME; Kristiansson, Kati K; Lim, Unhee U; Lotay, Vaneet V; Mangino, Massimo M; Leach, Irene Mateo IM; Medina-Gomez, Carolina C; Medland, Sarah E SE; Nalls, Michael A MA; Palmer, Cameron D CD; Pasko, Dorota D; Pechlivanis, Sonali S; Peters, Marjolein J MJ; Prokopenko, Inga I; Shungin, Dmitry D; Stančáková, Alena A; Strawbridge, Rona J RJ; Sung, Yun Ju YJ; Tanaka, Toshiko T; Teumer, Alexander A; Trompet, Stella S; van der Laan, Sander W SW; van Setten, Jessica J; Van Vliet-Ostaptchouk, Jana V JV; Wang, Zhaoming Z; Yengo, Loïc L; Zhang, Weihua W; Isaacs, Aaron A; Albrecht, Eva E; Ärnlöv, Johan J; Arscott, Gillian M GM; Attwood, Antony P AP; Bandinelli, Stefania S; Barrett, Amy A; Bas, Isabelita N IN; Bellis, Claire C; Bennett, Amanda J AJ; Berne, Christian C; Blagieva, Roza R; Blüher, Matthias M; Böhringer, Stefan S; Bonnycastle, Lori L LL; Böttcher, Yvonne Y; Boyd, Heather A HA; Bruinenberg, Marcel M; Caspersen, Ida H IH; Chen, Yii-Der Ida YI; Clarke, Robert R; Daw, E Warwick EW; de Craen, Anton J M AJM; Delgado, Graciela G; Dimitriou, Maria M; Doney, Alex S F ASF; Eklund, Niina N; Estrada, Karol K; Eury, Elodie E; Folkersen, Lasse L; Fraser, Ross M RM; Garcia, Melissa E ME; Geller, Frank F; Giedraitis, Vilmantas V; Gigante, Bruna B; Go, Alan S AS; Golay, Alain A; Goodall, Alison H AH; Gordon, Scott D SD; Gorski, Mathias M; Grabe, Hans-Jörgen HJ; Grallert, Harald H; Grammer, Tanja B TB; Gräßler, Jürgen J; Grönberg, Henrik H; Groves, Christopher J CJ; Gusto, Gaëlle G; Haessler, Jeffrey J; Hall, Per P; Haller, Toomas T; Hallmans, Goran G; Hartman, Catharina A CA; Hassinen, Maija M; Hayward, Caroline C; Heard-Costa, Nancy L NL; Helmer, Quinta Q; Hengstenberg, Christian C; Holmen, Oddgeir O; Hottenga, Jouke-Jan JJ; James, Alan L AL; Jeff, Janina M JM; Johansson, Åsa Å; Jolley, Jennifer J; Juliusdottir, Thorhildur T; Kinnunen, Leena L; Koenig, Wolfgang W; Koskenvuo, Markku M; Kratzer, Wolfgang W; Laitinen, Jaana J; Lamina, Claudia C; Leander, Karin K; Lee, Nanette R NR; Lichtner, Peter P; Lind, Lars L; Lindström, Jaana J; Lo, Ken Sin KS; Lobbens, Stéphane S; Lorbeer, Roberto R; Lu, Yingchang Y; Mach, François F; Magnusson, Patrik K E PKE; Mahajan, Anubha A; McArdle, Wendy L WL; McLachlan, Stela S; Menni, Cristina C; Merger, Sigrun S; Mihailov, Evelin E; Milani, Lili L; Moayyeri, Alireza A; Monda, Keri L KL; Morken, Mario A MA; Mulas, Antonella A; Müller, Gabriele G; Müller-Nurasyid, Martina M; Musk, Arthur W AW; Nagaraja, Ramaiah R; Nöthen, Markus M MM; Nolte, Ilja M IM; Pilz, Stefan S; Rayner, Nigel W NW; Renstrom, Frida F; Rettig, Rainer R; Ried, Janina S JS; Ripke, Stephan S; Robertson, Neil R NR; Rose, Lynda M LM; Sanna, Serena S; Scharnagl, Hubert H; Scholtens, Salome S; Schumacher, Fredrick R FR; Scott, William R WR; Seufferlein, Thomas T; Shi, Jianxin J; Smith, Albert Vernon AV; Smolonska, Joanna J; Stanton, Alice V AV; Steinthorsdottir, Valgerdur V; Stirrups, Kathleen K; Stringham, Heather M HM; Sundström, Johan J; Swertz, Morris A MA; Swift, Amy J AJ; Syvänen, Ann-Christine AC; Tan, Sian-Tsung ST; Tayo, Bamidele O BO; Thorand, Barbara B; Thorleifsson, Gudmar G; Tyrer, Jonathan P JP; Uh, Hae-Won HW; Vandenput, Liesbeth L; Verhulst, Frank C FC; Vermeulen, Sita H SH; Verweij, Niek N; Vonk, Judith M JM; Waite, Lindsay L LL; Warren, Helen R HR; Waterworth, Dawn D; Weedon, Michael N MN; Wilkens, Lynne R LR; Willenborg, Christina C; Wilsgaard, Tom T; Wojczynski, Mary K MK; Wong, Andrew A; Wright, Alan F AF; Zhang, Qunyuan Q; , ; Brennan, Eoin P EP; Choi, Murim M; Dastani, Zari Z; Drong, Alexander W AW; Eriksson, Per P; Franco-Cereceda, Anders A; Gådin, Jesper R JR; Gharavi, Ali G AG; Goddard, Michael E ME; Handsaker, Robert E RE; Huang, Jinyan J; Karpe, Fredrik F; Kathiresan, Sekar S; Keildson, Sarah S; Kiryluk, Krzysztof K; Kubo, Michiaki M; Lee, Jong-Young JY; Liang, Liming L; Lifton, Richard P RP; Ma, Baoshan B; McCarroll, Steven A SA; McKnight, Amy J AJ; Min, Josine L JL; Moffatt, Miriam F MF; Montgomery, Grant W GW; Murabito, Joanne M JM; Nicholson, George G; Nyholt, Dale R DR; Okada, Yukinori Y; Perry, John R B JRB; Dorajoo, Rajkumar R; Reinmaa, Eva E; Salem, Rany M RM; Sandholm, Niina N; Scott, Robert A RA; Stolk, Lisette L; Takahashi, Atsushi A; Tanaka, Toshihiro T; van 't Hooft, Ferdinand M FM; Vinkhuyzen, Anna A E AAE; Westra, Harm-Jan HJ; Zheng, Wei W; Zondervan, Krina T KT; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; Heath, Andrew C AC; Arveiler, Dominique D; Bakker, Stephan J L SJL; Beilby, John J; Bergman, Richard N RN; Blangero, John J; Bovet, Pascal P; Campbell, Harry H; Caulfield, Mark J MJ; Cesana, Giancarlo G; Chakravarti, Aravinda A; Chasman, Daniel I DI; Chines, Peter S PS; Collins, Francis S FS; Crawford, Dana C DC; Cupples, L Adrienne LA; Cusi, Daniele D; Danesh, John J; de Faire, Ulf U; den Ruijter, Hester M HM; Dominiczak, Anna F AF; Erbel, Raimund R; Erdmann, Jeanette J; Eriksson, Johan G JG; Farrall, Martin M; Felix, Stephan B SB; Ferrannini, Ele E; Ferrières, Jean J; Ford, Ian I; Forouhi, Nita G NG; Forrester, Terrence T; Franco, Oscar H OH; Gansevoort, Ron T RT; Gejman, Pablo V PV; Gieger, Christian C; Gottesman, Omri O; Gudnason, Vilmundur V; Gyllensten, Ulf U; Hall, Alistair S AS; Harris, Tamara B TB; Hattersley, Andrew T AT; Hicks, Andrew A AA; Hindorff, Lucia A LA; Hingorani, Aroon D AD; Hofman, Albert A; Homuth, Georg G; Hovingh, G Kees GK; Humphries, Steve E SE; Hunt, Steven C SC; Hyppönen, Elina E; Illig, Thomas T; Jacobs, Kevin B KB; Jarvelin, Marjo-Riitta MR; Jöckel, Karl-Heinz KH; Johansen, Berit B; Jousilahti, Pekka P; Jukema, J Wouter JW; Jula, Antti M AM; Kaprio, Jaakko J; Kastelein, John J P JJP; Keinanen-Kiukaanniemi, Sirkka M SM; Kiemeney, Lambertus A LA; Knekt, Paul P; Kooner, Jaspal S JS; Kooperberg, Charles C; Kovacs, Peter P; Kraja, Aldi T AT; Kumari, Meena M; Kuusisto, Johanna J; Lakka, Timo A TA; Langenberg, Claudia C; Marchand, Loic Le LL; Lehtimäki, Terho T; Lyssenko, Valeriya V; Männistö, Satu S; Marette, André A; Matise, Tara C TC; McKenzie, Colin A CA; McKnight, Barbara B; Moll, Frans L FL; Morris, Andrew D AD; Morris, Andrew P AP; Murray, Jeffrey C JC; Nelis, Mari M; Ohlsson, Claes C; Oldehinkel, Albertine J AJ; Ong, Ken K KK; Madden, Pamela A F PAF; Pasterkamp, Gerard G; Peden, John F JF; Peters, Annette A; Postma, Dirkje S DS; Pramstaller, Peter P PP; Price, Jackie F JF; Qi, Lu L; Raitakari, Olli T OT; Rankinen, Tuomo T; Rao, D C DC; Rice, Treva K TK; Ridker, Paul M PM; Rioux, John D JD; Ritchie, Marylyn D MD; Rudan, Igor I; Salomaa, Veikko V; Samani, Nilesh J NJ; Saramies, Jouko J; Sarzynski, Mark A MA; Schunkert, Heribert H; Schwarz, Peter E H PEH; Sever, Peter P; Shuldiner, Alan R AR; Sinisalo, Juha J; Stolk, Ronald P RP; Strauch, Konstantin K; Tönjes, Anke A; Trégouët, David-Alexandre DA; Tremblay, Angelo A; Tremoli, Elena E; Virtamo, Jarmo J; Vohl, Marie-Claude MC; Völker, Uwe U; Waeber, Gérard G; Willemsen, Gonneke G; Witteman, Jacqueline C JC; Zillikens, M Carola MC; Adair, Linda S LS; Amouyel, Philippe P; Asselbergs, Folkert W FW; Assimes, Themistocles L TL; Bochud, Murielle M; Boehm, Bernhard O BO; Boerwinkle, Eric E; Bornstein, Stefan R SR; Bottinger, Erwin P EP; Bouchard, Claude C; Cauchi, Stéphane S; Chambers, John C JC; Chanock, Stephen J SJ; Cooper, Richard S RS; de Bakker, Paul I W PIW; Dedoussis, George G; Ferrucci, Luigi L; Franks, Paul W PW; Froguel, Philippe P; Groop, Leif C LC; Haiman, Christopher A CA; Hamsten, Anders A; Hui, Jennie J; Hunter, David J DJ; Hveem, Kristian K; Kaplan, Robert C RC; Kivimaki, Mika M; Kuh, Diana D; Laakso, Markku M; Liu, Yongmei Y; Martin, Nicholas G NG; März, Winfried W; Melbye, Mads M; Metspalu, Andres A; Moebus, Susanne S; Munroe, Patricia B PB; Njølstad, Inger I; Oostra, Ben A BA; Palmer, Colin N A CNA; Pedersen, Nancy L NL; Perola, Markus M; Pérusse, Louis L; Peters, Ulrike U; Power, Chris C; Quertermous, Thomas T; Rauramaa, Rainer R; Rivadeneira, Fernando F; Saaristo, Timo E TE; Saleheen, Danish D; Sattar, Naveed N; Schadt, Eric E EE; Schlessinger, David D; Slagboom, P Eline PE; Snieder, Harold H; Spector, Tim D TD; Thorsteinsdottir, Unnur U; Stumvoll, Michael M; Tuomilehto, Jaakko J; Uitterlinden, André G AG; Uusitupa, Matti M; van der Harst, Pim P; Walker, Mark M; Wallaschofski, Henri H; Wareham, Nicholas J NJ; Watkins, Hugh H; Weir, David R DR; Wichmann, H-Erich HE; Wilson, James F JF; Zanen, Pieter P; Borecki, Ingrid B IB; Deloukas, Panos P; Fox, Caroline S CS; Heid, Iris M IM; O'Connell, Jeffrey R JR; Strachan, David P DP; Stefansson, Kari K; van Duijn, Cornelia M CM; Abecasis, Gonçalo R GR; Franke, Lude L; Frayling, Timothy M TM; McCarthy, Mark I MI; Visscher, Peter M PM; Scherag, André A; Willer, Cristen J CJ; Boehnke, Michael M; Mohlke, Karen L KL; Lindgren, Cecilia M CM; Beckmann, Jacques S JS; Barroso, Inês I; North, Kari E KE; Ingelsson, Erik E; Hirschhorn, Joel N JN; Loos, Ruth J F RJF; Speliotes, Elizabeth K EK
Publication Date: 2015-02-12

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 25673413
Variant Present in the following documents:
  • Main text
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Whole exome sequencing of a single osteosarcoma case--integrative analysis with whole transcriptome RNA-seq data.

Human Genomics
Reimann, Ene E; Kõks, Sulev S; Ho, Xuan Dung XD; Maasalu, Katre K; Märtson, Aare A
Publication Date: 2014-12-11

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 25496518
Variant Present in the following documents:
  • 40246_2014_20_MOESM1_ESM.xlsx, sheet 1
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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: STK36: G1003D; rs1863704
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
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Mutational analysis of hedgehog signaling pathway genes in human malignant mesothelioma.

Plos One
Lim, Chuan Bian CB; Prêle, Cecilia M CM; Cheah, Hui Min HM; Cheng, Yuen Yee YY; Klebe, Sonja S; Reid, Glen G; Watkins, D Neil DN; Baltic, Svetlana S; Thompson, Philip J PJ; Mutsaers, Steven E SE
Publication Date: 2013

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 23826113
Variant Present in the following documents:
  • Main text
  • pone.0066685.pdf
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Genome bioinformatic analysis of nonsynonymous SNPs.

Bmc Bioinformatics
Burke, David F DF; Worth, Catherine L CL; Priego, Eva-Maria EM; Cheng, Tammy T; Smink, Luc J LJ; Todd, John A JA; Blundell, Tom L TL
Publication Date: 2007-08-20

Variant appearance in text: STK36: G1003D; rs1863704
PubMed Link: 17708757
Variant Present in the following documents:
  • Main text
  • 1471-2105-8-301.pdf
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The FU gene and its possible protein isoforms.

Bmc Genomics
Østerlund, Torben T; Everman, David B DB; Betz, Regina C RC; Mosca, Monica M; Nöthen, Markus M MM; Schwartz, Charles E CE; Zaphiropoulos, Peter G PG; Toftgård, Rune R
Publication Date: 2004-07-22

Variant appearance in text: STK36: G1003D
PubMed Link: 15268766
Variant Present in the following documents:
  • Main text
  • 1471-2164-5-49.pdf
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