MYH9 c.4770+51C>T

Variant ID: 22-36684722-G-A

NM_002473.4(MYH9):c.4770+51C>T

This variant was identified in 15 publications

View GRCh38 version.




Publications:


JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: MYH9: 4770+51C>T; rs11912763
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
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An African perspective on the genetic risk of chronic kidney disease: a systematic review.

Bmc Medical Genetics
George, Cindy C; Yako, Yandiswa Y YY; Okpechi, Ikechi G IG; Matsha, Tandi E TE; Kaze Folefack, Francois J FJ; Kengne, Andre P AP
Publication Date: 2018-10-19

Variant appearance in text: rs11912763
PubMed Link: 30340464
Variant Present in the following documents:
  • Main text
  • 12881_2018_Article_702.pdf
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Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.

Omics : A Journal Of Integrative Biology
Geard, Amy A; Pule, Gift D GD; Chelo, David D; Bitoungui, Valentina Josiane Ngo VJ; Wonkam, Ambroise A
Publication Date: 2016-10

Variant appearance in text: rs11912763
PubMed Link: 27726639
Variant Present in the following documents:
  • Main text
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Genetic variants and cell-free hemoglobin processing in sickle cell nephropathy.

Haematologica
Saraf, Santosh L SL; Zhang, Xu X; Shah, Binal B; Kanias, Tamir T; Gudehithlu, Krishnamurthy P KP; Kittles, Rick R; Machado, Roberto F RF; Arruda, Jose A L JA; Gladwin, Mark T MT; Singh, Ashok K AK; Gordeuk, Victor R VR
Publication Date: 2015-10

Variant appearance in text: rs11912763
PubMed Link: 26206798
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic contribution and associated pathophysiology in end-stage renal disease.

The Application Of Clinical Genetics
Agrawal, Suraksha S; Agarwal, Ss S; Naik, Sita S
Publication Date: 2010

Variant appearance in text: rs11912763
PubMed Link: 23776353
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms in the non-muscle myosin heavy chain gene (MYH9) are associated with lower glomerular filtration rate in mixed ancestry diabetic subjects from South Africa.

Plos One
Matsha, Tandi Edith TE; Masconi, Katya K; Yako, Yandiswa Yolanda YY; Hassan, Mogamat Shafick MS; Macharia, Muiriri M; Erasmus, Rajiv Timothy RT; Kengne, Andre Pascal AP
Publication Date: 2012

Variant appearance in text: rs11912763
PubMed Link: 23285077
Variant Present in the following documents:
  • Main text
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Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians.

International Urology And Nephrology
Tayo, Bamidele O BO; Kramer, Holly H; Salako, Babatunde L BL; Gottesman, Omri O; McKenzie, Colin A CA; Ogunniyi, Adesola A; Bottinger, Erwin P EP; Cooper, Richard S RS
Publication Date: 2013-04

Variant appearance in text: rs11912763
PubMed Link: 22956460
Variant Present in the following documents:
  • Main text
View BVdb publication page



Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans.

Kidney International
Lipkowitz, Michael S MS; Freedman, Barry I BI; Langefeld, Carl D CD; Comeau, Mary E ME; Bowden, Donald W DW; Kao, W H Linda WH; Astor, Brad C BC; Bottinger, Erwin P EP; Iyengar, Sudha K SK; Klotman, Paul E PE; Freedman, Richard G RG; Zhang, Weijia W; Parekh, Rulan S RS; Choi, Michael J MJ; Nelson, George W GW; Winkler, Cheryl A CA; Kopp, Jeffrey B JB; ,
Publication Date: 2013-01

Variant appearance in text: rs11912763
PubMed Link: 22832513
Variant Present in the following documents:
  • Main text
  • nihms387629.pdf
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APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy.

Journal Of The American Society Of Nephrology : Jasn
Papeta, Natalia N; Kiryluk, Krzysztof K; Patel, Ami A; Sterken, Roel R; Kacak, Nilgun N; Snyder, Holly J HJ; Imus, Phil H PH; Mhatre, Anand N AN; Lawani, Anil K AK; Julian, Bruce A BA; Wyatt, Robert J RJ; Novak, Jan J; Wyatt, Christina M CM; Ross, Michael J MJ; Winston, Jonathan A JA; Klotman, Mary E ME; Cohen, David J DJ; Appel, Gerald B GB; D'Agati, Vivette D VD; Klotman, Paul E PE; Gharavi, Ali G AG
Publication Date: 2011-11

Variant appearance in text: rs11912763
PubMed Link: 21997397
Variant Present in the following documents:
  • Main text
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MYH9 and APOL1 are both associated with sickle cell disease nephropathy.

British Journal Of Haematology
Ashley-Koch, Allison E AE; Okocha, Emmanuel C EC; Garrett, Melanie E ME; Soldano, Karen K; De Castro, Laura M LM; Jonassaint, Jude C JC; Orringer, Eugene P EP; Eckman, James R JR; Telen, Marilyn J MJ
Publication Date: 2011-11

Variant appearance in text: rs11912763
PubMed Link: 21910715
Variant Present in the following documents:
  • Main text
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A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9.

Kidney International
Genovese, Giulio G; Tonna, Stephen J SJ; Knob, Andrea U AU; Appel, Gerald B GB; Katz, Avi A; Bernhardy, Andrea J AJ; Needham, Alexander W AW; Lazarus, Ross R; Pollak, Martin R MR
Publication Date: 2010-10

Variant appearance in text: rs11912763
PubMed Link: 20668430
Variant Present in the following documents:
  • Main text
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Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Human Genetics
Tzur, Shay S; Rosset, Saharon S; Shemer, Revital R; Yudkovsky, Guennady G; Selig, Sara S; Tarekegn, Ayele A; Bekele, Endashaw E; Bradman, Neil N; Wasser, Walter G WG; Behar, Doron M DM; Skorecki, Karl K
Publication Date: 2010-09

Variant appearance in text: rs11912763
PubMed Link: 20635188
Variant Present in the following documents:
  • Main text
  • 439_2010_Article_861.pdf
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The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans.

American Journal Of Nephrology
Freedman, Barry I BI; Edberg, Jeffrey C JC; Comeau, Mary E ME; Murea, Mariana M; Bowden, Donald W DW; Divers, Jasmin J; Alarcón, Graciela S GS; Brown, Elizabeth E EE; McGwin, Gerald G; Kopp, Jeffrey B JB; Winkler, Cheryl A CA; Nelson, George W GW; Illei, Gabor G; Petri, Michelle M; Ramsey-Goldman, Rosalind R; Reveille, John D JD; Vilá, Luis M LM; Langefeld, Carl D CD; Kimberly, Robert P RP; ,
Publication Date: 2010

Variant appearance in text: rs11912763
PubMed Link: 20523037
Variant Present in the following documents:
  • Main text
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African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.

Human Molecular Genetics
Behar, Doron M DM; Rosset, Saharon S; Tzur, Shay S; Selig, Sara S; Yudkovsky, Guennady G; Bercovici, Sivan S; Kopp, Jeffrey B JB; Winkler, Cheryl A CA; Nelson, George W GW; Wasser, Walter G WG; Skorecki, Karl K
Publication Date: 2010-05-01

Variant appearance in text: rs11912763
PubMed Link: 20144966
Variant Present in the following documents:
  • Main text
  • ddq040.pdf
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Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

Human Molecular Genetics
Nelson, George W GW; Freedman, Barry I BI; Bowden, Donald W DW; Langefeld, Carl D CD; An, Ping P; Hicks, Pamela J PJ; Bostrom, Meredith A MA; Johnson, Randall C RC; Kopp, Jeffrey B JB; Winkler, Cheryl A CA
Publication Date: 2010-05-01

Variant appearance in text: rs11912763
PubMed Link: 20124285
Variant Present in the following documents:
  • Main text
View BVdb publication page