AKAP6 c.3589-8138C>T

Variant ID: 14-33282470-C-T

NM_004274.4(AKAP6):c.3589-8138C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment.

Molecular Genetics & Genomic Medicine
Paolacci, Stefano S; Kiani, Aysha Karim AK; Manara, Elena E; Beccari, Tommaso T; Ceccarini, Maria Rachele MR; Stuppia, Liborio L; Chiurazzi, Pietro P; Dalla Ragione, Laura L; Bertelli, Matteo M
Publication Date: 2020-07

Variant appearance in text: rs2383378
PubMed Link: 32368866
Variant Present in the following documents:
  • Main text
  • MGG3-8-e1244.pdf
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Impact of AKAP6 polymorphisms on Glioma susceptibility and prognosis.

Bmc Neurology
Zhang, Ming M; Zhao, Yonglin Y; Zhao, Junjie J; Huang, Tingqin T; Wu, Yuan Y
Publication Date: 2019-11-23

Variant appearance in text: rs2383378
PubMed Link: 31759389
Variant Present in the following documents:
  • Main text
  • 12883_2019_Article_1504.pdf
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Human muscle-specific A-kinase anchoring protein polymorphisms modulate the susceptibility to cardiovascular diseases by altering cAMP/PKA signaling.

American Journal Of Physiology. Heart And Circulatory Physiology
Suryavanshi, Santosh V SV; Jadhav, Shweta M SM; Anderson, Kody L KL; Katsonis, Panagiotis P; Lichtarge, Olivier O; McConnell, Bradley K BK
Publication Date: 2018-07-01

Variant appearance in text: rs2383378
PubMed Link: 29600899
Variant Present in the following documents:
  • Main text
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Polymorphisms/Mutations in A-Kinase Anchoring Proteins (AKAPs): Role in the Cardiovascular System.

Journal Of Cardiovascular Development And Disease
Suryavanshi, Santosh V SV; Jadhav, Shweta M SM; McConnell, Bradley K BK
Publication Date: 2018-01-25

Variant appearance in text: rs2383378
PubMed Link: 29370121
Variant Present in the following documents:
  • Main text
  • jcdd-05-00007.pdf
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Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

Molecular Psychiatry
Davies, G G; Armstrong, N N; Bis, J C JC; Bressler, J J; Chouraki, V V; Giddaluru, S S; Hofer, E E; Ibrahim-Verbaas, C A CA; Kirin, M M; Lahti, J J; van der Lee, S J SJ; Le Hellard, S S; Liu, T T; Marioni, R E RE; Oldmeadow, C C; Postmus, I I; Smith, A V AV; Smith, J A JA; Thalamuthu, A A; Thomson, R R; Vitart, V V; Wang, J J; Yu, L L; Zgaga, L L; Zhao, W W; Boxall, R R; Harris, S E SE; Hill, W D WD; Liewald, D C DC; Luciano, M M; Adams, H H; Ames, D D; Amin, N N; Amouyel, P P; Assareh, A A AA; Au, R R; Becker, J T JT; Beiser, A A; Berr, C C; Bertram, L L; Boerwinkle, E E; Buckley, B M BM; Campbell, H H; Corley, J J; De Jager, P L PL; Dufouil, C C; Eriksson, J G JG; Espeseth, T T; Faul, J D JD; Ford, I I; , ; Gottesman, R F RF; Griswold, M E ME; Gudnason, V V; Harris, T B TB; Heiss, G G; Hofman, A A; Holliday, E G EG; Huffman, J J; Kardia, S L R SL; Kochan, N N; Knopman, D S DS; Kwok, J B JB; Lambert, J-C JC; Lee, T T; Li, G G; Li, S-C SC; Loitfelder, M M; Lopez, O L OL; Lundervold, A J AJ; Lundqvist, A A; Mather, K A KA; Mirza, S S SS; Nyberg, L L; Oostra, B A BA; Palotie, A A; Papenberg, G G; Pattie, A A; Petrovic, K K; Polasek, O O; Psaty, B M BM; Redmond, P P; Reppermund, S S; Rotter, J I JI; Schmidt, H H; Schuur, M M; Schofield, P W PW; Scott, R J RJ; Steen, V M VM; Stott, D J DJ; van Swieten, J C JC; Taylor, K D KD; Trollor, J J; Trompet, S S; Uitterlinden, A G AG; Weinstein, G G; Widen, E E; Windham, B G BG; Jukema, J W JW; Wright, A F AF; Wright, M J MJ; Yang, Q Q; Amieva, H H; Attia, J R JR; Bennett, D A DA; Brodaty, H H; de Craen, A J M AJ; Hayward, C C; Ikram, M A MA; Lindenberger, U U; Nilsson, L-G LG; Porteous, D J DJ; Räikkönen, K K; Reinvang, I I; Rudan, I I; Sachdev, P S PS; Schmidt, R R; Schofield, P R PR; Srikanth, V V; Starr, J M JM; Turner, S T ST; Weir, D R DR; Wilson, J F JF; van Duijn, C C; Launer, L L; Fitzpatrick, A L AL; Seshadri, S S; Mosley, T H TH; Deary, I J IJ
Publication Date: 2015-02

Variant appearance in text: rs2383378
PubMed Link: 25644384
Variant Present in the following documents:
  • Main text
  • mp2014188a.pdf
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Characterization of genetic variation in the VGLL4 gene in anorexia nervosa.

Psychiatric Genetics
Clarke, Toni-Kim TK; Crist, Richard C RC; Doyle, Glenn A GA; Weiss, Amy R D AR; Brandt, Harry H; Crawford, Steve S; Crow, Scott S; Fichter, Manfred M MM; Halmi, Katherine A KA; Johnson, Craig C; Kaplan, Allan S AS; La Via, Maria M; Mitchell, James E JE; Strober, Michael M; Rotondo, Alessandro A; Treasure, Janet J; Woodside, D Blake DB; Keel, Pamela P; Klump, Kelly L KL; Lilenfeld, Lisa L; Plotnicov, Katherine K; Magistretti, Pierre J PJ; Bergen, Andrew W AW; Kaye, Walter H WH; Schork, Nicholas J NJ; Berrettini, Wade H WH
Publication Date: 2014-08

Variant appearance in text: rs2383378
PubMed Link: 24983835
Variant Present in the following documents:
  • Main text
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Genetic variants associated with disordered eating.

The International Journal Of Eating Disorders
Wade, Tracey D TD; Gordon, Scott S; Medland, Sarah S; Bulik, Cynthia M CM; Heath, Andrew C AC; Montgomery, Grant W GW; Martin, Nicholas G NG
Publication Date: 2013-09

Variant appearance in text: rs2383378
PubMed Link: 23568457
Variant Present in the following documents:
  • Main text
View BVdb publication page