PBX1 c.266-37896G>T

Variant ID: 1-164723835-G-T

NM_002585.3(PBX1):c.266-37896G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate.

Birth Defects Research
Maili, Lorena L; Letra, Ariadne A; Silva, Renato R; Buchanan, Edward P EP; Mulliken, John B JB; Greives, Matthew R MR; Teichgraeber, John F JF; Blackwell, Steven J SJ; Ummer, Rohit R; Weber, Ryan R; Chiquet, Brett B; Blanton, Susan H SH; Hecht, Jacqueline T JT
Publication Date: 2020-02-01

Variant appearance in text: rs7543038
PubMed Link: 31825181
Variant Present in the following documents:
  • Main text
View BVdb publication page



Brief report: enrichment of associations in genes with fibrosis, apoptosis, and innate immunity functions with cardiac manifestations of neonatal lupus.

Arthritis And Rheumatism
Ramos, Paula S PS; Marion, Miranda C MC; Langefeld, Carl D CD; , ; Buyon, Jill P JP; Clancy, Robert M RM
Publication Date: 2012-12

Variant appearance in text: rs7543038
PubMed Link: 22886516
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluating the association of common PBX1 variants with type 2 diabetes.

Bmc Medical Genetics
Duesing, Konsta K; Charpentier, Guillaume G; Marre, Michel M; Tichet, Jean J; Hercberg, Serge S; Balkau, Beverley B; Froguel, Philippe P; Gibson, Fernando F
Publication Date: 2008-02-29

Variant appearance in text: rs7543038
PubMed Link: 18312624
Variant Present in the following documents:
View BVdb publication page