KMT2D c.1329_1332del ;(p.P444Rfs*485)

Variant ID: 12-49446134-CAGGT-C

NM_003482.3(KMT2D):c.1329_1332del;(p.P444Rfs*485)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: KMT2D: 1329_1332del; Pro444fs
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
  • 41588_2023_1327_MOESM5_ESM.xlsx, sheet 4
View BVdb publication page



Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities.

European Journal Of Human Genetics : Ejhg
Sobreira, Nara N; Brucato, Martha M; Zhang, Li L; Ladd-Acosta, Christine C; Ongaco, Chrissie C; Romm, Jane J; Doheny, Kimberly F KF; Mingroni-Netto, Regina C RC; Bertola, Debora D; Kim, Chong A CA; Perez, Ana Ba AB; Melaragno, Maria I MI; Valle, David D; Meloni, Vera A VA; Bjornsson, Hans T HT
Publication Date: 2017-12

Variant appearance in text: KMT2D: 1329_1332del
PubMed Link: 29255178
Variant Present in the following documents:
  • Main text
View BVdb publication page