From: Parental ages and levels of DNA methylation in the newborn are correlated
Gene | Phenotype/Function | OMIM Reference |
---|---|---|
KCNQ1 | Long QT Syndrome 1; Jervell and Lange-Nielsen Syndrome 1; Atrial fibrillation, familial 3; short QT Syndrome | 192500 220400 607554 609621 |
TUBB2A | Polymicrogyria, asymmetric | 610031 |
RAD51 | Breast cancer, familial | 114480 |
C19orf6 | Ovarian, breast, pancreatic and colorectal cancer expression | 611011 |
RAD54L | Adenocarcinoma, colonic, somatic; Lymphoma, non-Hodgkin; Breast cancer, invasive ductal | 603615 |
ACADS | SCAD deficiency | 201470 |
GM2A | Gangliosidase, AB variant | 272750 |
STAT5B | Growth hormone insensitivity with immunodeficiency | 245590 |
RET | Multiple endocrine neoplasia, type IIA; Hirschprung disease; Central hypoventilation syndrome; renal agenesis | 142623 209880 191830 |
ZFYVE26 | Spastic paraplegia 15, autosomal recessive | 270700 |
RBBP9 | Transformation to cancer | 602908 |
MRPS22 | Combined oxidative phosphorylation deficiency 5 | 611719 |
MYC | Burkitt lymphoma | 113970 |
RFXDC1 | Diabetes, neonatal, with pancreatic hypoplasia, intestinal atresia and gallbladder aplasia or hypoplasia | 601346 |
MYST1 | Histone acetyltransferase | 609912 |
RASSF1 | Tumor suppressor | 605082 |
ZBT16 | Skeletal defects, genital hypoplasia, and mental retardation | 612447 |
ACTN4 | Focal glomerulosclerosis 1 | 603278 |
NR0B2 | Obesity, mild, early-onset | 604630 |
ALX4 | Parietal foramina 2 | 609597 |