Human | GTF2H5 | 404672 | general transcription factor IIH, polypeptide 5 | |
Human | UBR1 | 197131 | ubiquitin protein ligase E3 component n-recognin 1 | |
Human | VPS13B | 157680 | vacuolar protein sorting 13 homolog B (yeast) | |
Human | MCPH1 | 79648 | microcephalin 1 | |
Human | TLR9 | 54106 | toll-like receptor 9 | TLR4 and TLR9 polymorphisms increased the risk of low birth weight in infants; polymorphisms of TLR4 increased the risk of maternal anemia |
Human | SBDS | 51119 | Shwachman-Bodian-Diamond syndrome | |
Human | LGALS13 | 29124 | lectin, galactoside-binding, soluble, 13 | Decreased levels of PP13 (placental protein 13) were not significantly correlated with the studied adverse pregnancy outcomes of intrauterine growth restriction, preterm delivery, low birth weight, and intrauterine fetal demise |
Human | CUL7 | 9820 | cullin 7 | |
Human | FZD4 | 8322 | frizzled family receptor 4 | Absence of premature birth, low birthweight, and exposure to oxygen |
Human | WHSC1 | 7468 | Wolf-Hirschhorn syndrome candidate 1 | |
Human | PHLDA2 | 7262 | pleckstrin homology-like domain, family A, member 2 | association with low birth weight |
Human | TSHR | 7253 | thyroid stimulating hormone receptor | |
Human | TNF | 7124 | tumor necrosis factor | placental TNF alpha associated with placental malaria and low birth weight in Malawian women |
Human | THRB | 7068 | thyroid hormone receptor, beta | Low birth weight for dates |
Human | ABCC8 | 6833 | ATP-binding cassette, sub-family C (CFTR/MRP), member 8 | |
Human | SLC12A1 | 6557 | solute carrier family 12 (sodium/potassium/chloride transporter), member 1 | |
Human | PPARG | 5468 | peroxisome proliferator-activated receptor gamma | There were no associations between low birth weight and blood lipids in any of the PPARgamma2 genotypes Hypertensive subjects with low birth weight or short length at birth and the Pro12Pro variant had raised systolic blood pressure |
Human | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma | Altered insulin activation of the PI3K/Akt but not the MAPK pathway precedes and may contribute to development of whole-body insulin resistance and type 2 diabetes in men with low birth weight |
Human | PDHA1 | 5160 | pyruvate dehydrogenase (lipoamide) alpha 1 | |
Human | SERPINE1 | 5054 | serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 | Together with low birth weight, increased plasma PAI-1-act levels in early pubertal precocious pubarche may indicate a greater risk of developing hyperinsulinemic-hyperandrogenism features of polycystic ovary syndrome The common promoter -675 4G/5G indel of the PAI-1 gene is not associated with PP but, in Catalan young women, the 5G allele enhances the risk for insulin resistance imposed by the sequence of a low birth weight (LBW) and a high BMI |
Human | NPHS1 | 4868 | nephrosis 1, congenital, Finnish type (nephrin) | |
Human | MYH3 | 4621 | myosin, heavy chain 3, skeletal muscle, embryonic | |
Human | MEST | 4232 | mesoderm specific transcript | Hypermethylation of paternally expressed genes including PEG1/MEST, which have growth-promoting effects, may be relevant to low birth weight in subjects conceived by assisted reproduction techniques |
Human | KCNJ11 | 3767 | potassium inwardly-rectifying channel, subfamily J, member 11 | |
Human | KCNJ1 | 3758 | potassium inwardly-rectifying channel, subfamily J, member 1 | |