Table 5. SMACv1.0 simple de novo outlier contigs from a genome-wide analysis of divergence with the zebra finch.
Predicted Outlier Contig Genes and Proteins1 | Known Function or GWAS Trait Classification | References |
EYA2, EPHB3, BCL6, NRP2, ALCAM | Neuronal Development | [118]–[120] |
SATB2 | Neuron Specification | [121] |
ALCAM, BCL6, NRP2, ALDH6A1, TP63, CUX1, ATXN1, | Neurological Disorders | [120], [122]–[132] |
VIPR2, WHSC1, BRSK2, CLINT1, DUSP8, ANKFN1, PI4KA | ||
ANKFN1, LPP, BOC | Human Developmental Anomalies | [133]–[135] |
ALDH6A1 | Hippocampal and Cognitive Aging | [122] |
UPF0632 Protein A | White Matter Integrity in Old Age | [136] |
VPS52 | Brian Striatal Volume, Cognition | [136]–[138] |
LDB2, DMXL2 | Susceptibility to Coronary Artery Disease | [139]–[140] |
SLC38A1 | Cardiovascular-Left Ventricular Mass | [141] |
ABCB8, RBM20, | Cardiomyopathy | [142]–[143] |
FOXC1 | Embryonic Cardiovascular Development | [144] |
VTI1A | Heart Ventricular Conduction | [96] |
TTN | Heart Q-wave T-wave Interval Length | [97] |
ZPLD1 | Cerebrovascular Developmental Disorders | [145] |
FOXF2 | Developmental Disorders of the Genitalia | [146] |
SATB2 | Osteogenic Differentiation, Regeneration | [147] |
MAP3K4 | Myogenesis | [148] |
DCT | Pigment Biosynthesis | [149] |
VSX2 | Eye Development-Microphthalmia | [150] |
EYA2 | Ocular Neural Pattern Development | [65] |
SCFD2 | Optic Disc Size-Cup Area | [151] |
SDF2L1 | Innate Immunity | [152] |
MKX | Tendon Differentiation and Development | [153] |
NGEF | Adiposity | [154] |
NPY2R | Feeding Behavior, Oral Feeding Success | [155] |
TCF7L2, Intergenic GPATCH2 and ESRRG, FOSL2, PPP1CB | Diabetes | [156]–[159] |
For outlier direction, see Table S14.