Table 3.
Category | Disease/Function Annotation |
p | pcor** | Genes |
---|---|---|---|---|
Neurological Disease |
Dysmetria | 4.5×10−5 | 0.025 | PRNP, SPRN |
Ataxia | 7.4×10−5 | 0.025 |
ATXN10,BID,KCNJ10 MOS, SLC4A7 |
|
Neurodegeneration of nervous tissue. |
3.78×10−3 | 0.046 | KCNJ10, MOS, SLC4A7 | |
Tissue Morphology |
Degeneration of organ of Corti |
7.22×10−5 | 0.025 | CLRN1,KCNJ10,SLC4A7 |
Quality of Chondrocytes |
8.33×10−5 | 0.025 | FGF18, FGF23, FOSL2 | |
Neurodegeneration of nervous tissue |
3.78×10−3 | 0.046 | KCNJ10, MOS, SLC4A7 | |
Connective Tissue Development and Function |
Quality of Chondrocytes |
8.33×10−5 | 0.025 | FGF18, FGF23, FOSL2 |
Proliferation of Chondrocytes |
2.59×10−3 | 0.046 | FGF18, FGF23, FOSL2 | |
Abnormal morphology of atlas. |
3.01×10−3 | 0.046 | HOXD3, SKI | |
Auditory Disease |
Collapse of Reissner’s Membrane |
1.49×10−3 | 0.036 | KCNJ10, SLC4A7 |
Degeneration of supporting cell layer of inner ear |
5.23×10−4 | 0.046 | CLRN1, SLC4A7 | |
Usher syndrome 3A | 3.91×10−3 | 0.046 | CLRN1 |
The complete list of target genes is presented in Supplementary Table 3.
pcor is the Benjamini Hochberg FDR corrected p-value.