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- Genome-wide Association Studies of ADHD
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- Data Summary
GO Report
Basic Info
| ID | GO:0007005 |
|---|---|
| Name | mitochondrion organization |
| Type | Biological Process |
| No. of Genes in ADHDgene | 5 |
| Source | Pathway by Database Search |
PBA Result (with statistical significance of FDR<0.05)
GO related genes in ADHDgene (count: 5)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 5)
| Approved Symbol | Approved Name | Source | Evidence[PMID] |
|---|---|---|---|
| OPA1 | optic atrophy 1 (autosomal dominant) | Mapped by CNV | NAS[11017080] |
| BCS1L | BCS1-like (S. cerevisiae) | Mapped by significant region | IMP[18628306] |
| TMEM11 | transmembrane protein 11 | Mapped by significant region | |
| SMCR7 | Smith-Magenis syndrome chromosome region, candidate 7 | Mapped by significant region | |
| SPG7 | spastic paraplegia 7 (pure and complicated autosomal recessive) | Mapped by significant region |