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- Data Summary
GO Report
Basic Info
| ID | GO:0016363 |
|---|---|
| Name | nuclear matrix |
| Type | Cellular Component |
| No. of Genes in ADHDgene | 16 |
| Source | Pathway by Database Search |
PBA Result (with statistical significance of FDR<0.05)
GO related genes in ADHDgene (count: 16)
Literature-origin genes (count: 2)
| Approved Symbol | Approved Name | Location | No. of Studies (significant/non-significant/trend)  |
Evidence[PMID] |
|---|---|---|---|---|
| GFI1B | growth factor independent 1B transcription repressor | 9q34.13 | 1(0/1/0) | IDA[12874834] |
| ATXN1 | ataxin 1 | 6p23 | 1(0/0/1) | IDA[9353120] |
Genes from other sources (count: 14)
| Approved Symbol | Approved Name | Source | Evidence[PMID] |
|---|---|---|---|
| CENPW | centromere protein W | Mapped by significant region | |
| TGFB1I1 | transforming growth factor beta 1 induced transcript 1 | Mapped by PBA pathway | |
| TINF2 | TERF1 (TRF1)-interacting nuclear factor 2 | Mapped by significant region | |
| CFL1 | cofilin 1 (non-muscle) | Mapped by significant region | |
| SMC3 | structural maintenance of chromosomes 3 | Mapped by PBA pathway | IDA[11590136] |
| SCAF8 | SR-related CTD-associated factor 8 | Mapped by LD-proxy; Mapped by literature SNP | |
| NUMA1 | nuclear mitotic apparatus protein 1 | Mapped by significant region | |
| ERCC8 | excision repair cross-complementing rodent repair deficiency, complementation group 8 | Mapped by CNV | IDA[11782547] |
| PSPC1 | paraspeckle component 1 | Mapped by significant region | |
| MEN1 | multiple endocrine neoplasia I | Mapped by significant region | IDA[12874027] |
| MYB | v-myb myeloblastosis viral oncogene homolog (avian) | Mapped by significant region | NAS[3014652] |
| CHMP1A | chromatin modifying protein 1A | Mapped by significant region | IDA[11559747] |
| PHF5A | PHD finger protein 5A | Mapped by PBA pathway | |
| SNW1 | SNW domain containing 1 | Mapped by PBA pathway | IDA[12840015] |