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ARHGAP11B is a human-specific gene that amplifies basal progenitors, controls neural progenitor proliferation, and contributes to neocortex folding. It is capable of causing neocortex folding in mice. This likely reflects a role for ARHGAP11B in development and evolutionary expansion of the human neocortex, a conclusion consistent with the finding that…
Function, Human evolution & Structure
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neocortex human gene activity bp arhgap11a rhogap folding development chr chromosome 15 function likely expansion evolution band rho nucleotide evolutionary
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| ARHGAP11B | Aliases | ARHGAP11B, B'-T, FAM7B1, Rho GTPase activating protein 11B, GAP (1-8), ArhGAP11B and human encephalisation | 1.00 | infobox |
| ARHGAP11B | Band | 15q13.2 | 1.00 | infobox |
| ARHGAP11B | Bgee | testicle | 1.00 | infobox |
| ARHGAP11B | Bgee | bone marrow | 1.00 | infobox |
| ARHGAP11B | Bgee | bone marrow cell | 1.00 | infobox |
| ARHGAP11B | Bgee | ganglionic eminence | 1.00 | infobox |
| ARHGAP11B | Bgee | stromal cell of endometrium | 1.00 | infobox |
| ARHGAP11B | Bgee | ventricular zone | 1.00 | infobox |
| ARHGAP11B | Bgee | gonad | 1.00 | infobox |
| ARHGAP11B | Bgee | lymph node | 1.00 | infobox |
| ARHGAP11B | Bgee | monocyte | 1.00 | infobox |
| ARHGAP11B | Bgee | appendix | 1.00 | infobox |
| ARHGAP11B | BioGPS | n/a | 1.00 | infobox |
| ARHGAP11B | Chr. | Chromosome 15 (human) | 1.00 | infobox |
| ARHGAP11B | Databases | NCBI: entry; OMA: entry | 1.00 | infobox |
| ARHGAP11B | End | 30,649,529 bp | 1.00 | infobox |
| ARHGAP11B | Ensembl | ENSG00000274734 ENSG00000286139 ENSG00000285077 | 1.00 | infobox |
| ARHGAP11B | Entrez | 89839 | 1.00 | infobox |
| ARHGAP11B | External IDs | OMIM: 616310; GeneCards: ARHGAP11B | 1.00 | infobox |
| ARHGAP11B | Gene location (Human) | Gene location (Human)Chr.Chromosome 15 (human)Band15q13.2Start30,624,494 bpEnd30,649,529 bp | 1.00 | infobox |
| ARHGAP11B | Gene ontology | GTPase activator activity | 1.00 | infobox |
| ARHGAP11B | Gene ontology | cytosol | 1.00 | infobox |
| ARHGAP11B | Gene ontology | regulation of small GTPase mediated signal transduction | 1.00 | infobox |
| ARHGAP11B | Gene ontology | signal transduction | 1.00 | infobox |
| ARHGAP11B | Gene ontology | cerebral cortex development | 1.00 | infobox |
| ARHGAP11B | Gene ontology | positive regulation of GTPase activity | 1.00 | infobox |
| ARHGAP11B | Location (UCSC) | Chr 15: 30.62 – 30.65 Mb | 1.00 | infobox |
| ARHGAP11B | Orthologs | OrthologsDatabasesNCBI: entry; OMA: entrySpeciesHumanMouseEntrez89839n/aEnsemblENSG00000274734 ENSG00000286139 ENSG00000285077n/aUniProtQ3KRB8n/aRefSeq (mRNA)NM_001039841n/aRefS… | 1.00 | infobox |
| ARHGAP11B | RefSeq (mRNA) | NM_001039841 | 1.00 | infobox |
| ARHGAP11B | RefSeq (protein) | NP_001034930 | 1.00 | infobox |
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