| human | 遺伝子名 | DAB1 |
| 同義語(エイリアス) | disabled (Drosophila) homolog 1; Disabled homolog 1; disabled homolog 1 (Drosophila) | |
| SWISS-PROTのID | SWISS-PROT:O75553 | |
| EntrezGeneのID | EntrezGene:1600 | |
| その他のDBのID | HGNC:2661 |
| human | 遺伝子名 | DAB1 |
| 同義語(エイリアス) | ZMPOMA1; OMA1; FLJ33782; 2010001O09Rik; YKR087C; MPRP-1 | |
| SWISS-PROTのID | --- | |
| EntrezGeneのID | EntrezGene:115209 | |
| その他のDBのID | HGNC:29661 |
| mouse | 遺伝子名 | Dab1 |
| 同義語(エイリアス) | scm; scr; disabled homolog 1 (Drosophila); Disabled homolog 1; yot; AI956902; scrambler; C630028C02Rik | |
| SWISS-PROTのID | SWISS-PROT:P97318 | |
| EntrezGeneのID | EntrezGene:13131 | |
| その他のDBのID | MGI:108554 |
| rat | 遺伝子名 | Dab1 |
| 同義語(エイリアス) | Disabled homolog 1; disabled homolog 1 (Drosophila) | |
| SWISS-PROTのID | SWISS-PROT:Q8CJH2 | |
| EntrezGeneのID | EntrezGene:266729 | |
| その他のDBのID | RGD:628770 |
| worm | 遺伝子名 | dab-1 |
| 同義語(エイリアス) | M110.5a.2; M110.5a.1; WP:CE37844; M110.5; M110.5a; CE37844; WP:CE36446; WP:CE36393; CE36393; M110.5b; CE36446; DAB (Drosophila disabled) homolog; M110.5c | |
| SWISS-PROTのID | --- | |
| EntrezGeneのID | EntrezGene:174323 | |
| その他のDBのID | WormBase:WBGene00000894 |
| zfish | 遺伝子名 | dab1 |
| 同義語(エイリアス) | disabled homolog 1 (Drosophila) | |
| SWISS-PROTのID | --- | |
| EntrezGeneのID | EntrezGene:692351 | |
| その他のDBのID | ZFIN:ZDB-GENE-060528-1 |
| zfish | 遺伝子名 | DAB1 |
| 同義語(エイリアス) | dab201; dab402; DAB; dab3*01; dab2*01; dab4*02; dab101; dab4*01; dab401; Brre-DAB1*04; major histocompatibility complex class II DAB gene; MHC Brre-DAB4; dab301; dab1*01; mhc2dab | |
| SWISS-PROTのID | --- | |
| EntrezGeneのID | EntrezGene:30762 | |
| その他のDBのID | ZFIN:ZDB-GENE-980526-200 |
本文中に表示されているデータベースの説明
出典:Wikipedia
出典:『Wikipedia』 (2011/05/02 20:07 UTC 版)
The Disabled-1 (Dab1) gene encodes a key regulator of Reelin signaling. Reelin is a large glycoprotein secreted by neurons of the developing brain, particularly Cajal-Retzius cells. DAB1 functions downstream of Reln in a signaling pathway that controls cell positioning in the developing brain and during adult neurogenesis. It docks to the intracellular part of the Reelin very low density lipoprotein receptor (VLDLR) and apoE receptor type 2 (ApoER2) and becomes tyrosine-phosphorylated following binding of Reelin to cortical neurons. In mice, mutations of Dab1 and Reelin generate identical phenotypes. In humans, Reelin mutations are associated with brain malformations and mental retardation. In mice, Dab1 mutation results in the scrambler mouse phenotype.