| Entrez Gene ID | 79191 |
|---|---|
| Official Gene Symbol | IRX3 (GeneCards) |
| Full name | iroquois homeobox 3 |
| Location | 16q12.2 |
| Other ids | Vega : OTTHUMG00000133200 MIM : 612985 HGNC : HGNC:14360 Ensembl : ENSG00000177508 |
| Other names | IRX-1, IRXB1 |
| Summary | IRX3 is a member of the Iroquois homeobox gene family (see IRX1; MIM 606197) and plays a role in an early step of neural development (Bellefroid et al., 1998 [PubMed 9427753]). Members of this family appear to play multiple roles during pattern formation of vertebrate embryos (Lewis et al., 1999 [PubMed 10370142]).[supplied by OMIM, Aug 2009] |
Found 6 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 19362 | 79191 | IRX3 | 16 | 54873537 | 54873537 | Asymptomatic | HiSeq X Ten |
| 19413 | 79191 | IRX3 | 16 | 54742552 | 54742552 | Asymptomatic | HiSeq X Ten |
| 19414 | 79191 | IRX3 | 16 | 54794032 | 54794032 | Asymptomatic | HiSeq X Ten |
| 19528 | 79191 | IRX3 | 16 | 54762029 | 54762029 | Asymptomatic | HiSeq X Ten |
| 19720 | 79191 | IRX3 | 16 | 54544674 | 54544674 | Cockayne syndrome | HiSeq X Ten |
| 23881 | 79191 | IRX3 | 16 | 54803677 | 54803677 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |