| Entrez gene ID | | 338917 |
| Official gene symbol | | VSX2 |
| Full name | | visual system homeobox 2 |
| Aliases | | ,CHX10,HOX10,MCOP2,MCOPCB3,RET1, |
| Gene summary | | This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq] |
| Location | | Chromosome: 14 Locus: 14q24.3 |
| Gene position | | 74706175 - 74729441 Map Viewer |
| Gene orientation | | plus |
| Gene size | | 23267 bp |
| Gene sequence |
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| OMIM ID | | 142993 |
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