| Entrez gene ID | | 5626 |
| Official gene symbol | | PROP1 |
| Full name | | PROP paired-like homeobox 1 |
| Aliases | | ,CPHD2, |
| Gene summary | | PROP1 has both DNA-binding and transcriptional activation ability. Its expression leads to ontogenesis of pituitary gonadotropes, as well as somatotropes, lactotropes, and caudomedial thyrotropes. Inactivating mutations in PROP1 result in deficiencies of luteinizing hormone (LH; MIM 152780), follicle-stimulating hormone (FSH; MIM 136530), growth hormone (GH; MIM 139250), prolactin (PRL; MIM 176760), and thyroid-stimulating hormone (TSH; MIM 188540). See combined pituitary hormone deficiency-2 (CPHD2; MIM 262600).[supplied by OMIM] |
| Location | | Chromosome: 5 Locus: 5q35.3 |
| Gene position | | 177423243 - 177419236 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 4008 bp |
| Gene sequence |
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| OMIM ID | | 601538 |
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