Entity Details
| Primary name |
LOXHD1 |
| Entity type |
gene |
| Source |
Source Link |
Details
| PrimaryID | 125336 |
| RefseqGene | NG_016646 |
| Symbol | LOXHD1 |
| Name | lipoxygenase homology PLAT domains 1 |
| Chromosome | 18 |
| Location | 18q21.1 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 2001-11-29 |
| ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 613079 | OMIM | Deafness, autosomal recessive, 77 (DFNB77) | A form of non-syndromic deafness characterized by preserved low-frequency hearing, and a trend toward mild to moderate mid-frequency and high-frequency hearing loss during childhood and adolescence. Hearing loss progresses to become moderate to severe at mid and high frequencies during adulthood. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
4 interactions