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Details of TRIOBP gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| TRIOBP | KIAA1662,TARA | Q9H2D6 | TARA_HUMAN | 11078 | ENSG00000100106 | TRIO and F-actin-binding protein | SPROT |
Disease |
Disease |
OMIM id |
Deafness, autosomal recessive, 28 (DFNB28) [MIM:609823]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Note=The disease is caused by mutations affecting the gene represented in this entry. |
609823 |
Phenotypes
Abnormality of the ear, Abnormality of the inner ear, Abnormality of the middle ear, Age of onset, All, Autosomal recessive inheritance, Bilateral conductive hearing impairment, Conductive hearing impairment, Functional abnormality of the inner ear, Functional abnormality of the middle ear, Hearing abnormality, Hearing impairment, Infantile onset, Mode of inheritance, Onset, Onset and clinical course, Phenotypic abnormality, Sensorineural hearing impairment, Severe sensorineural hearing impairment.
Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
Triobp | osp | --- | --- |