AudioGene
- Predicts the genetic cause of autosomal dominant non-syndromic hearing loss based on audiometric data
- Developed in collaboration with the Dept. of Biomedical Engineering
Deafness Variation Database
- Collates, annotates and classifies all genetic variants related to syndromic and non-syndromic hearing loss
- Developed in collaboration with the Dept. of Biomedical Engineering
Hereditary Hearing Loss Homepage
- Up-to-date overview of all known gene localizations and identifications for monogenic non-syndromic of hereditary hearing loss and common symptoms
MORL scRNA-Seq
- Contains cochlear single-cell RNA-sequencing datasets generated by the MORL
- Can be used to query gene expression and browse transcript structure from cochlear single-cell RNA-Seq datasets
Additional Resources:
- TMPRSS3 Hearing Loss Resource
- Navigate and make sense of the hearing loss related to the Transmembrane Serine Protease 3 / TMPRSS3 gene
- gEAR
- Visualization and analysis of multiomic data both in public and private domains allowing upload, visualization and analysis of scRNA-seq data
- The National Institute on Deafness and Other Communication Disorders
- Conducts and supports research in the normal and disordered processes of hearing, balance, taste, smell, voice, speech, and language
- World Health Organization
- UIHC Otolaryngology Clinic
- ENTs with UI Health Care diagnose and treat many conditions, including sinus infections, ear infections, tonsillitis, vertigo, and sore throat
- UIHC Hearing Loss Genetics Clinic
- The UIHC Hearing Loss Genetics Clinic provides comprehensive evaluation, genetic counseling, genetic testing, and management for genetic causes of hearing loss and deafness
- Usher Syndrome Coalition
- Raise awareness and accelerate research while providing information and support to individuals and families affected by Usher syndrome