Gene Symbol Report 
USH1C
| Approved Symbol |
USH1C |
|---|---|
| Approved Name |
Usher syndrome 1C (autosomal recessive, severe) |
| HGNC ID |
HGNC:12597 |
| Previous Symbols & Names |
"deafness, autosomal recessive 18", DFNB18 |
| Synonyms |
AIE-75, harmonin, NY-CO-37, NY-CO-38, PDZ-73, PDZ73 |
| Locus Type |
gene with protein product |
| Chromosomal Location |
11p14.3 |
| HOMOLOGS |
MGI:1919338 C Mouse Symbol: Ush1c RGD:1303329 D Rat Symbol: Ush1c HCOP D TreeFam D |
|
|---|---|---|
| NUCLEOTIDE SEQUENCES |
GenBank:AB006955 EMBL-Bank DDBJ C RefSeq:NM_005709 C CCDS:CCDS7825.1 C Vega:OTTHUMG00000166323 C |
|
| GENE RESOURCES |
Entrez Gene:10083 C Ensembl:ENSG00000006611 C UCSC:uc001mne.3 D Vega:OTTHUMG00000166323 C |
NCBI Sequence Viewer Ensembl Genome Browser UCSC Genome Browser Vega Genome Browser |
| PROTEIN RESOURCES |
UniProtKB:Q9Y6N9 D InterPro D |
|
| CLINICAL RESOURCES |
OMIM D GeneTests D Orphanet D DECIPHER D COSMIC D LSDB:Mutations of the Harmonin Gene C LSDB:CCHMC-BMI & UC Hearing Loss Mutation Database C Genetic Testing Registry C |
|
| REFERENCES |
PubMed Europe PMC C |
|
| OTHER DATABASE LINKS |
GENATLAS D GeneCards D GOPubmed D H-InvDB D QuickGO D Reactome D WikiGenes D |
|
