Usher Syndrome
| Gene Symbol | Aliases | Full Gene Name | Chr | Disorder | Mode of Inheritance | OMIM | HGNC ID |
| CDH23 | DFNB12; KIAA1774; KIAA1812; otocadherin; USH1D; cadherin-23; | cadherin-like 23 | 10q22.1 | Usher Syndrome Type 1D —————– DFNB12 Nonsyndromic Hearing Loss and Deafness |
autosomal recessive | *605516 | 13733 |
| MYO7A | NSRD2 | myosin VIIA | 11q13.5 | Usher Syndrome Type 1B —————– DFNA11 Nonsyndromic Hearing Loss and Deafness —————– DFNB2 Nonsyndromic Hearing Loss and Deafness |
autosomal recessive - —————– autosomal dominant - - —————– autosomal recessive |
*276903 | 7606 |
| PCDH15 | DFNB23; USH1F | protocadherin 15 | 10q21.1 | Usher Syndrome Type 1F —————– DFNB23 Nonsyndromic Hearing Loss and Deafness |
autosomal recessive | *605514 | 14674 |
| USH1C | PDZ73; harmonin; NY-CO-37; NY-CO-38; PDZ-73; AIE-75 | Usher syndrome 1C (autosomal recessive, severe) | 11p14.3 | Usher Syndrome Type 1C —————– DFNB18 Nonsyndromic Hearing Loss and Deafness |
autosomal recessive | *605242 | 12597 |
| USH1G | USH1G; FLJ33924; ANKS4A | scaffold protein containing ankyrin repeats and a SAM (sterile alpha motif) domain, Usher syndrome 1G | 17q25.2 | Usher Syndrome Type 1G | autosomal recessive | *607696 | 16356 |
| USH2A | RP39 | Usher syndrome 2A | 1q41 | Usher Syndrome Type 2A —————– Retinitis Pigmentosa |
autosomal recessive | +608400 | 12601 |
| DFNB31 | CIP98; WHRN; USH2D | deafness, autosomal recessive 31 | 9q32-q34 | Usher Syndrome Type 2D —————– DFNB31 Nonsyndromic Hearing Loss and Deafness |
autosomal recessive | *607928 | 16361 |
| GPR98 | DKFZp761P0710; KIAA0686; FEB4; VLGR1b | G protein-coupled receptor 98 | 5q13 | Usher Syndrome Type 2C | autosomal recessive | *602851 | 17416 |
| CLRN1 | USH3; CLARIN1 | clarin 1 | 3q21-q25 | Usher Syndrome Type 3A | autosomal recessive | *606397 | 12605 |
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