Oculopharyngeal Muscular Dystrophy(OPMD) Explore Disorder's Alias
An Autosomal dominant, Autosomal recessive mode(s) within the Neuromuscular disorders category
Candidate Gene Information
An Autosomal dominant, Autosomal recessive mode(s) within the Neuromuscular disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | PABPN1/8106 | poly(A) binding protein nuclear 1 | 14q11.2 | Chr14, NC_000014.9 (23321457..23326163) |
4707 nt | 6 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | ANXA11/311 | annexin A11 | 10q22.3 | Chr10, NC_000010.11 (80150889..80205808, complement) |
54920 nt | 21 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | HNRNPA2B1/3181 | heterogeneous nuclear ribonucleoprotein A2/B1 | 7p15.2 | Chr7, NC_000007.14 (26189927..26200746, complement) |
10820 nt | 12 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |