Dentinogenesis Imperfecta Type 2 Explore Disorder's Alias
An Autosomal dominant mode(s) within the Oral disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Oral 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 | DSPP/1834 | dentin sialophosphoprotein | 4q22.1 | Chr4, NC_000004.12 (87608529..87616873) |
8345 nt | 5 | 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 |