Autosomal Dominant Hypocalcemia(AD hypocalcemia) Explore Disorder's Alias
An Autosomal dominant mode(s) within the Metabolic disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Metabolic 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 | CASR/846 | calcium sensing receptor | 3q21.1 | Chr3, NC_000003.12 (122183668..122291629) |
107962 nt | 11 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | GNA11/2767 | G protein subunit alpha 11 | 19p13.3 | Chr19, NC_000019.10 (3094362..3123999) |
29638 nt | 7 | 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