Calcium and Phosphate disorders
Gene: DMP1EnsemblGeneIds (GRCh38): ENSG00000152592
EnsemblGeneIds (GRCh37): ENSG00000152592
OMIM: 600980, Gene2Phenotype
DMP1 is in 8 panels
1 review
Ain Roesley (Victorian Clinical Genetics Services)
Established associationCreated: 9 May 2022, 2:06 a.m. | Last Modified: 9 May 2022, 2:06 a.m.
Panel Version: 0.13955
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hypophosphatemic rickets MIM#241520
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- KidGen_CalcPhos v38.1.0
- Phenotypes
-
- Hypophosphatemic rickets MIM#241520
- OMIM
- 600980
- Clinvar variants
- Variants in DMP1
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: dmp1 has been classified as Green List (High Evidence).
Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)Phenotypes for gene: DMP1 were changed from to Hypophosphatemic rickets MIM#241520
Set publications
Bryony Thompson (Royal Melbourne Hospital)Publications for gene: DMP1 were set to
Set mode of inheritance
Bryony Thompson (Royal Melbourne Hospital)Mode of inheritance for gene: DMP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: DMP1 was added gene: DMP1 was added to Abnormalities of renal calcium and phosphate metabolism_KidGen. Sources: KidGen_CalcPhos v38.1.0,Expert Review Green Mode of inheritance for gene: DMP1 was set to Unknown