DSPP

dentin sialophosphoprotein
OMIM: 125485, ClinGen, DECIPHER

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green DSPP in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 39, with dentinogenesis - MIM#605594 Dentin dysplasia, type II - MIM#125420 Dentinogenesis imperfecta, Shields type II - MIM#125490 Dentinogenesis imperfecta, Shields type III - MIM#125500
Amber DSPP in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.210	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 39, with dentinogenesis, MIM# 605594
Green DSPP in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Radboud University Medical Center, Nijmegen Phenotypes Dentin dysplasia, type II, 125420 -3 Dentinogenesis imperfecta, Shields type III, 125500 Dentinogenesis imperfecta, Shields type II, 125490 Deafness, autosomal dominant 36, with dentinogenesis, 605594
Green DSPP in Amelogenesis imperfecta Level 2: Skeletal disorders Version 1.11	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Dentinogenesis imperfecta, Shields type II, OMIM #125490