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Medical condition
Mutations in the EDA, EDAR, and EDARADD genes cause hypohidrotic ectodermal dysplasia. The EDA, EDAR, and EDARADD genes provide instructions for making
Hypohidrotic ectodermal dysplasia
Hypohidrotic_ectodermal_dysplasia
Protein-coding gene in humans
receptor-associated adapter protein is a protein that in humans is encoded by the EDARADD gene. This gene was identified by its association with ectodermal dysplasia
EDARADD
Group of genetic conditions affecting the embryonic ectoderm
teeth, and glands during embryonic growth. Genes such as EDA, EDAR, and EDARADD are key players in this process, and variants in these genes disrupt normal
Ectodermal_dysplasia
Medical condition
a female carrier manifesting in males. Mutations in the EDA, EDAR, and EDARADD genes are known to cause HED, encoding for proteins critical during the
ANOTHER_syndrome
Absence of all primary or permanent teeth at birth
different genes found to be associated with anodontia including EDA, EDAR, and EDARADD genes. Other genes such as MSX1, PAX9, IRF6, GREM2, AXIN2, LRP6, SMOC2
Anodontia
anhidrotic, autosomal dominant; 129490; EDARADD Ectodermal dysplasia, anhidrotic, autosomal recessive; 224900; EDARADD Ectodermal dysplasia, anhidrotic, with
List_of_OMIM_disorder_codes
Q92838 4706 EDA2R HGNC:17756; Q9HAV5 4707 EDAR HGNC:2895; Q9UNE0 4708 EDARADD HGNC:14341; Q8WWZ3 4709 EDC3 HGNC:26114; Q96F86 4710 EDC4 HGNC:17157; Q6P2E9
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
Protein-coding gene in the species Homo sapiens
include GGT7, RNF5, ELOVL4, GPR42, BCL2L13, HEATR1, IZUMO4, ARID1B, SIAE, EDARADD, URB1, ZDHHC14, KIF11, RRM2, KCTD13, TMEM31, NDUFA3, SGPL1, CNR2, and GJA8
TMEM242
Protein-coding gene in humans
protein 3, CASP8AP2, CD134, CD137, CD27, CD40, CFLAR, CHUK, Caveolin 1, EDARADD, HIVEP3, IKK2, Low affinity nerve growth factor receptor, MAP3K14, MAP3K1
TRAF2
Use of DNA methylation patterns to predict phenotypes
with saliva samples and was based on 3 CpGs found in 3 gene promoters (EDARADD, TOM1L1, and NPTX2). Two years later, Steve Horvath generated epigenetic
Epiphenotyping
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