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EDARADD information


EDARADD
Identifiers
AliasesEDARADD, ECTD11A, ECTD11B, ED3, EDA3, EDAR-associated death domain, EDAR associated death domain
External IDsOMIM: 606603; MGI: 1931001; HomoloGene: 15430; GeneCards: EDARADD; OMA:EDARADD - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_145861
NM_080738

NM_133643

RefSeq (protein)

NP_542776
NP_665860

NP_598398

Location (UCSC)Chr 1: 236.35 – 236.5 MbChr 13: 12.49 – 12.54 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Ectodysplasin-A receptor-associated adapter protein is a protein that in humans is encoded by the EDARADD gene.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000186197 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000095105 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Headon DJ, Emmal SA, Ferguson BM, Tucker AS, Justice MJ, Sharpe PT, Zonana J, Overbeek PA (Jan 2002). "Gene defect in ectodermal dysplasia implicates a death domain adapter in development". Nature. 414 (6866): 913–6. doi:10.1038/414913a. PMID 11780064. S2CID 4380080.
  6. ^ Cite error: The named reference entrez was invoked but never defined (see the help page).

and 9 Related for: EDARADD information

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EDARADD

Last Update:

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...

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Hypohidrotic ectodermal dysplasia

Last Update:

needed] Mutations in the EDA, EDAR, and EDARADD genes cause hypohidrotic ectodermal dysplasia. The EDA, EDAR, and EDARADD genes provide instructions for making...

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Ectodermal dysplasia

Last Update:

Hypohidrotic ectodermal dysplasia can be associated with EDA, EDAR and EDARADD. Margarita Island ectodermal dysplasia is associated with PVRL1. Ectodermal...

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ANOTHER syndrome

Last Update:

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...

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Anodontia

Last Update:

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...

Word Count : 1970

TMEM242

Last Update:

include GGT7, RNF5, ELOVL4, GPR42, BCL2L13, HEATR1, IZUMO4, ARID1B, SIAE, EDARADD, URB1, ZDHHC14, KIF11, RRM2, KCTD13, TMEM31, NDUFA3, SGPL1, CNR2, and GJA8...

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Epiphenotyping

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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...

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TRAF2

Last Update:

protein 3, CASP8AP2, CD134, CD137, CD27, CD40, CFLAR, CHUK, Caveolin 1, EDARADD, HIVEP3, IKK2, Low affinity nerve growth factor receptor, MAP3K14, MAP3K1...

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List of OMIM disorder codes

Last Update:

anhidrotic, autosomal dominant; 129490; EDARADD Ectodermal dysplasia, anhidrotic, autosomal recessive; 224900; EDARADD Ectodermal dysplasia, anhidrotic, with...

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