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Results for the Protein: NP_001108454
169234665

tumor protein 63 isoform 6 [Homo sapiens]

Known Diseases associated with this Protein:
  3
  ADULT SYNDROME
  ADULT SYNDROME, INCLUDED
  ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME
  OROFACIAL CLEFT 8
  RAPP-HODGKIN SYNDROME, INCLUDED
  SPLIT-HAND/FOOT MALFORMATION 4
15
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15
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Default View:

P53 - pfam00870
P53 - cd08367
P53_tetramer - pfam07710




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
P53pfam008702.2e-14969265
P53_tetramerpfam077103.4e-20298338

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM603273.0006 Diseasep.ARG186CYSSPLIT-HAND/FOOT MALFORMATION 4
OMIM603273.0002 Diseasep.ARG110GLNECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3
OMIM603273.0024 Diseasep.ARG133GLNECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3||ADULT SYNDROME, INCLUDED
OMIM603273.0014 Diseasep.ARG204GLNADULT SYNDROME
OMIM603273.0008 Diseasep.ARG210GLNECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3
OMIM603273.0022 Diseasep.ARG204GLYADULT SYNDROME
OMIM603273.0021 Diseasep.ARG219GLYOROFACIAL CLEFT 8
OMIM603273.0007 Diseasep.ARG185HISECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3||RAPP-HODGKIN SYNDROME, INCLUDED
OMIM603273.0028 Diseasep.ARG133PROECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3
OMIM603273.0001 Diseasep.ARG110TRPECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3
OMIM603273.0015 Diseasep.ASP218GLYECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3
OMIM603273.0003 Diseasep.CYS212ARGECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3
OMIM603273.0005 Diseasep.LYS100GLUSPLIT-HAND/FOOT MALFORMATION 4
OMIM603273.0026 Diseasep.PRO33LEUADULT SYNDROME
OMIM603273.0020 Diseasep.VAL20METADULT SYNDROME



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