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Results for the Protein: NP_039230
7524356

paired box protein Pax-3 isoform PAX3b [Homo sapiens]

Known Diseases associated with this Protein:
  CRANIOFACIAL-DEAFNESS-HAND SYNDROME
  WAARDENBURG SYNDROME, TYPE 1
  WAARDENBURG SYNDROME, TYPE 1, INCLUDED
  WAARDENBURG SYNDROME, TYPE 3
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Default View:

PAX - smart00351
PAX - pfam00292
PAX - cd00131


RefSeq Protein: NP_039230
   Default View:





Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
PAXpfam002923.3e-9434159
PAXsmart003514.6e-9434159

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM606597.0014 Diseasep.ARG56LEUWAARDENBURG SYNDROME, TYPE 1
OMIM606597.0011 Diseasep.ASN47HISWAARDENBURG SYNDROME, TYPE 3
OMIM606597.0010 Diseasep.ASN47LYSCRANIOFACIAL-DEAFNESS-HAND SYNDROME
OMIM606597.0006 Diseasep.GLY81ALAWAARDENBURG SYNDROME, TYPE 1
OMIM606597.0015 Diseasep.HIS80ASPWAARDENBURG SYNDROME, TYPE 1
OMIM606597.0002 Diseasep.PRO50LEUWAARDENBURG SYNDROME, TYPE 1
OMIM606597.0009 Diseasep.SER84PHEWAARDENBURG SYNDROME, TYPE 3||WAARDENBURG SYNDROME, TYPE 1, INCLUDED
OMIM606597.0013 Diseasep.TYR90HISWAARDENBURG SYNDROME, TYPE 3



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