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Results for the Protein: NP_835365
30181242
DCX

neuronal migration protein doublecortin isoform b [Homo sapiens]

Known Diseases associated with this Protein:
  LISSENCEPHALY, X-LINKED, 1
  SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED
  SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED
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Default View:

DCX - smart00537
DCX - cd01617
DCX - pfam03607


RefSeq Protein: NP_835365
   Default View:





Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
DCXcd016171.7e-29180259
DCXpfam036071.4e-3370134
DCXpfam036073.3e-24197258
DCXsmart005372.5e-4948139
DCXsmart005372.8e-40175263

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM300121.0012 Diseasep.ARG8GLYSUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED
OMIM300121.0013 Diseasep.ARG115HISLISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED
OMIM300121.0002 Diseasep.ARG111TRPLISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED
OMIM300121.0006 Diseasep.THR122ARGLISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED
OMIM300121.0003 Diseasep.TYR44HISLISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED



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