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Results for the Protein: NP_001172004
297374777

fragile X mental retardation protein 1 isoform ISO6 [Homo sapiens]

Known Diseases associated with this Protein:
  FRAGILE X MENTAL RETARDATION SYNDROME
2
1
2
1
0
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Default View:

Agenet - pfam05641
KH - smart00322
KH_1 - pfam00013
KH-I - cd00105




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
KH_1pfam000135.9e-08220279
KH_1pfam000132e-05283333
Agenetpfam056411.2e-0959120
KHsmart003222.5e-05217284

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs29281 Polymorphismp.ALA145SERN/A
OMIM309550.0001 Diseasep.ILE304ASNFRAGILE X MENTAL RETARDATION SYNDROME
OMIM309550.0005 Diseasep.SER27TERFRAGILE X MENTAL RETARDATION SYNDROME



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