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Results for the Protein: P22626
133257

ROA2_HUMAN RecName: Full=Heterogeneous nuclear ribonucleoproteins A2/B1; Short=hnRNP A2/B1

Known Diseases associated with this Protein:
  DEMENTIA 2 (1 FAMILY)
  INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL
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Default View:

COG0724 - COG0724
- smart00362
RRM_SF - cd00590
RRM_1 - pfam00076
RRM - smart00360
HnRNPA1 - pfam11627


Swiss-Prot Protein: P22626
Identical to: NP_112533
   Default View:







Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
RRM_SFcd005906.2e-232295
RRM_SFcd005908.1e-19113186
RRM_1pfam000761.6e-202392
RRM_1pfam000761.1e-20114183
smart003625.3e-222294
RRMsmart003601.3e-222594
smart003621.8e-16113185
RRMsmart003606.1e-19116185
HnRNPA1pfam116272.4e-16297334

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM600124.0001 Diseasep.ASP290VALINCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL||DEMENTIA 2 (1 family)



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