Home News About DMDM Database Statistics Research Publications Contact  

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
1
0
1
0
0
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

 Clicking a check box will display or hide the correlated domain.

 To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic.



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 ↕
COG0724COG07241.8e-073322
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)



   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258