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Results for the Protein: NP_001243197
372220099

myopalladin isoform b [Homo sapiens]

Known Diseases associated with this Protein:
  CARDIOMYOPATHY, DILATED, 1KK
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22, INCLUDED
  CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4
5
0
5
0
0
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Default View:

I-set - pfam07679
IG_like - smart00410
IG - smart00409
IGc2 - smart00408
V-set - pfam07686




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
I-setpfam076794.8e-26141238
IGsmart004091.8e-19147239
IG_likesmart004101.8e-19147239
IGc2smart004081.3e-09154228
I-setpfam076796.2e-24651742
IGsmart004092e-15657743
IG_likesmart004102e-15657743
V-setpfam076860.0004659742
IGc2smart004084.2e-09664732
I-setpfam076796.9e-31779869
IGsmart004095.2e-15785870
IG_likesmart004105.2e-15785870
IGc2smart004081e-09792859
I-setpfam076796.1e-21878969
IGsmart004095.1e-15884970
IG_likesmart004105.1e-15884970
IGc2smart004087.2e-06891959

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM608517.0001 Diseasep.ARG794HISCARDIOMYOPATHY, DILATED, 1KK
OMIM608517.0005 Diseasep.GLN235TERCARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4
OMIM608517.0006 Diseasep.PRO667LEUCARDIOMYOPATHY, DILATED, 1KK
OMIM608517.0002 Diseasep.PRO818LEUCARDIOMYOPATHY, DILATED, 1KK||CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22, INCLUDED
OMIM608517.0003 Diseasep.VAL901METCARDIOMYOPATHY, DILATED, 1KK



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