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Results for the Protein: NP_001123476
194097350
87

alpha-actinin-1 isoform a [Homo sapiens]

Known Diseases associated with this Protein:
  BLEEDING DISORDER, PLATELET-TYPE, 15
6
0
6
0
0
Tips:
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Default View:

SAC6 - COG5069
CH - cd00014
CH - pfam00307
CH - smart00033
CAMSAP_CH - pfam11971
Spectrin - pfam00435
SPEC - cd00176
SPEC - smart00150
EFh - smart00054
EFh - cd00051
efhand - pfam00036
efhand_Ca_insen - pfam08726




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
CHcd000144e-35145250
SPECcd001765.8e-44395622
EFhcd000511.9e-11750839
SAC6COG50697.5e-3824602
CHpfam003074.4e-3032135
CHpfam003071.3e-36145250
Spectrinpfam004352e-14274384
Spectrinpfam004351.6e-33394499
Spectrinpfam004352.8e-19509620
Spectrinpfam004356.2e-15630733
efhandpfam000364.8e-06750778
CHsmart000337.4e-2533133
CHsmart000331.1e-26146245
CAMSAP_CHpfam119711.5e-11154230
SPECsmart001502.2e-26397498
SPECsmart001506.2e-07512619
EFhsmart000548.1e-07750778
efhand_Ca_insenpfam087263.1e-40844910

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM102575.0004 Diseasep.ARG46GLNBLEEDING DISORDER, PLATELET-TYPE, 15
OMIM102575.0003 Diseasep.ARG752GLNBLEEDING DISORDER, PLATELET-TYPE, 15
OMIM102575.0005 Diseasep.ARG738TRPBLEEDING DISORDER, PLATELET-TYPE, 15
OMIM102575.0002 Diseasep.GLN32LYSBLEEDING DISORDER, PLATELET-TYPE, 15
OMIM102575.0006 Diseasep.GLU225LYSBLEEDING DISORDER, PLATELET-TYPE, 15
OMIM102575.0001 Diseasep.VAL105ILEBLEEDING DISORDER, PLATELET-TYPE, 15



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