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Results for the Protein: P55291
1705553

CAD15_HUMAN RecName: Full=Cadherin-15; AltName: Full=Cadherin-14; AltName: Full=Muscle cadherin; Short=M-cadherin; Flags: Precursor

Known Diseases associated with this Protein:
  MENTAL RETARDATION, AUTOSOMAL DOMINANT 3
  MENTAL RETARDATION, AUTOSOMAL DOMINANT 3 (MRD3)
6
3
3
2
4
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

CA_like - cd00031
Cadherin - pfam00028
CA - smart00112
Cadherin_C - pfam01049


Swiss-Prot Protein: P55291
Identical to: NP_004924
   Default View:





Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
CA_likecd000316.3e-5749252
CA_likecd000311.2e-42261475
Cadherinpfam000283.9e-1350143
Cadherinpfam000283.3e-27157251
Cadherinpfam000284.7e-23265367
Cadherinpfam000285.4e-22380474
Cadherinpfam000282.1e-08487580
Cadherin_Cpfam010494.9e-70629783
CAsmart001122.2e-2068150
CAsmart001124.6e-26177258
CAsmart001128.4e-17284374
CAsmart001123.9e-15400481

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs2287359 Polymorphismp.ALA37SERN/A
Swiss-ProtVAR_054969Diseasep.ALA122VALMental retardation, autosomal dominant 3 (MRD3)
Swiss-ProtVAR_054967Diseasep.ARG60CYSMental retardation, autosomal dominant 3 (MRD3)
Swiss-ProtVAR_054968Diseasep.ARG92TRPMental retardation, autosomal dominant 3 (MRD3)
dbSNPrs75791347 Polymorphismp.LYS584GLNN/A
Swiss-ProtVAR_054966Polymorphismp.VAL8LEUN/A
OMIM114019.0003 Diseasep.ALA122VALMENTAL RETARDATION, AUTOSOMAL DOMINANT 3
OMIM114019.0001 Diseasep.ARG60CYSMENTAL RETARDATION, AUTOSOMAL DOMINANT 3
OMIM114019.0002 Diseasep.ARG92TRPMENTAL RETARDATION, AUTOSOMAL DOMINANT 3



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