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Results for the Protein: NP_001136239
218505783

protocadherin-15 isoform CD1-8 precursor [Homo sapiens]

Known Diseases associated with this Protein:
  DEAFNESS, AUTOSOMAL RECESSIVE 23
  USHER SYNDROME, TYPE IF
6
5
6
5
0
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Default View:

CA_like - cd00031
CA - smart00112
Cadherin - pfam00028




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
CA_likecd000318.6e-36362570
CA_likecd000315.3e-59583774
CA_likecd000313.6e-45786991
CA_likecd000311.4e-3710031207
Cadherinpfam000286.7e-05363463
Cadherinpfam000287e-10477569
Cadherinpfam000281.4e-17584671
Cadherinpfam000286.3e-21686773
Cadherinpfam000282.4e-12787880
Cadherinpfam000282.7e-11894990
Cadherinpfam000281e-1110041098
Cadherinpfam000280.0001111121206
CAsmart001122.3e-07270356
CAsmart001122.4e-09392470
CAsmart001125.6e-14497576
CAsmart001124.1e-20604678
CAsmart001121.3e-24705780
CAsmart001123.5e-15807887
CAsmart001123.4e-06914997
CAsmart001122.5e-1810211105
CAsmart001123.1e-0511321213

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs2135720 Polymorphismp.ARG892GLNN/A
dbSNPrs4935502 Polymorphismp.ASP398ALAN/A
dbSNPrs10825269 Polymorphismp.GLY343SERN/A
dbSNPrs79854148 Polymorphismp.ILE1863VALN/A
dbSNPrs11004439 Polymorphismp.SER19ALAN/A
OMIM605514.0007 Diseasep.ARG129GLYDEAFNESS, AUTOSOMAL RECESSIVE 23
OMIM605514.0004 Diseasep.ARG203TERUSHER SYNDROME, TYPE IF
OMIM605514.0002 Diseasep.ARG3TERUSHER SYNDROME, TYPE IF
OMIM605514.0006 Diseasep.GLY220ASPDEAFNESS, AUTOSOMAL RECESSIVE 23
OMIM605514.0009 Diseasep.SER605TERUSHER SYNDROME, TYPE IF
OMIM605514.0010 Diseasep.VAL486ASPDEAFNESS, AUTOSOMAL RECESSIVE 23



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