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Results for the Protein: Q9GZT5
14424011

WN10A_HUMAN RecName: Full=Protein Wnt-10a; Flags: Precursor

Known Diseases associated with this Protein:
  ODONTOONYCHODERMAL DYSPLASIA
  SCHOPF-SCHULZ-PASSARGE SYNDROME, INCLUDED;;
  TOOTH AGENESIS SELECTIVE 4 (STHAG4)
  TOOTH AGENESIS, SELECTIVE 4, INCLUDED
  TOOTH AGENESIS, SELECTIVE, 4
  TOOTH AGENESIS, SELECTIVE, 4, INCLUDED
12
7
8
0
11
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WNT1 - smart00097


Swiss-Prot Protein: Q9GZT5
Identical to: NP_079492
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Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
Swiss-ProtVAR_064839Polymorphismp.ARG360CYSN/A
Swiss-ProtVAR_062510Diseasep.ARG128GLNTooth agenesis selective 4 (STHAG4)
Swiss-ProtVAR_069172Polymorphismp.ARG163TRPN/A
Swiss-ProtVAR_069175Polymorphismp.ASN306LYSN/A
Swiss-ProtVAR_069173Diseasep.ASP217ASNTooth agenesis selective 4 (STHAG4)
Swiss-ProtVAR_069171Diseasep.GLU95LYSTooth agenesis selective 4 (STHAG4)
Swiss-ProtVAR_064837Polymorphismp.HIS143TYRN/A
Swiss-ProtVAR_062511Diseasep.PHE228ILETooth agenesis selective 4 (STHAG4)
Swiss-ProtVAR_013239Polymorphismp.PRO302THRN/A
Swiss-ProtVAR_069174Polymorphismp.TRP277CYSN/A
Swiss-ProtVAR_064838Polymorphismp.VAL145METN/A
OMIM606268.0004 Diseasep.ARG128GLNODONTOONYCHODERMAL DYSPLASIA||TOOTH AGENESIS, SELECTIVE, 4, INCLUDED
OMIM606268.0007 Diseasep.ASP217ASNTOOTH AGENESIS, SELECTIVE, 4
OMIM606268.0002 Diseasep.CYS107TERODONTOONYCHODERMAL DYSPLASIA||SCHOPF-SCHULZ-PASSARGE SYNDROME, INCLUDED;;||TOOTH AGENESIS, SELECTIVE 4, INCLUDED
OMIM606268.0005 Diseasep.CYS376TERODONTOONYCHODERMAL DYSPLASIA
OMIM606268.0001 Diseasep.GLU233TERODONTOONYCHODERMAL DYSPLASIA
OMIM606268.0008 Diseasep.GLY95LYSTOOTH AGENESIS, SELECTIVE, 4
OMIM606268.0003 Diseasep.PHE228ILEODONTOONYCHODERMAL DYSPLASIA||TOOTH AGENESIS, SELECTIVE, 4, INCLUDED
OMIM606268.0006 Diseasep.TRP9TERODONTOONYCHODERMAL DYSPLASIA



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