Home News About DMDM Database Statistics Research Publications Contact  

Results for the Protein: NP_002825
33356177

tyrosine-protein phosphatase non-receptor type 11 isoform 1 [Homo sapiens]

Known Diseases associated with this Protein:
  LEOPARD SYNDROME
  LEUKEMIA, JUVENILE MYELOMONOCYTIC, SOMATIC
  METACHONDROMATOSIS
  NOONAN SYNDROME
  NOONAN SYNDROME 1
26
0
26
0
0
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

 Clicking a check box will display or hide the correlated domain.

 To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic.



Default View:

SH2 - smart00252
SH2 - cd00173
SH2 - pfam00017
PTP2 - COG5599
PTPc - smart00194
Y_phosphatase - pfam00102
PTPc - cd00047
CDC14 - COG2453
PTPc_motif - smart00404
PTPc_DSPc - smart00012


RefSeq Protein: NP_002825
   Default View:









Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
SH2cd001731.6e-32111216
PTPccd000476.4e-129275520
SH2pfam000178.4e-37681
SH2pfam000177.7e-35112197
PTP2COG55997.9e-38227529
Y_phosphatasepfam001025.2e-121273520
CDC14COG24530.00053346538
SH2smart002521.6e-29487
SH2smart002526.7e-39110203
PTPcsmart001941.3e-135246520
PTPc_DSPcsmart000128.7e-46414520
PTPc_motifsmart004048.7e-46414520

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM176876.0002 Diseasep.ALA72GLYNOONAN SYNDROME 1
OMIM176876.0001 Diseasep.ALA72SERNOONAN SYNDROME 1
OMIM176876.0020 Diseasep.ALA461THRLEOPARD SYNDROME
OMIM176876.0026 Diseasep.ARG138TERMETACHONDROMATOSIS
OMIM176876.0003 Diseasep.ASN308ASPNOONAN SYNDROME 1
OMIM176876.0004 Diseasep.ASN308SERNOONAN SYNDROME 1
OMIM176876.0010 Diseasep.ASP61GLYNOONAN SYNDROME 1
OMIM176876.0023 Diseasep.GLN510ARGNOONAN SYNDROME
OMIM176876.0018 Diseasep.GLN79ARGNOONAN SYNDROME
OMIM176876.0022 Diseasep.GLN510PROLEOPARD SYNDROME
OMIM176876.0031 Diseasep.GLN506TERMETACHONDROMATOSIS
OMIM176876.0017 Diseasep.GLU76ALALEUKEMIA, JUVENILE MYELOMONOCYTIC, SOMATIC
OMIM176876.0016 Diseasep.GLU76GLYLEUKEMIA, JUVENILE MYELOMONOCYTIC, SOMATIC
OMIM176876.0014 Diseasep.GLU76LYSLEUKEMIA, JUVENILE MYELOMONOCYTIC, SOMATIC
OMIM176876.0015 Diseasep.GLU76VALLEUKEMIA, JUVENILE MYELOMONOCYTIC, SOMATIC
OMIM176876.0021 Diseasep.GLY464ALALEOPARD SYNDROME
OMIM176876.0034 Diseasep.LYS99TERMETACHONDROMATOSIS
OMIM176876.0012 Diseasep.PHE285SERNOONAN SYNDROME 1
OMIM176876.0007 Diseasep.SER502THRNOONAN SYNDROME 1
OMIM176876.0027 Diseasep.THR2ILENOONAN SYNDROME
OMIM176876.0011 Diseasep.THR73ILENOONAN SYNDROME 1
OMIM176876.0019 Diseasep.THR411METNOONAN SYNDROME
OMIM176876.0006 Diseasep.THR468METLEOPARD SYNDROME
OMIM176876.0009 Diseasep.TYR62ASPNOONAN SYNDROME 1
OMIM176876.0005 Diseasep.TYR279CYSLEOPARD SYNDROME
OMIM176876.0008 Diseasep.TYR63CYSNOONAN SYNDROME 1



   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258