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Results for the Protein: NP_001138498
222537743

phosphotidylinositol phosphatase PTPRQ precursor [Homo sapiens]

Known Diseases associated with this Protein:
  DEAFNESS, AUTOSOMAL RECESSIVE 84A
2
12
2
12
0
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

FN3 - cd00063
FN3 - smart00060
fn3 - pfam00041
PTP2 - COG5599
PTPc - smart00194
Y_phosphatase - pfam00102
PTPc - cd00047
PTPc_motif - smart00404
PTPc_DSPc - smart00012




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
FN3cd000631.1e-09305392
FN3cd000633e-18569660
FN3cd000633.6e-18665754
FN3cd000631.7e-15759849
FN3cd000638.8e-15854943
FN3cd000633.3e-139481048
FN3cd000631.5e-0710531145
FN3cd000631.1e-1111501237
FN3cd000637.8e-1312421335
FN3cd000632.2e-1513401424
FN3cd000632.4e-1114301533
FN3cd000632.4e-0815381636
FN3cd000634e-0716411740
PTPccd000471.9e-12520292258
fn3pfam000419.1e-1457143
fn3pfam000410.00011307386
fn3pfam000415.7e-12570651
fn3pfam000411.8e-13667744
fn3pfam000411.3e-08761842
fn3pfam000415.7e-12856935
fn3pfam000414.7e-069501040
fn3pfam000411.5e-0711521231
fn3pfam000415.5e-0912441328
fn3pfam000418e-1013411418
fn3pfam000412.5e-0514311526
fn3pfam000412.3e-0615401620
fn3pfam000412.7e-0516431733
PTP2COG55992e-4619892269
Y_phosphatasepfam001022.1e-10920272258
FN3smart000603.4e-1856140
FN3smart000603.2e-08306383
FN3smart000601.1e-14569648
FN3smart000604.5e-15666743
FN3smart000606.4e-10760839
FN3smart000601.1e-11855932
FN3smart000603.1e-089491037
FN3smart000602e-0710541134
FN3smart000605.5e-0911511228
FN3smart000602e-1112431324
FN3smart000602.5e-1113401415
FN3smart000601.1e-0814301523
FN3smart000602.2e-0715391620
FN3smart000608.9e-0616411731
PTPcsmart001941.3e-12620022258
PTPc_DSPcsmart000121.2e-4021572258
PTPc_motifsmart004041.2e-4021572258

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs7975340 Polymorphismp.ALA906PRON/A
dbSNPrs57971665 Polymorphismp.ARG259GLNN/A
dbSNPrs1163042 Polymorphismp.ARG1916LYSN/A
dbSNPrs17713202 Polymorphismp.ASN1030ASPN/A
dbSNPrs11114486 Polymorphismp.GLN619LYSN/A
dbSNPrs7963963 Polymorphismp.ILE1520THRN/A
dbSNPrs61729278 Polymorphismp.ILE842VALN/A
dbSNPrs6539524 Polymorphismp.PHE884LEUN/A
dbSNPrs60216135 Polymorphismp.THR17ILEN/A
dbSNPrs35189291 Polymorphismp.TYR915CYSN/A
dbSNPrs10778752 Polymorphismp.VAL473ASPN/A
dbSNPrs7965277 Polymorphismp.VAL647GLYN/A
OMIM603317.0002 Diseasep.ARG457GLYDEAFNESS, AUTOSOMAL RECESSIVE 84A
OMIM603317.0001 Diseasep.TYR497TERDEAFNESS, AUTOSOMAL RECESSIVE 84A



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