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Results for the Protein: Q8IY17
150403921

PLPL6_HUMAN RecName: Full=Neuropathy target esterase; AltName: Full=Patatin-like phospholipase domain-containing protein 6

Known Diseases associated with this Protein:
  SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE (SPG39)
2
2
0
0
4
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

Crp - COG0664
cNMP - smart00100
CAP_ED - cd00038
cNMP_binding - pfam00027
RssA - COG1752
Pat_PNPLA6_PNPLA7 - cd07225
Pat_Fungal_NTE1 - cd07227
Pat_hypo_W_succinoge - cd07210
Pat_NTE_like_bacteri - cd07228
Pat_PNPLA6_PNPLA7_NT - cd07205
Pat17_PNPLA8_PNPLA9_ - cd07199
Pat_ExoU_VipD_like - cd07207
Patatin_and_cPLA2 - cd01819
Pat_hypo_Ecoli_yjju_ - cd07208
Patatin - pfam01734
Patatin - cd07198
Pat_hypo_Ecoli_Z1214 - cd07209


Swiss-Prot Protein: Q8IY17
   Default View:















Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
CrpCOG06643.9e-07180388
CAP_EDcd000387.2e-24186307
CAP_EDcd000384.6e-19503618
CrpCOG06646.5e-10614846
CAP_EDcd000387.1e-24621734
RssACOG17521.3e-579341271
Pat_PNPLA6_PNPLA7cd072252.4e-2419551260
Pat_Fungal_NTE1cd072276.2e-1309601230
Pat_hypo_W_succinogecd072104e-109701216
Pat_NTE_like_bactericd072282.4e-329701150
Pat_PNPLA6_PNPLA7_NTcd072051.4e-819701150
Pat17_PNPLA8_PNPLA9_cd071993e-059711242
Pat_ExoU_VipD_likecd072078.9e-099711160
Patatin_and_cPLA2cd018197.2e-299721148
Pat_hypo_Ecoli_yjju_cd072081.1e-059721241
Patatincd071987.9e-499721148
Pat_hypo_Ecoli_Z1214cd072091.1e-149721185
cNMP_bindingpfam000277.6e-23204301
cNMP_bindingpfam000273.8e-21521612
cNMP_bindingpfam000271.4e-18638728
Patatinpfam017341.5e-319721138
cNMPsmart001001e-13186310
cNMPsmart001000.00016503621
cNMPsmart001001.3e-06622740

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
Swiss-ProtVAR_032949Polymorphismp.ALA403PRON/A
Swiss-ProtVAR_044409Diseasep.ARG929HISSpastic paraplegia 39, autosomal recessive (SPG39)
Swiss-ProtVAR_032950Polymorphismp.LYS1024ARGN/A
Swiss-ProtVAR_044410Diseasep.MET1051VALSpastic paraplegia 39, autosomal recessive (SPG39)



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