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Results for the Protein: P42261
116242505

GRIA1_HUMAN RecName: Full=Glutamate receptor 1; Short=GluR-1; AltName: Full=AMPA-selective glutamate receptor 1; AltName: Full=GluR-A; AltName: Full=GluR-K1; AltName: Full=Glutamate receptor ionotropic, AMPA 1; Short=GluA1; Flags: Precursor

Known Diseases associated with this Protein:
  VARIANT OF UNKNOWN SIGNIFICANCE
1
5
1
0
5
Tips:
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PBP1_iGluR_NMDA - cd06367
PBP1_iGluR_Kainate_G - cd06393
PBP1_iGluR_AMPA_GluR - cd06389
PBP1_iGluR_delta_lik - cd06381
PBP1_iGluR_AMPA_GluR - cd06390
PBP1_iGluR_delta_2 - cd06391
PBP1_iGluR_AMPA_GluR - cd06387
PBP1_iGluR_AMPA_GluR - cd06388
PBP1_iGluR_AMPA - cd06380
PBP1_iGluR_Kainate - cd06382
PBP1_ABC_transporter - cd04509
PBP1_iGluR_non_NMDA_ - cd06368
PBP1_glutamate_recep - cd06269
Periplasmic_Binding_ - cd01391
PBP1_GABAb_receptor - cd06366
PBP1_iGluR_N_LIVBP_l - cd06351
PBP1_GPCR_family_C_l - cd06350
ANF_receptor - pfam01094
PBPb - cd00134
SBP_bac_3 - pfam00497
Lig_chan-Glu_bd - pfam10613
Lig_chan - pfam00060
PBPe - smart00079


Swiss-Prot Protein: P42261
Identical to: NP_000818
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Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
PBP1_iGluR_NMDAcd063679.6e-0523397
PBP1_iGluR_Kainate_Gcd063931.4e-2423391
Periplasmic_Binding_cd013913.1e-3526366
PBP1_ABC_transportercd045097.5e-5926367
PBP1_glutamate_recepcd062691.5e-6526389
PBP1_GPCR_family_C_lcd063508.3e-0626392
PBP1_iGluR_N_LIVBP_lcd063511.5e-11926389
PBP1_GABAb_receptorcd063663.9e-0826392
PBP1_iGluR_non_NMDA_cd063685.9e-15926389
PBP1_iGluR_AMPAcd063803.1e-21226389
PBP1_iGluR_delta_likcd063817.2e-0626389
PBP1_iGluR_Kainatecd063821.3e-4726389
PBP1_iGluR_AMPA_GluRcd063891.5e-18226390
PBP1_iGluR_AMPA_GluRcd063906.3e-30226389
PBP1_iGluR_delta_2cd063911.5e-0626390
PBP1_iGluR_AMPA_GluRcd063887.9e-17026390
PBP1_iGluR_AMPA_GluRcd063871.1e-16626389
PBPbcd001343.9e-05409781
ANF_receptorpfam010945e-6537372
SBP_bac_3pfam004979.5e-19409783
Lig_chanpfam000604e-153536817
Lig_chan-Glu_bdpfam106133.3e-35418483
PBPesmart000795.2e-68646783

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
Swiss-ProtVAR_028073Polymorphismp.ALA536SERN/A
Swiss-ProtVAR_028071Polymorphismp.ASP487ASNN/A
Swiss-ProtVAR_028074Polymorphismp.ILE548METN/A
Swiss-ProtVAR_028075Polymorphismp.PHE588LEUN/A
Swiss-ProtVAR_028072Polymorphismp.PRO521THRN/A
OMIM138248.0001 Diseasep.ALA626THRVARIANT OF UNKNOWN SIGNIFICANCE



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