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Results for the Protein: P15153
131806

RAC2_HUMAN RecName: Full=Ras-related C3 botulinum toxin substrate 2; AltName: Full=GX; AltName: Full=Small G protein; AltName: Full=p21-Rac2; Flags: Precursor

Known Diseases associated with this Protein:
  NEUTROPHIL IMMUNODEFICIENCY SYNDROME
  NEUTROPHIL IMMUNODEFICIENCY SYNDROME (NEUID)
2
1
1
0
2
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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



Default View:

COG1100 - COG1100
Rab2 - cd01866
Rnd3_RhoE_Rho8 - cd04172
Rnd1_Rho6 - cd04174
Rab30 - cd04114
RhoG - cd01875
Rab14 - cd04122
Rit_Rin_Ric - cd04141
M_R_Ras_like - cd04145
Rab9 - cd04116
Rab33B_Rab33A - cd04115
Rab1_Ypt1 - cd01869
RhoBTB - cd01873
Rab8_Rab10_Rab13_lik - cd01867
Rab35 - cd04110
H_N_K_Ras_like - cd04138
Rap_like - cd04136
Rnd2_Rho7 - cd04173
Rap1 - cd04175
Rop_like - cd04133
Rap2 - cd04176
Rnd - cd04131
Rab5_related - cd01860
Rab3 - cd01865
Rac1_like - cd01871
Rho2 - cd04129
Cdc42 - cd01874
Rab20 - cd04126
Rab27A - cd04127
- cd04125
RJL - cd04119
Spg1 - cd04128
Rab21 - cd04123
RabL2 - cd04124
RalA_RalB - cd04139
RAS - smart00173
RAB - smart00175
Wrch_1 - cd04130
RRP22 - cd04142
Rho4_like - cd04132
Rab24 - cd04118
Tc10 - cd04135
Rab36_Rab34 - cd04108
Rab6 - cd01861
Rab18 - cd01863
Ran - cd00877
Rab - cd00154
Rab15 - cd04117
Rho - cd00157
Miro1 - cd01893
Rab7 - cd01862
Rab26 - cd04112
Rab4 - cd04113
RabL4 - cd04101
Rab28 - cd04109
Rab23_like - cd04106
Rab32_Rab38 - cd04107
Ras_dva - cd04147
RSR1 - cd04177
RERG_RasL11_like - cd04146
Miro - pfam08477
Ras - pfam00071
RhoA_like - cd01870
Rab11_like - cd01868
Rab19 - cd01864
Ras - cd00876
Ras2 - cd04144
Rho3 - cd04134
RheB - cd04137
ARHI_like - cd04140
RHO - smart00174
small_GTPase - smart00010
Rab39 - cd04111
Ras_like_GTPase - cd00882
RAN - smart00176


Swiss-Prot Protein: P15153
Identical to: NP_002863
   Default View:













































































Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
RhoGcd018754.3e-1221192
Rab30cd041148.9e-071176
Rnd3_RhoE_Rho8cd041727.2e-501179
Rnd1_Rho6cd041741.1e-311192
COG1100COG11005.1e-431191
Rab8_Rab10_Rab13_likcd018677.5e-132179
Rab1_Ypt1cd018693.4e-132179
RhoBTBcd018739.1e-312176
Rab35cd041106.8e-072189
Rab33B_Rab33Acd041151.7e-082185
Rab9cd041164e-092176
Rab14cd041228e-102179
Rit_Rin_Riccd041411.9e-132185
M_R_Ras_likecd041451.6e-232177
Rab5_relatedcd018602e-123177
Rab3cd018655e-093180
Rac1_likecd018712.8e-1333176
Cdc42cd018741.7e-1113177
Rho2cd041291e-633192
Rndcd041314.8e-563179
Rop_likecd041332.7e-923180
Rap_likecd041363.8e-173177
H_N_K_Ras_likecd041383.8e-223177
Rnd2_Rho7cd041734.4e-233192
Rap1cd041753.6e-163178
Rap2cd041765.1e-183177
Rabcd001541.6e-404174
Rhocd001573.5e-1284175
Rancd008771.1e-104154
Rab6cd018619.2e-114176
Rab7cd018621.3e-124182
Rab18cd018637.3e-124176
Miro1cd018937.6e-114179
RabL4cd041011.8e-074177
Rab23_likecd041061.7e-144154
Rab32_Rab38cd041072.3e-074191
Rab36_Rab34cd041080.000114191
Rab28cd041090.000554192
Rab26cd041128.2e-064189
Rab4cd041133e-114176
Rab15cd041173.5e-104176
Rab24cd041182.9e-074190
RJLcd041193.6e-064178
Rab21cd041232.7e-134177
RabL2cd041246.8e-074166
cd041257e-064192
Rab20cd041260.000144189
Rab27Acd041273.2e-084180
Spg1cd041288.5e-054149
Tc10cd041358.7e-1074177
Rho4_likecd041324.1e-864192
RalA_RalBcd041394.8e-114179
RRP22cd041420.000214192
Wrch_1cd041301.1e-924176
Rascd008763.1e-325176
Rab19cd018645.9e-065176
Rab11_likecd018682e-095177
RhoA_likecd018701.3e-825177
Rho3cd041346.3e-645192
RheBcd041371.1e-105192
ARHI_likecd041401.4e-065177
Ras2cd041441.4e-065192
RERG_RasL11_likecd041462.7e-105178
Ras_dvacd041471.1e-055192
RSR1cd041772.3e-055192
Rab39cd041112.7e-077190
Ras_like_GTPasecd008821.8e-528174
Raspfam000713e-865178
RASsmart001731.1e-184179
RABsmart001757.9e-194179
Miropfam084771.7e-135118
small_GTPasesmart000108.1e-526157
RHOsmart001745.1e-1356179
RANsmart001760.000149186

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
Swiss-ProtVAR_017452Diseasep.ASP57ASNNeutrophil immunodeficiency syndrome (NEUID)
Swiss-ProtVAR_036569Polymorphismp.PRO29LEUN/A
OMIM602049.0001 Diseasep.ASP57ASNNEUTROPHIL IMMUNODEFICIENCY SYNDROME



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