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Results for the Protein: NP_001243750
378744214

GTP-binding protein Rit1 isoform 1 [Homo sapiens]

Known Diseases associated with this Protein:
  NOONAN SYNDROME 8
4
0
4
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:

COG1100 - COG1100
Rab30 - cd04114
Rnd3_RhoE_Rho8 - cd04172
Rab9 - cd04116
Rab2 - cd01866
Rab8_Rab10_Rab13_lik - cd01867
small_GTPase - smart00010
RhoG - cd01875
M_R_Ras_like - cd04145
Rit_Rin_Ric - cd04141
Rab33B_Rab33A - cd04115
Rab35 - cd04110
RhoBTB - cd01873
ARHI_like - cd04140
RheB - cd04137
Rap1 - cd04175
RSR1 - cd04177
Rap_like - cd04136
Rap2 - cd04176
H_N_K_Ras_like - cd04138
Rab5_related - cd01860
Rab3 - cd01865
Rop_like - cd04133
RhoA_like - cd01870
Rac1_like - cd01871
Rnd - cd04131
Rho2 - cd04129
Cdc42 - cd01874
Rab20 - cd04126
- cd04125
RabL2 - cd04124
Rab12 - cd04120
RJL - cd04119
Wrch_1 - cd04130
Rab14 - cd04122
Rab21 - cd04123
RRP22 - cd04142
RAS - smart00173
RAB - smart00175
Rab24 - cd04118
RGK - cd04148
Rhes_like - cd04143
Tc10 - cd04135
RalA_RalB - cd04139
Rho4_like - cd04132
Rab23_like - cd04106
Rab7 - cd01862
Rab18 - cd01863
Rab19 - cd01864
Rab6 - cd01861
Rab15 - cd04117
Ran - cd00877
Rho - cd00157
Rab - cd00154
Rab1_Ypt1 - cd01869
Rab11_like - cd01868
Rab39 - cd04111
Rab26 - cd04112
Rab4 - cd04113
Rab36_Rab34 - cd04108
Rab28 - cd04109
RabL4 - cd04101
Rab32_Rab38 - cd04107
Centaurin_gamma - cd04103
Arl10_like - cd04159
Ras - pfam00071
Miro - pfam08477
Ras_dva - cd04147
Ras - cd00876
Miro1 - cd01893
Arf_Arl - cd00878
RERG_RasL11_like - cd04146
Rab27A - cd04127
Rho3 - cd04134
Ras2 - cd04144
RHO - smart00174
Ras_like_GTPase - cd00882
RAN - smart00176




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
Rab30cd041142.3e-1233200
Rab9cd041165.6e-2034199
Rnd3_RhoE_Rho8cd041726.7e-0534202
Rab2cd018662.9e-3135202
Rab8_Rab10_Rab13_likcd018671.8e-3536202
RhoGcd018751.4e-1136209
RhoBTBcd018730.0002237199
Rab35cd041107.7e-2037234
Rab33B_Rab33Acd041151.6e-1237214
Rit_Rin_Riccd041412.8e-12237208
M_R_Ras_likecd041456.9e-7637200
Rab5_relatedcd018605.3e-1538200
Rab3cd018654.4e-2138202
RhoA_likecd018701.5e-1838200
Rac1_likecd018711.6e-1738199
Cdc42cd018744.2e-1438199
Rho2cd041292e-1038235
Rndcd041319.7e-0638201
Rop_likecd041331.3e-0638225
Rap_likecd041361.1e-7938200
RheBcd041371.2e-4438221
H_N_K_Ras_likecd041387.8e-7538200
ARHI_likecd041406.1e-3838200
Rap1cd041754.4e-6638201
Rap2cd041765.5e-6538200
RSR1cd041774.9e-4638236
Rabcd001541.8e-4339197
Rhocd001571.4e-2239198
Rancd008773.7e-1139207
Rab6cd018612.6e-1639199
Rab7cd018622e-1339205
Rab18cd018631.5e-2339199
Rab19cd018641.1e-1039199
Rab11_likecd018686.6e-1739200
Rab1_Ypt1cd018696.6e-3239202
RabL4cd041014.4e-0739200
Centaurin_gammacd041030.0001139199
Rab23_likecd041061.3e-1739199
Rab32_Rab38cd041071.4e-0839235
Rab36_Rab34cd041089.7e-0539236
Rab28cd041093.8e-0739236
Rab39cd041114.3e-0939236
Rab26cd041121.6e-0839227
Rab4cd041131.1e-1339199
Rab15cd041174.4e-2039199
Rab24cd041181.5e-0839236
RJLcd041197.2e-1039201
Rab12cd041205.7e-0639234
Rab14cd041221.6e-2239202
Rab21cd041234.7e-2839200
RabL2cd041241.9e-0639202
cd041253.4e-0939230
Rab20cd041266.2e-0739224
Wrch_1cd041302.1e-1439199
Rho4_likecd041322.8e-1139236
Tc10cd041353.6e-1239196
RalA_RalBcd041394.6e-6239202
RRP22cd041424.9e-0839210
Rhes_likecd041432.9e-1239236
RGKcd041487.3e-1439236
Rascd008762.8e-9540199
Arf_Arlcd008788.8e-0540201
Miro1cd018932e-0640194
Rab27Acd041274.8e-1140203
Rho3cd041341.5e-0640210
Ras2cd041445.9e-5440236
RERG_RasL11_likecd041462.2e-5240201
Ras_dvacd041471.3e-1440236
Arl10_likecd041592e-0540198
Ras_like_GTPasecd008823.4e-5343197
Raspfam000711.2e-7240201
small_GTPasesmart000101.3e-4436203
RASsmart001736.8e-11239202
RABsmart001756e-3239202
Miropfam084771e-1440154
RHOsmart001741.3e-1141202
RANsmart001766.6e-0644234

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
OMIM609591.0001 Diseasep.ALA57GLYNOONAN SYNDROME 8
OMIM609591.0002 Diseasep.GLU81GLYNOONAN SYNDROME 8
OMIM609591.0004 Diseasep.GLY95ALANOONAN SYNDROME 8
OMIM609591.0003 Diseasep.PHE82LEUNOONAN SYNDROME 8



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