Incidental Mutation 'R4824:Rnd2'
ID 374246
Institutional Source Beutler Lab
Gene Symbol Rnd2
Ensembl Gene ENSMUSG00000001313
Gene Name Rho family GTPase 2
Synonyms Rohn, Arhn
MMRRC Submission 042440-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4824 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 101359001-101362679 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 101359825 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 57 (L57F)
Ref Sequence ENSEMBL: ENSMUSP00000001347 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000001347] [ENSMUST00000040430]
AlphaFold Q9QYM5
Predicted Effect probably damaging
Transcript: ENSMUST00000001347
AA Change: L57F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000001347
Gene: ENSMUSG00000001313
AA Change: L57F

DomainStartEndE-ValueType
RHO 10 184 5.22e-100 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000040430
SMART Domains Protein: ENSMUSP00000048350
Gene: ENSMUSG00000034993

DomainStartEndE-ValueType
low complexity region 3 31 N/A INTRINSIC
low complexity region 41 60 N/A INTRINSIC
Pfam:ADH_N 89 157 8.8e-11 PFAM
Pfam:ADH_zinc_N 213 355 2.1e-21 PFAM
Pfam:ADH_zinc_N_2 245 398 6.9e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134980
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153185
Meta Mutation Damage Score 0.1630 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.0%
Validation Efficiency 98% (123/126)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Rho GTPase family, whose members play a key role in the regulation of actin cytoskeleton organization in response to extracellular growth factors. This particular family member has been implicated in the regulation of neuronal morphology and endosomal trafficking. The gene localizes to chromosome 17 and is the centromeric neighbor of the breast-ovarian cancer susceptibility gene BRCA1. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 107 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A G 3: 137,771,437 (GRCm39) T209A probably benign Het
1700086D15Rik T C 11: 65,043,441 (GRCm39) probably benign Het
A130010J15Rik G A 1: 192,856,965 (GRCm39) V106I probably benign Het
Abca16 C A 7: 120,074,702 (GRCm39) N580K possibly damaging Het
Actrt2 A T 4: 154,751,344 (GRCm39) F264Y probably damaging Het
Adh4 G A 3: 138,134,807 (GRCm39) S327N possibly damaging Het
Alkbh5 T C 11: 60,444,697 (GRCm39) probably null Het
Anapc1 T A 2: 128,470,610 (GRCm39) T1507S possibly damaging Het
Anapc2 A G 2: 25,167,764 (GRCm39) R444G probably damaging Het
Apoh G T 11: 108,305,087 (GRCm39) W335L probably benign Het
B4galt7 A T 13: 55,752,162 (GRCm39) H71L possibly damaging Het
Bicd2 A G 13: 49,532,488 (GRCm39) E358G probably damaging Het
Bmper T A 9: 23,134,956 (GRCm39) V7D possibly damaging Het
Brca2 T C 5: 150,463,200 (GRCm39) F988S probably damaging Het
Brix1 A G 15: 10,485,828 (GRCm39) V49A possibly damaging Het
Brpf3 T C 17: 29,025,460 (GRCm39) S178P probably benign Het
Btaf1 A G 19: 36,958,448 (GRCm39) Y655C possibly damaging Het
C1rl C G 6: 124,486,040 (GRCm39) Y470* probably null Het
Cacnb4 A G 2: 52,565,822 (GRCm39) V21A probably benign Het
Caskin1 C A 17: 24,720,103 (GRCm39) P437T probably benign Het
Casz1 C A 4: 149,029,028 (GRCm39) P1158T probably damaging Het
Ccdc141 T A 2: 76,954,680 (GRCm39) Q189L probably damaging Het
Ccr3 T C 9: 123,828,809 (GRCm39) V48A probably damaging Het
Cebpd G A 16: 15,705,978 (GRCm39) G264S probably benign Het
Cert1 C T 13: 96,752,995 (GRCm39) P350S probably benign Het
Cfap20dc A T 14: 8,665,997 (GRCm38) M1K probably null Het
Chd1 C A 17: 15,953,386 (GRCm39) S440R probably damaging Het
Clip1 T A 5: 123,769,086 (GRCm39) E504D probably damaging Het
Cmya5 T C 13: 93,230,082 (GRCm39) R1669G probably benign Het
Col11a2 T A 17: 34,269,937 (GRCm39) F456I probably damaging Het
Ctnna2 A T 6: 76,957,764 (GRCm39) M130K probably damaging Het
Elmo2 A T 2: 165,133,922 (GRCm39) probably benign Het
F11 T C 8: 45,708,379 (GRCm39) D27G probably damaging Het
Faap100 A T 11: 120,266,412 (GRCm39) probably null Het
Fat1 A G 8: 45,442,151 (GRCm39) E1151G probably damaging Het
Fbll1 T A 11: 35,688,652 (GRCm39) I204F probably damaging Het
Gle1 T A 2: 29,830,215 (GRCm39) V257D possibly damaging Het
Hoxc9 T A 15: 102,890,225 (GRCm39) C47* probably null Het
Hsd17b6 A G 10: 127,829,524 (GRCm39) V226A probably benign Het
Hsd17b7 C T 1: 169,788,764 (GRCm39) R151Q probably benign Het
Hsh2d G A 8: 72,954,304 (GRCm39) D229N probably benign Het
Ido2 A G 8: 25,023,875 (GRCm39) I321T probably benign Het
Irf2bp2 T C 8: 127,318,172 (GRCm39) T465A probably benign Het
Kdm2a A G 19: 4,412,815 (GRCm39) M34T probably damaging Het
Klhl6 C T 16: 19,775,778 (GRCm39) R260H probably damaging Het
Kntc1 T A 5: 123,928,196 (GRCm39) L1231* probably null Het
Lca5l A C 16: 95,963,229 (GRCm39) Y412* probably null Het
Lipt1 T C 1: 37,914,513 (GRCm39) S190P possibly damaging Het
Ly6f T A 15: 75,143,569 (GRCm39) V92D probably damaging Het
Matn4 T A 2: 164,235,151 (GRCm39) M433L probably benign Het
Mbtd1 C A 11: 93,816,528 (GRCm39) P370T probably benign Het
Mcph1 T A 8: 18,682,703 (GRCm39) probably null Het
Muc5b T A 7: 141,417,922 (GRCm39) C3623S probably damaging Het
Myt1l C A 12: 29,899,399 (GRCm39) H134N probably benign Het
Nav2 A T 7: 49,058,749 (GRCm39) probably benign Het
Ndufaf8 T C 11: 119,989,992 (GRCm39) C35R probably damaging Het
Neb G A 2: 52,094,891 (GRCm39) T5130I possibly damaging Het
Nlrp9c T C 7: 26,079,989 (GRCm39) N624S possibly damaging Het
Nr0b2 C A 4: 133,283,334 (GRCm39) H190Q probably damaging Het
Nrg4 A G 9: 55,156,405 (GRCm39) probably benign Het
Nup88 A T 11: 70,852,450 (GRCm39) V215E probably benign Het
Oas2 T G 5: 120,876,411 (GRCm39) T511P probably benign Het
Or1e25 A G 11: 73,493,426 (GRCm39) T7A possibly damaging Het
Or2t6 A G 14: 14,175,885 (GRCm38) S66P probably damaging Het
Or5d14 A C 2: 87,880,432 (GRCm39) F179V probably damaging Het
Or5w8 T C 2: 87,687,621 (GRCm39) V34A probably benign Het
Or8g26 A G 9: 39,095,501 (GRCm39) N9S probably benign Het
Or9q1 A C 19: 13,805,718 (GRCm39) L14R probably damaging Het
Pcdhgb2 T A 18: 37,823,502 (GRCm39) N164K probably damaging Het
Pde4d C G 13: 109,253,400 (GRCm39) P76A probably benign Het
Phlda1 T C 10: 111,343,516 (GRCm39) probably benign Het
Plekhh1 A G 12: 79,101,577 (GRCm39) T216A probably benign Het
Plppr3 T A 10: 79,701,507 (GRCm39) E445V possibly damaging Het
Prom1 A G 5: 44,191,732 (GRCm39) V337A probably damaging Het
Prr14l T C 5: 33,001,743 (GRCm39) probably benign Het
Psmd1 A G 1: 86,064,820 (GRCm39) I951V probably benign Het
Rab35 T G 5: 115,781,454 (GRCm39) I85M possibly damaging Het
Rad9a A T 19: 4,250,536 (GRCm39) S93T probably benign Het
Ric1 G A 19: 29,563,242 (GRCm39) C555Y probably damaging Het
Ror2 T A 13: 53,264,719 (GRCm39) Q791L probably benign Het
Rps8 G C 4: 117,012,352 (GRCm39) probably benign Het
Sdr16c5 C T 4: 4,016,216 (GRCm39) W70* probably null Het
Senp3 A G 11: 69,568,821 (GRCm39) V408A probably benign Het
Sh2d4b C A 14: 40,562,301 (GRCm39) W288L probably benign Het
Slc38a9 A T 13: 112,859,832 (GRCm39) D422V probably damaging Het
Slc4a2 T C 5: 24,645,141 (GRCm39) F1104L probably damaging Het
Slc4a3 A G 1: 75,527,267 (GRCm39) K113E possibly damaging Het
Spata3 G A 1: 85,952,048 (GRCm39) probably null Het
Spata31d1d A T 13: 59,877,055 (GRCm39) V160E possibly damaging Het
Sprr2f A G 3: 92,273,203 (GRCm39) M1V probably null Het
Sptbn1 A G 11: 30,068,295 (GRCm39) V1733A possibly damaging Het
Syce1 C A 7: 140,359,809 (GRCm39) L83F probably damaging Het
Tardbp A G 4: 148,702,050 (GRCm39) I295T probably benign Het
Tmem212 A G 3: 27,939,157 (GRCm39) S110P probably damaging Het
Tnc G A 4: 63,935,857 (GRCm39) Q360* probably null Het
Tnrc6c C A 11: 117,613,731 (GRCm39) Q630K probably damaging Het
Ttc19 G A 11: 62,199,922 (GRCm39) R235H probably benign Het
Ube3b T A 5: 114,553,787 (GRCm39) probably null Het
Vmn2r31 C T 7: 7,390,062 (GRCm39) probably null Het
Vmn2r92 T A 17: 18,372,183 (GRCm39) probably benign Het
Washc5 A T 15: 59,205,485 (GRCm39) Y685* probably null Het
Wdr93 T A 7: 79,399,817 (GRCm39) Y135* probably null Het
Wdr95 T A 5: 149,518,797 (GRCm39) I546K probably damaging Het
Zbtb38 T A 9: 96,570,254 (GRCm39) T277S probably benign Het
Zfp13 T C 17: 23,795,797 (GRCm39) D258G possibly damaging Het
Zfp397 T A 18: 24,093,249 (GRCm39) S245T probably benign Het
Zfp646 T C 7: 127,482,907 (GRCm39) Y1695H probably benign Het
Other mutations in Rnd2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00596:Rnd2 APN 11 101,362,017 (GRCm39) missense possibly damaging 0.81
IGL01964:Rnd2 APN 11 101,361,632 (GRCm39) splice site probably null
Atkins UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R1581:Rnd2 UTSW 11 101,362,022 (GRCm39) missense probably benign
R4606:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R4797:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R4825:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R4931:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5005:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5078:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5079:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5402:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5405:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5497:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5498:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5501:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5534:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5619:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5666:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5669:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5670:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5671:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5786:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5788:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5844:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5845:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5857:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5989:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5991:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R5992:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6018:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6019:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6020:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6122:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6144:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6148:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6208:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6209:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6226:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6230:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6332:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6333:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6335:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6491:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6541:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6605:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6606:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6607:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6677:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6678:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6726:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6796:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R6797:Rnd2 UTSW 11 101,359,825 (GRCm39) missense probably damaging 1.00
R8415:Rnd2 UTSW 11 101,362,011 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CTTCTGTCTAGGGACTGAGCTG -3'
(R):5'- GCCGATATTAGACTTCCTACGTG -3'

Sequencing Primer
(F):5'- TCTAGGGACTGAGCTGGACCG -3'
(R):5'- GGTTTCTGTCAGGCCTAAGAAACTC -3'
Posted On 2016-03-01