Incidental Mutation 'R4433:Rhob'
ID328714
Institutional Source Beutler Lab
Gene Symbol Rhob
Ensembl Gene ENSMUSG00000054364
Gene Nameras homolog family member B
SynonymsArhb
MMRRC Submission 041147-MU
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.418) question?
Stock #R4433 (G1)
Quality Score225
Status Validated
Chromosome12
Chromosomal Location8497661-8500009 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 8499533 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Histidine at position 34 (Y34H)
Ref Sequence ENSEMBL: ENSMUSP00000067013 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067384]
Predicted Effect possibly damaging
Transcript: ENSMUST00000067384
AA Change: Y34H

PolyPhen 2 Score 0.728 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000067013
Gene: ENSMUSG00000054364
AA Change: Y34H

DomainStartEndE-ValueType
RHO 8 181 1.13e-127 SMART
Meta Mutation Damage Score 0.7659 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.7%
Validation Efficiency 98% (59/60)
MGI Phenotype PHENOTYPE: Homozygous mutation of this gene results in increased incidence of DMBA-induced skin tumors. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc5 A T 16: 20,368,187 probably null Het
Acsm2 A G 7: 119,554,509 H14R unknown Het
Adamtsl4 T C 3: 95,681,759 probably null Het
Ak5 A G 3: 152,655,880 I135T probably damaging Het
Alk G T 17: 71,899,241 S1038* probably null Het
Ank2 A T 3: 126,947,806 probably benign Het
Ap2m1 A T 16: 20,543,384 H414L possibly damaging Het
Atp13a5 A T 16: 29,282,024 M649K probably damaging Het
Atp4a G A 7: 30,720,225 R671Q probably benign Het
Cdc25b A G 2: 131,191,698 S186G probably benign Het
Ceacam16 A G 7: 19,853,589 V418A possibly damaging Het
Cntnap3 A C 13: 64,778,853 S568A possibly damaging Het
Col24a1 G T 3: 145,314,383 V172F possibly damaging Het
E430018J23Rik T G 7: 127,393,002 Q87P possibly damaging Het
Eef2 CCC CCCC 10: 81,178,768 probably null Het
Esp36 T A 17: 38,418,956 T15S unknown Het
Fam126a A C 5: 23,979,581 C218G possibly damaging Het
Fam26f T A 10: 34,127,831 T27S probably damaging Het
Fat2 A T 11: 55,309,640 H869Q possibly damaging Het
Fat3 A G 9: 16,031,152 V1308A probably damaging Het
Gimap3 T C 6: 48,765,946 T17A possibly damaging Het
Hnrnpr A G 4: 136,317,148 K13R probably benign Het
Kdr A G 5: 75,943,925 M1133T possibly damaging Het
Mgarp A G 3: 51,396,260 probably benign Het
Neto2 G A 8: 85,641,083 T337I probably damaging Het
Nfib C T 4: 82,498,435 R137Q probably damaging Het
Nr3c2 A G 8: 77,217,467 E890G probably damaging Het
Nsun4 A G 4: 116,040,130 V228A possibly damaging Het
Nt5c1a T A 4: 123,215,896 S263T probably benign Het
Ntm A T 9: 29,012,220 Y45* probably null Het
Nts A G 10: 102,485,027 V67A probably benign Het
Olfr1288 T A 2: 111,479,412 C209* probably null Het
Olfr378 A T 11: 73,425,711 S91T possibly damaging Het
Olfr384 A G 11: 73,602,886 Y102C probably damaging Het
Olfr610 T A 7: 103,506,139 K269M probably benign Het
Ostm1 C A 10: 42,679,123 A47E probably benign Het
Otol1 G A 3: 70,018,548 V19M probably benign Het
Pcdhb15 A G 18: 37,475,512 N599S probably damaging Het
Pcdhgb1 T C 18: 37,681,251 I265T probably damaging Het
Pdzd3 T C 9: 44,247,988 *499W probably null Het
Pex14 T C 4: 148,961,510 E321G possibly damaging Het
Phactr3 C A 2: 178,283,132 R251S probably damaging Het
Pkdcc C T 17: 83,221,141 T313M probably benign Het
Plce1 A T 19: 38,767,301 E1911V probably damaging Het
Ptprv G T 1: 135,114,570 noncoding transcript Het
Rab36 G A 10: 75,044,496 V63I probably damaging Het
Slc27a3 G A 3: 90,387,340 T408M probably damaging Het
Slc9c1 A T 16: 45,599,466 I1000F possibly damaging Het
Tcf7 G T 11: 52,261,615 P36T probably benign Het
Tcf7l1 C G 6: 72,788,769 E62Q probably damaging Het
Tctex1d4 C T 4: 117,128,123 R48C probably damaging Het
Tll2 A G 19: 41,121,348 S326P probably benign Het
Tubgcp4 A G 2: 121,184,473 N288S probably benign Het
Zfhx3 G A 8: 108,955,637 R3236H unknown Het
Zgrf1 A G 3: 127,562,078 T318A probably benign Het
Other mutations in Rhob
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0084:Rhob UTSW 12 8499107 missense probably benign 0.39
R1442:Rhob UTSW 12 8499325 missense possibly damaging 0.76
R1484:Rhob UTSW 12 8499388 missense probably damaging 0.97
R2071:Rhob UTSW 12 8499232 missense probably benign 0.00
R4569:Rhob UTSW 12 8499373 missense probably damaging 0.97
R5263:Rhob UTSW 12 8499232 missense probably benign
R6478:Rhob UTSW 12 8499585 nonsense probably null
Z1176:Rhob UTSW 12 8499326 missense not run
Predicted Primers PCR Primer
(F):5'- TGTTGGCCACCAGGATGATG -3'
(R):5'- ACACTCAGTGCACCGTATG -3'

Sequencing Primer
(F):5'- AGAAGTGCTTTACCTCGGGC -3'
(R):5'- AGTTAGCGAGCCTAGCCC -3'
Posted On2015-07-21