Incidental Mutation 'R3829:Ralb'
ID273870
Institutional Source Beutler Lab
Gene Symbol Ralb
Ensembl Gene ENSMUSG00000004451
Gene Namev-ral simian leukemia viral oncogene B
Synonyms5730472O18Rik
MMRRC Submission 040776-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R3829 (G1)
Quality Score225
Status Validated
Chromosome1
Chromosomal Location119470305-119504794 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 119471717 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Serine at position 204 (C204S)
Ref Sequence ENSEMBL: ENSMUSP00000004565 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000004565]
Predicted Effect probably benign
Transcript: ENSMUST00000004565
AA Change: C204S

PolyPhen 2 Score 0.041 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000004565
Gene: ENSMUSG00000004451
AA Change: C204S

DomainStartEndE-ValueType
RAS 12 179 1.83e-95 SMART
low complexity region 191 198 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000142945
SMART Domains Protein: ENSMUSP00000119849
Gene: ENSMUSG00000004451

DomainStartEndE-ValueType
small_GTPase 2 127 1.15e-37 SMART
Meta Mutation Damage Score 0.0816 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.7%
  • 20x: 96.1%
Validation Efficiency 100% (54/54)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a GTP-binding protein that belongs to the small GTPase superfamily and Ras family of proteins. GTP-binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit no obvious abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931414P19Rik G T 14: 54,584,509 H466Q probably damaging Het
4933411K16Rik A T 19: 42,052,883 H151L probably damaging Het
A330008L17Rik A G 8: 99,421,757 noncoding transcript Het
Abcc5 C A 16: 20,365,865 V1015L probably benign Het
Bach2 T A 4: 32,563,150 L539H probably damaging Het
Birc6 A G 17: 74,655,178 K3929R probably damaging Het
C1qtnf2 A G 11: 43,491,321 D320G probably benign Het
Cbr2 A T 11: 120,730,452 H140Q probably benign Het
Cbs T C 17: 31,617,381 probably benign Het
Cdc42bpg T C 19: 6,317,645 V1015A probably damaging Het
Cep104 T G 4: 153,984,943 M207R probably damaging Het
Chil6 A T 3: 106,405,958 M25K probably benign Het
Cln5 A G 14: 103,073,359 D154G probably damaging Het
Col4a1 C A 8: 11,209,650 G1341V probably damaging Het
Commd9 C A 2: 101,897,141 N93K probably benign Het
Cx3cl1 A T 8: 94,777,306 probably benign Het
Cyct T C 2: 76,354,168 K80E probably damaging Het
Dhx37 T C 5: 125,431,613 K86R probably benign Het
Dnah17 G A 11: 118,041,158 probably benign Het
Etl4 T C 2: 20,785,421 V628A probably benign Het
Fam234a T C 17: 26,218,189 E172G probably benign Het
Foxp2 C T 6: 15,379,831 probably benign Het
Frem1 A T 4: 82,998,930 F592Y probably damaging Het
Gm10259 T G 3: 25,212,529 noncoding transcript Het
Gm17521 C A X: 123,029,225 G149C unknown Het
Gpat4 G A 8: 23,180,155 P286L probably damaging Het
Grpel1 T A 5: 36,469,483 N36K probably benign Het
Hap1 G T 11: 100,356,021 D19E probably damaging Het
Lpcat1 T C 13: 73,489,093 I114T possibly damaging Het
Mast4 G T 13: 102,738,811 H1350N probably damaging Het
Mrpl50 T C 4: 49,514,539 E44G probably damaging Het
Myg1 G C 15: 102,337,736 G349R probably damaging Het
Myh1 A G 11: 67,205,597 I301V probably benign Het
Ncapg2 A T 12: 116,407,318 probably benign Het
Ncor2 T C 5: 125,118,692 probably benign Het
Neo1 A G 9: 58,913,169 Y824H possibly damaging Het
Olfr99 T A 17: 37,280,249 Y57F probably damaging Het
Orc1 T A 4: 108,605,631 M635K probably damaging Het
Phip A G 9: 82,871,645 I1682T probably benign Het
Ppp2r1b A G 9: 50,862,494 N223S probably benign Het
Rgs12 G A 5: 34,966,015 V381M possibly damaging Het
Rsg1 C T 4: 141,218,589 R148C probably damaging Het
Rtkn2 A T 10: 67,997,626 probably null Het
Srrm3 A G 5: 135,857,214 D336G probably damaging Het
Stk11 T C 10: 80,127,948 probably null Het
Svep1 A G 4: 58,096,177 L1481P probably damaging Het
Tiam2 C G 17: 3,507,701 probably benign Het
Tmem59l A G 8: 70,487,301 L6S unknown Het
Tmprss11b T C 5: 86,661,590 T348A probably damaging Het
Ube3b C A 5: 114,399,951 Q368K probably damaging Het
Veph1 T A 3: 66,159,327 E413D possibly damaging Het
Vmn2r91 T G 17: 18,105,497 W126G probably damaging Het
Yrdc T A 4: 124,851,761 M1K probably null Het
Zfp445 T C 9: 122,853,077 M600V probably benign Het
Other mutations in Ralb
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00227:Ralb APN 1 119476040 missense probably benign 0.26
IGL00927:Ralb APN 1 119471776 missense probably benign 0.00
IGL01607:Ralb APN 1 119483549 missense probably damaging 0.96
IGL01805:Ralb APN 1 119475995 missense probably benign 0.03
IGL02330:Ralb APN 1 119471720 missense probably damaging 0.98
R0393:Ralb UTSW 1 119478126 splice site probably null
R1616:Ralb UTSW 1 119478014 missense probably damaging 1.00
R1854:Ralb UTSW 1 119476067 missense possibly damaging 0.94
R4097:Ralb UTSW 1 119483498 missense probably benign 0.03
R4352:Ralb UTSW 1 119483552 missense probably benign 0.09
R4854:Ralb UTSW 1 119475915 missense probably benign 0.12
R5567:Ralb UTSW 1 119483535 missense probably damaging 1.00
R5683:Ralb UTSW 1 119475956 missense possibly damaging 0.86
R6153:Ralb UTSW 1 119478140 unclassified probably null
R6358:Ralb UTSW 1 119476005 missense probably damaging 1.00
R6408:Ralb UTSW 1 119478109 nonsense probably null
R6816:Ralb UTSW 1 119477982 nonsense probably null
R7371:Ralb UTSW 1 119472399 missense
Predicted Primers PCR Primer
(F):5'- AGGGCAGACTCTCAAAGCTC -3'
(R):5'- CTGTACATAAGAGTTGAGTGCAC -3'

Sequencing Primer
(F):5'- ACAGACAAAGGCGTCTTTCTTCTG -3'
(R):5'- TAAGAGTTGAGTGCACCCCAC -3'
Posted On2015-04-02