Incidental Mutation 'R0502:Rerg'
ID47195
Institutional Source Beutler Lab
Gene Symbol Rerg
Ensembl Gene ENSMUSG00000030222
Gene NameRAS-like, estrogen-regulated, growth-inhibitor
Synonyms
MMRRC Submission 038697-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.120) question?
Stock #R0502 (G1)
Quality Score225
Status Validated
Chromosome6
Chromosomal Location137054825-137170497 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 137056307 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Stop codon at position 123 (C123*)
Ref Sequence ENSEMBL: ENSMUSP00000113702 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032347] [ENSMUST00000117919] [ENSMUST00000119610] [ENSMUST00000203003]
Predicted Effect probably null
Transcript: ENSMUST00000032347
AA Change: C142*
SMART Domains Protein: ENSMUSP00000032347
Gene: ENSMUSG00000030222
AA Change: C142*

DomainStartEndE-ValueType
RAS 4 170 7.2e-71 SMART
Predicted Effect probably null
Transcript: ENSMUST00000117919
AA Change: C142*
SMART Domains Protein: ENSMUSP00000113105
Gene: ENSMUSG00000030222
AA Change: C142*

DomainStartEndE-ValueType
RAS 4 170 7.2e-71 SMART
Predicted Effect probably null
Transcript: ENSMUST00000119610
AA Change: C123*
SMART Domains Protein: ENSMUSP00000113702
Gene: ENSMUSG00000030222
AA Change: C123*

DomainStartEndE-ValueType
RAS 4 151 8.5e-50 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000203003
SMART Domains Protein: ENSMUSP00000144823
Gene: ENSMUSG00000030222

DomainStartEndE-ValueType
Pfam:Ras 1 59 3.4e-9 PFAM
Meta Mutation Damage Score 0.644 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 94.7%
Validation Efficiency 100% (63/63)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] RERG, a member of the RAS superfamily of GTPases, inhibits cell proliferation and tumor formation (Finlin et al., 2001 [PubMed 11533059]).[supplied by OMIM, Mar 2009]
Allele List at MGI
Other mutations in this stock
Total: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930111J21Rik1 T C 11: 48,947,495 H755R possibly damaging Het
Ano1 A G 7: 144,597,215 L821P probably damaging Het
Apol10b T A 15: 77,592,149 probably benign Het
Atp2c2 A G 8: 119,734,577 E279G probably null Het
Ccar2 A G 14: 70,140,982 S625P probably benign Het
Ccdc110 A G 8: 45,934,724 probably benign Het
Cep350 A T 1: 155,900,883 probably null Het
Chd3 A G 11: 69,354,105 V1203A probably damaging Het
Col24a1 A G 3: 145,545,316 probably benign Het
Col6a6 A T 9: 105,767,351 M1246K probably benign Het
Crot A G 5: 8,976,075 V304A possibly damaging Het
D10Wsu102e A G 10: 83,362,056 D42G probably damaging Het
Dapk1 T A 13: 60,730,848 probably null Het
Dicer1 A T 12: 104,705,060 S984T probably damaging Het
Diexf A T 1: 193,114,828 probably benign Het
Dmbt1 G A 7: 131,097,673 probably null Het
Dnah7b A T 1: 46,219,544 E1965V probably damaging Het
Dpp4 G T 2: 62,364,988 N315K probably damaging Het
Fam102b G A 3: 108,992,685 R116C probably damaging Het
Fat4 T A 3: 39,002,924 S4256R probably damaging Het
Fcho1 C T 8: 71,712,560 A418T probably benign Het
Gpatch4 A G 3: 88,055,365 D295G probably benign Het
Gpbar1 A T 1: 74,279,392 I265F probably benign Het
Gria1 T G 11: 57,189,716 V175G probably damaging Het
Hacl1 A T 14: 31,622,984 probably benign Het
Hnrnpc A G 14: 52,075,172 probably benign Het
Hoxa13 CCG CCGCG 6: 52,260,635 probably null Het
Ifnar1 T A 16: 91,501,751 C419S probably damaging Het
Irx4 T A 13: 73,266,584 probably null Het
Itga2 T G 13: 114,845,856 N1038H probably benign Het
Kif16b C T 2: 142,712,155 D908N probably benign Het
Lamc1 A G 1: 153,246,932 probably benign Het
Lrig3 A G 10: 126,008,736 T690A probably damaging Het
Lrp2 T C 2: 69,511,017 K940E probably damaging Het
Macf1 A G 4: 123,469,815 S1775P probably damaging Het
Mrps27 G T 13: 99,409,795 probably benign Het
Ncam1 A G 9: 49,569,818 probably benign Het
Olfr30 T C 11: 58,455,314 I212V possibly damaging Het
Olfr586 A T 7: 103,122,436 M112K possibly damaging Het
Pbrm1 T G 14: 31,064,820 D631E probably benign Het
Pdc A T 1: 150,328,414 probably benign Het
Pkd1 T C 17: 24,574,792 S1818P probably damaging Het
Ptpru T C 4: 131,793,643 N784S probably benign Het
Rab35 G A 5: 115,645,664 R170Q probably benign Het
Ros1 A G 10: 52,194,823 probably benign Het
Siglece A G 7: 43,659,931 Y68H probably damaging Het
Slc28a2 T A 2: 122,458,281 probably null Het
Slc4a11 T C 2: 130,688,157 K234E probably damaging Het
Sqor C T 2: 122,798,050 P158S probably benign Het
Tcerg1 C T 18: 42,522,956 P110S unknown Het
Tm6sf2 T A 8: 70,077,941 Y224N probably damaging Het
Tmem39b A C 4: 129,686,986 Y238D possibly damaging Het
Ttll10 T C 4: 156,047,548 probably benign Het
Ubap2l A T 3: 90,009,213 L898Q probably damaging Het
Uggt1 A T 1: 36,159,946 V1207E probably damaging Het
Uhrf2 A G 19: 30,092,776 D775G probably damaging Het
Vmn1r196 G A 13: 22,293,387 M65I probably benign Het
Vmn1r87 T G 7: 13,131,656 T235P probably damaging Het
Vmn2r96 T A 17: 18,584,000 M504K probably benign Het
Zdbf2 A T 1: 63,305,290 I943F possibly damaging Het
Zfp78 A G 7: 6,373,158 D22G probably damaging Het
Zfp827 C T 8: 79,179,077 probably null Het
Zfyve9 A T 4: 108,719,764 L40* probably null Het
Other mutations in Rerg
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01799:Rerg APN 6 137056378 nonsense probably null
R1370:Rerg UTSW 6 137057801 splice site probably benign
R2056:Rerg UTSW 6 137057880 missense probably benign 0.00
R4919:Rerg UTSW 6 137056144 missense probably damaging 0.99
R6651:Rerg UTSW 6 137056386 missense probably damaging 1.00
R7089:Rerg UTSW 6 137067035 missense possibly damaging 0.84
Predicted Primers PCR Primer
(F):5'- AGCACATTTCGGCAAGACCTCTAAC -3'
(R):5'- CGTTCATCCAGGAAGACAGCCAAG -3'

Sequencing Primer
(F):5'- ATTTCGGCAAGACCTCTAACTACTG -3'
(R):5'- TTCTTTGCCCACAGGAAGAC -3'
Posted On2013-06-12