Incidental Mutation 'R1126:Rem1'
ID 96134
Institutional Source Beutler Lab
Gene Symbol Rem1
Ensembl Gene ENSMUSG00000000359
Gene Name rad and gem related GTP binding protein 1
Synonyms E030011C07Rik
MMRRC Submission 039199-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R1126 (G1)
Quality Score 148
Status Not validated
Chromosome 2
Chromosomal Location 152468928-152477111 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 152476455 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Methionine at position 238 (V238M)
Ref Sequence ENSEMBL: ENSMUSP00000000369 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000369]
AlphaFold O35929
Predicted Effect probably damaging
Transcript: ENSMUST00000000369
AA Change: V238M

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000000369
Gene: ENSMUSG00000000359
AA Change: V238M

DomainStartEndE-ValueType
low complexity region 64 77 N/A INTRINSIC
Pfam:Roc 82 198 1e-10 PFAM
Pfam:Ras 82 244 2.6e-32 PFAM
low complexity region 258 290 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139370
Meta Mutation Damage Score 0.2146 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a GTPase and member of the RAS-like GTP-binding protein family. The encoded protein is expressed in endothelial cells, where it promotes reorganization of the actin cytoskeleton and morphological changes in the cells. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 T C 7: 45,759,062 (GRCm39) E1226G probably damaging Het
Arhgef40 G T 14: 52,234,583 (GRCm39) S962I probably damaging Het
Atp9b A T 18: 80,822,169 (GRCm39) M477K probably damaging Het
Enpp2 C T 15: 54,770,222 (GRCm39) probably null Het
Ephb3 T A 16: 21,041,226 (GRCm39) M727K possibly damaging Het
Exo5 A T 4: 120,779,322 (GRCm39) I181N probably damaging Het
Fbn1 T C 2: 125,163,112 (GRCm39) probably null Het
Gas6 T C 8: 13,533,700 (GRCm39) N103S probably benign Het
Gm11596 A T 11: 99,683,699 (GRCm39) C140* probably null Het
Il6st T C 13: 112,640,266 (GRCm39) Y681H probably damaging Het
Itih4 T C 14: 30,611,918 (GRCm39) probably null Het
Kdm5b C T 1: 134,541,729 (GRCm39) A768V possibly damaging Het
Krt87 A T 15: 101,385,363 (GRCm39) N336K probably damaging Het
Mfsd6 A G 1: 52,748,670 (GRCm39) V65A probably benign Het
Nipsnap1 A G 11: 4,834,081 (GRCm39) N90S probably benign Het
Nlrp9a C A 7: 26,260,166 (GRCm39) D640E probably benign Het
Or11h4b C T 14: 50,918,720 (GRCm39) A124T possibly damaging Het
Or1l4 A T 2: 37,092,113 (GRCm39) M287L probably benign Het
Or2j3 A G 17: 38,615,579 (GRCm39) C258R probably damaging Het
Or5p53 A C 7: 107,533,578 (GRCm39) M284L possibly damaging Het
Parp9 G A 16: 35,768,110 (GRCm39) V97I possibly damaging Het
Pdzd2 T C 15: 12,458,306 (GRCm39) T12A possibly damaging Het
Penk T C 4: 4,138,119 (GRCm39) T9A probably benign Het
Pilrb2 T C 5: 137,869,222 (GRCm39) D126G probably damaging Het
Pkdrej A T 15: 85,700,515 (GRCm39) V1807E probably damaging Het
Ppp1r9a A G 6: 4,906,795 (GRCm39) E450G possibly damaging Het
Rag1 T C 2: 101,473,034 (GRCm39) R703G probably damaging Het
Rmdn3 T C 2: 118,984,476 (GRCm39) D92G probably benign Het
Rp1l1 G A 14: 64,267,918 (GRCm39) G1168D probably damaging Het
Saxo1 T A 4: 86,397,224 (GRCm39) T105S probably benign Het
Slc39a2 G A 14: 52,131,602 (GRCm39) G58R probably damaging Het
Tbx6 C T 7: 126,383,891 (GRCm39) T315I probably damaging Het
Tcf12 A G 9: 71,907,715 (GRCm39) M99T probably benign Het
Tdrd3 A G 14: 87,718,210 (GRCm39) D197G probably damaging Het
Tnc T C 4: 63,936,357 (GRCm39) N193S probably damaging Het
Ttn A G 2: 76,680,347 (GRCm39) probably benign Het
Vmn1r225 A G 17: 20,722,588 (GRCm39) I10V probably benign Het
Zp3r A G 1: 130,546,079 (GRCm39) L77P probably damaging Het
Other mutations in Rem1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1121:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1122:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1233:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1235:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1378:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1709:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1713:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1911:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R1912:Rem1 UTSW 2 152,476,455 (GRCm39) missense probably damaging 0.96
R5442:Rem1 UTSW 2 152,469,977 (GRCm39) critical splice acceptor site probably null
R5853:Rem1 UTSW 2 152,470,200 (GRCm39) missense possibly damaging 0.92
R6062:Rem1 UTSW 2 152,470,017 (GRCm39) start codon destroyed probably null 1.00
R6072:Rem1 UTSW 2 152,476,437 (GRCm39) missense probably benign
R7215:Rem1 UTSW 2 152,470,069 (GRCm39) missense probably damaging 1.00
R7635:Rem1 UTSW 2 152,476,585 (GRCm39) missense probably damaging 1.00
R9276:Rem1 UTSW 2 152,469,969 (GRCm39) splice site probably benign
X0057:Rem1 UTSW 2 152,471,111 (GRCm39) missense probably benign 0.32
Predicted Primers PCR Primer
(F):5'- TGCTTCCTGAGAGTTTGAACACA -3'
(R):5'- CTTTTCTCCTCAGTGGCACCATA -3'

Sequencing Primer
(F):5'- CATCTCTTCCCACCTTTATC -3'
(R):5'- ATAGTGTCCCATCACCCCAG -3'
Posted On 2014-01-05