Incidental Mutation 'R2873:Ralgds'
ID 260378
Institutional Source Beutler Lab
Gene Symbol Ralgds
Ensembl Gene ENSMUSG00000026821
Gene Name ral guanine nucleotide dissociation stimulator
Synonyms RalGDS, Rgds, Gnds
MMRRC Submission 040461-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.148) question?
Stock # R2873 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 28403137-28443093 bp(+) (GRCm39)
Type of Mutation splice site (4 bp from exon)
DNA Base Change (assembly) A to G at 28438781 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000109526 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028170] [ENSMUST00000100241] [ENSMUST00000113893] [ENSMUST00000140704]
AlphaFold Q03385
Predicted Effect probably null
Transcript: ENSMUST00000028170
SMART Domains Protein: ENSMUSP00000028170
Gene: ENSMUSG00000026821

DomainStartEndE-ValueType
RasGEFN 56 194 4.02e-37 SMART
low complexity region 239 285 N/A INTRINSIC
RasGEF 320 587 5.28e-118 SMART
low complexity region 613 626 N/A INTRINSIC
low complexity region 646 655 N/A INTRINSIC
low complexity region 683 712 N/A INTRINSIC
low complexity region 716 726 N/A INTRINSIC
RA 736 823 6.51e-22 SMART
Predicted Effect probably null
Transcript: ENSMUST00000100241
SMART Domains Protein: ENSMUSP00000097812
Gene: ENSMUSG00000026821

DomainStartEndE-ValueType
RasGEFN 111 249 4.02e-37 SMART
low complexity region 294 340 N/A INTRINSIC
RasGEF 375 642 5.28e-118 SMART
low complexity region 668 681 N/A INTRINSIC
low complexity region 701 710 N/A INTRINSIC
low complexity region 738 767 N/A INTRINSIC
low complexity region 771 781 N/A INTRINSIC
RA 791 878 6.51e-22 SMART
Predicted Effect probably null
Transcript: ENSMUST00000113893
SMART Domains Protein: ENSMUSP00000109526
Gene: ENSMUSG00000026821

DomainStartEndE-ValueType
RasGEFN 111 237 1.25e-42 SMART
low complexity region 282 328 N/A INTRINSIC
RasGEF 363 630 5.28e-118 SMART
low complexity region 656 669 N/A INTRINSIC
low complexity region 689 698 N/A INTRINSIC
low complexity region 726 755 N/A INTRINSIC
low complexity region 759 769 N/A INTRINSIC
RA 779 866 6.51e-22 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128680
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130281
Predicted Effect probably benign
Transcript: ENSMUST00000137215
SMART Domains Protein: ENSMUSP00000116215
Gene: ENSMUSG00000026821

DomainStartEndE-ValueType
RasGEFN 1 107 5.55e-8 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137513
Predicted Effect probably benign
Transcript: ENSMUST00000140704
SMART Domains Protein: ENSMUSP00000118966
Gene: ENSMUSG00000026821

DomainStartEndE-ValueType
low complexity region 4 13 N/A INTRINSIC
RA 36 123 6.51e-22 SMART
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 100% (81/81)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Guanine nucleotide dissociation stimulators (GDSs, or exchange factors), such as RALGDS, are effectors of Ras-related GTPases (see MIM 190020) that participate in signaling for a variety of cellular processes.[supplied by OMIM, Nov 2010]
PHENOTYPE: Homozygous mutant mice exhibit reduced tumor incidence, size and progression to malignancy in multistage skin carcinogenesis. [provided by MGI curators]
Allele List at MGI

All alleles(16) : Targeted(5) Gene trapped(11)

Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b A G 11: 109,846,002 (GRCm39) C811R possibly damaging Het
Acvr1 G A 2: 58,367,808 (GRCm39) Q118* probably null Het
Als2 A G 1: 59,250,296 (GRCm39) S483P probably damaging Het
Ankrd40 T C 11: 94,224,771 (GRCm39) V60A possibly damaging Het
Armc2 C T 10: 41,842,696 (GRCm39) probably null Het
Atp12a A G 14: 56,624,407 (GRCm39) R952G possibly damaging Het
Atp13a2 T C 4: 140,730,294 (GRCm39) I773T probably benign Het
Atp6v1g1 A G 4: 63,468,258 (GRCm39) Y87C probably benign Het
Ccdc162 G T 10: 41,531,095 (GRCm39) T537N possibly damaging Het
Ccdc59 A T 10: 105,677,388 (GRCm39) K9M possibly damaging Het
Cd101 A T 3: 100,911,164 (GRCm39) D831E probably benign Het
Ch25h T A 19: 34,452,210 (GRCm39) H106L probably benign Het
Chek2 C A 5: 111,011,202 (GRCm39) Y333* probably null Het
Cimap1d G A 10: 79,481,487 (GRCm39) T14I probably benign Het
Csmd2 T C 4: 128,451,511 (GRCm39) F113S unknown Het
Cyp4a14 C A 4: 115,344,498 (GRCm39) G456W probably damaging Het
Cyp4a30b A G 4: 115,315,559 (GRCm39) H260R possibly damaging Het
Dennd2b A T 7: 109,156,637 (GRCm39) Y38N probably benign Het
Eif4enif1 C T 11: 3,192,586 (GRCm39) P805S probably damaging Het
Fan1 A G 7: 64,012,938 (GRCm39) I668T probably benign Het
Flnc A G 6: 29,447,542 (GRCm39) D1115G probably damaging Het
Ftdc1 A T 16: 58,434,342 (GRCm39) I125K probably benign Het
Gbp11 C T 5: 105,478,866 (GRCm39) D191N probably benign Het
Gm5519 A C 19: 33,802,410 (GRCm39) D151A possibly damaging Het
Grid2ip C A 5: 143,343,684 (GRCm39) Q127K probably benign Het
Hdhd2 T C 18: 77,042,702 (GRCm39) F44L probably damaging Het
Hmcn1 A T 1: 150,614,467 (GRCm39) V1313D possibly damaging Het
Kpna7 T C 5: 144,930,745 (GRCm39) T367A probably benign Het
Matr3 T A 18: 35,705,349 (GRCm39) S91R probably benign Het
Mdm1 A G 10: 117,986,847 (GRCm39) T267A probably benign Het
Mlxip A G 5: 123,590,730 (GRCm39) M878V probably benign Het
Mtor T A 4: 148,624,487 (GRCm39) M2089K probably benign Het
Myo9b G A 8: 71,786,981 (GRCm39) R721Q probably benign Het
Ndufs1 A G 1: 63,203,882 (GRCm39) probably benign Het
Nlrp4b C T 7: 10,444,170 (GRCm39) Q40* probably null Het
Nomo1 C A 7: 45,696,361 (GRCm39) T293N probably damaging Het
Notch1 A G 2: 26,350,247 (GRCm39) C2298R possibly damaging Het
Notum A G 11: 120,551,022 (GRCm39) V48A probably benign Het
Or10g1 T G 14: 52,648,318 (GRCm39) T4P probably benign Het
Or10z1 T C 1: 174,078,092 (GRCm39) S134G probably benign Het
Or6c211 A T 10: 129,505,628 (GRCm39) C253* probably null Het
Ostc T C 3: 130,497,157 (GRCm39) N80S probably damaging Het
Palmd T C 3: 116,717,400 (GRCm39) R366G possibly damaging Het
Parp1 A G 1: 180,401,230 (GRCm39) D45G probably damaging Het
Pcdhga9 T A 18: 37,870,524 (GRCm39) Y118N possibly damaging Het
Pes1 C A 11: 3,926,834 (GRCm39) T372K probably benign Het
Plcl1 A T 1: 55,736,309 (GRCm39) D550V probably benign Het
Plekhg5 T A 4: 152,191,960 (GRCm39) C433S probably benign Het
Plin2 A G 4: 86,586,915 (GRCm39) M1T probably null Het
Pms2 G A 5: 143,848,732 (GRCm39) probably benign Het
Ppp1r7 T A 1: 93,285,585 (GRCm39) probably null Het
Psmb8 T C 17: 34,419,144 (GRCm39) I146T probably damaging Het
Ptger4 T C 15: 5,264,286 (GRCm39) R457G probably benign Het
Pzp A T 6: 128,462,519 (GRCm39) probably null Het
Rnf6 T C 5: 146,147,215 (GRCm39) Y601C probably benign Het
Sgk2 A G 2: 162,836,449 (GRCm39) probably benign Het
Shoc1 A C 4: 59,093,850 (GRCm39) L226R probably damaging Het
Slc39a8 T A 3: 135,592,554 (GRCm39) probably null Het
Slc4a4 G T 5: 89,283,623 (GRCm39) V481L probably damaging Het
Slc5a8 A G 10: 88,740,825 (GRCm39) I247V probably benign Het
Slit3 G T 11: 35,435,620 (GRCm39) E184* probably null Het
Sppl2c C T 11: 104,078,141 (GRCm39) P314S probably benign Het
St7 C T 6: 17,819,276 (GRCm39) P60L probably damaging Het
Tafa2 A T 10: 123,540,270 (GRCm39) H42L possibly damaging Het
Tbc1d8 A G 1: 39,444,398 (GRCm39) F187S probably damaging Het
Tet2 C T 3: 133,192,715 (GRCm39) G573E probably damaging Het
Tnni3k C T 3: 154,644,387 (GRCm39) probably null Het
Trpa1 A G 1: 14,957,844 (GRCm39) C705R probably damaging Het
Usp9y T A Y: 1,310,502 (GRCm39) probably benign Het
Vmn2r68 A C 7: 84,882,834 (GRCm39) M306R probably benign Het
Vwa7 G A 17: 35,240,218 (GRCm39) M395I probably damaging Het
Ybx3 G A 6: 131,347,376 (GRCm39) A253V probably damaging Het
Zfp53 A T 17: 21,728,340 (GRCm39) E124D probably benign Het
Other mutations in Ralgds
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00426:Ralgds APN 2 28,442,230 (GRCm39) missense probably damaging 1.00
IGL01774:Ralgds APN 2 28,440,554 (GRCm39) nonsense probably null
IGL02747:Ralgds APN 2 28,438,122 (GRCm39) unclassified probably benign
IGL03135:Ralgds APN 2 28,439,100 (GRCm39) missense probably damaging 0.99
PIT4458001:Ralgds UTSW 2 28,432,486 (GRCm39) missense probably damaging 1.00
PIT4531001:Ralgds UTSW 2 28,435,226 (GRCm39) nonsense probably null
R0049:Ralgds UTSW 2 28,432,391 (GRCm39) synonymous silent
R0052:Ralgds UTSW 2 28,434,400 (GRCm39) critical splice donor site probably null
R0052:Ralgds UTSW 2 28,434,400 (GRCm39) critical splice donor site probably null
R0285:Ralgds UTSW 2 28,440,581 (GRCm39) splice site probably null
R0665:Ralgds UTSW 2 28,435,218 (GRCm39) missense probably damaging 0.98
R0718:Ralgds UTSW 2 28,439,128 (GRCm39) missense probably benign 0.37
R1755:Ralgds UTSW 2 28,440,558 (GRCm39) missense probably damaging 0.99
R1966:Ralgds UTSW 2 28,435,887 (GRCm39) missense probably damaging 0.96
R2874:Ralgds UTSW 2 28,438,781 (GRCm39) splice site probably null
R4082:Ralgds UTSW 2 28,442,283 (GRCm39) utr 3 prime probably benign
R4342:Ralgds UTSW 2 28,442,107 (GRCm39) missense probably damaging 1.00
R4344:Ralgds UTSW 2 28,442,107 (GRCm39) missense probably damaging 1.00
R4647:Ralgds UTSW 2 28,435,532 (GRCm39) critical splice donor site probably null
R4738:Ralgds UTSW 2 28,435,428 (GRCm39) missense probably damaging 1.00
R4762:Ralgds UTSW 2 28,442,164 (GRCm39) missense probably damaging 0.97
R5027:Ralgds UTSW 2 28,442,102 (GRCm39) critical splice acceptor site probably null
R5320:Ralgds UTSW 2 28,435,224 (GRCm39) missense probably damaging 1.00
R5738:Ralgds UTSW 2 28,432,538 (GRCm39) intron probably benign
R5969:Ralgds UTSW 2 28,432,426 (GRCm39) missense probably damaging 1.00
R6014:Ralgds UTSW 2 28,433,673 (GRCm39) missense probably damaging 0.97
R6136:Ralgds UTSW 2 28,440,577 (GRCm39) critical splice donor site probably null
R6137:Ralgds UTSW 2 28,437,600 (GRCm39) missense probably damaging 0.99
R6583:Ralgds UTSW 2 28,423,656 (GRCm39) missense probably damaging 0.99
R6618:Ralgds UTSW 2 28,440,523 (GRCm39) missense probably benign 0.09
R6801:Ralgds UTSW 2 28,438,448 (GRCm39) missense probably damaging 1.00
R7046:Ralgds UTSW 2 28,430,741 (GRCm39) missense probably damaging 1.00
R7095:Ralgds UTSW 2 28,439,320 (GRCm39) missense possibly damaging 0.83
R7276:Ralgds UTSW 2 28,435,884 (GRCm39) missense probably damaging 1.00
R7399:Ralgds UTSW 2 28,433,667 (GRCm39) missense possibly damaging 0.95
R7446:Ralgds UTSW 2 28,435,901 (GRCm39) missense probably damaging 0.99
R7560:Ralgds UTSW 2 28,437,607 (GRCm39) missense probably damaging 1.00
R8384:Ralgds UTSW 2 28,437,182 (GRCm39) missense probably damaging 1.00
R9422:Ralgds UTSW 2 28,435,184 (GRCm39) missense probably benign
X0028:Ralgds UTSW 2 28,438,711 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CATGATGTCATCACTGTTGCC -3'
(R):5'- ACAGGAAACACTTGGCTTACTCTC -3'

Sequencing Primer
(F):5'- TGGTGACAGCTGCGTATCCAG -3'
(R):5'- AAACACTTGGCTTACTCTCAGGGTC -3'
Posted On 2015-01-23