Incidental Mutation 'R7640:Rragd'
ID 590174
Institutional Source Beutler Lab
Gene Symbol Rragd
Ensembl Gene ENSMUSG00000028278
Gene Name Ras-related GTP binding D
Synonyms D4Ertd174e, C030003H22Rik, 5730543C08Rik
MMRRC Submission
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock # R7640 (G1)
Quality Score 115.008
Status Validated
Chromosome 4
Chromosomal Location 32983037-33022180 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 32983527 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 22 (D22V)
Ref Sequence ENSEMBL: ENSMUSP00000095792 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029946] [ENSMUST00000084747] [ENSMUST00000098190]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000029946
AA Change: D22V

PolyPhen 2 Score 0.662 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000029946
Gene: ENSMUSG00000028278
AA Change: D22V

DomainStartEndE-ValueType
low complexity region 12 23 N/A INTRINSIC
Pfam:Arf 105 291 9.5e-9 PFAM
Pfam:SRPRB 114 220 1.2e-7 PFAM
Pfam:Gtr1_RagA 118 344 3.2e-74 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000084747
AA Change: M1L
SMART Domains Protein: ENSMUSP00000081799
Gene: ENSMUSG00000028278
AA Change: M1L

DomainStartEndE-ValueType
Pfam:Gtr1_RagA 24 169 1.5e-41 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000098190
AA Change: D22V

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000095792
Gene: ENSMUSG00000028278
AA Change: D22V

DomainStartEndE-ValueType
low complexity region 12 23 N/A INTRINSIC
Pfam:Arf 51 236 8.2e-9 PFAM
Pfam:SRPRB 59 166 9.5e-8 PFAM
Pfam:Gtr1_RagA 63 289 9.9e-75 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 99% (68/69)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] RRAGD is a monomeric guanine nucleotide-binding protein, or G protein. By binding GTP or GDP, small G proteins act as molecular switches in numerous cell processes and signaling pathways.[supplied by OMIM, Apr 2004]
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700013G24Rik A T 4: 137,454,594 N20I probably damaging Het
1700020D05Rik T A 19: 5,503,007 S249C probably damaging Het
4930558K02Rik A G 1: 161,957,149 S74P probably benign Het
4932415D10Rik T A 10: 82,294,656 N840I probably damaging Het
Abcb6 A T 1: 75,174,845 probably null Het
Adamts14 C A 10: 61,246,057 A234S probably benign Het
Ankrd42 A G 7: 92,619,635 S167P probably benign Het
Ap3m1 T C 14: 21,038,175 I272V probably benign Het
Armt1 T C 10: 4,453,572 F219S probably damaging Het
Atr T G 9: 95,907,293 probably null Het
Cep72 G A 13: 74,058,488 Q72* probably null Het
Clock G T 5: 76,248,378 L175M possibly damaging Het
Cnmd T A 14: 79,661,534 Y26F possibly damaging Het
Col6a6 A T 9: 105,785,744 M198K possibly damaging Het
Cuta C T 17: 26,938,422 V135I probably benign Het
Ddx41 A T 13: 55,534,239 M241K possibly damaging Het
Dnajc22 A G 15: 99,101,114 N60S probably damaging Het
Drc3 A G 11: 60,388,904 M432V probably benign Het
Eef1d C A 15: 75,902,707 G368C probably damaging Het
En2 A T 5: 28,170,166 K236* probably null Het
Fas A G 19: 34,307,164 T24A possibly damaging Het
Gm13078 T C 4: 143,726,706 V128A probably benign Het
Golga2 T C 2: 32,306,239 V930A probably benign Het
Gprin2 G T 14: 34,195,753 A20D probably benign Het
Ighv14-4 A T 12: 114,176,444 C115* probably null Het
Impdh2 T C 9: 108,565,181 Y459H possibly damaging Het
Klhdc7b G T 15: 89,387,260 V124L possibly damaging Het
L2hgdh A T 12: 69,721,357 Y122* probably null Het
Lamc2 A T 1: 153,136,804 I708N possibly damaging Het
Large2 T C 2: 92,374,705 M1V probably null Het
Lrit2 T C 14: 37,072,124 W382R probably damaging Het
Mcee T A 7: 64,411,968 V173E probably damaging Het
Mcph1 T A 8: 18,632,326 V493E probably benign Het
Mfap4 A G 11: 61,487,087 N118D probably damaging Het
Mknk2 T C 10: 80,668,566 S301G probably benign Het
Mlf1 G A 3: 67,392,933 M94I possibly damaging Het
Mrc2 T A 11: 105,332,295 S455T possibly damaging Het
Mrgprb5 T G 7: 48,168,259 I243L probably benign Het
Muc4 C A 16: 32,760,105 P360T Het
Nat10 G A 2: 103,743,090 A354V probably damaging Het
Nts T C 10: 102,490,304 Q7R possibly damaging Het
Oas1b T C 5: 120,821,414 L288P probably damaging Het
Olfr1076 A G 2: 86,508,943 I161M possibly damaging Het
Olfr1131 A G 2: 87,629,092 I94V probably benign Het
Olfr1196 T A 2: 88,700,886 I148L probably benign Het
Olfr633 A T 7: 103,946,943 I126F probably damaging Het
Otoa A G 7: 121,145,626 E869G probably damaging Het
Pcdhac2 T C 18: 37,144,525 L186P probably damaging Het
Plekhh2 A G 17: 84,610,776 E1271G possibly damaging Het
Pmepa1 C T 2: 173,276,163 A8T probably benign Het
Rc3h2 A G 2: 37,377,849 probably null Het
Rlf T A 4: 121,146,801 M1771L possibly damaging Het
Rpap1 G A 2: 119,764,410 P1372L possibly damaging Het
Sema3f A T 9: 107,683,575 S644R probably benign Het
Sp110 G A 1: 85,579,092 R417C probably benign Het
Specc1l T A 10: 75,257,869 N717K probably damaging Het
Sphkap C T 1: 83,278,928 D367N possibly damaging Het
Tbc1d21 C T 9: 58,361,261 V272M probably damaging Het
Tmem132c A G 5: 127,563,006 D747G probably damaging Het
Tmem56 A G 3: 121,235,041 probably null Het
Trim2 C A 3: 84,190,906 V372F probably benign Het
Ttc34 A G 4: 154,861,384 T292A probably benign Het
Ube3b A G 5: 114,415,323 T919A probably benign Het
Wdr34 T G 2: 30,031,768 D527A probably benign Het
Zfhx4 T C 3: 5,412,480 I3385T probably benign Het
Zfp423 T C 8: 87,781,277 K813R probably damaging Het
Zfp850 T C 7: 27,989,209 T525A probably benign Het
Zfp873 T C 10: 82,060,275 I280T possibly damaging Het
Zkscan7 A G 9: 122,896,056 T697A possibly damaging Het
Other mutations in Rragd
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00434:Rragd APN 4 33007219 splice site probably benign
R0432:Rragd UTSW 4 33004332 missense probably damaging 0.98
R0542:Rragd UTSW 4 33007103 missense probably damaging 1.00
R1521:Rragd UTSW 4 32996005 missense probably damaging 0.96
R4090:Rragd UTSW 4 33007155 missense probably damaging 1.00
R4272:Rragd UTSW 4 32996099 critical splice donor site probably null
R4812:Rragd UTSW 4 33018766 missense probably benign 0.11
R4817:Rragd UTSW 4 32995072 missense probably benign
R6235:Rragd UTSW 4 32995985 missense possibly damaging 0.78
R7124:Rragd UTSW 4 32996027 missense possibly damaging 0.83
R7532:Rragd UTSW 4 33004166 missense possibly damaging 0.72
R8280:Rragd UTSW 4 32995112 missense probably benign
R8479:Rragd UTSW 4 33018734 missense probably benign
R8813:Rragd UTSW 4 33012953 missense possibly damaging 0.59
R9027:Rragd UTSW 4 32996083 missense probably damaging 0.96
R9220:Rragd UTSW 4 32995924 missense probably damaging 1.00
R9643:Rragd UTSW 4 33012998 missense probably benign 0.00
RF040:Rragd UTSW 4 32995150 intron probably benign
RF061:Rragd UTSW 4 32995150 intron probably benign
Z1177:Rragd UTSW 4 33005141 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACACCCGAATTCTCTCTAGGGG -3'
(R):5'- TTTAGCTCGACATCCGACCC -3'

Sequencing Primer
(F):5'- CCGAATTCTCTCTAGGGGGAGAAC -3'
(R):5'- CGACATCCGACCCTGCTC -3'
Posted On 2019-10-24