Incidental Mutation 'R1710:Arhgap29'
ID 190407
Institutional Source Beutler Lab
Gene Symbol Arhgap29
Ensembl Gene ENSMUSG00000039831
Gene Name Rho GTPase activating protein 29
Synonyms C76601, Parg1, B130017I01Rik, 6720461J18Rik
MMRRC Submission 039743-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1710 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 121746752-121810326 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 121801729 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 748 (Y748N)
Ref Sequence ENSEMBL: ENSMUSP00000044624 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037958] [ENSMUST00000197155]
AlphaFold Q8CGF1
Predicted Effect probably damaging
Transcript: ENSMUST00000037958
AA Change: Y748N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000044624
Gene: ENSMUSG00000039831
AA Change: Y748N

DomainStartEndE-ValueType
low complexity region 5 12 N/A INTRINSIC
PDB:3QWE|A 193 469 5e-41 PDB
Blast:RhoGAP 412 595 9e-84 BLAST
C1 613 659 2.48e-6 SMART
RhoGAP 684 885 1.92e-68 SMART
low complexity region 947 961 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000197155
AA Change: Y748N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000142945
Gene: ENSMUSG00000039831
AA Change: Y748N

DomainStartEndE-ValueType
low complexity region 5 12 N/A INTRINSIC
PDB:3QWE|A 193 469 8e-42 PDB
Blast:RhoGAP 412 595 2e-87 BLAST
C1 613 659 2.48e-6 SMART
RhoGAP 684 780 1.14e-6 SMART
Predicted Effect unknown
Transcript: ENSMUST00000198914
AA Change: Y340N
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199550
Meta Mutation Damage Score 0.9534 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.5%
Validation Efficiency 98% (117/120)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Rap1 is a small GTPase that, through effectors, regulates Rho GTPase signaling. These effectors- Rasip1, Radil, and the protein encoded by this gene- translocate to the cell membrane, where they form a multiprotein complex. This complex is necessary for Rap1-induced inhibition of Rho signaling. Defects in this gene may be a cause of nonsyndromic cleft lip with or without cleft palate. [provided by RefSeq, Jun 2016]
Allele List at MGI
Other mutations in this stock
Total: 114 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503L19Rik A T 18: 70,601,134 (GRCm39) S249R possibly damaging Het
Acadvl T A 11: 69,901,181 (GRCm39) I638F probably damaging Het
Acnat2 T A 4: 49,380,587 (GRCm39) T264S probably benign Het
Acrv1 C T 9: 36,605,551 (GRCm39) Q33* probably null Het
Actrt3 T A 3: 30,653,901 (GRCm39) N33I probably damaging Het
Alyref2 T C 1: 171,331,168 (GRCm39) probably benign Het
Ank2 C A 3: 126,726,709 (GRCm39) E3712* probably null Het
Ano7 C A 1: 93,313,346 (GRCm39) H161Q probably benign Het
Arhgap10 C A 8: 78,085,216 (GRCm39) E451* probably null Het
Arhgap45 C T 10: 79,853,932 (GRCm39) Q149* probably null Het
Asap2 C T 12: 21,274,393 (GRCm39) H371Y probably damaging Het
Atp6v1b1 T C 6: 83,735,372 (GRCm39) I480T probably benign Het
BC034090 T C 1: 155,101,610 (GRCm39) D218G possibly damaging Het
Brdt A T 5: 107,491,450 (GRCm39) D74V probably damaging Het
C4b A G 17: 34,962,638 (GRCm39) probably benign Het
Card11 T A 5: 140,888,660 (GRCm39) K233* probably null Het
Catip T G 1: 74,401,929 (GRCm39) F35V possibly damaging Het
Ccdc13 C T 9: 121,648,647 (GRCm39) G247R probably damaging Het
Cep97 T A 16: 55,735,385 (GRCm39) D471V probably damaging Het
Col17a1 A T 19: 47,659,370 (GRCm39) L403Q probably damaging Het
Crbn A G 6: 106,767,906 (GRCm39) S194P possibly damaging Het
Degs1l A G 1: 180,878,884 (GRCm39) M1V probably null Het
Dennd10 A G 19: 60,806,021 (GRCm39) Y102C probably damaging Het
Dhx58 T A 11: 100,594,400 (GRCm39) H97L probably benign Het
Dnah8 T C 17: 31,073,914 (GRCm39) I4528T probably damaging Het
Dpyd A G 3: 118,404,092 (GRCm39) probably null Het
Entpd1 A T 19: 40,714,680 (GRCm39) Q263L probably benign Het
Entrep1 A T 19: 23,957,059 (GRCm39) I317N probably damaging Het
Esyt3 T C 9: 99,218,244 (GRCm39) I130M probably benign Het
Etv1 T C 12: 38,902,261 (GRCm39) F264S probably benign Het
Fat1 T C 8: 45,463,519 (GRCm39) S1354P probably benign Het
Fat4 C A 3: 39,005,304 (GRCm39) T1901N probably damaging Het
Fbxw13 C T 9: 109,010,586 (GRCm39) V351I probably damaging Het
Fmo3 A G 1: 162,795,356 (GRCm39) F160L possibly damaging Het
Fyb2 T A 4: 104,861,113 (GRCm39) D592E probably damaging Het
Gjb4 T C 4: 127,245,663 (GRCm39) M93V possibly damaging Het
Gm5089 C A 14: 122,673,566 (GRCm39) G52* probably null Het
Gm6401 G T 14: 41,788,840 (GRCm39) N76K probably benign Het
Gm6871 A G 7: 41,195,901 (GRCm39) S279P probably damaging Het
Gtf2ird2 T G 5: 134,240,081 (GRCm39) V301G probably benign Het
H2bw2 A C X: 135,828,216 (GRCm39) D35A unknown Het
Hfm1 A G 5: 107,028,380 (GRCm39) F817L probably damaging Het
Hfm1 T C 5: 107,043,869 (GRCm39) E589G probably damaging Het
Hivep2 A T 10: 14,005,249 (GRCm39) K616* probably null Het
Hmcn1 A T 1: 150,551,735 (GRCm39) I2623N probably damaging Het
Igf2bp3 G T 6: 49,082,565 (GRCm39) A339E probably damaging Het
Insyn2b T A 11: 34,354,263 (GRCm39) probably null Het
Irx4 T C 13: 73,415,757 (GRCm39) I182T possibly damaging Het
Jcad T C 18: 4,674,511 (GRCm39) S758P probably damaging Het
Klhdc4 A T 8: 122,526,226 (GRCm39) Y304* probably null Het
Lama1 A G 17: 68,060,786 (GRCm39) I705V probably benign Het
Mbd5 A G 2: 49,147,044 (GRCm39) N418S probably benign Het
Mmp21 C T 7: 133,279,014 (GRCm39) V279I probably damaging Het
Morc4 A C X: 138,755,279 (GRCm39) C272W probably damaging Het
Mrm1 A T 11: 84,709,518 (GRCm39) C180S probably damaging Het
Ncor1 T C 11: 62,313,831 (GRCm39) D103G probably damaging Het
Ndrg4 A G 8: 96,437,314 (GRCm39) D251G probably damaging Het
Ndufaf5 T C 2: 140,035,522 (GRCm39) V246A possibly damaging Het
Noa1 T C 5: 77,457,572 (GRCm39) E111G possibly damaging Het
Nod1 C A 6: 54,921,044 (GRCm39) V425F probably damaging Het
Nos1 A T 5: 118,033,984 (GRCm39) I369F probably damaging Het
Nsun5 C T 5: 135,400,170 (GRCm39) H98Y probably damaging Het
Optn G A 2: 5,057,941 (GRCm39) T76I possibly damaging Het
Or14c39 G A 7: 86,344,318 (GRCm39) R218H probably benign Het
Or4k15c C G 14: 50,321,827 (GRCm39) V104L probably benign Het
Or5k1b A G 16: 58,581,504 (GRCm39) F12L probably benign Het
Or8d1b A G 9: 38,887,202 (GRCm39) I77V probably damaging Het
Or8g28 T C 9: 39,169,867 (GRCm39) I37V probably benign Het
Or9g19 C T 2: 85,600,199 (GRCm39) T18I probably benign Het
Oscar C T 7: 3,614,855 (GRCm39) W22* probably null Het
Palmd T A 3: 116,717,306 (GRCm39) Y397F probably damaging Het
Plk1 A G 7: 121,768,121 (GRCm39) D447G probably damaging Het
Plscr5 T A 9: 92,087,581 (GRCm39) N183K probably damaging Het
Polk T G 13: 96,625,712 (GRCm39) D364A probably damaging Het
Polr3d T C 14: 70,680,450 (GRCm39) T36A probably benign Het
Ppp1r10 A T 17: 36,237,428 (GRCm39) R199S probably damaging Het
Prkcz C T 4: 155,346,969 (GRCm39) D388N probably damaging Het
Prrc2b T C 2: 32,102,234 (GRCm39) L769P probably damaging Het
Psg26 A G 7: 18,213,966 (GRCm39) V232A probably damaging Het
Pth2r T C 1: 65,375,997 (GRCm39) V85A possibly damaging Het
Rbpms2 T C 9: 65,566,494 (GRCm39) probably benign Het
Reps1 A T 10: 17,994,698 (GRCm39) D514V possibly damaging Het
Riok3 G T 18: 12,276,018 (GRCm39) R238L probably benign Het
Rnf19a T C 15: 36,244,353 (GRCm39) Q569R probably damaging Het
Rorb G A 19: 18,937,865 (GRCm39) T267I probably damaging Het
Rrm2b A T 15: 37,929,340 (GRCm39) M70K probably damaging Het
Rsf1 A T 7: 97,311,556 (GRCm39) E762V possibly damaging Het
S100a2 G A 3: 90,498,699 (GRCm39) V67I probably benign Het
Skp1 T A 11: 52,133,442 (GRCm39) D42E probably benign Het
Slc22a4 A T 11: 53,918,801 (GRCm39) M1K probably null Het
Slc2a9 T A 5: 38,539,387 (GRCm39) Q371L probably damaging Het
Slc4a9 A G 18: 36,665,075 (GRCm39) T475A probably benign Het
Slc8b1 A G 5: 120,657,717 (GRCm39) N60S probably damaging Het
Slx4 A C 16: 3,817,022 (GRCm39) D66E probably benign Het
Smg8 A T 11: 86,977,113 (GRCm39) I156N probably damaging Het
Snx25 A T 8: 46,569,244 (GRCm39) C218S possibly damaging Het
Sulf2 T C 2: 165,920,992 (GRCm39) I784V probably benign Het
Tatdn2 G T 6: 113,674,888 (GRCm39) R72L possibly damaging Het
Tbc1d8 T C 1: 39,445,918 (GRCm39) D91G possibly damaging Het
Tifab C A 13: 56,324,433 (GRCm39) R3S probably benign Het
Tm4sf1 A T 3: 57,200,304 (GRCm39) S104T probably damaging Het
Tmem132e T A 11: 82,334,343 (GRCm39) I618N probably damaging Het
Ttc7b A T 12: 100,369,667 (GRCm39) D367E probably damaging Het
Txlnb A G 10: 17,719,203 (GRCm39) D678G possibly damaging Het
Vgll4 A G 6: 114,934,895 (GRCm39) probably null Het
Vmn2r124 A T 17: 18,282,187 (GRCm39) probably benign Het
Vmn2r2 T C 3: 64,024,820 (GRCm39) D587G probably benign Het
Vmn2r84 G A 10: 130,226,968 (GRCm39) A290V probably benign Het
Vps13c T A 9: 67,818,811 (GRCm39) S1077R probably benign Het
Vsig10 C T 5: 117,489,719 (GRCm39) A495V probably benign Het
Vwa3a A T 7: 120,403,254 (GRCm39) probably null Het
Zfhx2 C A 14: 55,303,455 (GRCm39) A1510S possibly damaging Het
Zfp142 T A 1: 74,611,389 (GRCm39) D601V probably damaging Het
Zfp62 T C 11: 49,108,510 (GRCm39) I867T probably benign Het
Other mutations in Arhgap29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00492:Arhgap29 APN 3 121,796,961 (GRCm39) nonsense probably null
IGL01121:Arhgap29 APN 3 121,803,512 (GRCm39) missense probably damaging 1.00
IGL01622:Arhgap29 APN 3 121,767,773 (GRCm39) splice site probably benign
IGL01623:Arhgap29 APN 3 121,767,773 (GRCm39) splice site probably benign
IGL01995:Arhgap29 APN 3 121,807,977 (GRCm39) missense probably benign 0.00
IGL02120:Arhgap29 APN 3 121,797,906 (GRCm39) missense probably benign 0.05
IGL02554:Arhgap29 APN 3 121,786,173 (GRCm39) unclassified probably benign
IGL02931:Arhgap29 APN 3 121,786,509 (GRCm39) missense probably benign
IGL02937:Arhgap29 APN 3 121,767,698 (GRCm39) missense probably damaging 0.99
PIT4362001:Arhgap29 UTSW 3 121,796,861 (GRCm39) missense probably benign 0.42
R0022:Arhgap29 UTSW 3 121,782,586 (GRCm39) missense possibly damaging 0.61
R0574:Arhgap29 UTSW 3 121,801,274 (GRCm39) missense probably benign 0.01
R0601:Arhgap29 UTSW 3 121,784,759 (GRCm39) missense probably damaging 1.00
R0639:Arhgap29 UTSW 3 121,801,290 (GRCm39) missense probably damaging 1.00
R0881:Arhgap29 UTSW 3 121,808,328 (GRCm39) missense probably damaging 1.00
R1232:Arhgap29 UTSW 3 121,796,989 (GRCm39) missense probably damaging 1.00
R1295:Arhgap29 UTSW 3 121,786,044 (GRCm39) missense probably benign 0.27
R1296:Arhgap29 UTSW 3 121,786,044 (GRCm39) missense probably benign 0.27
R1403:Arhgap29 UTSW 3 121,767,578 (GRCm39) missense probably damaging 1.00
R1403:Arhgap29 UTSW 3 121,767,578 (GRCm39) missense probably damaging 1.00
R1470:Arhgap29 UTSW 3 121,785,968 (GRCm39) unclassified probably benign
R1878:Arhgap29 UTSW 3 121,805,020 (GRCm39) missense probably damaging 1.00
R2051:Arhgap29 UTSW 3 121,775,509 (GRCm39) missense probably benign 0.01
R2112:Arhgap29 UTSW 3 121,805,210 (GRCm39) missense probably benign 0.03
R2188:Arhgap29 UTSW 3 121,784,658 (GRCm39) missense probably damaging 1.00
R2240:Arhgap29 UTSW 3 121,805,102 (GRCm39) missense probably benign 0.12
R2420:Arhgap29 UTSW 3 121,767,629 (GRCm39) missense probably benign
R3618:Arhgap29 UTSW 3 121,782,176 (GRCm39) missense possibly damaging 0.62
R4673:Arhgap29 UTSW 3 121,808,620 (GRCm39) missense probably damaging 1.00
R4717:Arhgap29 UTSW 3 121,803,607 (GRCm39) missense possibly damaging 0.82
R5028:Arhgap29 UTSW 3 121,803,709 (GRCm39) critical splice donor site probably null
R5043:Arhgap29 UTSW 3 121,767,653 (GRCm39) missense probably benign 0.00
R5045:Arhgap29 UTSW 3 121,796,244 (GRCm39) missense probably benign 0.28
R5463:Arhgap29 UTSW 3 121,782,200 (GRCm39) missense possibly damaging 0.94
R5495:Arhgap29 UTSW 3 121,808,578 (GRCm39) missense probably damaging 1.00
R5743:Arhgap29 UTSW 3 121,775,560 (GRCm39) missense probably damaging 1.00
R5791:Arhgap29 UTSW 3 121,807,894 (GRCm39) missense probably damaging 0.98
R5896:Arhgap29 UTSW 3 121,805,736 (GRCm39) missense possibly damaging 0.78
R6083:Arhgap29 UTSW 3 121,786,397 (GRCm39) missense probably benign 0.00
R6355:Arhgap29 UTSW 3 121,804,907 (GRCm39) missense possibly damaging 0.46
R6451:Arhgap29 UTSW 3 121,787,230 (GRCm39) missense probably damaging 1.00
R6528:Arhgap29 UTSW 3 121,808,351 (GRCm39) missense probably benign 0.13
R7239:Arhgap29 UTSW 3 121,782,599 (GRCm39) missense probably benign 0.16
R7669:Arhgap29 UTSW 3 121,786,461 (GRCm39) missense probably damaging 1.00
R7807:Arhgap29 UTSW 3 121,807,981 (GRCm39) missense probably benign 0.01
R8045:Arhgap29 UTSW 3 121,801,211 (GRCm39) synonymous silent
R8048:Arhgap29 UTSW 3 121,786,550 (GRCm39) missense probably damaging 1.00
R8165:Arhgap29 UTSW 3 121,782,222 (GRCm39) missense probably damaging 0.98
R9001:Arhgap29 UTSW 3 121,775,523 (GRCm39) missense probably benign 0.03
R9032:Arhgap29 UTSW 3 121,808,249 (GRCm39) missense probably benign
R9060:Arhgap29 UTSW 3 121,783,973 (GRCm39) missense probably damaging 0.99
R9085:Arhgap29 UTSW 3 121,808,249 (GRCm39) missense probably benign
R9717:Arhgap29 UTSW 3 121,797,920 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- ACCAGATGGCATCCCTTTTGTACTG -3'
(R):5'- ACTGATCCAAACAACACTCTGCTTGTG -3'

Sequencing Primer
(F):5'- AATAGAGCCTTGTGTCTCCAG -3'
(R):5'- GGGTTCAACACTGGCCTCTC -3'
Posted On 2014-05-14