Incidental Mutation 'R0730:Macrod2'
ID 67441
Institutional Source Beutler Lab
Gene Symbol Macrod2
Ensembl Gene ENSMUSG00000068205
Gene Name mono-ADP ribosylhydrolase 2
Synonyms 1110033L15Rik, 2900006F19Rik, 2610107G07Rik
MMRRC Submission 038911-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0730 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 140237229-142234886 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 142059594 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000078027] [ENSMUST00000110064] [ENSMUST00000110067]
AlphaFold Q3UYG8
Predicted Effect probably benign
Transcript: ENSMUST00000078027
SMART Domains Protein: ENSMUSP00000077174
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
A1pp 71 201 5.72e-45 SMART
low complexity region 266 293 N/A INTRINSIC
low complexity region 307 319 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000110064
SMART Domains Protein: ENSMUSP00000105691
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
A1pp 71 201 5.72e-45 SMART
low complexity region 266 293 N/A INTRINSIC
low complexity region 307 319 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000110067
SMART Domains Protein: ENSMUSP00000105694
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
A1pp 71 201 5.72e-45 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138786
Predicted Effect probably benign
Transcript: ENSMUST00000156619
SMART Domains Protein: ENSMUSP00000121013
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
PDB:4IQY|B 2 24 3e-8 PDB
low complexity region 47 65 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.8%
  • 20x: 96.1%
Validation Efficiency 99% (99/100)
Allele List at MGI
Other mutations in this stock
Total: 99 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam9 A T 8: 25,486,774 (GRCm39) I168N probably benign Het
Adamts20 G A 15: 94,245,571 (GRCm39) A577V probably benign Het
Agtr1a A T 13: 30,565,279 (GRCm39) S115C probably damaging Het
Ankrd11 T C 8: 123,618,692 (GRCm39) Y1720C probably damaging Het
Ano6 A T 15: 95,818,252 (GRCm39) T353S probably damaging Het
App A G 16: 84,876,840 (GRCm39) F184L probably damaging Het
Arhgef38 T A 3: 132,843,232 (GRCm39) Y446F probably benign Het
Aspg T A 12: 112,078,693 (GRCm39) Y57* probably null Het
Atp1a4 G A 1: 172,067,774 (GRCm39) probably benign Het
Bdp1 G A 13: 100,195,459 (GRCm39) probably benign Het
Bicd2 T A 13: 49,531,717 (GRCm39) S246T possibly damaging Het
Brd10 T A 19: 29,695,381 (GRCm39) I1438F probably benign Het
Bsn T A 9: 107,984,011 (GRCm39) M3348L unknown Het
Cacna1c C T 6: 118,589,586 (GRCm39) R1446H probably damaging Het
Cacna2d3 T C 14: 28,704,322 (GRCm39) I820V probably benign Het
Cdc40 A G 10: 40,720,952 (GRCm39) probably benign Het
Cdh23 T C 10: 60,159,493 (GRCm39) E2094G probably damaging Het
Celsr2 T A 3: 108,305,922 (GRCm39) N2061Y probably damaging Het
Cfap206 G A 4: 34,711,391 (GRCm39) A502V probably benign Het
Cfap54 T C 10: 92,870,599 (GRCm39) T29A probably benign Het
Cfap57 T C 4: 118,470,117 (GRCm39) probably null Het
Chd5 A G 4: 152,432,441 (GRCm39) E43G possibly damaging Het
Clk1 G A 1: 58,453,558 (GRCm39) H343Y probably benign Het
Cntn4 A C 6: 106,527,447 (GRCm39) K443T probably damaging Het
Csn2 G A 5: 87,842,811 (GRCm39) A72V possibly damaging Het
Ctdp1 T A 18: 80,493,457 (GRCm39) H346L probably benign Het
Ctif A T 18: 75,698,083 (GRCm39) N192K probably damaging Het
Ddr2 G A 1: 169,823,135 (GRCm39) A383V probably benign Het
Derl3 C T 10: 75,731,076 (GRCm39) probably benign Het
Dgkh T C 14: 78,821,919 (GRCm39) I865V probably damaging Het
Dip2b C T 15: 100,069,532 (GRCm39) A619V probably damaging Het
Elapor1 T A 3: 108,376,851 (GRCm39) H509L probably benign Het
Eml1 A G 12: 108,496,585 (GRCm39) T614A possibly damaging Het
Eogt G C 6: 97,092,970 (GRCm39) Y402* probably null Het
Erbb4 A G 1: 68,298,449 (GRCm39) V647A probably damaging Het
Esm1 G T 13: 113,350,036 (GRCm39) probably null Het
Fbxo31 A G 8: 122,282,103 (GRCm39) probably benign Het
Fbxw5 T A 2: 25,394,630 (GRCm39) D201E possibly damaging Het
Fgfr1 G A 8: 26,045,760 (GRCm39) D123N probably benign Het
G530012D18Rik A C 1: 85,504,757 (GRCm39) probably benign Het
Gnat1 G A 9: 107,556,662 (GRCm39) T29I probably damaging Het
Gtf2ird2 A T 5: 134,221,597 (GRCm39) R67* probably null Het
Il22b A T 10: 118,130,142 (GRCm39) D87E probably benign Het
Kcnq3 T C 15: 65,867,457 (GRCm39) T729A probably benign Het
Klrc2 A T 6: 129,635,659 (GRCm39) S156R probably damaging Het
Krt76 A T 15: 101,795,784 (GRCm39) L462Q probably damaging Het
Lama3 C A 18: 12,589,907 (GRCm39) probably benign Het
Lin28a A T 4: 133,735,319 (GRCm39) S56T probably damaging Het
Macf1 A G 4: 123,276,323 (GRCm39) probably benign Het
Mansc1 C T 6: 134,594,424 (GRCm39) probably benign Het
Map1b G T 13: 99,566,274 (GRCm39) S2149* probably null Het
Mgst1 A T 6: 138,124,667 (GRCm39) T34S probably benign Het
Mlf2 C T 6: 124,911,354 (GRCm39) T123M probably damaging Het
Mospd2 C T X: 163,731,253 (GRCm39) probably benign Het
Mrpl15 A T 1: 4,847,834 (GRCm39) V155E probably damaging Het
Mstn A T 1: 53,100,953 (GRCm39) Y10F possibly damaging Het
Myo1g C T 11: 6,470,794 (GRCm39) V21M probably damaging Het
Myom2 T C 8: 15,149,326 (GRCm39) I599T probably benign Het
Ndc80 A T 17: 71,803,241 (GRCm39) N633K probably benign Het
Nhs C A X: 160,620,296 (GRCm39) V1487L possibly damaging Het
Npc1 T C 18: 12,352,382 (GRCm39) T106A probably benign Het
Nup133 C T 8: 124,675,747 (GRCm39) V57M probably benign Het
Nup98 T A 7: 101,809,923 (GRCm39) T536S probably damaging Het
Oprm1 T C 10: 6,782,652 (GRCm39) probably benign Het
Or5j1 T C 2: 86,879,492 (GRCm39) I29M probably benign Het
Or6c219 T A 10: 129,780,980 (GRCm39) H317L probably benign Het
Or8j3 A G 2: 86,029,069 (GRCm39) V9A probably benign Het
Ostf1 C T 19: 18,581,571 (GRCm39) V14I unknown Het
Pcdhb14 C A 18: 37,581,921 (GRCm39) D342E probably damaging Het
Pdia3 G A 2: 121,262,858 (GRCm39) G275S probably damaging Het
Pdpr T C 8: 111,852,387 (GRCm39) probably null Het
Plce1 G A 19: 38,705,135 (GRCm39) V847M probably damaging Het
Pon3 A G 6: 5,230,444 (GRCm39) M288T probably benign Het
Psd2 A T 18: 36,111,627 (GRCm39) D84V possibly damaging Het
Ptpro T A 6: 137,420,592 (GRCm39) V1007D probably damaging Het
Ralgapa1 T C 12: 55,712,448 (GRCm39) K1808E probably damaging Het
Ramp3 T C 11: 6,626,476 (GRCm39) probably benign Het
Rasgrf1 T A 9: 89,833,062 (GRCm39) probably benign Het
Rictor A G 15: 6,803,467 (GRCm39) probably benign Het
Rptor A T 11: 119,775,780 (GRCm39) I984F probably benign Het
Slc1a6 C T 10: 78,631,842 (GRCm39) P223S probably benign Het
Taar8b A C 10: 23,967,924 (GRCm39) V90G probably damaging Het
Tbc1d21 A G 9: 58,267,160 (GRCm39) V327A probably benign Het
Tex21 T C 12: 76,250,940 (GRCm39) T499A probably benign Het
Tg A T 15: 66,550,638 (GRCm39) D256V probably damaging Het
Tmf1 A G 6: 97,153,453 (GRCm39) S207P probably benign Het
Tpr A G 1: 150,269,158 (GRCm39) probably benign Het
Ufd1 A G 16: 18,633,637 (GRCm39) T21A probably damaging Het
Unc13a T C 8: 72,108,929 (GRCm39) D115G possibly damaging Het
Usb1 T A 8: 96,070,669 (GRCm39) F198L probably damaging Het
Utrn A T 10: 12,573,902 (GRCm39) probably benign Het
Vars1 A G 17: 35,233,276 (GRCm39) N954S probably damaging Het
Wdr17 C T 8: 55,146,131 (GRCm39) A90T possibly damaging Het
Wdr33 C T 18: 31,968,429 (GRCm39) probably benign Het
Zfp236 A G 18: 82,658,369 (GRCm39) probably benign Het
Zfp445 A T 9: 122,690,823 (GRCm39) V124E probably damaging Het
Zfp616 A T 11: 73,975,648 (GRCm39) H639L probably damaging Het
Zfyve16 C A 13: 92,657,985 (GRCm39) S642I probably damaging Het
Zswim5 C T 4: 116,842,943 (GRCm39) T896I possibly damaging Het
Other mutations in Macrod2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00574:Macrod2 APN 2 140,242,797 (GRCm39) missense probably damaging 0.99
IGL00661:Macrod2 APN 2 140,261,824 (GRCm39) critical splice acceptor site probably null
IGL00788:Macrod2 APN 2 142,052,069 (GRCm39) splice site probably benign
IGL00840:Macrod2 APN 2 142,018,578 (GRCm39) missense possibly damaging 0.53
IGL01160:Macrod2 APN 2 140,666,962 (GRCm39) splice site probably benign
IGL01357:Macrod2 APN 2 142,226,250 (GRCm39) missense probably damaging 1.00
IGL01453:Macrod2 APN 2 140,294,492 (GRCm39) splice site probably benign
IGL01910:Macrod2 APN 2 142,138,485 (GRCm39) missense probably benign 0.04
IGL02208:Macrod2 APN 2 142,216,196 (GRCm39) missense possibly damaging 0.55
IGL03013:Macrod2 APN 2 141,357,147 (GRCm39) missense probably benign 0.02
R0196:Macrod2 UTSW 2 142,018,545 (GRCm39) missense probably damaging 1.00
R0415:Macrod2 UTSW 2 142,052,065 (GRCm39) critical splice donor site probably null
R0699:Macrod2 UTSW 2 140,260,836 (GRCm39) critical splice donor site probably null
R1119:Macrod2 UTSW 2 140,242,826 (GRCm39) missense probably benign 0.00
R1124:Macrod2 UTSW 2 140,294,547 (GRCm39) missense probably damaging 1.00
R1422:Macrod2 UTSW 2 140,261,861 (GRCm39) splice site probably null
R3707:Macrod2 UTSW 2 141,652,549 (GRCm39) missense probably damaging 1.00
R3708:Macrod2 UTSW 2 141,652,549 (GRCm39) missense probably damaging 1.00
R3745:Macrod2 UTSW 2 141,652,549 (GRCm39) missense probably damaging 1.00
R4409:Macrod2 UTSW 2 140,260,777 (GRCm39) missense possibly damaging 0.66
R4666:Macrod2 UTSW 2 142,059,519 (GRCm39) missense probably damaging 0.99
R4782:Macrod2 UTSW 2 140,261,858 (GRCm39) missense possibly damaging 0.81
R4885:Macrod2 UTSW 2 140,261,985 (GRCm39) missense possibly damaging 0.66
R5180:Macrod2 UTSW 2 140,237,636 (GRCm39) missense probably damaging 1.00
R5524:Macrod2 UTSW 2 142,159,863 (GRCm39) missense possibly damaging 0.82
R5677:Macrod2 UTSW 2 142,018,587 (GRCm39) missense probably damaging 1.00
R5735:Macrod2 UTSW 2 140,260,809 (GRCm39) missense possibly damaging 0.66
R5750:Macrod2 UTSW 2 141,357,240 (GRCm39) missense probably benign 0.41
R5770:Macrod2 UTSW 2 141,074,102 (GRCm39) intron probably benign
R6029:Macrod2 UTSW 2 142,160,367 (GRCm39) missense probably damaging 0.99
R6174:Macrod2 UTSW 2 140,242,895 (GRCm39) start codon destroyed probably null
R6453:Macrod2 UTSW 2 142,018,545 (GRCm39) missense probably damaging 1.00
R6830:Macrod2 UTSW 2 140,294,602 (GRCm39) missense probably damaging 1.00
R6927:Macrod2 UTSW 2 142,098,441 (GRCm39) missense probably damaging 1.00
R6932:Macrod2 UTSW 2 140,261,833 (GRCm39) missense probably damaging 0.97
R7020:Macrod2 UTSW 2 142,231,795 (GRCm39) makesense probably null
R7886:Macrod2 UTSW 2 141,566,565 (GRCm39) missense probably damaging 1.00
R9245:Macrod2 UTSW 2 141,652,534 (GRCm39) missense probably benign 0.35
Z1176:Macrod2 UTSW 2 140,866,010 (GRCm39) missense probably damaging 1.00
Z1176:Macrod2 UTSW 2 140,548,128 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AAAGGCAGAATGCCCTGGACTTC -3'
(R):5'- GCATTGGTCATCATGTGTAGGCCAC -3'

Sequencing Primer
(F):5'- tgtgtgtgtgtgtgtTGGG -3'
(R):5'- GCCATGCATAGAACGTGACTTTG -3'
Posted On 2013-09-03