Incidental Mutation 'IGL00788:Macrod2'
ID 11882
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Macrod2
Ensembl Gene ENSMUSG00000068205
Gene Name mono-ADP ribosylhydrolase 2
Synonyms 1110033L15Rik, 2900006F19Rik, 2610107G07Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00788
Quality Score
Status
Chromosome 2
Chromosomal Location 140237229-142234886 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 142052069 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
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap9 A G 5: 4,110,480 (GRCm39) E3061G probably damaging Het
Armh3 C T 19: 45,920,789 (GRCm39) probably null Het
Casd1 A G 6: 4,624,400 (GRCm39) T398A probably benign Het
Ceacam2 C T 7: 25,237,998 (GRCm39) probably null Het
Chst9 A G 18: 15,586,087 (GRCm39) Y159H probably benign Het
Cip2a T A 16: 48,829,432 (GRCm39) probably benign Het
Cops4 A G 5: 100,681,421 (GRCm39) E152G probably damaging Het
Crygd C T 1: 65,101,250 (GRCm39) R115Q probably benign Het
Dpy19l1 A G 9: 24,373,864 (GRCm39) probably benign Het
Gbp8 T A 5: 105,198,863 (GRCm39) E17D probably benign Het
Grik5 G A 7: 24,764,818 (GRCm39) H108Y probably damaging Het
Gsap G A 5: 21,426,303 (GRCm39) probably benign Het
Gsap G A 5: 21,459,022 (GRCm39) V496M probably damaging Het
Hectd1 C T 12: 51,795,571 (GRCm39) S2286N probably damaging Het
Hgf A T 5: 16,803,228 (GRCm39) Q380L probably damaging Het
Hsd11b1 C T 1: 192,923,766 (GRCm39) M1I probably null Het
Kank2 A G 9: 21,691,775 (GRCm39) probably benign Het
Klhl6 G A 16: 19,775,812 (GRCm39) L249F probably benign Het
Lrba A T 3: 86,234,992 (GRCm39) M846L probably damaging Het
Mroh9 A T 1: 162,852,227 (GRCm39) S821T probably benign Het
Myo5a A G 9: 75,076,241 (GRCm39) T819A probably benign Het
Neb A T 2: 52,095,744 (GRCm39) probably benign Het
Pcyt1b T C X: 92,778,515 (GRCm39) F255L probably benign Het
Rttn T A 18: 88,990,633 (GRCm39) S57T probably benign Het
Senp2 A G 16: 21,837,114 (GRCm39) D121G probably damaging Het
Slc25a21 A T 12: 56,760,597 (GRCm39) probably benign Het
Sorbs1 A G 19: 40,325,487 (GRCm39) probably benign Het
Spats2l T A 1: 57,924,864 (GRCm39) N87K probably damaging Het
Sulf1 A G 1: 12,918,673 (GRCm39) D99G probably damaging Het
Sytl2 T A 7: 90,031,906 (GRCm39) probably benign Het
Trim13 T C 14: 61,843,119 (GRCm39) F379L probably benign 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
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
R0730:Macrod2 UTSW 2 142,059,594 (GRCm39) splice site probably benign
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
Posted On 2012-12-06