Incidental Mutation 'IGL00661:Macrod2'
ID 11886
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 # IGL00661
Quality Score
Status
Chromosome 2
Chromosomal Location 140237229-142234886 bp(+) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) G to A at 140261824 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000105689 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043836] [ENSMUST00000078027] [ENSMUST00000110061] [ENSMUST00000110062] [ENSMUST00000110063] [ENSMUST00000110064] [ENSMUST00000110067]
AlphaFold Q3UYG8
Predicted Effect probably null
Transcript: ENSMUST00000043836
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: ENSMUST00000110061
SMART Domains Protein: ENSMUSP00000105688
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
PDB:4IQY|B 21 54 5e-13 PDB
Predicted Effect probably null
Transcript: ENSMUST00000110062
SMART Domains Protein: ENSMUSP00000105689
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
PDB:4IQY|B 21 54 5e-13 PDB
Predicted Effect probably benign
Transcript: ENSMUST00000110063
SMART Domains Protein: ENSMUSP00000105690
Gene: ENSMUSG00000068205

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
PDB:4IQY|B 21 107 1e-36 PDB
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 noncoding transcript
Transcript: ENSMUST00000124403
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150460
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138485
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154505
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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AAdacl4fm3 A G 4: 144,430,263 (GRCm39) V242A possibly damaging Het
Antxr2 T C 5: 98,152,155 (GRCm39) D152G probably benign Het
Blmh A T 11: 76,856,758 (GRCm39) K118* probably null Het
Bnip3 G A 7: 138,499,801 (GRCm39) P62L probably damaging Het
Catsperb A T 12: 101,554,357 (GRCm39) T684S probably damaging Het
Chd3 C A 11: 69,248,209 (GRCm39) K894N possibly damaging Het
Chkb T A 15: 89,311,794 (GRCm39) R133S probably benign Het
Dennd5a T C 7: 109,507,579 (GRCm39) N803S probably benign Het
Dync2li1 A T 17: 84,956,668 (GRCm39) D276V possibly damaging Het
Erap1 T C 13: 74,822,908 (GRCm39) probably benign Het
Hgsnat C T 8: 26,462,965 (GRCm39) V70M probably benign Het
Leprot T C 4: 101,509,673 (GRCm39) probably null Het
Lhcgr G A 17: 89,057,546 (GRCm39) A315V probably benign Het
Lrrn4 C T 2: 132,712,588 (GRCm39) V412I probably benign Het
Mmaa G A 8: 80,008,199 (GRCm39) R13C probably damaging Het
Plpp4 T A 7: 128,918,023 (GRCm39) I66N probably damaging Het
Prl4a1 T C 13: 28,205,359 (GRCm39) V108A probably benign Het
Prss1 G T 6: 41,439,553 (GRCm39) K95N possibly damaging Het
Rasa2 C T 9: 96,459,606 (GRCm39) probably benign Het
Relb A G 7: 19,350,336 (GRCm39) V208A possibly damaging Het
Sema3d T C 5: 12,555,806 (GRCm39) S178P probably damaging Het
Slc18a1 A T 8: 69,526,383 (GRCm39) W102R probably benign Het
Slc39a8 A C 3: 135,563,873 (GRCm39) K239N probably benign Het
Stap1 A G 5: 86,229,132 (GRCm39) H100R probably benign Het
Suz12 T A 11: 79,889,918 (GRCm39) V143E probably damaging Het
Tmf1 A G 6: 97,153,455 (GRCm39) V206A probably benign Het
Trim16 T A 11: 62,728,058 (GRCm39) probably benign Het
Ube2b C T 11: 51,891,119 (GRCm39) probably null Het
Vmn1r223 T C 13: 23,434,254 (GRCm39) S283P probably damaging Het
Wrn T A 8: 33,809,173 (GRCm39) probably benign Het
Other mutations in Macrod2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00574:Macrod2 APN 2 140,242,797 (GRCm39) missense probably damaging 0.99
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
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