Incidental Mutation 'IGL01018:Armt1'
ID 53831
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Armt1
Ensembl Gene ENSMUSG00000061759
Gene Name acidic residue methyltransferase 1
Synonyms 1700052N19Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.124) question?
Stock # IGL01018
Quality Score
Status
Chromosome 10
Chromosomal Location 4432467-4455141 bp(+) (GRCm38)
Type of Mutation unclassified
DNA Base Change (assembly) C to T at 4454237 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000115624 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095893] [ENSMUST00000118544] [ENSMUST00000152294]
AlphaFold A6H630
Predicted Effect probably benign
Transcript: ENSMUST00000095893
SMART Domains Protein: ENSMUSP00000093581
Gene: ENSMUSG00000061759

DomainStartEndE-ValueType
Pfam:DUF89 20 417 1.3e-125 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000118544
SMART Domains Protein: ENSMUSP00000114073
Gene: ENSMUSG00000061759

DomainStartEndE-ValueType
Pfam:DUF89 20 187 1.2e-33 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143037
Predicted Effect probably benign
Transcript: ENSMUST00000152294
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931408C20Rik T C 1: 26,682,910 E1063G probably damaging Het
5530400C23Rik G T 6: 133,294,497 R168I probably benign Het
5530400C23Rik A T 6: 133,294,498 R168S probably benign Het
9230019H11Rik A G 10: 3,120,231 noncoding transcript Het
9230019H11Rik A G 10: 3,120,209 noncoding transcript Het
9230019H11Rik G A 10: 3,125,031 noncoding transcript Het
9230019H11Rik C T 10: 3,125,193 noncoding transcript Het
Ccdc170 T C 10: 4,512,788 W35R probably benign Het
Ccdc170 G T 10: 4,514,155 A99S probably benign Het
Ccdc170 T C 10: 4,514,114 V31A probably benign Het
Glp2r C A 11: 67,709,644 V460F probably benign Het
Gm21411 T C 4: 146,892,577 Q80R probably benign Het
Gm21411 C T 4: 146,892,610 S69N possibly damaging Het
Gm21671 G T 5: 25,950,723 H208N probably benign Het
Gm21738 G A 14: 19,418,856 P24L probably benign Het
H2-M10.6 C T 17: 36,812,220 A15V probably benign Het
H60c T C 10: 3,259,766 M174V probably benign Het
H60c A C 10: 3,260,343 F69V probably benign Het
Ipcef1 C T 10: 6,919,968 R144Q probably damaging Het
Ipcef1 G A 10: 6,890,551 A382V probably benign Het
Mapk8ip3 T G 17: 24,899,719 probably benign Het
Mthfd1l T C 10: 3,978,708 V100A probably benign Het
Mthfd1l T C 10: 4,007,800 V279A probably benign Het
Mthfd1l T C 10: 4,032,345 probably benign Het
Mtrf1l A G 10: 5,814,180 probably benign Het
Myo18b T C 5: 112,809,747 E1450G probably damaging Het
Obscn C T 11: 59,128,069 V973M probably damaging Het
Olfr414 G A 1: 174,431,342 V305I probably benign Het
Oprm1 T C 10: 7,037,170 probably benign Het
Pou5f2 A G 13: 78,025,938 probably benign Het
Ralgapa2 G A 2: 146,410,193 H891Y probably benign Het
Ralgapa2 T G 2: 146,410,192 H806P probably benign Het
Rmnd1 A T 10: 4,427,290 S130T probably benign Het
Rmnd1 A G 10: 4,427,392 W96R probably benign Het
Trappc12 A C 12: 28,691,854 probably benign Het
Vip A G 10: 5,642,480 D40G probably benign Het
Vmn2r125 T A 4: 156,351,226 L300M probably benign Het
Vmn2r125 T C 4: 156,350,612 probably benign Het
Vmn2r125 C T 4: 156,351,038 T237I probably benign Het
Vmn2r125 A T 4: 156,351,037 T237S probably benign Het
Vmn2r125 A C 4: 156,350,900 Q191P probably benign Het
Vmn2r125 C A 4: 156,350,899 Q191K probably benign Het
Vmn2r125 A G 4: 156,350,845 N173D probably damaging Het
Vmn2r40 G A 7: 8,908,176 S706F probably damaging Het
Vmn2r-ps159 G A 4: 156,334,605 noncoding transcript Het
Vmn2r-ps159 A T 4: 156,338,146 noncoding transcript Het
Vmn2r-ps159 C A 4: 156,338,435 noncoding transcript Het
Vmn2r-ps159 T C 4: 156,334,263 noncoding transcript Het
Vmn2r-ps159 T C 4: 156,335,590 noncoding transcript Het
Zfp14 T A 7: 30,038,101 R486S probably damaging Het
Other mutations in Armt1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00907:Armt1 APN 10 4454051 missense possibly damaging 0.50
IGL01018:Armt1 APN 10 4450732 missense probably benign
IGL02198:Armt1 APN 10 4454064 missense possibly damaging 0.95
IGL02980:Armt1 APN 10 4450643 splice site probably benign
IGL03104:Armt1 APN 10 4439615 missense possibly damaging 0.94
R0620:Armt1 UTSW 10 4432689 missense probably benign 0.38
R4248:Armt1 UTSW 10 4439687 missense probably benign 0.00
R5709:Armt1 UTSW 10 4434903 missense probably damaging 0.97
R6058:Armt1 UTSW 10 4453488 missense probably damaging 1.00
R6318:Armt1 UTSW 10 4450859 missense probably benign 0.01
R6410:Armt1 UTSW 10 4453826 missense probably benign
R6998:Armt1 UTSW 10 4453937 missense probably benign 0.03
R7242:Armt1 UTSW 10 4453475 missense probably damaging 1.00
R7268:Armt1 UTSW 10 4450855 missense possibly damaging 0.75
R7432:Armt1 UTSW 10 4432706 missense probably benign 0.00
R7640:Armt1 UTSW 10 4453572 missense probably damaging 0.97
R7715:Armt1 UTSW 10 4450751 missense probably benign 0.01
R8877:Armt1 UTSW 10 4450864 missense possibly damaging 0.66
R8968:Armt1 UTSW 10 4454150 missense probably damaging 1.00
R8973:Armt1 UTSW 10 4439550 missense probably damaging 0.99
R9096:Armt1 UTSW 10 4434829 missense probably damaging 1.00
R9404:Armt1 UTSW 10 4450848 frame shift probably null
R9405:Armt1 UTSW 10 4450848 frame shift probably null
R9408:Armt1 UTSW 10 4450848 frame shift probably null
R9563:Armt1 UTSW 10 4450848 frame shift probably null
R9785:Armt1 UTSW 10 4439606 missense probably damaging 1.00
Posted On 2013-06-28