Incidental Mutation 'IGL01777:Moxd1'
ID 154132
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Moxd1
Ensembl Gene ENSMUSG00000020000
Gene Name monooxygenase, DBH-like 1
Synonyms 3230402N08Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01777
Quality Score
Status
Chromosome 10
Chromosomal Location 24099415-24178681 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 24128494 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 182 (T182K)
Ref Sequence ENSEMBL: ENSMUSP00000093460 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095784]
AlphaFold Q9CXI3
Predicted Effect probably benign
Transcript: ENSMUST00000095784
AA Change: T182K

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000093460
Gene: ENSMUSG00000020000
AA Change: T182K

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
DoH 59 148 7.89e-15 SMART
Pfam:Cu2_monooxygen 186 315 2.7e-50 PFAM
Pfam:Cu2_monoox_C 334 491 2.1e-48 PFAM
low complexity region 602 613 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2 T C 3: 59,932,205 (GRCm39) V240A possibly damaging Het
Aftph A T 11: 20,676,554 (GRCm39) C352S possibly damaging Het
Cand2 T C 6: 115,769,818 (GRCm39) V876A probably damaging Het
Ccar1 T C 10: 62,616,356 (GRCm39) I125V possibly damaging Het
Celsr3 A T 9: 108,713,141 (GRCm39) M1858L probably benign Het
Csmd3 A T 15: 47,561,594 (GRCm39) N2134K probably benign Het
Dhx29 A G 13: 113,067,406 (GRCm39) I96V probably benign Het
Dst A G 1: 34,238,478 (GRCm39) T3727A probably benign Het
Elavl4 T A 4: 110,063,858 (GRCm39) probably null Het
Eno2 C T 6: 124,743,600 (GRCm39) G113D probably damaging Het
Esf1 A C 2: 139,999,092 (GRCm39) probably null Het
Frmd4b T C 6: 97,272,905 (GRCm39) D783G probably benign Het
Grin2a C T 16: 9,461,994 (GRCm39) V713I probably benign Het
Impa1 C T 3: 10,388,008 (GRCm39) G138D probably damaging Het
Kcnt2 A G 1: 140,523,736 (GRCm39) T1079A probably benign Het
Kmt2a A G 9: 44,760,302 (GRCm39) S549P probably damaging Het
Magoh C A 4: 107,740,373 (GRCm39) Q86K probably benign Het
Or5p55 A G 7: 107,566,709 (GRCm39) Y35C probably damaging Het
Pramel25 T G 4: 143,521,688 (GRCm39) C435G possibly damaging Het
Rab3b A T 4: 108,786,607 (GRCm39) Q119L probably damaging Het
Snap47 T A 11: 59,312,477 (GRCm39) probably null Het
Taar3 A G 10: 23,825,903 (GRCm39) R150G probably benign Het
Tas2r102 C T 6: 132,739,815 (GRCm39) T241I probably damaging Het
Tas2r114 C T 6: 131,666,664 (GRCm39) W121* probably null Het
Trak1 G A 9: 121,260,626 (GRCm39) probably null Het
Ubn1 T C 16: 4,890,013 (GRCm39) V426A possibly damaging Het
Vmn1r40 T C 6: 89,691,204 (GRCm39) L7P probably benign Het
Vmn2r43 T C 7: 8,258,272 (GRCm39) I314V probably damaging Het
Vrtn T G 12: 84,695,696 (GRCm39) S149A probably benign Het
Other mutations in Moxd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00091:Moxd1 APN 10 24,155,762 (GRCm39) missense probably damaging 1.00
IGL00227:Moxd1 APN 10 24,158,491 (GRCm39) missense probably damaging 1.00
IGL00331:Moxd1 APN 10 24,158,453 (GRCm39) splice site probably benign
IGL01074:Moxd1 APN 10 24,155,282 (GRCm39) missense probably benign 0.45
IGL01462:Moxd1 APN 10 24,120,286 (GRCm39) critical splice donor site probably null
IGL02051:Moxd1 APN 10 24,128,916 (GRCm39) splice site probably null
IGL02272:Moxd1 APN 10 24,158,598 (GRCm39) nonsense probably null
IGL02343:Moxd1 APN 10 24,155,762 (GRCm39) missense probably damaging 1.00
IGL02425:Moxd1 APN 10 24,155,334 (GRCm39) missense probably benign 0.01
IGL02448:Moxd1 APN 10 24,158,617 (GRCm39) missense probably damaging 0.99
IGL02452:Moxd1 APN 10 24,158,650 (GRCm39) missense probably damaging 1.00
IGL03301:Moxd1 APN 10 24,155,382 (GRCm39) missense probably damaging 0.99
R0631:Moxd1 UTSW 10 24,128,852 (GRCm39) missense probably damaging 1.00
R1436:Moxd1 UTSW 10 24,120,256 (GRCm39) missense probably damaging 1.00
R1484:Moxd1 UTSW 10 24,099,758 (GRCm39) missense probably damaging 1.00
R1574:Moxd1 UTSW 10 24,176,217 (GRCm39) missense probably damaging 1.00
R1574:Moxd1 UTSW 10 24,176,217 (GRCm39) missense probably damaging 1.00
R1713:Moxd1 UTSW 10 24,157,394 (GRCm39) missense probably damaging 1.00
R1954:Moxd1 UTSW 10 24,155,781 (GRCm39) missense probably benign 0.17
R3115:Moxd1 UTSW 10 24,177,429 (GRCm39) nonsense probably null
R3116:Moxd1 UTSW 10 24,177,429 (GRCm39) nonsense probably null
R5183:Moxd1 UTSW 10 24,163,034 (GRCm39) missense probably damaging 1.00
R5183:Moxd1 UTSW 10 24,155,445 (GRCm39) critical splice donor site probably null
R5322:Moxd1 UTSW 10 24,120,151 (GRCm39) missense possibly damaging 0.88
R5728:Moxd1 UTSW 10 24,099,581 (GRCm39) missense possibly damaging 0.92
R5824:Moxd1 UTSW 10 24,162,995 (GRCm39) missense probably damaging 1.00
R6158:Moxd1 UTSW 10 24,160,675 (GRCm39) missense probably damaging 1.00
R6322:Moxd1 UTSW 10 24,160,709 (GRCm39) missense probably damaging 1.00
R6662:Moxd1 UTSW 10 24,160,658 (GRCm39) missense probably damaging 1.00
R6827:Moxd1 UTSW 10 24,155,748 (GRCm39) missense probably benign 0.29
R6928:Moxd1 UTSW 10 24,176,186 (GRCm39) missense probably damaging 1.00
R7048:Moxd1 UTSW 10 24,157,374 (GRCm39) missense probably damaging 1.00
R7320:Moxd1 UTSW 10 24,177,363 (GRCm39) missense probably benign 0.05
R7736:Moxd1 UTSW 10 24,158,608 (GRCm39) missense probably damaging 1.00
R8060:Moxd1 UTSW 10 24,177,510 (GRCm39) missense unknown
R8073:Moxd1 UTSW 10 24,128,848 (GRCm39) missense probably damaging 1.00
R8089:Moxd1 UTSW 10 24,157,417 (GRCm39) missense probably benign 0.43
R8255:Moxd1 UTSW 10 24,099,700 (GRCm39) missense probably benign 0.02
R8314:Moxd1 UTSW 10 24,128,438 (GRCm39) missense possibly damaging 0.81
R9039:Moxd1 UTSW 10 24,155,251 (GRCm39) splice site probably benign
R9099:Moxd1 UTSW 10 24,155,762 (GRCm39) missense probably damaging 1.00
R9306:Moxd1 UTSW 10 24,128,824 (GRCm39) splice site probably benign
R9657:Moxd1 UTSW 10 24,128,485 (GRCm39) missense probably benign 0.16
X0063:Moxd1 UTSW 10 24,128,398 (GRCm39) missense probably benign 0.18
Z1177:Moxd1 UTSW 10 24,160,702 (GRCm39) missense probably benign
Posted On 2014-02-04