Incidental Mutation 'R2040:Moxd2'
ID 225518
Institutional Source Beutler Lab
Gene Symbol Moxd2
Ensembl Gene ENSMUSG00000029885
Gene Name monooxygenase, DBH-like 2
Synonyms Dbhl1
MMRRC Submission 040047-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R2040 (G1)
Quality Score 225
Status Validated
Chromosome 6
Chromosomal Location 40855728-40864428 bp(-) (GRCm39)
Type of Mutation splice site (3 bp from exon)
DNA Base Change (assembly) T to C at 40861887 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000031937 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031937]
AlphaFold Q7TT41
Predicted Effect probably null
Transcript: ENSMUST00000031937
SMART Domains Protein: ENSMUSP00000031937
Gene: ENSMUSG00000029885

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
DoH 66 156 1.43e-12 SMART
Pfam:Cu2_monooxygen 192 316 8.3e-39 PFAM
Pfam:Cu2_monoox_C 336 493 1.8e-37 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192446
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.1%
Validation Efficiency 99% (67/68)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700028K03Rik A T 5: 107,693,607 (GRCm39) I75L probably benign Het
Abca2 T C 2: 25,333,817 (GRCm39) L1755P probably damaging Het
Adam6b A T 12: 113,454,364 (GRCm39) I394L probably benign Het
Ano2 T A 6: 126,016,471 (GRCm39) N1001K probably benign Het
Arap2 A T 5: 62,906,259 (GRCm39) N253K probably damaging Het
Ascc3 T C 10: 50,604,227 (GRCm39) C1316R probably benign Het
Atox1 T C 11: 55,341,343 (GRCm39) Y64C probably benign Het
Atp13a1 A G 8: 70,259,702 (GRCm39) T1098A possibly damaging Het
Casr T C 16: 36,330,728 (GRCm39) E202G possibly damaging Het
Cct2 T C 10: 116,889,018 (GRCm39) T494A probably benign Het
Cd209e T A 8: 3,899,158 (GRCm39) N185Y probably damaging Het
Celsr1 A G 15: 85,917,088 (GRCm39) L295P probably damaging Het
Cyp26a1 A G 19: 37,686,499 (GRCm39) T48A possibly damaging Het
Elovl3 A G 19: 46,121,567 (GRCm39) S37G probably benign Het
Fbh1 T G 2: 11,774,706 (GRCm39) D13A possibly damaging Het
Fpr-rs4 CAGGAA CA 17: 18,242,596 (GRCm39) probably null Het
Frem3 G T 8: 81,342,455 (GRCm39) V1583L possibly damaging Het
Gm21863 C A 12: 20,004,515 (GRCm39) Q4K possibly damaging Het
Gm266 T C 12: 111,452,132 (GRCm39) T25A possibly damaging Het
Gm8674 T C 13: 50,055,705 (GRCm39) noncoding transcript Het
Greb1 T C 12: 16,752,651 (GRCm39) H897R probably damaging Het
Hells A G 19: 38,943,474 (GRCm39) D565G probably damaging Het
Hfm1 C T 5: 107,049,684 (GRCm39) V426I probably damaging Het
Ints6 G A 14: 62,951,138 (GRCm39) T297I probably damaging Het
Itga10 C T 3: 96,559,054 (GRCm39) probably benign Het
Kmt2b A T 7: 30,268,845 (GRCm39) M2628K probably damaging Het
Ktn1 T G 14: 47,938,069 (GRCm39) probably benign Het
Lyst T A 13: 13,815,807 (GRCm39) D1230E probably benign Het
Mboat1 T C 13: 30,425,300 (GRCm39) probably null Het
Mtmr4 T C 11: 87,495,916 (GRCm39) M527T probably damaging Het
Myt1 T A 2: 181,467,717 (GRCm39) N1050K probably damaging Het
Ncoa6 A T 2: 155,248,000 (GRCm39) V1768E probably damaging Het
Nelfcd G A 2: 174,261,875 (GRCm39) C48Y probably damaging Het
Opn3 G A 1: 175,491,145 (GRCm39) A296V possibly damaging Het
Or13a22 T C 7: 140,073,295 (GRCm39) I248T probably benign Het
Or2z8 T A 8: 72,811,607 (GRCm39) F28I possibly damaging Het
Pam T C 1: 97,792,167 (GRCm39) E418G possibly damaging Het
Prrc2c A T 1: 162,525,126 (GRCm39) N493K probably damaging Het
Ptpn18 A G 1: 34,509,300 (GRCm39) Q165R probably damaging Het
Ptpro C A 6: 137,363,162 (GRCm39) probably benign Het
Ralgapa1 A G 12: 55,833,107 (GRCm39) F132S probably damaging Het
Robo1 T C 16: 72,730,630 (GRCm39) C244R probably damaging Het
Robo3 A C 9: 37,338,760 (GRCm39) V316G probably damaging Het
Rsl1 T C 13: 67,330,145 (GRCm39) S198P probably damaging Het
Rsph9 T C 17: 46,445,910 (GRCm39) D220G probably damaging Het
Rxfp2 A C 5: 149,993,677 (GRCm39) I580L probably benign Het
Septin7 G A 9: 25,199,532 (GRCm39) A144T possibly damaging Het
Sfn T C 4: 133,328,603 (GRCm39) K160E probably benign Het
Ski A G 4: 155,306,029 (GRCm39) Y317H probably damaging Het
Skic3 A C 13: 76,328,222 (GRCm39) R1423S probably damaging Het
Slc22a22 A T 15: 57,110,936 (GRCm39) Y430* probably null Het
Src A G 2: 157,299,030 (GRCm39) K9R probably benign Het
Srm C T 4: 148,678,453 (GRCm39) P255L possibly damaging Het
Stpg4 T A 17: 87,730,075 (GRCm39) N90I probably damaging Het
Sytl2 T A 7: 90,031,069 (GRCm39) probably benign Het
Tbpl2 T C 2: 23,984,871 (GRCm39) K92R probably benign Het
Tlcd4 G T 3: 121,024,975 (GRCm39) probably benign Het
Tmem38a T A 8: 73,335,096 (GRCm39) N178K probably damaging Het
Tnfaip3 T C 10: 18,883,900 (GRCm39) D160G possibly damaging Het
Vegfb T A 19: 6,963,407 (GRCm39) H119L possibly damaging Het
Vmn2r111 T A 17: 22,767,395 (GRCm39) I701F probably damaging Het
Vmn2r95 C T 17: 18,661,561 (GRCm39) L436F probably damaging Het
Wdr47 T C 3: 108,530,688 (GRCm39) C394R probably benign Het
Ythdc2 T A 18: 44,988,241 (GRCm39) Y16* probably null Het
Zer1 G A 2: 29,998,286 (GRCm39) L342F probably damaging Het
Zfp353-ps A G 8: 42,535,333 (GRCm39) noncoding transcript Het
Other mutations in Moxd2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00885:Moxd2 APN 6 40,861,113 (GRCm39) splice site probably benign
IGL02113:Moxd2 APN 6 40,862,338 (GRCm39) missense probably benign 0.06
IGL02223:Moxd2 APN 6 40,861,967 (GRCm39) missense probably damaging 1.00
IGL03204:Moxd2 APN 6 40,864,239 (GRCm39) missense probably benign 0.04
IGL03385:Moxd2 APN 6 40,855,952 (GRCm39) missense probably damaging 1.00
R0084:Moxd2 UTSW 6 40,856,342 (GRCm39) missense probably null 0.01
R1213:Moxd2 UTSW 6 40,868,831 (GRCm39) unclassified probably benign
R1326:Moxd2 UTSW 6 40,857,288 (GRCm39) missense probably benign 0.00
R1652:Moxd2 UTSW 6 40,864,337 (GRCm39) missense probably damaging 1.00
R1940:Moxd2 UTSW 6 40,860,466 (GRCm39) missense probably damaging 1.00
R2088:Moxd2 UTSW 6 40,861,901 (GRCm39) missense probably damaging 1.00
R3018:Moxd2 UTSW 6 40,855,820 (GRCm39) missense probably benign 0.01
R3962:Moxd2 UTSW 6 40,862,331 (GRCm39) missense probably benign
R4248:Moxd2 UTSW 6 40,855,933 (GRCm39) missense probably damaging 1.00
R4438:Moxd2 UTSW 6 40,860,996 (GRCm39) missense probably damaging 1.00
R4715:Moxd2 UTSW 6 40,864,181 (GRCm39) missense probably damaging 1.00
R4732:Moxd2 UTSW 6 40,855,793 (GRCm39) missense probably benign
R4733:Moxd2 UTSW 6 40,855,793 (GRCm39) missense probably benign
R4760:Moxd2 UTSW 6 40,868,537 (GRCm39) missense probably benign 0.06
R4851:Moxd2 UTSW 6 40,855,756 (GRCm39) missense probably damaging 1.00
R5087:Moxd2 UTSW 6 40,856,270 (GRCm39) missense probably damaging 1.00
R5187:Moxd2 UTSW 6 40,856,271 (GRCm39) missense probably benign 0.18
R5339:Moxd2 UTSW 6 40,862,354 (GRCm39) missense probably damaging 1.00
R5452:Moxd2 UTSW 6 40,859,048 (GRCm39) splice site probably null
R5860:Moxd2 UTSW 6 40,857,341 (GRCm39) missense probably damaging 1.00
R5973:Moxd2 UTSW 6 40,855,744 (GRCm39) missense probably damaging 0.96
R6015:Moxd2 UTSW 6 40,860,688 (GRCm39) missense probably damaging 1.00
R6316:Moxd2 UTSW 6 40,860,481 (GRCm39) missense probably damaging 1.00
R7500:Moxd2 UTSW 6 40,868,746 (GRCm39) missense probably benign
R7561:Moxd2 UTSW 6 40,864,337 (GRCm39) missense probably damaging 1.00
R7840:Moxd2 UTSW 6 40,862,378 (GRCm39) missense possibly damaging 0.95
R8042:Moxd2 UTSW 6 40,862,301 (GRCm39) missense probably benign 0.40
R9147:Moxd2 UTSW 6 40,860,978 (GRCm39) missense probably damaging 1.00
R9148:Moxd2 UTSW 6 40,860,978 (GRCm39) missense probably damaging 1.00
R9169:Moxd2 UTSW 6 40,860,490 (GRCm39) missense possibly damaging 0.94
R9259:Moxd2 UTSW 6 40,860,969 (GRCm39) missense probably damaging 1.00
R9291:Moxd2 UTSW 6 40,857,362 (GRCm39) missense probably damaging 1.00
R9448:Moxd2 UTSW 6 40,864,160 (GRCm39) missense probably benign 0.01
R9522:Moxd2 UTSW 6 40,857,375 (GRCm39) missense probably benign 0.13
R9635:Moxd2 UTSW 6 40,863,000 (GRCm39) missense possibly damaging 0.93
X0052:Moxd2 UTSW 6 40,859,462 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CCCCAGAAATTATGTGGCTTCC -3'
(R):5'- AGTTACTATGAGTTCCCTTGACCC -3'

Sequencing Primer
(F):5'- GAAATTATGTGGCTTCCAACCC -3'
(R):5'- AGTTCCCTTGACCCTGTGAGAAG -3'
Posted On 2014-08-25