Incidental Mutation 'R6747:Nos2'
ID 530604
Institutional Source Beutler Lab
Gene Symbol Nos2
Ensembl Gene ENSMUSG00000020826
Gene Name nitric oxide synthase 2, inducible
Synonyms iNOS, Nos-2, Nos2a, NOS-II
MMRRC Submission 044864-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6747 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 78920787-78960254 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 78952954 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 909 (D909G)
Ref Sequence ENSEMBL: ENSMUSP00000018610 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018610] [ENSMUST00000214397]
AlphaFold P29477
PDB Structure MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN (DELTA 114) (N-[(1,3-BENZODIOXOL-5-YL)METHYL]-1-[2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL]-4-(METHOXYCARBONYL)-PIPERAZINE-2-ACETAMIDE COMPLEX [X-RAY DIFFRACTION]
MURINE INOSOXY DIMER WITH ISOTHIOUREA BOUND IN THE ACTIVE SITE [X-RAY DIFFRACTION]
MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DIMER N-HYDROXYARGININE AND 4-AMINO TETRAHYDROBIOPTERIN [X-RAY DIFFRACTION]
MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DIMER N-HYDROXYARGININE AND DIHYDROBIOPTERIN [X-RAY DIFFRACTION]
MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DIMER N-HYDROXYARGININE AND TETRAHYDROBIOPTERIN [X-RAY DIFFRACTION]
Murine Inducible Nitric Oxide Synthase Oxygenase Dimer (Delta 65) with W457F Mutation at Tetrahydrobiopterin Binding Site [X-RAY DIFFRACTION]
Murine Inducible Nitric Oxide Synthase Oxygenase Dimer (Delta 65) with W457A Mutation at Tetrahydrobiopterin Binding Site [X-RAY DIFFRACTION]
inducible nitric oxide synthase with Chlorzoxazone bound [X-RAY DIFFRACTION]
inducible nitric oxide synthase with 7-nitroindazole bound [X-RAY DIFFRACTION]
inducible nitric oxide synthase with 6-nitroindazole bound [X-RAY DIFFRACTION]
>> 40 additional structures at PDB <<
Predicted Effect probably damaging
Transcript: ENSMUST00000018610
AA Change: D909G

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000018610
Gene: ENSMUSG00000020826
AA Change: D909G

DomainStartEndE-ValueType
Pfam:NO_synthase 129 491 6.7e-189 PFAM
Pfam:Flavodoxin_1 535 666 5.5e-43 PFAM
Pfam:FAD_binding_1 719 941 8.8e-79 PFAM
Pfam:NAD_binding_1 973 1087 4.1e-24 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214397
AA Change: D796G

PolyPhen 2 Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
Meta Mutation Damage Score 0.2154 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 96.0%
Validation Efficiency 97% (68/70)
MGI Phenotype FUNCTION: Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. This gene encodes a nitric oxide synthase that is inducible by a combination of lipopolysaccharide and certain cytokines. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygous deletion of this gene alters susceptibility to infection, response to injury, sepsis and sensory stimuli, cardiac function, osteoclast, platelet and mammary gland physiology, tumor growth, testis and uterus morphology, diet-induced atherosclerosis, and blood, urine and glucose metabolism. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 C T 3: 122,126,313 (GRCm38) probably null Het
Acyp1 C T 12: 85,278,905 (GRCm38) V107I probably null Het
Aftph T C 11: 20,726,144 (GRCm38) probably null Het
Agtpbp1 A T 13: 59,544,353 (GRCm38) probably null Het
Arhgap15 C A 2: 44,116,677 (GRCm38) P269T probably damaging Het
Arhgap30 T C 1: 171,407,729 (GRCm38) V557A probably damaging Het
Asb3 T A 11: 31,081,493 (GRCm38) M410K probably benign Het
B4galnt2 T C 11: 95,868,634 (GRCm38) probably null Het
Birc3 A G 9: 7,860,261 (GRCm38) probably null Het
Cav2 A T 6: 17,286,951 (GRCm38) N69Y probably damaging Het
Cc2d2b G A 19: 40,795,667 (GRCm38) C826Y probably benign Het
Cenpf T A 1: 189,652,854 (GRCm38) T2410S probably benign Het
Chchd1 A G 14: 20,703,380 (GRCm38) D24G probably benign Het
Cmip G A 8: 117,436,879 (GRCm38) G450S probably benign Het
Col11a1 C T 3: 114,212,450 (GRCm38) Q534* probably null Het
Col3a1 G T 1: 45,338,622 (GRCm38) probably benign Het
Cox4i1 T C 8: 120,673,230 (GRCm38) I31T possibly damaging Het
Cstf3 G T 2: 104,646,767 (GRCm38) V168F probably damaging Het
Dapk1 T C 13: 60,725,340 (GRCm38) I352T probably benign Het
Ddx52 T C 11: 83,955,302 (GRCm38) V456A probably damaging Het
Dmxl2 A T 9: 54,416,088 (GRCm38) H1337Q probably damaging Het
Dnah7a T C 1: 53,636,062 (GRCm38) T369A probably benign Het
Dppa1 T A 11: 46,625,595 (GRCm38) I8F unknown Het
Ebf1 G T 11: 44,883,814 (GRCm38) V213F probably damaging Het
Foxb2 C A 19: 16,872,833 (GRCm38) E270* probably null Het
Gclc A T 9: 77,788,245 (GRCm38) R450W probably damaging Het
Gm13128 T C 4: 144,332,978 (GRCm38) W420R probably benign Het
Grin2d T C 7: 45,862,268 (GRCm38) E251G probably damaging Het
Hal A T 10: 93,500,677 (GRCm38) N423Y probably damaging Het
Krtap4-8 T A 11: 99,780,091 (GRCm38) I185F unknown Het
Lrp3 T A 7: 35,211,437 (GRCm38) Q61L probably benign Het
Met A C 6: 17,571,467 (GRCm38) Q1296H probably damaging Het
Mphosph9 T A 5: 124,297,699 (GRCm38) N557I possibly damaging Het
Mrpl46 C A 7: 78,782,981 (GRCm38) W16C probably benign Het
Myh13 G A 11: 67,350,419 (GRCm38) R874Q probably damaging Het
Nelfb G A 2: 25,203,381 (GRCm38) T453I probably benign Het
Nr5a2 T C 1: 136,882,344 (GRCm38) E431G possibly damaging Het
Nsmce2 A G 15: 59,591,724 (GRCm38) D149G probably benign Het
Olfr203 T C 16: 59,303,641 (GRCm38) F164L probably benign Het
Olfr690 C T 7: 105,330,027 (GRCm38) R55H probably benign Het
Pcbp4 C A 9: 106,460,648 (GRCm38) probably null Het
Peg10 A G 6: 4,757,137 (GRCm38) probably benign Het
Pms2 C T 5: 143,925,419 (GRCm38) P154L probably benign Het
Pou6f2 A C 13: 18,129,187 (GRCm38) L112R probably benign Het
Prdm6 A T 18: 53,465,046 (GRCm38) probably benign Het
Prob1 G A 18: 35,655,154 (GRCm38) R12W probably damaging Het
Rif1 T A 2: 52,078,263 (GRCm38) probably null Het
Rpl9-ps6 A G 19: 32,466,143 (GRCm38) S137P probably benign Het
Rsf1 GGCG GGCGACGGCAGCG 7: 97,579,906 (GRCm38) probably benign Homo
Sec23ip A G 7: 128,752,849 (GRCm38) silent Het
Slc38a9 T C 13: 112,690,180 (GRCm38) C151R probably benign Het
Slc39a8 T C 3: 135,849,180 (GRCm38) probably null Het
Slc6a18 C A 13: 73,677,991 (GRCm38) probably benign Het
Snw1 T C 12: 87,464,710 (GRCm38) D57G probably damaging Het
Sox6 C G 7: 115,541,731 (GRCm38) R505P probably damaging Het
Speg T C 1: 75,410,395 (GRCm38) probably null Het
Spire2 C T 8: 123,356,846 (GRCm38) R190C probably damaging Het
Stard9 A C 2: 120,698,383 (GRCm38) H1707P possibly damaging Het
Tenm3 G T 8: 48,343,243 (GRCm38) T237K probably damaging Het
Themis2 T A 4: 132,796,262 (GRCm38) E31V possibly damaging Het
Trim56 T G 5: 137,114,521 (GRCm38) Q47P probably damaging Het
Trim58 T C 11: 58,651,264 (GRCm38) I350T probably benign Het
Ttll7 C T 3: 146,944,056 (GRCm38) P639S probably benign Het
Ubxn6 A G 17: 56,070,650 (GRCm38) probably null Het
Vmn2r114 A T 17: 23,309,876 (GRCm38) F417L probably benign Het
Vmn2r29 T A 7: 7,231,422 (GRCm38) M822L probably benign Het
Vps9d1 T C 8: 123,254,007 (GRCm38) D27G probably damaging Het
Wdr3 C T 3: 100,138,724 (GRCm38) R931Q probably damaging Het
Whamm G A 7: 81,578,302 (GRCm38) probably null Het
Zcchc24 T C 14: 25,757,033 (GRCm38) H142R probably damaging Het
Zfp292 T C 4: 34,806,894 (GRCm38) K2050R probably damaging Het
Other mutations in Nos2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01388:Nos2 APN 11 78,957,452 (GRCm38) missense probably damaging 0.96
IGL01503:Nos2 APN 11 78,945,863 (GRCm38) splice site probably benign
IGL01789:Nos2 APN 11 78,944,657 (GRCm38) splice site probably benign
IGL02797:Nos2 APN 11 78,940,344 (GRCm38) missense probably damaging 1.00
IGL02968:Nos2 APN 11 78,937,637 (GRCm38) missense probably damaging 1.00
R6762_Nos2_754 UTSW 11 78,959,748 (GRCm38) missense possibly damaging 0.90
R0035:Nos2 UTSW 11 78,945,727 (GRCm38) missense probably damaging 1.00
R0265:Nos2 UTSW 11 78,937,602 (GRCm38) missense probably damaging 0.98
R0441:Nos2 UTSW 11 78,928,583 (GRCm38) missense probably benign 0.10
R0504:Nos2 UTSW 11 78,940,077 (GRCm38) missense probably damaging 1.00
R0570:Nos2 UTSW 11 78,935,361 (GRCm38) missense possibly damaging 0.49
R1356:Nos2 UTSW 11 78,952,803 (GRCm38) missense probably benign 0.00
R1538:Nos2 UTSW 11 78,956,570 (GRCm38) missense probably benign 0.00
R3414:Nos2 UTSW 11 78,957,588 (GRCm38) missense probably benign 0.14
R3418:Nos2 UTSW 11 78,959,695 (GRCm38) missense possibly damaging 0.47
R4279:Nos2 UTSW 11 78,929,776 (GRCm38) missense probably benign 0.01
R4492:Nos2 UTSW 11 78,950,095 (GRCm38) missense probably benign
R4632:Nos2 UTSW 11 78,957,591 (GRCm38) missense possibly damaging 0.95
R4686:Nos2 UTSW 11 78,928,630 (GRCm38) missense possibly damaging 0.65
R5038:Nos2 UTSW 11 78,922,314 (GRCm38) missense probably benign
R5214:Nos2 UTSW 11 78,955,441 (GRCm38) missense probably damaging 1.00
R5377:Nos2 UTSW 11 78,957,491 (GRCm38) missense probably benign 0.00
R5777:Nos2 UTSW 11 78,940,152 (GRCm38) missense probably null 1.00
R5834:Nos2 UTSW 11 78,928,579 (GRCm38) missense probably benign 0.01
R5930:Nos2 UTSW 11 78,937,915 (GRCm38) missense probably damaging 1.00
R6511:Nos2 UTSW 11 78,955,464 (GRCm38) splice site probably null
R6706:Nos2 UTSW 11 78,944,723 (GRCm38) missense possibly damaging 0.60
R6762:Nos2 UTSW 11 78,959,748 (GRCm38) missense possibly damaging 0.90
R6817:Nos2 UTSW 11 78,945,266 (GRCm38) missense possibly damaging 0.64
R6868:Nos2 UTSW 11 78,957,506 (GRCm38) missense probably benign 0.02
R6917:Nos2 UTSW 11 78,951,227 (GRCm38) missense possibly damaging 0.50
R7082:Nos2 UTSW 11 78,928,579 (GRCm38) missense probably benign 0.02
R7286:Nos2 UTSW 11 78,929,854 (GRCm38) missense probably damaging 1.00
R7367:Nos2 UTSW 11 78,950,090 (GRCm38) missense possibly damaging 0.77
R7398:Nos2 UTSW 11 78,936,471 (GRCm38) nonsense probably null
R7411:Nos2 UTSW 11 78,944,855 (GRCm38) critical splice donor site probably null
R7469:Nos2 UTSW 11 78,952,971 (GRCm38) missense possibly damaging 0.94
R7736:Nos2 UTSW 11 78,922,366 (GRCm38) nonsense probably null
R8694:Nos2 UTSW 11 78,945,689 (GRCm38) missense possibly damaging 0.93
R8832:Nos2 UTSW 11 78,955,464 (GRCm38) splice site probably null
R8872:Nos2 UTSW 11 78,949,123 (GRCm38) missense probably damaging 0.99
R8952:Nos2 UTSW 11 78,945,263 (GRCm38) missense probably benign 0.00
R9433:Nos2 UTSW 11 78,959,664 (GRCm38) missense probably damaging 1.00
R9580:Nos2 UTSW 11 78,937,631 (GRCm38) missense probably benign 0.01
R9612:Nos2 UTSW 11 78,949,158 (GRCm38) missense probably damaging 1.00
R9727:Nos2 UTSW 11 78,952,999 (GRCm38) missense possibly damaging 0.51
R9747:Nos2 UTSW 11 78,931,646 (GRCm38) missense probably damaging 0.96
X0063:Nos2 UTSW 11 78,922,367 (GRCm38) missense probably benign 0.01
Z1177:Nos2 UTSW 11 78,931,672 (GRCm38) missense probably benign
Predicted Primers PCR Primer
(F):5'- TGGATAGCGCCCGTCTTTTG -3'
(R):5'- ATCTTGCCCTAAAGTGGTGGC -3'

Sequencing Primer
(F):5'- CGTTTGTTGAAGGAATGAATGGATAC -3'
(R):5'- CCCTAAAGTGGTGGCAGTCAG -3'
Posted On 2018-08-01