Incidental Mutation 'R4227:Naip5'
ID 320105
Institutional Source Beutler Lab
Gene Symbol Naip5
Ensembl Gene ENSMUSG00000071203
Gene Name NLR family, apoptosis inhibitory protein 5
Synonyms Birc1e, Lgn1, Naip-rs3
MMRRC Submission 041047-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # R4227 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 100211739-100246323 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 100212768 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 1351 (S1351P)
Ref Sequence ENSEMBL: ENSMUSP00000058611 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049789]
AlphaFold Q9R016
Predicted Effect probably damaging
Transcript: ENSMUST00000049789
AA Change: S1351P

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000058611
Gene: ENSMUSG00000071203
AA Change: S1351P

DomainStartEndE-ValueType
low complexity region 36 51 N/A INTRINSIC
BIR 58 129 1.08e-19 SMART
BIR 157 229 1.06e-36 SMART
BIR 276 347 2.14e-32 SMART
Pfam:NACHT 464 618 1.7e-36 PFAM
low complexity region 851 862 N/A INTRINSIC
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency 97% (56/58)
MGI Phenotype PHENOTYPE: This locus controls resistance to Legionella pneumophila, the organism responsible for Legionnaire's disease. Cultured peritoneal macrophages from A/J mice are susceptible, supporting bacterial proliferation; other strains, e.g., C57BL/6 are resistant. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T C 2: 69,284,776 T609A probably damaging Het
Agbl2 T G 2: 90,801,453 L385R probably damaging Het
Arfgef2 A T 2: 166,867,324 D1107V probably damaging Het
Arhgef5 C T 6: 43,279,498 A1180V probably damaging Het
B9d1 C G 11: 61,512,657 R160G probably damaging Het
Birc6 T C 17: 74,619,840 probably null Het
Capn11 A G 17: 45,642,466 probably null Het
Ceacam12 G T 7: 18,071,753 M288I probably benign Het
Cfhr3 T A 1: 139,608,308 noncoding transcript Het
Copa A G 1: 172,118,115 probably benign Het
Cypt4 A G 9: 24,625,492 M93V probably benign Het
Fat3 G A 9: 16,377,693 T178I probably damaging Het
Gm15931 A G 7: 4,274,794 noncoding transcript Het
Gm9871 A G 6: 101,796,693 noncoding transcript Het
Gpsm1 T C 2: 26,339,626 probably benign Het
Grhl1 A G 12: 24,611,851 T510A probably benign Het
Kcnn3 A C 3: 89,521,175 H236P possibly damaging Het
Kif21b T A 1: 136,154,093 probably null Het
Lcn3 G T 2: 25,766,111 M59I probably benign Het
Mrps27 C G 13: 99,411,340 P253A probably damaging Het
Mug2 A T 6: 122,040,732 D476V probably benign Het
Naca A T 10: 128,041,661 probably benign Het
Odf2 A G 2: 29,901,284 probably benign Het
Olfr1143 T A 2: 87,802,875 I162N probably damaging Het
Olfr1284 A G 2: 111,379,065 K22E probably benign Het
Olfr444 A G 6: 42,955,714 Y72C possibly damaging Het
Olfr598 A T 7: 103,328,819 H111L probably damaging Het
P3h2 G T 16: 26,105,453 D77E probably benign Het
Pcbp2 A G 15: 102,478,631 M87V probably benign Het
Plekhg6 A G 6: 125,378,805 L12P probably damaging Het
Plekhh2 A G 17: 84,566,795 T503A probably benign Het
Pnpla3 C A 15: 84,179,190 N256K probably benign Het
Polh A G 17: 46,172,594 S582P probably benign Het
Ptprb T C 10: 116,302,225 Y345H possibly damaging Het
Rasl11b T A 5: 74,198,191 I119N probably damaging Het
Rnaseh2a G A 8: 84,960,073 T149I possibly damaging Het
Serpina10 A G 12: 103,628,415 Y182H probably damaging Het
Serpina1d A G 12: 103,767,481 V188A probably benign Het
Setd1a C A 7: 127,796,647 probably benign Het
Slc17a8 T C 10: 89,598,713 N184S probably damaging Het
Spen C T 4: 141,522,147 S110N unknown Het
Tas1r1 T C 4: 152,028,272 I775V probably damaging Het
Tktl2 A G 8: 66,513,699 probably null Het
Tmem181a T A 17: 6,295,786 L185H probably damaging Het
Tmprss6 C T 15: 78,446,699 V43M probably damaging Het
Try5 A G 6: 41,313,467 Y28H possibly damaging Het
Urad A T 5: 147,315,290 F117L probably damaging Het
Vegfc A G 8: 54,159,410 Y156C probably damaging Het
Vmn2r45 A T 7: 8,483,278 V337E probably damaging Het
Vmn2r6 A T 3: 64,537,948 F696L probably damaging Het
Wnk2 C T 13: 49,090,837 D508N probably damaging Het
Zfp131 T C 13: 119,766,746 D455G probably damaging Het
Other mutations in Naip5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00096:Naip5 APN 13 100,246,175 (GRCm38) nonsense probably null
IGL00493:Naip5 APN 13 100,230,771 (GRCm38) missense probably damaging 0.96
IGL01294:Naip5 APN 13 100,217,080 (GRCm38) missense probably damaging 0.99
IGL01405:Naip5 APN 13 100,221,945 (GRCm38) missense probably benign 0.11
IGL01568:Naip5 APN 13 100,217,101 (GRCm38) missense probably benign 0.26
IGL01804:Naip5 APN 13 100,221,584 (GRCm38) missense probably damaging 1.00
IGL02012:Naip5 APN 13 100,223,339 (GRCm38) missense probably benign 0.01
IGL02183:Naip5 APN 13 100,221,642 (GRCm38) missense probably benign 0.41
IGL02449:Naip5 APN 13 100,222,175 (GRCm38) missense probably benign 0.34
IGL02815:Naip5 APN 13 100,222,731 (GRCm38) missense probably benign
IGL02992:Naip5 APN 13 100,223,028 (GRCm38) missense probably damaging 1.00
IGL03027:Naip5 APN 13 100,223,016 (GRCm38) missense probably benign 0.00
IGL03234:Naip5 APN 13 100,212,627 (GRCm38) missense probably damaging 1.00
inwood2 UTSW 13 100,223,014 (GRCm38) nonsense probably null
inwood3 UTSW 13 100,221,903 (GRCm38) nonsense probably null
Nuchal UTSW 13 100,214,663 (GRCm38) missense possibly damaging 0.82
PIT4131001:Naip5 UTSW 13 100,219,760 (GRCm38) missense probably benign 0.00
PIT4131001:Naip5 UTSW 13 100,219,739 (GRCm38) missense probably benign
R0001:Naip5 UTSW 13 100,223,114 (GRCm38) missense probably benign
R0001:Naip5 UTSW 13 100,214,650 (GRCm38) critical splice donor site probably null
R0462:Naip5 UTSW 13 100,221,732 (GRCm38) missense probably damaging 1.00
R0636:Naip5 UTSW 13 100,219,688 (GRCm38) missense probably benign
R0674:Naip5 UTSW 13 100,223,199 (GRCm38) missense probably benign 0.04
R0764:Naip5 UTSW 13 100,217,105 (GRCm38) missense probably benign 0.03
R0837:Naip5 UTSW 13 100,230,743 (GRCm38) missense probably benign
R1179:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R1302:Naip5 UTSW 13 100,221,591 (GRCm38) missense possibly damaging 0.91
R1441:Naip5 UTSW 13 100,219,717 (GRCm38) missense possibly damaging 0.95
R1513:Naip5 UTSW 13 100,222,206 (GRCm38) missense probably benign
R1638:Naip5 UTSW 13 100,212,669 (GRCm38) missense probably damaging 1.00
R1651:Naip5 UTSW 13 100,221,911 (GRCm38) missense probably benign 0.41
R1707:Naip5 UTSW 13 100,242,855 (GRCm38) missense probably damaging 1.00
R1835:Naip5 UTSW 13 100,223,218 (GRCm38) nonsense probably null
R1836:Naip5 UTSW 13 100,219,687 (GRCm38) missense probably benign 0.18
R1972:Naip5 UTSW 13 100,212,770 (GRCm38) missense probably damaging 0.98
R2080:Naip5 UTSW 13 100,221,533 (GRCm38) missense probably damaging 1.00
R2333:Naip5 UTSW 13 100,223,171 (GRCm38) missense probably damaging 1.00
R2348:Naip5 UTSW 13 100,219,738 (GRCm38) missense probably benign 0.01
R3055:Naip5 UTSW 13 100,221,878 (GRCm38) missense probably benign 0.23
R3401:Naip5 UTSW 13 100,221,903 (GRCm38) nonsense probably null
R3723:Naip5 UTSW 13 100,223,014 (GRCm38) nonsense probably null
R3775:Naip5 UTSW 13 100,223,394 (GRCm38) missense probably benign 0.00
R3775:Naip5 UTSW 13 100,223,375 (GRCm38) missense probably benign 0.00
R4019:Naip5 UTSW 13 100,223,375 (GRCm38) missense probably benign 0.00
R4019:Naip5 UTSW 13 100,223,394 (GRCm38) missense probably benign 0.00
R4020:Naip5 UTSW 13 100,223,394 (GRCm38) missense probably benign 0.00
R4020:Naip5 UTSW 13 100,223,375 (GRCm38) missense probably benign 0.00
R4074:Naip5 UTSW 13 100,246,064 (GRCm38) missense probably damaging 1.00
R4082:Naip5 UTSW 13 100,245,830 (GRCm38) missense probably damaging 1.00
R4105:Naip5 UTSW 13 100,219,739 (GRCm38) missense probably benign
R4639:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R4640:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R4641:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R4644:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R4645:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R4700:Naip5 UTSW 13 100,223,414 (GRCm38) missense possibly damaging 0.62
R4727:Naip5 UTSW 13 100,221,870 (GRCm38) missense possibly damaging 0.81
R4729:Naip5 UTSW 13 100,222,131 (GRCm38) missense possibly damaging 0.75
R4816:Naip5 UTSW 13 100,219,681 (GRCm38) missense probably benign 0.32
R4816:Naip5 UTSW 13 100,219,687 (GRCm38) missense probably benign 0.01
R4816:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R4869:Naip5 UTSW 13 100,245,131 (GRCm38) missense probably damaging 1.00
R5162:Naip5 UTSW 13 100,223,406 (GRCm38) missense possibly damaging 0.78
R5244:Naip5 UTSW 13 100,245,662 (GRCm38) missense probably benign 0.08
R5411:Naip5 UTSW 13 100,245,746 (GRCm38) missense possibly damaging 0.54
R5632:Naip5 UTSW 13 100,230,662 (GRCm38) splice site probably null
R5760:Naip5 UTSW 13 100,242,838 (GRCm38) missense probably damaging 1.00
R5916:Naip5 UTSW 13 100,222,701 (GRCm38) missense probably benign 0.02
R6302:Naip5 UTSW 13 100,223,166 (GRCm38) missense possibly damaging 0.76
R6304:Naip5 UTSW 13 100,223,166 (GRCm38) missense possibly damaging 0.76
R6411:Naip5 UTSW 13 100,223,405 (GRCm38) missense probably benign 0.01
R6474:Naip5 UTSW 13 100,214,663 (GRCm38) missense possibly damaging 0.82
R6499:Naip5 UTSW 13 100,221,594 (GRCm38) missense probably benign
R6544:Naip5 UTSW 13 100,223,144 (GRCm38) missense possibly damaging 0.50
R6827:Naip5 UTSW 13 100,245,929 (GRCm38) missense possibly damaging 0.48
R6954:Naip5 UTSW 13 100,223,414 (GRCm38) missense probably damaging 0.99
R7052:Naip5 UTSW 13 100,222,347 (GRCm38) missense probably benign 0.01
R7138:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R7141:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R7375:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7375:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7401:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7401:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7447:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7447:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7466:Naip5 UTSW 13 100,221,986 (GRCm38) nonsense probably null
R7491:Naip5 UTSW 13 100,217,071 (GRCm38) missense probably benign 0.18
R7559:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7559:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7562:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7562:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7588:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7588:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7589:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7589:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7590:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7590:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
R7742:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R7886:Naip5 UTSW 13 100,246,181 (GRCm38) missense probably benign 0.28
R7996:Naip5 UTSW 13 100,221,656 (GRCm38) missense probably damaging 1.00
R8026:Naip5 UTSW 13 100,245,898 (GRCm38) missense probably damaging 1.00
R8046:Naip5 UTSW 13 100,222,233 (GRCm38) missense probably benign
R8319:Naip5 UTSW 13 100,221,659 (GRCm38) missense probably benign 0.12
R8471:Naip5 UTSW 13 100,221,645 (GRCm38) missense probably damaging 0.99
R8480:Naip5 UTSW 13 100,222,235 (GRCm38) missense probably damaging 1.00
R8496:Naip5 UTSW 13 100,212,739 (GRCm38) missense probably benign 0.00
R8500:Naip5 UTSW 13 100,222,712 (GRCm38) missense probably damaging 0.98
R8712:Naip5 UTSW 13 100,223,096 (GRCm38) missense possibly damaging 0.61
R8780:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R8781:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R8788:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R8817:Naip5 UTSW 13 100,212,699 (GRCm38) missense probably benign 0.01
R8833:Naip5 UTSW 13 100,222,934 (GRCm38) missense probably damaging 0.97
R8835:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R8958:Naip5 UTSW 13 100,217,609 (GRCm38) nonsense probably null
R9031:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9032:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9074:Naip5 UTSW 13 100,221,756 (GRCm38) missense possibly damaging 0.92
R9098:Naip5 UTSW 13 100,229,619 (GRCm38) missense possibly damaging 0.67
R9204:Naip5 UTSW 13 100,222,500 (GRCm38) missense probably damaging 1.00
R9223:Naip5 UTSW 13 100,227,676 (GRCm38) missense probably benign 0.05
R9358:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9389:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9403:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9518:Naip5 UTSW 13 100,221,859 (GRCm38) missense probably benign
R9568:Naip5 UTSW 13 100,223,313 (GRCm38) missense probably benign 0.00
R9568:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9569:Naip5 UTSW 13 100,223,313 (GRCm38) missense probably benign 0.00
R9569:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9570:Naip5 UTSW 13 100,223,313 (GRCm38) missense probably benign 0.00
R9572:Naip5 UTSW 13 100,223,313 (GRCm38) missense probably benign 0.00
R9581:Naip5 UTSW 13 100,214,686 (GRCm38) missense probably benign 0.11
R9627:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
R9725:Naip5 UTSW 13 100,222,276 (GRCm38) missense possibly damaging 0.94
R9763:Naip5 UTSW 13 100,230,761 (GRCm38) missense probably damaging 0.99
R9764:Naip5 UTSW 13 100,230,761 (GRCm38) missense probably damaging 0.99
R9765:Naip5 UTSW 13 100,230,761 (GRCm38) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- CAGTAGTCTTCAGGAGCATCC -3'
(R):5'- CATACGTGTTTTGTTTTCAGCCAGG -3'

Sequencing Primer
(F):5'- TCCTTTACTCCAGGATAACAGGAGAG -3'
(R):5'- GGCGGCAACCAGTGGAG -3'
Posted On 2015-06-12