Incidental Mutation 'R7886:Naip5'
ID 609080
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 045938-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # R7886 (G1)
Quality Score 225.009
Status Validated
Chromosome 13
Chromosomal Location 100211739-100246323 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 100246181 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 7 (S7T)
Ref Sequence ENSEMBL: ENSMUSP00000058611 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049789]
AlphaFold Q9R016
Predicted Effect probably benign
Transcript: ENSMUST00000049789
AA Change: S7T

PolyPhen 2 Score 0.276 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000058611
Gene: ENSMUSG00000071203
AA Change: S7T

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (53/53)
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A730049H05Rik T G 6: 92,834,456 I130S unknown Het
Ano5 A G 7: 51,570,393 H427R probably benign Het
Atad2 A T 15: 58,126,136 V182E probably damaging Het
B4galnt1 T C 10: 127,167,054 Y147H probably damaging Het
C1s2 T C 6: 124,628,330 S349G possibly damaging Het
Ccdc51 G T 9: 109,091,587 A181S probably damaging Het
Dcc G A 18: 71,954,868 Q100* probably null Het
Dchs2 A T 3: 83,305,085 I2064F probably damaging Het
Depdc1a G A 3: 159,516,069 V217I probably benign Het
Dnajc7 A T 11: 100,601,803 F31I probably benign Het
Eftud2 C T 11: 102,840,108 R825H probably damaging Het
Fam184a T C 10: 53,675,160 E237G probably damaging Het
Fdx1l A T 9: 21,073,327 probably null Het
Frem1 T C 4: 83,016,406 D106G possibly damaging Het
Gabrg3 G A 7: 56,724,481 R446W probably damaging Het
Gm42669 A G 5: 107,508,706 E362G Het
Hmcn1 A T 1: 150,657,470 I3022N possibly damaging Het
Ifna2 C A 4: 88,683,269 V171F probably damaging Het
Igsf10 T C 3: 59,328,327 N1478D probably benign Het
Kcnc1 C A 7: 46,427,621 D282E probably damaging Het
Klhdc2 G A 12: 69,304,632 probably null Het
Macrod2 G A 2: 141,724,645 G188S probably damaging Het
Mapkbp1 T C 2: 120,012,647 F186L possibly damaging Het
Mettl21a T C 1: 64,615,184 E58G probably damaging Het
Muc16 A T 9: 18,585,982 C6625S probably benign Het
Nfs1 T A 2: 156,142,061 D132V unknown Het
Nlgn1 T C 3: 25,435,907 D552G probably damaging Het
Numa1 C T 7: 102,013,865 T2066I probably benign Het
Olfr1355 A G 10: 78,879,823 Y217C possibly damaging Het
Olfr330 C A 11: 58,529,054 V311L probably benign Het
Olfr370 T C 8: 83,541,947 S268P possibly damaging Het
Olfr730 A T 14: 50,186,564 Y219N probably damaging Het
Olfr847 A T 9: 19,375,906 probably null Het
Pde11a C T 2: 76,291,203 V345I probably benign Het
Pglyrp2 A G 17: 32,418,761 S98P possibly damaging Het
Pik3c3 C T 18: 30,319,588 Q643* probably null Het
Pold2 T C 11: 5,872,714 Y402C probably damaging Het
Pom121 T C 5: 135,381,994 T770A unknown Het
Pou4f1 A T 14: 104,466,792 V68E probably damaging Het
Ppfia1 G T 7: 144,519,283 Q265K probably benign Het
Pygl A G 12: 70,206,356 probably null Het
Rdh19 A G 10: 127,850,300 T94A probably benign Het
Scgb1b12 A G 7: 32,334,497 T61A probably damaging Het
Sirpb1c C T 3: 15,832,202 A337T probably benign Het
Sltm C G 9: 70,586,673 P802R possibly damaging Het
Tbc1d23 T C 16: 57,189,383 E381G possibly damaging Het
Tnik A G 3: 28,666,139 I1304V probably damaging Het
Tpmt C A 13: 47,040,162 G54C probably damaging Het
Usp25 A T 16: 77,113,771 Q905L probably damaging Het
Vmn1r91 T A 7: 20,101,565 N136K probably benign Het
Wdr70 C T 15: 8,079,249 E138K probably benign Het
Wrb T A 16: 96,145,568 L31Q possibly damaging Het
Zbed3 A G 13: 95,336,125 D19G possibly damaging Het
Zfp369 A G 13: 65,292,054 K184R possibly 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
R4227:Naip5 UTSW 13 100,212,768 (GRCm38) missense probably damaging 0.99
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 13 100,219,697 (GRCm38) missense not run
R7447:Naip5 UTSW 13 100,219,696 (GRCm38) missense probably benign 0.00
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 13 100,219,696 (GRCm38) missense probably benign 0.00
R7590:Naip5 UTSW 13 100,219,697 (GRCm38) missense not run
R7742:Naip5 UTSW 13 100,219,830 (GRCm38) missense probably benign
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'- TTGGCTTCACTGCGCATCTG -3'
(R):5'- TATGCAGTAACAGGGGTGGC -3'

Sequencing Primer
(F):5'- CTGCGCATCTGTGAGTTAAAACC -3'
(R):5'- TAAGCCTGTGAGCAGCATC -3'
Posted On 2019-12-20