Incidental Mutation 'R1419:Nlrp4g'
ID 159999
Institutional Source Beutler Lab
Gene Symbol Nlrp4g
Ensembl Gene ENSMUSG00000079741
Gene Name NLR family, pyrin domain containing 4G
Synonyms nalp4g
MMRRC Submission 039475-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R1419 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 124117991-124126089 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 124349434 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000067621
SMART Domains Protein: ENSMUSP00000065508
Gene: ENSMUSG00000079741

DomainStartEndE-ValueType
Pfam:NACHT 69 238 1.5e-39 PFAM
Blast:LRR 555 582 9e-10 BLAST
Blast:LRR 610 637 7e-10 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214229
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215276
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215602
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216416
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217178
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217183
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.5%
  • 20x: 90.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 T A 7: 119,974,125 (GRCm39) M894K probably benign Het
Ablim1 C A 19: 57,123,065 (GRCm39) C173F probably damaging Het
Abtb2 G T 2: 103,539,765 (GRCm39) R710L probably benign Het
Arap3 T C 18: 38,111,485 (GRCm39) T1144A possibly damaging Het
Arhgef12 A T 9: 42,938,516 (GRCm39) V92D probably damaging Het
Ash1l T G 3: 88,892,204 (GRCm39) M1361R probably damaging Het
Atm A C 9: 53,368,789 (GRCm39) N2337K probably benign Het
Cog7 T C 7: 121,555,215 (GRCm39) E316G probably damaging Het
Dsp A G 13: 38,370,671 (GRCm39) Y858C probably damaging Het
Enc1 G T 13: 97,382,692 (GRCm39) G401C probably damaging Het
Gata6 T C 18: 11,064,706 (GRCm39) V506A probably benign Het
Gm16380 C T 9: 53,791,471 (GRCm39) noncoding transcript Het
Hsd17b8 G A 17: 34,246,617 (GRCm39) R89C probably benign Het
Hsh2d G A 8: 72,954,304 (GRCm39) D229N probably benign Het
Ift80 T A 3: 68,847,531 (GRCm39) N322Y probably damaging Het
Igsf9 T A 1: 172,325,578 (GRCm39) V1082E probably damaging Het
Katnal2 A T 18: 77,065,128 (GRCm39) L481Q possibly damaging Het
Kcnma1 T C 14: 23,417,710 (GRCm39) T713A probably damaging Het
Kif13a T C 13: 46,978,711 (GRCm39) T230A probably damaging Het
Klhl14 C A 18: 21,785,250 (GRCm39) R59L probably damaging Het
Mecom A G 3: 30,035,038 (GRCm39) C213R probably damaging Het
Mrpl13 T A 15: 55,397,717 (GRCm39) M178L probably benign Het
Myof T C 19: 37,890,359 (GRCm39) E1971G probably damaging Het
Naa10 A G X: 72,961,522 (GRCm39) V133A probably damaging Het
Ofcc1 C T 13: 40,362,305 (GRCm39) G206R probably benign Het
Oplah T C 15: 76,182,120 (GRCm39) I1047V probably benign Het
Or4a15 T C 2: 89,193,666 (GRCm39) T36A probably damaging Het
Or4k47 A T 2: 111,451,640 (GRCm39) F260I probably benign Het
Or5al1 A G 2: 85,989,773 (GRCm39) *314Q probably null Het
Paip1 A G 13: 119,593,553 (GRCm39) D189G probably damaging Het
Pkn1 A G 8: 84,400,151 (GRCm39) F624L probably damaging Het
Plxnb1 C A 9: 108,943,454 (GRCm39) P1899H probably damaging Het
Rpa3 T A 6: 8,257,720 (GRCm39) E47D probably benign Het
Shoc1 T C 4: 59,064,457 (GRCm39) T826A possibly damaging Het
Snai2 C T 16: 14,526,044 (GRCm39) H232Y possibly damaging Het
Spint5 T C 2: 164,557,331 (GRCm39) S23P possibly damaging Het
St8sia2 G A 7: 73,616,742 (GRCm39) Q78* probably null Het
Tktl2 A G 8: 66,965,690 (GRCm39) N416S probably damaging Het
Tm7sf3 T A 6: 146,505,475 (GRCm39) I494F possibly damaging Het
Trf C T 9: 103,103,307 (GRCm39) V119M probably damaging Het
Other mutations in Nlrp4g
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01066:Nlrp4g APN 9 124,349,526 (GRCm38) unclassified noncoding transcript
IGL01087:Nlrp4g APN 9 124,353,858 (GRCm38) critical splice acceptor site noncoding transcript
IGL01106:Nlrp4g APN 9 124,350,452 (GRCm38) unclassified noncoding transcript
IGL01938:Nlrp4g APN 9 124,349,068 (GRCm38) unclassified noncoding transcript
IGL02088:Nlrp4g APN 9 124,350,453 (GRCm38) unclassified noncoding transcript
IGL02170:Nlrp4g APN 9 124,348,980 (GRCm38) unclassified noncoding transcript
IGL02582:Nlrp4g APN 9 124,349,764 (GRCm38) unclassified noncoding transcript
IGL02588:Nlrp4g APN 9 124,348,843 (GRCm38) unclassified noncoding transcript
IGL02931:Nlrp4g APN 9 124,348,940 (GRCm38) unclassified noncoding transcript
IGL03111:Nlrp4g APN 9 124,353,978 (GRCm38) exon noncoding transcript
IGL03373:Nlrp4g APN 9 124,349,853 (GRCm38) unclassified noncoding transcript
R0617:Nlrp4g UTSW 9 124,349,540 (GRCm38) unclassified noncoding transcript
R2060:Nlrp4g UTSW 9 124,349,693 (GRCm38) unclassified noncoding transcript
R2152:Nlrp4g UTSW 9 124,353,339 (GRCm38) exon noncoding transcript
R2356:Nlrp4g UTSW 9 124,349,306 (GRCm38) unclassified noncoding transcript
R2384:Nlrp4g UTSW 9 124,349,707 (GRCm38) unclassified noncoding transcript
R2698:Nlrp4g UTSW 9 124,349,630 (GRCm38) unclassified noncoding transcript
R3878:Nlrp4g UTSW 9 124,349,362 (GRCm38) unclassified noncoding transcript
R4640:Nlrp4g UTSW 9 124,349,153 (GRCm38) unclassified noncoding transcript
R4745:Nlrp4g UTSW 9 124,349,515 (GRCm38) unclassified noncoding transcript
R4754:Nlrp4g UTSW 9 124,349,788 (GRCm38) unclassified noncoding transcript
R4937:Nlrp4g UTSW 9 124,354,005 (GRCm38) exon noncoding transcript
R5024:Nlrp4g UTSW 9 124,350,155 (GRCm38) unclassified noncoding transcript
R5162:Nlrp4g UTSW 9 124,350,394 (GRCm38) unclassified noncoding transcript
R5407:Nlrp4g UTSW 9 124,349,930 (GRCm38) unclassified noncoding transcript
R5521:Nlrp4g UTSW 9 124,350,020 (GRCm38) unclassified noncoding transcript
R8224:Nlrp4g UTSW 9 124,353,374 (GRCm38) missense noncoding transcript
R8259:Nlrp4g UTSW 9 124,353,392 (GRCm38) missense noncoding transcript
Z1088:Nlrp4g UTSW 9 124,349,201 (GRCm38) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- AAGCAGTTGAAGACAGCCAGCC -3'
(R):5'- GCCCTCAGCAGCTAGAGAACATAAG -3'

Sequencing Primer
(F):5'- CTGAACTTATCTCCAGAGAGTGGC -3'
(R):5'- AGACAGAGACTGGGTCTCCTC -3'
Posted On 2014-03-14