Incidental Mutation 'IGL03373:Nlrp4g'
ID 420376
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nlrp4g
Ensembl Gene ENSMUSG00000079741
Gene Name NLR family, pyrin domain containing 4G
Synonyms nalp4g
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # IGL03373
Quality Score
Status
Chromosome 9
Chromosomal Location 124117991-124126089 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 124349853 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
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam6a A T 12: 113,509,172 (GRCm39) Y515F possibly damaging Het
Adgrv1 A G 13: 81,711,751 (GRCm39) V1075A probably damaging Het
Alox8 T C 11: 69,077,443 (GRCm39) T436A probably benign Het
Cdc7 T A 5: 107,120,785 (GRCm39) probably benign Het
Cdhr1 T A 14: 36,818,257 (GRCm39) D65V possibly damaging Het
Dnase1 A G 16: 3,857,707 (GRCm39) E278G probably damaging Het
Eif3g A T 9: 20,805,722 (GRCm39) probably benign Het
Flnb G A 14: 7,890,867 (GRCm38) probably null Het
Hars2 G T 18: 36,918,998 (GRCm39) R86L probably damaging Het
Lmod1 C T 1: 135,292,264 (GRCm39) A373V possibly damaging Het
Mdga2 A G 12: 66,763,496 (GRCm39) I200T probably damaging Het
Mup1 T G 4: 60,457,849 (GRCm39) probably benign Het
Nat8f5 A C 6: 85,794,529 (GRCm39) S144A probably benign Het
Ndnf A C 6: 65,681,272 (GRCm39) Y517S possibly damaging Het
Nedd4l G A 18: 65,314,391 (GRCm39) probably benign Het
Nob1 C T 8: 108,144,678 (GRCm39) probably benign Het
Nploc4 G A 11: 120,300,455 (GRCm39) R326* probably null Het
Obox3 A T 7: 15,359,715 (GRCm39) V318D probably benign Het
Or10a3m G A 7: 108,313,339 (GRCm39) V248I probably damaging Het
Or10ag57 T C 2: 87,218,577 (GRCm39) F176S probably damaging Het
Pgm1 T C 4: 99,818,741 (GRCm39) I130T probably damaging Het
Ptprk A T 10: 28,442,533 (GRCm39) D845V probably damaging Het
Ptx4 T A 17: 25,339,873 (GRCm39) S17T probably benign Het
Rasgrf1 T C 9: 89,899,084 (GRCm39) probably benign Het
Rfx6 A G 10: 51,596,096 (GRCm39) T426A probably damaging Het
Sfpq C A 4: 126,920,578 (GRCm39) R564S possibly damaging Het
Spint2 A G 7: 28,957,634 (GRCm39) probably benign Het
Vmn1r27 A G 6: 58,192,689 (GRCm39) I105T probably damaging Het
Vmn1r78 T C 7: 11,887,270 (GRCm39) S294P possibly damaging Het
Vmn2r40 T C 7: 8,923,092 (GRCm39) D423G probably benign 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
R0617:Nlrp4g UTSW 9 124,349,540 (GRCm38) unclassified noncoding transcript
R1419:Nlrp4g UTSW 9 124,349,434 (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
Posted On 2016-08-02