Incidental Mutation 'IGL02931:Nlrp4g'
ID 364079
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 # IGL02931
Quality Score
Status
Chromosome 9
Chromosomal Location 124117991-124126089 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 124348940 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: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy1 G A 11: 7,029,012 (GRCm39) R254Q probably benign Het
Adgrv1 T C 13: 81,727,833 (GRCm39) Y269C probably damaging Het
Apol7a C A 15: 77,277,650 (GRCm39) E33* probably null Het
Arhgap29 T C 3: 121,786,509 (GRCm39) V358A probably benign Het
B3galt1 T C 2: 67,948,728 (GRCm39) S148P probably damaging Het
BC061237 A G 14: 44,740,779 (GRCm39) N60D possibly damaging Het
Bcl9l C T 9: 44,412,047 (GRCm39) P11L probably damaging Het
Ccdc89 A C 7: 90,076,110 (GRCm39) K107Q probably benign Het
Col27a1 T C 4: 63,249,663 (GRCm39) probably benign Het
Col5a2 T C 1: 45,424,225 (GRCm39) D1067G probably damaging Het
Col9a2 A T 4: 120,910,389 (GRCm39) R511S probably benign Het
Disp3 G A 4: 148,333,658 (GRCm39) S1060F possibly damaging Het
Dusp8 T C 7: 141,636,667 (GRCm39) T308A probably benign Het
Ern1 T C 11: 106,314,266 (GRCm39) N178S probably damaging Het
Gas6 C A 8: 13,527,136 (GRCm39) C204F probably damaging Het
Gga1 T C 15: 78,777,522 (GRCm39) S558P possibly damaging Het
Gli1 T C 10: 127,168,279 (GRCm39) T525A probably benign Het
Gse1 A G 8: 121,304,808 (GRCm39) probably benign Het
Hmcn1 G A 1: 150,532,958 (GRCm39) S3075L probably benign Het
Hnf4a G A 2: 163,408,037 (GRCm39) probably benign Het
Htt A T 5: 35,034,097 (GRCm39) E1894D probably damaging Het
Kcnh8 G A 17: 53,263,650 (GRCm39) E716K probably benign Het
Kntc1 A G 5: 123,937,874 (GRCm39) Y1524C probably damaging Het
Krtap9-5 A G 11: 99,839,931 (GRCm39) T211A unknown Het
Lin54 T C 5: 100,628,180 (GRCm39) I8V possibly damaging Het
Lipe A G 7: 25,082,760 (GRCm39) probably benign Het
Lpin2 T A 17: 71,545,678 (GRCm39) V508E probably damaging Het
Lrrc9 C A 12: 72,500,923 (GRCm39) H216Q probably damaging Het
Lrrn1 T C 6: 107,544,709 (GRCm39) L169P probably damaging Het
Map9 C A 3: 82,284,428 (GRCm39) T334K possibly damaging Het
Msantd5f1 G A 4: 73,605,602 (GRCm39) A338T probably damaging Het
Mst1 A T 9: 107,961,841 (GRCm39) probably null Het
Mtor T A 4: 148,549,421 (GRCm39) F602I probably benign Het
Mylpf T A 7: 126,812,798 (GRCm39) D98E probably benign Het
Naca C A 10: 127,883,551 (GRCm39) Q2059K probably damaging Het
Nefh G A 11: 4,891,356 (GRCm39) T421I possibly damaging Het
Npat C T 9: 53,482,341 (GRCm39) Q1350* probably null Het
Oaz3 T C 3: 94,342,287 (GRCm39) N123S probably benign Het
Patj A G 4: 98,299,410 (GRCm39) probably benign Het
Pgap6 T A 17: 26,336,923 (GRCm39) F280L probably benign Het
Piezo1 A C 8: 123,210,258 (GRCm39) D2224E probably damaging Het
Pnpla7 A T 2: 24,905,241 (GRCm39) I610F possibly damaging Het
Psapl1 A T 5: 36,362,233 (GRCm39) D275V probably damaging Het
Ptpdc1 T A 13: 48,744,095 (GRCm39) probably benign Het
Rac2 T C 15: 78,454,947 (GRCm39) E31G possibly damaging Het
Sdhc T C 1: 170,971,124 (GRCm39) probably benign Het
Smim23 G T 11: 32,770,667 (GRCm39) P80T probably damaging Het
Snupn C T 9: 56,864,364 (GRCm39) T21I probably benign Het
Tjp2 A G 19: 24,073,996 (GRCm39) V1097A probably benign Het
Ttc16 A G 2: 32,661,939 (GRCm39) Y164H probably damaging Het
Txlnb A G 10: 17,703,730 (GRCm39) E296G probably damaging Het
Ube2l6 G A 2: 84,633,195 (GRCm39) V34M probably damaging Het
Vwf A C 6: 125,592,931 (GRCm39) S764R possibly damaging Het
Zfand3 A G 17: 30,411,611 (GRCm39) S146G probably benign Het
Zfp280d T G 9: 72,203,307 (GRCm39) F18L 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
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
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 2015-12-18