Incidental Mutation 'IGL01087:Nlrp4g'
ID 51890
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 # IGL01087
Quality Score
Chromosome 9
Chromosomal Location 124117991-124126089 bp(-) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) A to G at 124353858 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

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: ENSMUST00000215602
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700003E16Rik A T 6: 83,139,770 (GRCm39) probably null Het
Abca6 C A 11: 110,082,476 (GRCm39) A1166S probably benign Het
Arhgdib C A 6: 136,910,622 (GRCm39) K46N probably damaging Het
Ash1l T A 3: 88,971,209 (GRCm39) V2507D probably damaging Het
B4galnt1 A T 10: 127,002,060 (GRCm39) I63F probably damaging Het
Bclaf1 A G 10: 20,201,056 (GRCm39) D394G probably damaging Het
Btbd10 T C 7: 112,915,763 (GRCm39) D442G probably damaging Het
Cd44 A T 2: 102,652,607 (GRCm39) L492H probably damaging Het
Cfap206 C T 4: 34,721,562 (GRCm39) S162N probably damaging Het
Chsy1 T G 7: 65,821,874 (GRCm39) V703G possibly damaging Het
Clrn2 T C 5: 45,621,311 (GRCm39) probably benign Het
Crtc3 T C 7: 80,248,487 (GRCm39) probably benign Het
Cul1 A G 6: 47,485,978 (GRCm39) T342A probably benign Het
Dgki T C 6: 36,989,846 (GRCm39) D631G probably damaging Het
Eif3b T C 5: 140,426,862 (GRCm39) I706T probably damaging Het
Fam120a A G 13: 49,055,549 (GRCm39) L713P probably damaging Het
I830077J02Rik C A 3: 105,836,049 (GRCm39) probably null Het
Jmjd8 A C 17: 26,048,145 (GRCm39) probably benign Het
Kmt5a T C 5: 124,589,443 (GRCm39) probably benign Het
Krt87 C A 15: 101,329,706 (GRCm39) C486F probably benign Het
Lrp2 A T 2: 69,354,417 (GRCm39) N470K probably damaging Het
Med1 C A 11: 98,071,111 (GRCm39) D79Y probably damaging Het
Myo1d A G 11: 80,573,261 (GRCm39) S189P probably damaging Het
Myo9a T A 9: 59,697,361 (GRCm39) Y381N possibly damaging Het
Nipbl C A 15: 8,379,981 (GRCm39) S937I possibly damaging Het
Nutm2 A G 13: 50,623,665 (GRCm39) T121A probably damaging Het
Opa1 C T 16: 29,405,815 (GRCm39) P127S probably damaging Het
Or2h1b C T 17: 37,462,332 (GRCm39) C177Y probably damaging Het
Pcdh15 A T 10: 74,178,464 (GRCm39) I574F possibly damaging Het
Pcnx1 G A 12: 82,042,113 (GRCm39) probably benign Het
Prex2 A G 1: 11,138,328 (GRCm39) T136A probably benign Het
Prph2 A G 17: 47,222,085 (GRCm39) T155A probably damaging Het
Rsl1d1 T C 16: 11,012,539 (GRCm39) K296E possibly damaging Het
Syne1 A T 10: 5,375,708 (GRCm39) I128N probably damaging Het
Tlk1 A T 2: 70,582,660 (GRCm39) N156K possibly damaging Het
Trem2 C T 17: 48,658,956 (GRCm39) T222I probably damaging Het
Trip12 A T 1: 84,735,580 (GRCm39) F872L probably damaging Het
Trrap T A 5: 144,783,349 (GRCm39) S3393T probably damaging Het
Vwa8 T A 14: 79,172,669 (GRCm39) S304T probably benign Het
Zc3h7a T C 16: 10,971,046 (GRCm39) T328A probably benign Het
Other mutations in Nlrp4g
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01066:Nlrp4g APN 9 124,349,526 (GRCm38) unclassified 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
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 2013-06-21