Incidental Mutation 'IGL01386:Fpr-rs7'
ID 79036
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fpr-rs7
Ensembl Gene ENSMUSG00000071276
Gene Name formyl peptide receptor, related sequence 7
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.084) question?
Stock # IGL01386
Quality Score
Status
Chromosome 17
Chromosomal Location 20333472-20334488 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 20334454 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Leucine at position 12 (S12L)
Ref Sequence ENSEMBL: ENSMUSP00000093297 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095637]
AlphaFold Q71MR7
Predicted Effect probably damaging
Transcript: ENSMUST00000095637
AA Change: S12L

PolyPhen 2 Score 0.977 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000093297
Gene: ENSMUSG00000071276
AA Change: S12L

DomainStartEndE-ValueType
Pfam:7tm_1 43 297 1.2e-38 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000176711
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn1 T C 12: 80,240,446 (GRCm39) R214G probably benign Het
Cacna1e T A 1: 154,348,123 (GRCm39) K817N probably benign Het
Cyp3a16 A G 5: 145,377,244 (GRCm39) F448L probably damaging Het
Dpp6 T A 5: 27,869,760 (GRCm39) probably null Het
Eif2ak3 C T 6: 70,869,710 (GRCm39) T799M probably damaging Het
Erbb4 A T 1: 68,383,090 (GRCm39) S302R probably damaging Het
Fam217a T A 13: 35,099,632 (GRCm39) probably benign Het
Flt4 C A 11: 49,528,162 (GRCm39) A995D probably benign Het
Fsd1 C T 17: 56,303,733 (GRCm39) S491F probably damaging Het
Hpcal4 T C 4: 123,083,035 (GRCm39) probably null Het
Intu A T 3: 40,647,017 (GRCm39) D630V probably damaging Het
Jak3 A G 8: 72,136,933 (GRCm39) D703G probably damaging Het
Lama4 A G 10: 38,887,060 (GRCm39) I122V probably benign Het
Mrpl11 A C 19: 5,013,409 (GRCm39) K92T probably null Het
Mtarc2 A G 1: 184,551,413 (GRCm39) probably benign Het
Mylk A G 16: 34,791,610 (GRCm39) probably null Het
Or52ab4 A T 7: 102,987,974 (GRCm39) K238* probably null Het
Parpbp A C 10: 87,975,848 (GRCm39) Y88* probably null Het
Plod2 G A 9: 92,488,655 (GRCm39) R627Q probably damaging Het
Rapsn G T 2: 90,867,144 (GRCm39) A149S probably damaging Het
Ripk3 T G 14: 56,023,484 (GRCm39) Q109P probably damaging Het
Scaf11 T C 15: 96,318,361 (GRCm39) D401G probably damaging Het
Serpine2 G A 1: 79,779,268 (GRCm39) T150I probably damaging Het
Sh2d6 T A 6: 72,495,945 (GRCm39) T98S probably benign Het
Slc28a1 G T 7: 80,814,427 (GRCm39) A513S probably benign Het
Tanc2 T C 11: 105,777,207 (GRCm39) F795S probably damaging Het
Tcim T A 8: 24,928,705 (GRCm39) I70F probably benign Het
Thbd G A 2: 148,249,602 (GRCm39) Q89* probably null Het
Tmem115 C T 9: 107,411,859 (GRCm39) T61I probably damaging Het
Tsc2 A T 17: 24,832,259 (GRCm39) V650E probably damaging Het
Tubgcp6 A T 15: 88,992,199 (GRCm39) Y595* probably null Het
Uroc1 C T 6: 90,323,747 (GRCm39) A398V probably damaging Het
Vmn1r31 T C 6: 58,449,587 (GRCm39) T93A probably benign Het
Vmn2r113 A G 17: 23,175,024 (GRCm39) E545G possibly damaging Het
Vps13a A G 19: 16,678,516 (GRCm39) V1155A possibly damaging Het
Zfp667 A G 7: 6,307,869 (GRCm39) H179R probably benign Het
Other mutations in Fpr-rs7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00332:Fpr-rs7 APN 17 20,333,480 (GRCm39) nonsense probably null
IGL02293:Fpr-rs7 APN 17 20,334,232 (GRCm39) missense probably benign 0.01
IGL03303:Fpr-rs7 APN 17 20,334,001 (GRCm39) missense possibly damaging 0.55
R0731:Fpr-rs7 UTSW 17 20,334,116 (GRCm39) missense probably benign 0.00
R0826:Fpr-rs7 UTSW 17 20,333,888 (GRCm39) missense probably benign 0.01
R1439:Fpr-rs7 UTSW 17 20,333,869 (GRCm39) missense probably benign 0.10
R1590:Fpr-rs7 UTSW 17 20,333,678 (GRCm39) missense probably benign 0.05
R1778:Fpr-rs7 UTSW 17 20,334,277 (GRCm39) missense probably damaging 1.00
R4715:Fpr-rs7 UTSW 17 20,333,690 (GRCm39) missense probably benign 0.00
R4744:Fpr-rs7 UTSW 17 20,334,265 (GRCm39) missense probably benign 0.17
R4921:Fpr-rs7 UTSW 17 20,334,082 (GRCm39) missense possibly damaging 0.70
R5540:Fpr-rs7 UTSW 17 20,334,356 (GRCm39) missense probably damaging 1.00
R5677:Fpr-rs7 UTSW 17 20,334,365 (GRCm39) missense probably benign
R5959:Fpr-rs7 UTSW 17 20,334,011 (GRCm39) missense probably benign 0.01
R6042:Fpr-rs7 UTSW 17 20,333,477 (GRCm39) missense probably benign 0.00
R7921:Fpr-rs7 UTSW 17 20,333,667 (GRCm39) missense probably benign 0.03
R7984:Fpr-rs7 UTSW 17 20,333,671 (GRCm39) missense probably benign 0.01
R8137:Fpr-rs7 UTSW 17 20,334,055 (GRCm39) missense possibly damaging 0.49
R8172:Fpr-rs7 UTSW 17 20,334,443 (GRCm39) missense probably benign 0.04
R8762:Fpr-rs7 UTSW 17 20,333,789 (GRCm39) missense probably benign 0.07
R9134:Fpr-rs7 UTSW 17 20,334,325 (GRCm39) missense probably damaging 1.00
Z1176:Fpr-rs7 UTSW 17 20,333,655 (GRCm39) missense probably benign 0.02
Posted On 2013-11-05