Incidental Mutation 'IGL03166:Smpdl3b'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Smpdl3b
Ensembl Gene ENSMUSG00000028885
Gene Namesphingomyelin phosphodiesterase, acid-like 3B
Synonyms1110054A24Rik, Asml3b
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.088) question?
Stock #IGL03166
Quality Score
Chromosomal Location132732966-132757252 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 132741531 bp
Amino Acid Change Aspartic acid to Glycine at position 125 (D125G)
Ref Sequence ENSEMBL: ENSMUSP00000030709 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030709]
Predicted Effect probably benign
Transcript: ENSMUST00000030709
AA Change: D125G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000030709
Gene: ENSMUSG00000028885
AA Change: D125G

signal peptide 1 18 N/A INTRINSIC
Pfam:Metallophos 21 281 1.9e-20 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele are viable and overtly normal but exhibit an enhanced inflammatory response in models of Toll-like receptor (TLR)-dependent peritonitis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3110079O15Rik A C 1: 87,475,211 probably benign Het
Acvr1b A G 15: 101,203,078 R374G probably damaging Het
Ankfn1 G T 11: 89,538,438 A40D probably benign Het
Arhgap20 T A 9: 51,849,777 I940K possibly damaging Het
Arhgap24 T C 5: 102,875,686 probably benign Het
Bdp1 T C 13: 100,035,800 T2103A probably benign Het
Cep350 A G 1: 155,863,600 S2166P possibly damaging Het
Dlg2 T C 7: 91,900,730 probably benign Het
Fam160b2 A T 14: 70,590,176 C160S probably damaging Het
Fyco1 A T 9: 123,828,387 L908H probably benign Het
Gprc5b C A 7: 118,983,999 A216S probably benign Het
Lamc1 A G 1: 153,332,301 V80A probably benign Het
Lilra6 T C 7: 3,912,627 I370V possibly damaging Het
Lim2 T A 7: 43,430,623 C11* probably null Het
Lrp1b T A 2: 41,111,038 H2058L probably damaging Het
Lrp3 G T 7: 35,202,480 L659I probably benign Het
Lrrc8a T G 2: 30,255,365 S64A probably benign Het
Lsr C T 7: 30,962,097 probably null Het
Lyl1 C T 8: 84,702,671 P3L possibly damaging Het
Man2c1 T A 9: 57,139,098 V479E probably damaging Het
Mtf2 T A 5: 108,106,720 D462E probably benign Het
Mx2 T C 16: 97,546,790 I205T probably damaging Het
Nos1 T A 5: 117,914,452 probably benign Het
Olfr78 T C 7: 102,742,047 N319D probably benign Het
Optc C T 1: 133,903,792 probably benign Het
Orm1 C A 4: 63,344,594 probably benign Het
Pdzd8 T C 19: 59,300,508 E820G probably damaging Het
Pkp1 A T 1: 135,878,124 M612K probably damaging Het
Pno1 T A 11: 17,204,513 probably null Het
Rbm34 T C 8: 126,970,856 Q35R probably damaging Het
Ryr3 A T 2: 112,641,112 Y4564* probably null Het
Slc34a3 T C 2: 25,232,174 I140V probably damaging Het
Slc43a1 T C 2: 84,857,356 I419T possibly damaging Het
Sltm C A 9: 70,542,969 A17E possibly damaging Het
Supt3 G T 17: 44,923,219 A48S probably damaging Het
Tlr3 A G 8: 45,402,928 F72L probably benign Het
Trim36 T C 18: 46,212,321 E15G probably benign Het
Tubb4b-ps1 A T 5: 7,179,965 probably benign Het
Vmn2r68 T C 7: 85,222,123 T651A probably benign Het
Wdr76 G T 2: 121,534,306 V462F possibly damaging Het
Wnk2 C A 13: 49,071,044 G1112* probably null Het
Zfp868 A C 8: 69,612,314 C123W probably damaging Het
Zyg11b T A 4: 108,265,889 M294L probably benign Het
Other mutations in Smpdl3b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02057:Smpdl3b APN 4 132733713 missense probably benign 0.11
R0321:Smpdl3b UTSW 4 132741444 missense probably damaging 0.99
R0450:Smpdl3b UTSW 4 132745138 missense probably damaging 1.00
R0510:Smpdl3b UTSW 4 132745138 missense probably damaging 1.00
R1462:Smpdl3b UTSW 4 132746614 missense probably damaging 1.00
R1462:Smpdl3b UTSW 4 132746614 missense probably damaging 1.00
R4725:Smpdl3b UTSW 4 132745178 missense probably damaging 0.97
R4844:Smpdl3b UTSW 4 132738058 missense probably damaging 1.00
R6290:Smpdl3b UTSW 4 132738275 missense possibly damaging 0.67
R6992:Smpdl3b UTSW 4 132745141 missense possibly damaging 0.94
Posted On2016-08-02