Incidental Mutation 'R6747:Spire2'
ID530594
Institutional Source Beutler Lab
Gene Symbol Spire2
Ensembl Gene ENSMUSG00000010154
Gene Namespire type actin nucleation factor 2
SynonymsSpir-2
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.164) question?
Stock #R6747 (G1)
Quality Score225.009
Status Validated
Chromosome8
Chromosomal Location123332713-123369515 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 123356846 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Cysteine at position 190 (R190C)
Ref Sequence ENSEMBL: ENSMUSP00000148710 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000010298] [ENSMUST00000127664] [ENSMUST00000212404]
Predicted Effect probably damaging
Transcript: ENSMUST00000010298
AA Change: R290C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000010298
Gene: ENSMUSG00000010154
AA Change: R290C

DomainStartEndE-ValueType
low complexity region 2 23 N/A INTRINSIC
KIND 26 207 2.63e-82 SMART
PDB:4EFH|B 310 360 8e-8 PDB
low complexity region 419 431 N/A INTRINSIC
low complexity region 496 513 N/A INTRINSIC
SCOP:d1zbdb_ 540 636 7e-8 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000127664
SMART Domains Protein: ENSMUSP00000118564
Gene: ENSMUSG00000092329

DomainStartEndE-ValueType
Pfam:Glycos_transf_2 104 287 7.4e-31 PFAM
Pfam:Glyco_transf_7C 261 331 4.9e-8 PFAM
RICIN 406 531 9.28e-27 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000212404
AA Change: R190C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 96.0%
Validation Efficiency 97% (68/70)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 C T 3: 122,126,313 probably null Het
Acyp1 C T 12: 85,278,905 V107I probably null Het
Aftph T C 11: 20,726,144 probably null Het
Agtpbp1 A T 13: 59,544,353 probably null Het
Arhgap15 C A 2: 44,116,677 P269T probably damaging Het
Arhgap30 T C 1: 171,407,729 V557A probably damaging Het
Asb3 T A 11: 31,081,493 M410K probably benign Het
B4galnt2 T C 11: 95,868,634 probably null Het
Birc3 A G 9: 7,860,261 probably null Het
Cav2 A T 6: 17,286,951 N69Y probably damaging Het
Cc2d2b G A 19: 40,795,667 C826Y probably benign Het
Cenpf T A 1: 189,652,854 T2410S probably benign Het
Chchd1 A G 14: 20,703,380 D24G probably benign Het
Cmip G A 8: 117,436,879 G450S probably benign Het
Col11a1 C T 3: 114,212,450 Q534* probably null Het
Col3a1 G T 1: 45,338,622 probably benign Het
Cox4i1 T C 8: 120,673,230 I31T possibly damaging Het
Cstf3 G T 2: 104,646,767 V168F probably damaging Het
Dapk1 T C 13: 60,725,340 I352T probably benign Het
Ddx52 T C 11: 83,955,302 V456A probably damaging Het
Dmxl2 A T 9: 54,416,088 H1337Q probably damaging Het
Dnah7a T C 1: 53,636,062 T369A probably benign Het
Dppa1 T A 11: 46,625,595 I8F unknown Het
Ebf1 G T 11: 44,883,814 V213F probably damaging Het
Foxb2 C A 19: 16,872,833 E270* probably null Het
Gclc A T 9: 77,788,245 R450W probably damaging Het
Gm13128 T C 4: 144,332,978 W420R probably benign Het
Grin2d T C 7: 45,862,268 E251G probably damaging Het
Hal A T 10: 93,500,677 N423Y probably damaging Het
Krtap4-8 T A 11: 99,780,091 I185F unknown Het
Lrp3 T A 7: 35,211,437 Q61L probably benign Het
Met A C 6: 17,571,467 Q1296H probably damaging Het
Mphosph9 T A 5: 124,297,699 N557I possibly damaging Het
Mrpl46 C A 7: 78,782,981 W16C probably benign Het
Myh13 G A 11: 67,350,419 R874Q probably damaging Het
Nelfb G A 2: 25,203,381 T453I probably benign Het
Nos2 A G 11: 78,952,954 D909G probably damaging Het
Nr5a2 T C 1: 136,882,344 E431G possibly damaging Het
Nsmce2 A G 15: 59,591,724 D149G probably benign Het
Olfr203 T C 16: 59,303,641 F164L probably benign Het
Olfr690 C T 7: 105,330,027 R55H probably benign Het
Pcbp4 C A 9: 106,460,648 probably null Het
Peg10 A G 6: 4,757,137 probably benign Het
Pms2 C T 5: 143,925,419 P154L probably benign Het
Pou6f2 A C 13: 18,129,187 L112R probably benign Het
Prdm6 A T 18: 53,465,046 probably benign Het
Prob1 G A 18: 35,655,154 R12W probably damaging Het
Rif1 T A 2: 52,078,263 probably null Het
Rpl9-ps6 A G 19: 32,466,143 S137P probably benign Het
Rsf1 GGCG GGCGACGGCAGCG 7: 97,579,906 probably benign Homo
Sec23ip A G 7: 128,752,849 silent Het
Slc38a9 T C 13: 112,690,180 C151R probably benign Het
Slc39a8 T C 3: 135,849,180 probably null Het
Slc6a18 C A 13: 73,677,991 probably benign Het
Snw1 T C 12: 87,464,710 D57G probably damaging Het
Sox6 C G 7: 115,541,731 R505P probably damaging Het
Speg T C 1: 75,410,395 probably null Het
Stard9 A C 2: 120,698,383 H1707P possibly damaging Het
Tenm3 G T 8: 48,343,243 T237K probably damaging Het
Themis2 T A 4: 132,796,262 E31V possibly damaging Het
Trim56 T G 5: 137,114,521 Q47P probably damaging Het
Trim58 T C 11: 58,651,264 I350T probably benign Het
Ttll7 C T 3: 146,944,056 P639S probably benign Het
Ubxn6 A G 17: 56,070,650 probably null Het
Vmn2r114 A T 17: 23,309,876 F417L probably benign Het
Vmn2r29 T A 7: 7,231,422 M822L probably benign Het
Vps9d1 T C 8: 123,254,007 D27G probably damaging Het
Wdr3 C T 3: 100,138,724 R931Q probably damaging Het
Whamm G A 7: 81,578,302 probably null Het
Zcchc24 T C 14: 25,757,033 H142R probably damaging Het
Zfp292 T C 4: 34,806,894 K2050R probably damaging Het
Other mutations in Spire2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00091:Spire2 APN 8 123354059 missense probably damaging 1.00
IGL01610:Spire2 APN 8 123356763 missense probably damaging 1.00
IGL01611:Spire2 APN 8 123359398 missense probably damaging 1.00
IGL01776:Spire2 APN 8 123359392 missense probably damaging 0.98
IGL02164:Spire2 APN 8 123332964 missense probably damaging 0.99
IGL03005:Spire2 APN 8 123363368 missense probably benign 0.16
R0127:Spire2 UTSW 8 123358097 splice site probably benign
R0194:Spire2 UTSW 8 123363011 splice site probably benign
R0571:Spire2 UTSW 8 123354116 missense probably damaging 1.00
R1386:Spire2 UTSW 8 123361366 critical splice donor site probably null
R1526:Spire2 UTSW 8 123368763 missense probably benign 0.08
R1538:Spire2 UTSW 8 123358156 missense probably damaging 1.00
R1917:Spire2 UTSW 8 123363071 missense probably benign 0.00
R1919:Spire2 UTSW 8 123363071 missense probably benign 0.00
R2018:Spire2 UTSW 8 123332918 missense probably damaging 1.00
R2019:Spire2 UTSW 8 123332918 missense probably damaging 1.00
R4524:Spire2 UTSW 8 123360235 missense probably benign
R4672:Spire2 UTSW 8 123358111 missense probably benign 0.06
R4931:Spire2 UTSW 8 123368784 missense possibly damaging 0.54
R4973:Spire2 UTSW 8 123356844 missense probably damaging 1.00
R5057:Spire2 UTSW 8 123358201 missense probably damaging 1.00
R5702:Spire2 UTSW 8 123346663 missense probably benign 0.07
R5899:Spire2 UTSW 8 123354094 missense probably damaging 1.00
R6816:Spire2 UTSW 8 123359413 missense probably benign 0.12
R6823:Spire2 UTSW 8 123356727 missense probably damaging 1.00
R7146:Spire2 UTSW 8 123369250 missense probably benign 0.08
R7903:Spire2 UTSW 8 123368750 missense probably benign
R7934:Spire2 UTSW 8 123356699 splice site probably null
R7986:Spire2 UTSW 8 123368750 missense probably benign
Predicted Primers PCR Primer
(F):5'- AGACTGGGTAAGACGCACAC -3'
(R):5'- GCCCTAATTTAAACTCTGATCAAGCAC -3'

Sequencing Primer
(F):5'- GAGCACGGTACACCCAGAG -3'
(R):5'- GCACAAGCGAAGGGACAAG -3'
Posted On2018-08-01