Incidental Mutation 'IGL01385:Spmip3'
ID 79003
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Spmip3
Ensembl Gene ENSMUSG00000015962
Gene Name sperm microtubule inner protein 3
Synonyms 1700016C15Rik
Accession Numbers
Essential gene? Not available question?
Stock # IGL01385
Quality Score
Status
Chromosome 1
Chromosomal Location 177557380-177580890 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 177568640 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Arginine at position 46 (G46R)
Ref Sequence ENSEMBL: ENSMUSP00000016106 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000016106]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000016106
AA Change: G46R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000016106
Gene: ENSMUSG00000015962
AA Change: G46R

DomainStartEndE-ValueType
low complexity region 75 86 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI

none

Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim1 A T 19: 57,057,346 (GRCm39) S292R probably damaging Het
Adamts19 A G 18: 59,105,851 (GRCm39) T749A probably damaging Het
Agap2 A T 10: 126,923,865 (GRCm39) I747F unknown Het
Arhgap35 T A 7: 16,298,399 (GRCm39) N222I probably damaging Het
Atp10b A G 11: 43,125,256 (GRCm39) E1074G probably damaging Het
Brd3 T C 2: 27,354,101 (GRCm39) T4A possibly damaging Het
Col6a6 A G 9: 105,660,865 (GRCm39) S415P probably damaging Het
Dennd2a A G 6: 39,500,070 (GRCm39) V165A probably damaging Het
Dnm1l T A 16: 16,159,317 (GRCm39) E95V probably damaging Het
Dock9 A G 14: 121,817,995 (GRCm39) Y1609H possibly damaging Het
Esm1 A C 13: 113,353,216 (GRCm39) E166A possibly damaging Het
F2rl2 A C 13: 95,837,836 (GRCm39) I294L probably benign Het
Gstt3 A G 10: 75,610,822 (GRCm39) S187P probably benign Het
Katna1 T C 10: 7,628,574 (GRCm39) C268R probably damaging Het
Mbd5 T A 2: 49,140,233 (GRCm39) C66S possibly damaging Het
Naa35 G A 13: 59,748,880 (GRCm39) E167K probably damaging Het
Or10ak16 T C 4: 118,750,748 (GRCm39) L156S probably benign Het
Osbpl2 A G 2: 179,778,873 (GRCm39) N2S probably benign Het
Parp6 T C 9: 59,537,895 (GRCm39) probably benign Het
Pcdhb5 T A 18: 37,455,267 (GRCm39) V549E probably benign Het
Pcnx4 T C 12: 72,620,520 (GRCm39) L780P probably damaging Het
Plcb3 A T 19: 6,935,276 (GRCm39) D851E probably benign Het
Ppfia2 A G 10: 106,749,560 (GRCm39) S1149G probably damaging Het
Prkca A G 11: 107,869,178 (GRCm39) V469A probably damaging Het
Ryr1 A T 7: 28,756,410 (GRCm39) V3468D probably damaging Het
Stxbp4 A G 11: 90,431,074 (GRCm39) V412A possibly damaging Het
Vmn1r238 G T 18: 3,122,770 (GRCm39) Q215K possibly damaging Het
Wdr11 A G 7: 129,209,637 (GRCm39) M482V probably benign Het
Wdr72 T C 9: 74,086,788 (GRCm39) probably benign Het
Xirp2 T C 2: 67,340,021 (GRCm39) L754P probably damaging Het
Zmym6 G A 4: 127,017,899 (GRCm39) G1135S probably benign Het
Other mutations in Spmip3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01542:Spmip3 APN 1 177,570,950 (GRCm39) missense possibly damaging 0.94
IGL02329:Spmip3 APN 1 177,570,867 (GRCm39) missense probably benign 0.05
N/A:Spmip3 UTSW 1 177,561,100 (GRCm39) missense probably damaging 0.99
R0850:Spmip3 UTSW 1 177,568,571 (GRCm39) missense probably benign
R7739:Spmip3 UTSW 1 177,570,828 (GRCm39) missense probably damaging 0.97
R9426:Spmip3 UTSW 1 177,570,834 (GRCm39) nonsense probably null
R9485:Spmip3 UTSW 1 177,580,545 (GRCm39) missense possibly damaging 0.90
Z1176:Spmip3 UTSW 1 177,568,583 (GRCm39) missense possibly damaging 0.95
Posted On 2013-11-05