Incidental Mutation 'IGL01568:Spmip4'
ID 91074
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Spmip4
Ensembl Gene ENSMUSG00000029828
Gene Name sperm microtubule inner protein 4
Synonyms 4921507P07Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # IGL01568
Quality Score
Status
Chromosome 6
Chromosomal Location 50550282-50573612 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 50550678 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000031852 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031852]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000031852
SMART Domains Protein: ENSMUSP00000031852
Gene: ENSMUSG00000029828

DomainStartEndE-ValueType
Pfam:DUF4555 1 283 2e-149 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126537
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147260
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184470
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap13 T A 7: 75,258,270 (GRCm39) L298* probably null Het
Capn15 G T 17: 26,184,419 (GRCm39) R21S probably damaging Het
Cbs A G 17: 31,840,488 (GRCm39) L290P possibly damaging Het
Dnah5 T C 15: 28,229,798 (GRCm39) I144T probably benign Het
Dok4 T A 8: 95,593,430 (GRCm39) I119F probably benign Het
Dpp9 T C 17: 56,498,159 (GRCm39) N599S probably benign Het
Ep400 T C 5: 110,867,361 (GRCm39) T984A unknown Het
Fcrl2 T C 3: 87,163,986 (GRCm39) N381S probably damaging Het
Fhod3 A G 18: 25,253,219 (GRCm39) I1390V probably benign Het
Gabbr1 A G 17: 37,381,561 (GRCm39) Y775C probably damaging Het
Gimap9 A G 6: 48,654,550 (GRCm39) T46A probably benign Het
Gm3696 T C 14: 18,435,020 (GRCm39) N88S probably benign Het
Gm5277 A G 3: 78,799,743 (GRCm39) noncoding transcript Het
Gpr153 C A 4: 152,366,825 (GRCm39) probably null Het
Hgf A T 5: 16,769,812 (GRCm39) K95N probably damaging Het
Igf2r A G 17: 12,902,872 (GRCm39) S2393P possibly damaging Het
Ikbke C A 1: 131,185,633 (GRCm39) probably null Het
Il17re G T 6: 113,447,013 (GRCm39) R588L probably damaging Het
Itch T C 2: 155,054,382 (GRCm39) probably benign Het
Krt1c T A 15: 101,721,646 (GRCm39) D465V probably damaging Het
Krt28 G T 11: 99,262,243 (GRCm39) P249Q probably damaging Het
Lax1 A T 1: 133,608,038 (GRCm39) D234E probably benign Het
Mtmr3 A G 11: 4,477,861 (GRCm39) I61T probably damaging Het
Naip5 G T 13: 100,353,609 (GRCm39) Q1217K probably benign Het
Nt5dc3 A G 10: 86,669,802 (GRCm39) T466A probably benign Het
Or5bw2 A T 7: 6,573,569 (GRCm39) H193L possibly damaging Het
Or8s2 T C 15: 98,276,787 (GRCm39) D68G probably damaging Het
Pcdhb3 T C 18: 37,435,054 (GRCm39) V340A possibly damaging Het
Pclo C T 5: 14,728,443 (GRCm39) probably benign Het
Piezo2 C T 18: 63,163,463 (GRCm39) V2152I probably benign Het
Pip4k2b A T 11: 97,620,378 (GRCm39) probably null Het
Ptprs G A 17: 56,720,958 (GRCm39) H1432Y probably damaging Het
Rars1 A G 11: 35,716,808 (GRCm39) probably benign Het
Scrn1 A G 6: 54,499,739 (GRCm39) probably benign Het
Sdr42e1 T C 8: 118,390,182 (GRCm39) Y153C probably damaging Het
Slc18a1 A T 8: 69,518,278 (GRCm39) S245R probably damaging Het
Tns1 T G 1: 73,992,668 (GRCm39) D670A probably damaging Het
Trim16 T A 11: 62,711,684 (GRCm39) D118E probably benign Het
Trpv1 A G 11: 73,129,269 (GRCm39) D62G probably benign Het
Tyr A G 7: 87,087,156 (GRCm39) L452P probably damaging Het
Ubr4 T C 4: 139,148,684 (GRCm39) C1723R probably damaging Het
Uqcrb G A 13: 67,049,459 (GRCm39) probably benign Het
Vax2 G T 6: 83,688,519 (GRCm39) V81L possibly damaging Het
Zan A G 5: 137,463,106 (GRCm39) V691A unknown Het
Zfp335 A G 2: 164,736,708 (GRCm39) S976P possibly damaging Het
Zfp384 C T 6: 125,001,095 (GRCm39) P56S probably damaging Het
Other mutations in Spmip4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00852:Spmip4 APN 6 50,566,164 (GRCm39) critical splice acceptor site probably null
IGL01310:Spmip4 APN 6 50,551,175 (GRCm39) missense probably benign
IGL01794:Spmip4 APN 6 50,554,826 (GRCm39) missense probably damaging 1.00
IGL02718:Spmip4 APN 6 50,561,367 (GRCm39) missense probably damaging 1.00
IGL03146:Spmip4 APN 6 50,550,853 (GRCm39) missense probably damaging 0.97
IGL03381:Spmip4 APN 6 50,566,116 (GRCm39) missense probably damaging 1.00
R1173:Spmip4 UTSW 6 50,566,121 (GRCm39) missense probably damaging 0.98
R1174:Spmip4 UTSW 6 50,566,121 (GRCm39) missense probably damaging 0.98
R1175:Spmip4 UTSW 6 50,566,121 (GRCm39) missense probably damaging 0.98
R1769:Spmip4 UTSW 6 50,568,801 (GRCm39) splice site probably benign
R1883:Spmip4 UTSW 6 50,551,433 (GRCm39) missense probably benign 0.01
R2056:Spmip4 UTSW 6 50,550,725 (GRCm39) missense possibly damaging 0.71
R2437:Spmip4 UTSW 6 50,560,959 (GRCm39) missense probably damaging 1.00
R2929:Spmip4 UTSW 6 50,551,285 (GRCm39) missense probably benign 0.07
R4357:Spmip4 UTSW 6 50,551,190 (GRCm39) missense probably benign
R4666:Spmip4 UTSW 6 50,572,808 (GRCm39) missense possibly damaging 0.69
R4791:Spmip4 UTSW 6 50,572,817 (GRCm39) missense probably damaging 1.00
R4827:Spmip4 UTSW 6 50,572,836 (GRCm39) missense possibly damaging 0.76
R4976:Spmip4 UTSW 6 50,566,164 (GRCm39) critical splice acceptor site probably null
R5453:Spmip4 UTSW 6 50,572,776 (GRCm39) critical splice donor site probably null
R6689:Spmip4 UTSW 6 50,566,089 (GRCm39) critical splice donor site probably null
R6897:Spmip4 UTSW 6 50,566,145 (GRCm39) missense possibly damaging 0.82
R7718:Spmip4 UTSW 6 50,566,078 (GRCm39) splice site probably null
R8475:Spmip4 UTSW 6 50,566,107 (GRCm39) missense probably damaging 0.99
R8885:Spmip4 UTSW 6 50,551,028 (GRCm39) missense possibly damaging 0.95
R8975:Spmip4 UTSW 6 50,561,391 (GRCm39) missense probably damaging 1.00
R9626:Spmip4 UTSW 6 50,550,930 (GRCm39) missense
X0021:Spmip4 UTSW 6 50,550,906 (GRCm39) missense probably benign
Z1176:Spmip4 UTSW 6 50,551,001 (GRCm39) missense possibly damaging 0.55
Z1177:Spmip4 UTSW 6 50,568,672 (GRCm39) missense probably benign 0.17
Posted On 2013-12-09