Incidental Mutation 'IGL01346:Stpg2'
ID 75066
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Stpg2
Ensembl Gene ENSMUSG00000047940
Gene Name sperm tail PG rich repeat containing 2
Synonyms LOC381476, B930007M17Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL01346
Quality Score
Status
Chromosome 3
Chromosomal Location 138910953-139415185 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 139125635 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101846 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062306] [ENSMUST00000106239]
AlphaFold Q8C8J0
Predicted Effect probably benign
Transcript: ENSMUST00000062306
SMART Domains Protein: ENSMUSP00000051539
Gene: ENSMUSG00000047940

DomainStartEndE-ValueType
Pfam:SHIPPO-rpt 20 50 1.1e1 PFAM
Pfam:SHIPPO-rpt 62 92 1.3e1 PFAM
Pfam:SHIPPO-rpt 97 127 9.1e1 PFAM
Pfam:SHIPPO-rpt 162 193 1.3e2 PFAM
Pfam:SHIPPO-rpt 200 235 1.7e0 PFAM
Pfam:SHIPPO-rpt 249 285 1.2e-2 PFAM
Pfam:SHIPPO-rpt 292 315 3.2e1 PFAM
Pfam:SHIPPO-rpt 334 371 2.1e0 PFAM
Pfam:SHIPPO-rpt 421 462 3.8e0 PFAM
Pfam:SHIPPO-rpt 471 497 2.9e1 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083741
Predicted Effect probably benign
Transcript: ENSMUST00000106239
SMART Domains Protein: ENSMUSP00000101846
Gene: ENSMUSG00000047940

DomainStartEndE-ValueType
Pfam:SHIPPO-rpt 200 220 6.9e-1 PFAM
Pfam:SHIPPO-rpt 249 285 8.8e-2 PFAM
Pfam:SHIPPO-rpt 334 371 5.4e-2 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3300002I08Rik A G 2: 150,152,980 (GRCm39) V135A unknown Het
Cnot4 A T 6: 35,047,183 (GRCm39) I143N probably damaging Het
Cnot6l A T 5: 96,234,105 (GRCm39) M302K probably damaging Het
Dmxl2 T C 9: 54,322,759 (GRCm39) T1542A probably damaging Het
Dnaaf9 A G 2: 130,633,766 (GRCm39) probably benign Het
Dnhd1 T C 7: 105,363,116 (GRCm39) S3893P probably benign Het
Duox2 A T 2: 122,117,683 (GRCm39) probably benign Het
Dusp1 T C 17: 26,725,295 (GRCm39) N355D probably benign Het
Fam76b T C 9: 13,741,046 (GRCm39) C60R probably damaging Het
Gnptab G A 10: 88,272,041 (GRCm39) V944I possibly damaging Het
Gys1 A G 7: 45,091,961 (GRCm39) Y249C probably damaging Het
Ift88 A T 14: 57,681,862 (GRCm39) E215D probably damaging Het
Kcnu1 T C 8: 26,424,551 (GRCm39) probably benign Het
Lmln C A 16: 32,937,490 (GRCm39) N618K probably benign Het
Lrrc75a T C 11: 62,496,813 (GRCm39) T250A probably damaging Het
Mpp4 A G 1: 59,164,719 (GRCm39) S435P probably damaging Het
Myo1c T A 11: 75,563,076 (GRCm39) V1036E probably damaging Het
Nlrp12 T G 7: 3,289,316 (GRCm39) T399P probably damaging Het
Or2y16 A G 11: 49,335,595 (GRCm39) R306G probably benign Het
Or4c118 A G 2: 88,974,575 (GRCm39) F264S possibly damaging Het
Parp8 A T 13: 117,031,600 (GRCm39) C332S possibly damaging Het
Pdcd11 G A 19: 47,098,053 (GRCm39) V780I probably benign Het
Plekha5 A G 6: 140,480,292 (GRCm39) probably benign Het
Ppt1 T A 4: 122,737,848 (GRCm39) I62K probably damaging Het
Proser3 T C 7: 30,249,071 (GRCm39) N7S probably benign Het
Ptk2b A G 14: 66,414,567 (GRCm39) L311P possibly damaging Het
Rasal2 T C 1: 156,988,786 (GRCm39) N706S probably benign Het
Ripk2 A G 4: 16,132,775 (GRCm39) probably null Het
Setx T A 2: 29,034,821 (GRCm39) H435Q probably damaging Het
Smurf2 T A 11: 106,721,741 (GRCm39) probably benign Het
Snx32 A G 19: 5,547,764 (GRCm39) L182P possibly damaging Het
Taar2 A G 10: 23,816,997 (GRCm39) Y179C probably damaging Het
Tenm2 G A 11: 35,918,232 (GRCm39) R1843* probably null Het
Tmco4 T C 4: 138,748,260 (GRCm39) I280T probably damaging Het
Tuba4a C A 1: 75,193,921 (GRCm39) C46F probably damaging Het
Ubr1 A G 2: 120,703,603 (GRCm39) probably null Het
Vldlr A T 19: 27,217,081 (GRCm39) I45L possibly damaging Het
Vmn2r120 C A 17: 57,852,232 (GRCm39) G28V probably benign Het
Vmn2r37 C A 7: 9,209,680 (GRCm39) V611L probably benign Het
Vmn2r67 A G 7: 84,786,127 (GRCm39) L626P probably damaging Het
Wdr19 C T 5: 65,379,082 (GRCm39) probably benign Het
Zfp595 T A 13: 67,464,749 (GRCm39) K505* probably null Het
Other mutations in Stpg2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01505:Stpg2 APN 3 139,023,214 (GRCm39) missense probably benign 0.02
IGL01649:Stpg2 APN 3 139,125,623 (GRCm39) missense probably damaging 1.00
IGL03264:Stpg2 APN 3 139,014,970 (GRCm39) missense possibly damaging 0.72
PIT4687001:Stpg2 UTSW 3 138,921,026 (GRCm39) missense possibly damaging 0.89
R0053:Stpg2 UTSW 3 138,918,082 (GRCm39) missense probably benign 0.00
R0099:Stpg2 UTSW 3 138,948,954 (GRCm39) splice site probably benign
R0417:Stpg2 UTSW 3 138,924,082 (GRCm39) missense probably damaging 1.00
R1646:Stpg2 UTSW 3 139,125,463 (GRCm39) splice site probably benign
R1719:Stpg2 UTSW 3 138,937,960 (GRCm39) missense probably benign 0.11
R1791:Stpg2 UTSW 3 139,023,162 (GRCm39) missense probably benign 0.00
R1799:Stpg2 UTSW 3 139,125,542 (GRCm39) missense probably damaging 1.00
R1912:Stpg2 UTSW 3 139,228,742 (GRCm39) splice site probably null
R1974:Stpg2 UTSW 3 139,014,944 (GRCm39) nonsense probably null
R3725:Stpg2 UTSW 3 139,023,238 (GRCm39) missense probably benign 0.00
R3727:Stpg2 UTSW 3 139,004,257 (GRCm39) missense probably damaging 1.00
R4225:Stpg2 UTSW 3 138,921,053 (GRCm39) missense probably damaging 0.97
R4694:Stpg2 UTSW 3 139,023,177 (GRCm39) missense possibly damaging 0.94
R4698:Stpg2 UTSW 3 139,014,990 (GRCm39) missense probably damaging 1.00
R4879:Stpg2 UTSW 3 138,921,134 (GRCm39) missense probably benign 0.03
R5236:Stpg2 UTSW 3 138,937,984 (GRCm39) missense probably damaging 1.00
R5476:Stpg2 UTSW 3 138,948,899 (GRCm39) missense probably benign 0.03
R5567:Stpg2 UTSW 3 139,125,547 (GRCm39) missense probably benign 0.22
R6297:Stpg2 UTSW 3 139,407,432 (GRCm39) missense possibly damaging 0.91
R6692:Stpg2 UTSW 3 139,228,738 (GRCm39) critical splice donor site probably null
R7113:Stpg2 UTSW 3 139,407,535 (GRCm39) critical splice donor site probably null
R7154:Stpg2 UTSW 3 138,921,056 (GRCm39) missense probably benign 0.44
R7553:Stpg2 UTSW 3 138,924,098 (GRCm39) missense probably damaging 1.00
R7660:Stpg2 UTSW 3 139,407,458 (GRCm39) missense probably damaging 0.98
R8105:Stpg2 UTSW 3 138,948,925 (GRCm39) missense probably damaging 1.00
R8154:Stpg2 UTSW 3 139,014,938 (GRCm39) missense probably damaging 1.00
R8902:Stpg2 UTSW 3 139,004,170 (GRCm39) missense probably damaging 1.00
R9165:Stpg2 UTSW 3 139,014,993 (GRCm39) missense possibly damaging 0.57
RF021:Stpg2 UTSW 3 138,918,011 (GRCm39) critical splice acceptor site probably null
X0009:Stpg2 UTSW 3 139,004,223 (GRCm39) missense probably benign 0.00
X0018:Stpg2 UTSW 3 138,948,851 (GRCm39) missense probably benign 0.44
Z1176:Stpg2 UTSW 3 139,407,401 (GRCm39) nonsense probably null
Posted On 2013-10-07