Incidental Mutation 'R0148:Spata17'
ID 60854
Institutional Source Beutler Lab
Gene Symbol Spata17
Ensembl Gene ENSMUSG00000026611
Gene Name spermatogenesis associated 17
Synonyms 4930513F16Rik, 4930504I07Rik, 1700065F16Rik
MMRRC Submission 038432-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R0148 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 186776845-186947662 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 186844798 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 111 (V111A)
Ref Sequence ENSEMBL: ENSMUSP00000139073 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000027908] [ENSMUST00000183819] [ENSMUST00000183931] [ENSMUST00000183996]
AlphaFold Q9D552
Predicted Effect possibly damaging
Transcript: ENSMUST00000027908
AA Change: V267A

PolyPhen 2 Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000027908
Gene: ENSMUSG00000026611
AA Change: V267A

DomainStartEndE-ValueType
IQ 47 69 5.27e0 SMART
IQ 70 92 1.77e-2 SMART
IQ 106 128 1.4e1 SMART
coiled coil region 133 174 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000159848
AA Change: V267A

PolyPhen 2 Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000123771
Gene: ENSMUSG00000026611
AA Change: V267A

DomainStartEndE-ValueType
IQ 47 69 5.27e0 SMART
IQ 70 92 1.77e-2 SMART
IQ 106 128 1.4e1 SMART
coiled coil region 133 174 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000183819
AA Change: V267A

PolyPhen 2 Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000138855
Gene: ENSMUSG00000026611
AA Change: V267A

DomainStartEndE-ValueType
IQ 47 69 5.27e0 SMART
IQ 70 92 1.77e-2 SMART
IQ 106 128 1.4e1 SMART
coiled coil region 133 174 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000183931
SMART Domains Protein: ENSMUSP00000139329
Gene: ENSMUSG00000026611

DomainStartEndE-ValueType
low complexity region 39 63 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000183996
AA Change: V111A

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000139073
Gene: ENSMUSG00000026611
AA Change: V111A

DomainStartEndE-ValueType
low complexity region 2 16 N/A INTRINSIC
Meta Mutation Damage Score 0.1696 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 96.0%
  • 20x: 91.8%
Validation Efficiency 86% (30/35)
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m T C 6: 121,639,405 (GRCm39) probably null Het
Agtr1a T C 13: 30,565,927 (GRCm39) S331P probably benign Het
Ank1 T A 8: 23,613,993 (GRCm39) N1545K probably damaging Het
Bahcc1 A T 11: 120,159,230 (GRCm39) Q152H probably damaging Het
Bend3 T A 10: 43,387,946 (GRCm39) Y780N probably damaging Het
Bod1l G T 5: 41,976,040 (GRCm39) A1758E possibly damaging Het
Ctcfl T C 2: 172,960,340 (GRCm39) D81G possibly damaging Het
Ddx39a C T 8: 84,449,105 (GRCm39) R298C possibly damaging Het
Dock8 T C 19: 25,096,823 (GRCm39) L577P probably benign Het
Drc1 A T 5: 30,486,487 (GRCm39) N13I possibly damaging Het
Efl1 T C 7: 82,320,878 (GRCm39) S104P probably damaging Het
Eml4 T A 17: 83,729,081 (GRCm39) N85K probably damaging Het
Epb41l4a T C 18: 33,931,853 (GRCm39) T581A probably damaging Het
Epha3 T C 16: 63,433,307 (GRCm39) D446G possibly damaging Het
Fam209 G T 2: 172,315,900 (GRCm39) G92C probably damaging Het
Fbln1 G A 15: 85,115,027 (GRCm39) R193H probably damaging Het
Fbxw21 A G 9: 108,977,085 (GRCm39) probably null Het
Fgf17 C T 14: 70,876,313 (GRCm39) R49Q probably damaging Het
Flnb T C 14: 7,939,077 (GRCm38) S2307P probably benign Het
Galr1 A G 18: 82,423,695 (GRCm39) L194P probably benign Het
Gar1 T C 3: 129,623,122 (GRCm39) H89R probably damaging Het
Gbp4 T A 5: 105,267,362 (GRCm39) Y519F probably benign Het
Git1 A G 11: 77,396,554 (GRCm39) T601A probably benign Het
Gm10722 T "C,A" 9: 3,001,405 (GRCm39) probably null Het
Gm5142 C T 14: 59,416,119 (GRCm39) R13H possibly damaging Het
Gria2 A C 3: 80,615,038 (GRCm39) W481G probably damaging Het
Homer2 T C 7: 81,274,026 (GRCm39) T57A probably benign Het
Hpse2 A C 19: 42,920,099 (GRCm39) probably null Het
Hspb7 T C 4: 141,151,302 (GRCm39) I148T probably damaging Het
Htr1d C A 4: 136,170,788 (GRCm39) T339K probably damaging Het
Il4ra T A 7: 125,174,709 (GRCm39) C306S probably damaging Het
Kansl3 A T 1: 36,392,897 (GRCm39) C225S probably damaging Het
Lama3 G A 18: 12,581,329 (GRCm39) C596Y probably damaging Het
Lama5 T C 2: 179,832,199 (GRCm39) H1714R probably benign Het
Marchf6 C T 15: 31,490,758 (GRCm39) V293M probably damaging Het
Med12l A G 3: 58,945,075 (GRCm39) D100G probably damaging Het
Mettl14 G A 3: 123,165,043 (GRCm39) T316I probably damaging Het
Mmp15 A T 8: 96,098,945 (GRCm39) N591Y probably benign Het
Mrpl53 T C 6: 83,086,518 (GRCm39) L74P probably damaging Het
Mvp C T 7: 126,589,037 (GRCm39) V577M probably damaging Het
Neb T C 2: 52,139,388 (GRCm39) K140E probably damaging Het
Nfya A G 17: 48,706,026 (GRCm39) V48A possibly damaging Het
Ngf G T 3: 102,417,119 (GRCm39) probably benign Het
Nipsnap3b C T 4: 53,017,088 (GRCm39) A104V possibly damaging Het
Nlrp14 A G 7: 106,781,928 (GRCm39) Y375C probably benign Het
Nod1 A G 6: 54,915,202 (GRCm39) Y764H probably damaging Het
Or13d1 A T 4: 52,971,232 (GRCm39) I204F probably benign Het
Or2w25 G A 11: 59,504,320 (GRCm39) V177M probably damaging Het
Or7e177 T G 9: 20,212,387 (GRCm39) M297R probably damaging Het
Pcdhb19 A T 18: 37,630,235 (GRCm39) Q10L probably benign Het
Pdcl T C 2: 37,242,142 (GRCm39) I203V probably benign Het
Peg10 C A 6: 4,755,711 (GRCm39) R96S possibly damaging Het
Pknox1 T A 17: 31,823,764 (GRCm39) N379K probably benign Het
Prodh T G 16: 17,895,677 (GRCm39) Q360P probably damaging Het
Raf1 C T 6: 115,609,934 (GRCm39) G202S probably benign Het
Rgs11 T A 17: 26,426,433 (GRCm39) probably null Het
Rilp A T 11: 75,401,059 (GRCm39) H29L probably damaging Het
Rtel1 T C 2: 180,962,839 (GRCm39) C31R probably damaging Het
Rubcnl T A 14: 75,279,898 (GRCm39) I427K probably damaging Het
Ryr1 C A 7: 28,751,460 (GRCm39) R3706L probably damaging Het
Ryr2 T C 13: 11,729,434 (GRCm39) D2396G probably damaging Het
Slc45a2 T C 15: 11,025,954 (GRCm39) S435P probably damaging Het
Svep1 C T 4: 58,116,608 (GRCm39) D881N possibly damaging Het
Sypl2 T A 3: 108,126,411 (GRCm39) N67I possibly damaging Het
Tenm3 T C 8: 48,689,755 (GRCm39) Y1944C probably damaging Het
Tep1 A T 14: 51,062,246 (GRCm39) D2535E possibly damaging Het
Tkt T A 14: 30,294,177 (GRCm39) I529N probably damaging Het
Trp53i11 T G 2: 93,028,080 (GRCm39) V39G probably damaging Het
Trpm2 C T 10: 77,761,659 (GRCm39) G997D probably damaging Het
Usp3 A G 9: 66,447,449 (GRCm39) V219A possibly damaging Het
Usp4 T A 9: 108,268,870 (GRCm39) probably null Het
Wdfy3 A G 5: 102,065,277 (GRCm39) V1297A probably benign Het
Wdr46 T A 17: 34,159,997 (GRCm39) F70I probably benign Het
Xkr6 T C 14: 64,056,998 (GRCm39) V303A unknown Het
Zdbf2 C T 1: 63,343,165 (GRCm39) Q515* probably null Het
Zfhx2 A G 14: 55,310,354 (GRCm39) Y731H possibly damaging Het
Other mutations in Spata17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00662:Spata17 APN 1 186,849,536 (GRCm39) missense probably benign 0.34
IGL02101:Spata17 APN 1 186,849,657 (GRCm39) missense probably benign 0.40
IGL02268:Spata17 APN 1 186,872,595 (GRCm39) missense probably damaging 0.97
IGL02406:Spata17 APN 1 186,849,458 (GRCm39) critical splice donor site probably null
IGL02429:Spata17 APN 1 186,872,631 (GRCm39) missense possibly damaging 0.66
IGL03333:Spata17 APN 1 186,872,667 (GRCm39) start codon destroyed probably null
R0147:Spata17 UTSW 1 186,844,798 (GRCm39) missense probably damaging 1.00
R0269:Spata17 UTSW 1 186,830,069 (GRCm39) missense probably benign 0.02
R1521:Spata17 UTSW 1 186,926,191 (GRCm39) missense probably damaging 0.96
R1620:Spata17 UTSW 1 186,915,412 (GRCm39) intron probably benign
R2017:Spata17 UTSW 1 186,780,650 (GRCm39) missense possibly damaging 0.73
R2113:Spata17 UTSW 1 186,830,108 (GRCm39) missense possibly damaging 0.93
R2251:Spata17 UTSW 1 186,780,670 (GRCm39) missense possibly damaging 0.96
R4260:Spata17 UTSW 1 186,780,677 (GRCm39) missense possibly damaging 0.53
R4572:Spata17 UTSW 1 186,926,193 (GRCm39) missense possibly damaging 0.91
R4894:Spata17 UTSW 1 186,872,643 (GRCm39) missense probably benign 0.00
R4910:Spata17 UTSW 1 186,926,208 (GRCm39) missense probably damaging 0.98
R6277:Spata17 UTSW 1 186,926,151 (GRCm39) nonsense probably null
R7200:Spata17 UTSW 1 186,844,700 (GRCm39) missense probably benign 0.00
R7621:Spata17 UTSW 1 186,854,833 (GRCm39) splice site probably null
R7735:Spata17 UTSW 1 186,872,577 (GRCm39) missense unknown
R7990:Spata17 UTSW 1 186,872,592 (GRCm39) missense unknown
R8115:Spata17 UTSW 1 186,849,653 (GRCm39) missense probably damaging 1.00
R8833:Spata17 UTSW 1 186,915,436 (GRCm39) missense probably damaging 1.00
R9288:Spata17 UTSW 1 186,844,756 (GRCm39) missense possibly damaging 0.85
R9481:Spata17 UTSW 1 186,844,756 (GRCm39) missense possibly damaging 0.85
R9588:Spata17 UTSW 1 186,849,471 (GRCm39) missense possibly damaging 0.91
V7732:Spata17 UTSW 1 186,780,677 (GRCm39) missense possibly damaging 0.53
X0027:Spata17 UTSW 1 186,926,156 (GRCm39) missense probably damaging 0.97
Z1177:Spata17 UTSW 1 186,872,626 (GRCm39) nonsense probably null
Z1177:Spata17 UTSW 1 186,849,525 (GRCm39) missense possibly damaging 0.86
Predicted Primers PCR Primer
(F):5'- AATTTGAAACATGGCTCAGCTAAGCAC -3'
(R):5'- CTGGGGAAGTCTGCCAAGTCTTAAAG -3'

Sequencing Primer
(F):5'- TGGCTCAGCTAAGCACTTACATC -3'
(R):5'- tttgtttgtttgtttgttgtgtttc -3'
Posted On 2013-07-24