Incidental Mutation 'R4794:Spata31e4'
ID 368875
Institutional Source Beutler Lab
Gene Symbol Spata31e4
Ensembl Gene ENSMUSG00000094918
Gene Name spermatogenesis associated 31 subfamily E member 4
Synonyms Gm8765
MMRRC Submission 042420-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # R4794 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 50852348-50857471 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to G at 50857275 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Arginine at position 971 (P971R)
Ref Sequence ENSEMBL: ENSMUSP00000097118 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099518]
AlphaFold B7ZWJ3
Predicted Effect probably benign
Transcript: ENSMUST00000099518
AA Change: P971R

PolyPhen 2 Score 0.069 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000097118
Gene: ENSMUSG00000094918
AA Change: P971R

DomainStartEndE-ValueType
low complexity region 69 82 N/A INTRINSIC
Pfam:FAM75 95 418 1.1e-15 PFAM
SCOP:d1i5pa1 811 874 9e-3 SMART
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 92.5%
Validation Efficiency 97% (75/77)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam4 A T 12: 81,468,198 (GRCm39) I141K probably damaging Het
Adgrb1 A G 15: 74,459,978 (GRCm39) E537G probably damaging Het
Asic3 C T 5: 24,620,895 (GRCm39) A259V probably damaging Het
Bcar1 G A 8: 112,447,552 (GRCm39) Q142* probably null Het
Bcas3 T C 11: 85,400,294 (GRCm39) V200A probably damaging Het
Cd302 A T 2: 60,102,493 (GRCm39) I42N probably benign Het
Colec12 C A 18: 9,848,984 (GRCm39) N387K probably damaging Het
Copa T A 1: 171,946,888 (GRCm39) I1032N probably damaging Het
D630003M21Rik G C 2: 158,038,059 (GRCm39) T1129S probably benign Het
D630045J12Rik G A 6: 38,171,420 (GRCm39) T916I possibly damaging Het
Dnajb13 C T 7: 100,153,199 (GRCm39) A241T probably damaging Het
Dyrk4 G T 6: 126,862,300 (GRCm39) N397K possibly damaging Het
Eftud2 T A 11: 102,761,003 (GRCm39) Y114F probably benign Het
Elp1 ACTTCTTCTTCTTCTTCTTCTTC ACTTCTTCTTCTTCTTCTTC 4: 56,781,176 (GRCm39) probably benign Het
Epm2a A G 10: 11,266,597 (GRCm39) D114G probably benign Het
Exoc5 T C 14: 49,286,357 (GRCm39) probably null Het
Fam135a G A 1: 24,068,241 (GRCm39) T706I probably benign Het
Fasn A G 11: 120,702,121 (GRCm39) V1845A probably benign Het
Fscn3 A G 6: 28,430,595 (GRCm39) E255G probably damaging Het
Galnt7 A T 8: 57,998,397 (GRCm39) Y311N probably damaging Het
Grid1 T C 14: 34,544,579 (GRCm39) L50P probably damaging Het
Hepacam2 A G 6: 3,475,933 (GRCm39) F331L probably damaging Het
Kalrn C T 16: 33,810,180 (GRCm39) D2525N possibly damaging Het
Kif1a T C 1: 92,953,449 (GRCm39) Y1245C probably damaging Het
Ltbp3 T C 19: 5,806,707 (GRCm39) F1022L probably damaging Het
Med16 G T 10: 79,735,951 (GRCm39) T399N probably damaging Het
Mfsd14a A T 3: 116,439,155 (GRCm39) probably benign Het
Myh7b G A 2: 155,465,186 (GRCm39) V681I probably benign Het
Ndc1 A G 4: 107,247,419 (GRCm39) E409G probably benign Het
Necap2 A G 4: 140,798,912 (GRCm39) probably benign Het
Or2a57 T A 6: 43,212,629 (GRCm39) L29H probably damaging Het
Or4p21 A T 2: 88,276,691 (GRCm39) M197K probably benign Het
Or7g29 C T 9: 19,286,841 (GRCm39) S112N probably benign Het
Parp12 G A 6: 39,094,744 (GRCm39) T117I probably benign Het
Pars2 C A 4: 106,511,407 (GRCm39) C396* probably null Het
Prg4 A T 1: 150,330,297 (GRCm39) probably benign Het
Prkg2 G A 5: 99,114,492 (GRCm39) T523I probably damaging Het
Prph T A 15: 98,955,308 (GRCm39) L425Q probably damaging Het
Ranbp9 A G 13: 43,567,552 (GRCm39) Y549H probably damaging Het
Rbm12 A T 2: 155,937,489 (GRCm39) probably benign Het
Reln T C 5: 22,549,183 (GRCm39) Y75C probably damaging Het
Rock2 G A 12: 16,990,408 (GRCm39) R110H probably damaging Het
Samd1 G A 8: 84,726,346 (GRCm39) E468K probably damaging Het
Samd11 T A 4: 156,333,922 (GRCm39) Q173L probably damaging Het
Scgb2b20 C A 7: 33,065,151 (GRCm39) G37V probably damaging Het
Sf1 C A 19: 6,425,694 (GRCm39) probably benign Het
Slc17a5 T A 9: 78,481,997 (GRCm39) H183L probably damaging Het
Slco1a7 A G 6: 141,713,288 (GRCm39) V31A probably benign Het
Smgc T A 15: 91,725,657 (GRCm39) S13T probably benign Het
Snapin A G 3: 90,398,092 (GRCm39) probably benign Het
Ssc5d C T 7: 4,946,744 (GRCm39) P1033S probably benign Het
Strn3 T C 12: 51,696,954 (GRCm39) E259G probably benign Het
Tbc1d32 A G 10: 56,072,932 (GRCm39) F238L possibly damaging Het
Tbck G A 3: 132,392,729 (GRCm39) V57M possibly damaging Het
Tgm3 A G 2: 129,883,875 (GRCm39) D511G probably benign Het
Tlr5 T C 1: 182,801,461 (GRCm39) V241A probably benign Het
Tmem181c-ps A G 17: 6,887,754 (GRCm39) noncoding transcript Het
Tnfrsf1a G A 6: 125,335,047 (GRCm39) C168Y probably damaging Het
Tph2 G T 10: 115,018,675 (GRCm39) L79I possibly damaging Het
Tsc1 G A 2: 28,551,702 (GRCm39) probably null Het
Ttc14 A T 3: 33,857,298 (GRCm39) M215L probably benign Het
Ube3c A G 5: 29,802,083 (GRCm39) N120S probably benign Het
Ubr2 A T 17: 47,241,371 (GRCm39) W1728R probably damaging Het
Vnn1 A G 10: 23,776,602 (GRCm39) T318A probably benign Het
Washc2 T C 6: 116,235,610 (GRCm39) V941A probably benign Het
Wdfy3 A G 5: 102,091,809 (GRCm39) V510A probably damaging Het
Wdsub1 A T 2: 59,693,188 (GRCm39) V272E possibly damaging Het
Xylt1 A C 7: 117,236,862 (GRCm39) D537A probably benign Het
Zfp57 A G 17: 37,321,022 (GRCm39) N292S possibly damaging Het
Other mutations in Spata31e4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01548:Spata31e4 APN 13 50,854,414 (GRCm39) missense probably benign 0.18
IGL02452:Spata31e4 APN 13 50,857,113 (GRCm39) missense probably damaging 0.99
IGL02610:Spata31e4 APN 13 50,855,748 (GRCm39) missense possibly damaging 0.91
IGL03171:Spata31e4 APN 13 50,856,388 (GRCm39) missense probably benign 0.23
IGL03369:Spata31e4 APN 13 50,857,200 (GRCm39) missense possibly damaging 0.74
PIT4382001:Spata31e4 UTSW 13 50,855,007 (GRCm39) missense probably damaging 0.99
R0346:Spata31e4 UTSW 13 50,857,346 (GRCm39) missense probably benign 0.12
R1015:Spata31e4 UTSW 13 50,855,664 (GRCm39) missense possibly damaging 0.92
R1054:Spata31e4 UTSW 13 50,856,432 (GRCm39) missense probably benign 0.01
R1102:Spata31e4 UTSW 13 50,857,118 (GRCm39) missense probably benign 0.00
R1519:Spata31e4 UTSW 13 50,854,443 (GRCm39) critical splice donor site probably null
R1628:Spata31e4 UTSW 13 50,856,324 (GRCm39) missense probably benign 0.25
R1754:Spata31e4 UTSW 13 50,855,123 (GRCm39) missense probably damaging 0.98
R4212:Spata31e4 UTSW 13 50,854,388 (GRCm39) missense possibly damaging 0.94
R4672:Spata31e4 UTSW 13 50,857,208 (GRCm39) missense probably benign
R4780:Spata31e4 UTSW 13 50,855,116 (GRCm39) missense probably damaging 0.97
R5171:Spata31e4 UTSW 13 50,854,414 (GRCm39) missense possibly damaging 0.85
R6240:Spata31e4 UTSW 13 50,855,453 (GRCm39) missense probably damaging 0.97
R6366:Spata31e4 UTSW 13 50,855,972 (GRCm39) missense probably benign 0.01
R6421:Spata31e4 UTSW 13 50,855,987 (GRCm39) missense probably benign 0.35
R6644:Spata31e4 UTSW 13 50,856,071 (GRCm39) missense possibly damaging 0.54
R6678:Spata31e4 UTSW 13 50,855,946 (GRCm39) missense probably benign 0.14
R6788:Spata31e4 UTSW 13 50,857,131 (GRCm39) missense probably damaging 0.99
R7030:Spata31e4 UTSW 13 50,857,019 (GRCm39) missense possibly damaging 0.52
R7513:Spata31e4 UTSW 13 50,856,909 (GRCm39) missense probably benign 0.01
R7681:Spata31e4 UTSW 13 50,856,290 (GRCm39) missense possibly damaging 0.70
R7753:Spata31e4 UTSW 13 50,855,817 (GRCm39) missense probably damaging 1.00
R7794:Spata31e4 UTSW 13 50,856,344 (GRCm39) missense probably damaging 0.98
R7994:Spata31e4 UTSW 13 50,856,900 (GRCm39) missense probably benign 0.04
R8021:Spata31e4 UTSW 13 50,855,130 (GRCm39) missense possibly damaging 0.50
R8858:Spata31e4 UTSW 13 50,855,423 (GRCm39) missense probably benign 0.07
R9027:Spata31e4 UTSW 13 50,857,007 (GRCm39) nonsense probably null
R9037:Spata31e4 UTSW 13 50,856,944 (GRCm39) missense probably benign 0.09
R9047:Spata31e4 UTSW 13 50,856,128 (GRCm39) nonsense probably null
R9065:Spata31e4 UTSW 13 50,856,276 (GRCm39) missense probably benign 0.01
R9476:Spata31e4 UTSW 13 50,856,149 (GRCm39) missense possibly damaging 0.70
R9495:Spata31e4 UTSW 13 50,855,465 (GRCm39) missense possibly damaging 0.82
R9510:Spata31e4 UTSW 13 50,856,149 (GRCm39) missense possibly damaging 0.70
Z1177:Spata31e4 UTSW 13 50,856,180 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCTGACATCCCACTCTTCTGAG -3'
(R):5'- CTAGGACAATGGCTGGCAAG -3'

Sequencing Primer
(F):5'- GTCTGTATGACACAAACTATAGCAG -3'
(R):5'- TGGCTGGCAAGATGGGAC -3'
Posted On 2016-02-04