Incidental Mutation 'R7187:Spats2'
ID 559385
Institutional Source Beutler Lab
Gene Symbol Spats2
Ensembl Gene ENSMUSG00000051934
Gene Name spermatogenesis associated, serine-rich 2
Synonyms p59, 59kDa, 2700012F11Rik, Scr59
MMRRC Submission 045377-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.364) question?
Stock # R7187 (G1)
Quality Score 225.009
Status Validated
Chromosome 15
Chromosomal Location 99023797-99111096 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 99110054 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 484 (S484P)
Ref Sequence ENSEMBL: ENSMUSP00000070549 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063517]
AlphaFold Q8K1N4
Predicted Effect probably benign
Transcript: ENSMUST00000063517
AA Change: S484P

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000070549
Gene: ENSMUSG00000051934
AA Change: S484P

DomainStartEndE-ValueType
Pfam:DUF1387 81 385 8.1e-125 PFAM
low complexity region 391 413 N/A INTRINSIC
low complexity region 517 528 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (59/59)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 A G 2: 25,327,733 (GRCm39) Y716C probably damaging Het
Abcc1 A G 16: 14,284,861 (GRCm39) I1237V probably benign Het
Adam34 C T 8: 44,105,565 (GRCm39) A27T probably benign Het
Aff3 T C 1: 38,257,478 (GRCm39) S415G probably damaging Het
Ak7 T C 12: 105,711,532 (GRCm39) Y390H probably benign Het
Arap2 A C 5: 62,826,396 (GRCm39) M1056R probably damaging Het
Brf1 T C 12: 112,923,945 (GRCm39) Y676C unknown Het
Cachd1 T A 4: 100,833,552 (GRCm39) H776Q possibly damaging Het
Cacng7 T C 7: 3,385,183 (GRCm39) V28A probably damaging Het
Camk2g A T 14: 20,792,780 (GRCm39) D359E probably benign Het
Cd209b T C 8: 3,976,638 (GRCm39) D16G probably benign Het
Ceacam5 A G 7: 17,493,410 (GRCm39) E811G possibly damaging Het
Cecr2 T A 6: 120,733,647 (GRCm39) S545T probably benign Het
Cep55 T C 19: 38,048,806 (GRCm39) probably null Het
Ctif C A 18: 75,770,290 (GRCm39) V32L probably damaging Het
Cwc27 G A 13: 104,797,900 (GRCm39) A353V probably benign Het
Dclk3 T A 9: 111,314,064 (GRCm39) S713R probably damaging Het
Dlec1 C T 9: 118,941,214 (GRCm39) H255Y probably benign Het
Dlgap1 A G 17: 70,823,093 (GRCm39) H26R possibly damaging Het
Dydc1 C T 14: 40,800,051 (GRCm39) T19I possibly damaging Het
Efcab12 G A 6: 115,800,474 (GRCm39) P183L not run Het
Eif1ad19 T C 12: 87,740,708 (GRCm39) probably benign Het
Eri3 C A 4: 117,446,343 (GRCm39) Q219K probably benign Het
Fam135a A G 1: 24,083,295 (GRCm39) L310P probably damaging Het
Fgd5 T A 6: 91,965,272 (GRCm39) S502T possibly damaging Het
Fgf8 A G 19: 45,730,106 (GRCm39) S57P probably benign Het
Gls T C 1: 52,259,139 (GRCm39) E154G probably damaging Het
Gm28042 T C 2: 119,870,176 (GRCm39) L705P probably damaging Het
Golgb1 C A 16: 36,736,512 (GRCm39) Q1961K probably benign Het
Herc3 C A 6: 58,833,616 (GRCm39) Q168K probably benign Het
Il31ra C A 13: 112,682,845 (GRCm39) C168F probably benign Het
Ino80 A T 2: 119,257,072 (GRCm39) D860E probably benign Het
Iqcm T G 8: 76,480,044 (GRCm39) L334R probably benign Het
Lrrk2 A G 15: 91,641,204 (GRCm39) D1587G possibly damaging Het
Map4 T A 9: 109,882,201 (GRCm39) V355E probably benign Het
Mapk13 T A 17: 28,995,361 (GRCm39) I194N probably damaging Het
Mtus2 A G 5: 148,013,515 (GRCm39) T103A probably benign Het
Naglu G T 11: 100,961,158 (GRCm39) G70W probably benign Het
Nlrp4f A T 13: 65,343,201 (GRCm39) M126K possibly damaging Het
Or4c120 T C 2: 89,001,714 (GRCm39) probably benign Het
Or5p61 A T 7: 107,758,585 (GRCm39) V165E probably benign Het
Pdia4 T C 6: 47,790,193 (GRCm39) T16A unknown Het
Pou6f2 G A 13: 18,414,298 (GRCm39) A159V Het
Ripor1 A G 8: 106,344,506 (GRCm39) T547A probably benign Het
Rundc3b A G 5: 8,542,506 (GRCm39) S389P probably damaging Het
Sorbs1 G C 19: 40,365,244 (GRCm39) R180G probably benign Het
Supv3l1 G A 10: 62,271,328 (GRCm39) T403I probably damaging Het
Tacstd2 G A 6: 67,512,180 (GRCm39) R171W probably damaging Het
Taok2 A T 7: 126,471,552 (GRCm39) F542L probably damaging Het
Tbc1d31 T A 15: 57,801,459 (GRCm39) N331K possibly damaging Het
Tff2 A T 17: 31,361,200 (GRCm39) C118S probably damaging Het
Tmprss7 G A 16: 45,498,317 (GRCm39) T354I possibly damaging Het
Tmtc3 A T 10: 100,313,774 (GRCm39) F33I probably damaging Het
Tpbpa G A 13: 61,088,399 (GRCm39) probably benign Het
Ube3a G T 7: 58,925,653 (GRCm39) V165F probably benign Het
Vmn2r4 T G 3: 64,322,681 (GRCm39) T13P probably benign Het
Wnt8b A G 19: 44,500,121 (GRCm39) D236G probably benign Het
Ythdf3 C A 3: 16,258,451 (GRCm39) D210E probably benign Het
Zfp110 T A 7: 12,583,753 (GRCm39) Y800* probably null Het
Other mutations in Spats2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Spats2 APN 15 99,078,474 (GRCm39) missense possibly damaging 0.88
IGL00696:Spats2 APN 15 99,108,775 (GRCm39) missense probably damaging 1.00
IGL01524:Spats2 APN 15 99,110,127 (GRCm39) missense probably benign 0.00
IGL02496:Spats2 APN 15 99,071,329 (GRCm39) missense probably damaging 1.00
IGL03031:Spats2 APN 15 99,078,569 (GRCm39) missense probably benign 0.00
R0067:Spats2 UTSW 15 99,110,168 (GRCm39) missense possibly damaging 0.64
R0067:Spats2 UTSW 15 99,110,168 (GRCm39) missense possibly damaging 0.64
R0630:Spats2 UTSW 15 99,083,909 (GRCm39) splice site probably null
R1577:Spats2 UTSW 15 99,076,333 (GRCm39) missense possibly damaging 0.94
R2012:Spats2 UTSW 15 99,076,375 (GRCm39) missense probably damaging 0.97
R2229:Spats2 UTSW 15 99,072,334 (GRCm39) critical splice donor site probably null
R2982:Spats2 UTSW 15 99,108,927 (GRCm39) missense probably benign
R3743:Spats2 UTSW 15 99,108,795 (GRCm39) missense probably benign 0.09
R4679:Spats2 UTSW 15 99,078,603 (GRCm39) missense possibly damaging 0.62
R4857:Spats2 UTSW 15 99,072,301 (GRCm39) missense probably damaging 1.00
R4962:Spats2 UTSW 15 99,110,157 (GRCm39) missense probably benign 0.00
R5291:Spats2 UTSW 15 99,076,422 (GRCm39) missense probably benign 0.16
R6879:Spats2 UTSW 15 99,071,293 (GRCm39) missense probably damaging 1.00
R7476:Spats2 UTSW 15 99,110,022 (GRCm39) missense probably benign 0.00
R8084:Spats2 UTSW 15 99,064,961 (GRCm39) missense possibly damaging 0.94
R8239:Spats2 UTSW 15 99,106,776 (GRCm39) missense probably damaging 1.00
R8338:Spats2 UTSW 15 99,076,340 (GRCm39) missense probably damaging 1.00
R8979:Spats2 UTSW 15 99,110,123 (GRCm39) missense possibly damaging 0.92
R9013:Spats2 UTSW 15 99,097,128 (GRCm39) missense probably damaging 1.00
R9050:Spats2 UTSW 15 99,110,010 (GRCm39) missense possibly damaging 0.78
R9433:Spats2 UTSW 15 99,076,446 (GRCm39) nonsense probably null
X0062:Spats2 UTSW 15 99,076,413 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- CGGTTTTGCTATCAGAACACTG -3'
(R):5'- TCAGGAGTTCGCAGCTTCAG -3'

Sequencing Primer
(F):5'- TTGCTATCAGAACACTGCTATAACC -3'
(R):5'- TTCGCAGCTTCAGCCTGAGAG -3'
Posted On 2019-06-26