Incidental Mutation 'R4685:Sspo'
ID 353599
Institutional Source Beutler Lab
Gene Symbol Sspo
Ensembl Gene ENSMUSG00000029797
Gene Name SCO-spondin
Synonyms C79529, Scospondin
MMRRC Submission 041936-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4685 (G1)
Quality Score 225
Status Validated
Chromosome 6
Chromosomal Location 48425163-48478184 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 48469828 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 4500 (S4500G)
Ref Sequence ENSEMBL: ENSMUSP00000148570 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043676] [ENSMUST00000169350] [ENSMUST00000185370] [ENSMUST00000188970] [ENSMUST00000212740]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000043676
AA Change: S4366G

PolyPhen 2 Score 0.159 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000047991
Gene: ENSMUSG00000029797
AA Change: S4366G

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
low complexity region 126 135 N/A INTRINSIC
Pfam:VWD 154 219 7.4e-11 PFAM
C8 267 346 2.3e-10 SMART
Pfam:TIL 349 404 3.2e-13 PFAM
VWC 406 448 2e-1 SMART
VWD 433 593 5.08e-29 SMART
C8 631 703 2.14e-28 SMART
Pfam:TIL 706 759 5.8e-11 PFAM
VWC 856 924 4.76e-2 SMART
VWD 883 1042 9.59e-48 SMART
C8 1076 1150 3.62e-26 SMART
Pfam:TIL 1153 1209 2.6e-13 PFAM
LDLa 1253 1291 2.29e-13 SMART
LDLa 1293 1328 1.87e-9 SMART
LDLa 1329 1366 5.77e-10 SMART
LDLa 1369 1408 1.52e-9 SMART
LDLa 1442 1479 2.55e-11 SMART
LDLa 1480 1520 5.6e-8 SMART
LDLa 1533 1574 2.29e-4 SMART
TSP1 1575 1626 6.47e-13 SMART
TSP1 1631 1686 1.35e-10 SMART
Pfam:TIL 1690 1746 3.1e-9 PFAM
TSP1 1774 1827 6.94e-2 SMART
VWC 1829 1886 4.95e-9 SMART
low complexity region 1901 1911 N/A INTRINSIC
FA58C 1928 2085 1.4e-2 SMART
LDLa 2091 2128 1.48e-7 SMART
LDLa 2242 2279 5.68e-9 SMART
LDLa 2299 2336 5.77e-10 SMART
TSP1 2339 2389 1.42e-9 SMART
TSP1 2394 2446 6.36e-21 SMART
Pfam:TIL 2460 2511 5.7e-10 PFAM
VWC 2513 2567 2.48e-1 SMART
TSP1 2554 2605 3.07e-14 SMART
TSP1 2611 2664 4.05e-5 SMART
TSP1 2669 2719 1.83e-12 SMART
EGF_like 2733 2776 5.45e1 SMART
VWC 2783 2836 2.73e-11 SMART
TSP1 2823 2875 3.72e-13 SMART
TSP1 2878 2919 6.05e-4 SMART
Pfam:TIL 2926 2978 1.1e-11 PFAM
VWC 2980 3035 9.77e-2 SMART
TSP1 3022 3086 6.68e-6 SMART
TSP1 3091 3143 1.08e-14 SMART
Pfam:TIL 3147 3201 2.2e-9 PFAM
VWC 3203 3260 2.72e-1 SMART
TSP1 3247 3306 3.72e-4 SMART
TSP1 3311 3363 5.27e-4 SMART
Pfam:TIL 3365 3421 4.2e-9 PFAM
TSP1 3484 3529 1.87e-9 SMART
low complexity region 3591 3601 N/A INTRINSIC
TSP1 3660 3713 5.02e-10 SMART
TSP1 3730 3779 2.95e-7 SMART
TSP1 3796 3849 1.99e-13 SMART
TSP1 3854 3906 2.51e-10 SMART
Pfam:TIL 3909 3964 3.4e-11 PFAM
VWC 3966 4022 1.26e0 SMART
TSP1 4009 4059 4.05e-5 SMART
TSP1 4103 4155 3.19e-12 SMART
TSP1 4161 4213 2.87e-2 SMART
TSP1 4218 4269 1.45e-6 SMART
Pfam:TIL 4273 4328 2.1e-10 PFAM
TSP1 4468 4516 7.56e-5 SMART
low complexity region 4551 4562 N/A INTRINSIC
VWC 4578 4652 5.21e-1 SMART
TSP1 4619 4669 3.92e-12 SMART
Pfam:TIL 4671 4725 1.5e-11 PFAM
Pfam:TIL 4777 4835 3.1e-9 PFAM
VWC 4837 4892 1.8e-11 SMART
GHB 4904 4997 1.02e0 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000169350
AA Change: S4509G

PolyPhen 2 Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000131401
Gene: ENSMUSG00000029797
AA Change: S4509G

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
low complexity region 126 135 N/A INTRINSIC
VWD 185 341 4.36e-28 SMART
C8 390 469 2.3e-10 SMART
Pfam:TIL 472 527 8.6e-13 PFAM
VWC 529 571 2e-1 SMART
VWD 556 716 5.08e-29 SMART
C8 754 826 2.14e-28 SMART
Pfam:TIL 829 882 1.6e-10 PFAM
VWC 979 1047 4.76e-2 SMART
VWD 1006 1165 9.59e-48 SMART
C8 1201 1275 3.62e-26 SMART
Pfam:TIL 1278 1334 7e-13 PFAM
LDLa 1378 1416 2.29e-13 SMART
LDLa 1418 1453 1.87e-9 SMART
LDLa 1454 1491 5.77e-10 SMART
LDLa 1494 1533 1.52e-9 SMART
LDLa 1567 1604 2.55e-11 SMART
LDLa 1605 1645 5.6e-8 SMART
LDLa 1658 1699 2.29e-4 SMART
TSP1 1700 1751 6.47e-13 SMART
TSP1 1756 1811 1.35e-10 SMART
Pfam:TIL 1815 1871 8.3e-9 PFAM
VWC 1873 1928 2.42e-1 SMART
TSP1 1915 1968 6.94e-2 SMART
VWC 1970 2027 4.95e-9 SMART
low complexity region 2042 2052 N/A INTRINSIC
FA58C 2069 2226 1.4e-2 SMART
LDLa 2232 2269 1.48e-7 SMART
LDLa 2387 2424 5.68e-9 SMART
LDLa 2444 2481 5.77e-10 SMART
TSP1 2484 2534 1.42e-9 SMART
TSP1 2539 2591 6.36e-21 SMART
Pfam:TIL 2606 2656 1.8e-9 PFAM
VWC 2658 2712 2.48e-1 SMART
TSP1 2699 2750 3.07e-14 SMART
TSP1 2756 2809 4.05e-5 SMART
TSP1 2814 2864 1.83e-12 SMART
EGF_like 2878 2921 5.45e1 SMART
VWC 2928 2981 2.73e-11 SMART
TSP1 2968 3020 3.72e-13 SMART
TSP1 3023 3064 6.05e-4 SMART
Pfam:TIL 3071 3123 3e-11 PFAM
VWC 3125 3180 9.77e-2 SMART
TSP1 3167 3231 6.68e-6 SMART
TSP1 3236 3288 1.08e-14 SMART
Pfam:TIL 3292 3346 6e-9 PFAM
VWC 3348 3405 2.72e-1 SMART
TSP1 3392 3451 3.72e-4 SMART
TSP1 3456 3508 5.27e-4 SMART
Pfam:TIL 3510 3566 1.1e-8 PFAM
TSP1 3629 3674 1.87e-9 SMART
low complexity region 3734 3744 N/A INTRINSIC
TSP1 3803 3856 5.02e-10 SMART
TSP1 3873 3922 2.95e-7 SMART
TSP1 3939 3992 1.99e-13 SMART
TSP1 3997 4049 2.51e-10 SMART
Pfam:TIL 4052 4107 9.1e-11 PFAM
VWC 4109 4165 1.26e0 SMART
TSP1 4152 4202 4.05e-5 SMART
TSP1 4246 4298 3.19e-12 SMART
TSP1 4304 4356 2.87e-2 SMART
TSP1 4361 4412 1.45e-6 SMART
Pfam:TIL 4416 4471 5.6e-10 PFAM
TSP1 4611 4659 7.56e-5 SMART
low complexity region 4694 4705 N/A INTRINSIC
VWC 4721 4795 5.21e-1 SMART
TSP1 4762 4812 3.92e-12 SMART
Pfam:TIL 4814 4868 4e-11 PFAM
Pfam:TIL 4920 4978 8.4e-9 PFAM
VWC 4980 5035 1.8e-11 SMART
GHB 5050 5143 1.02e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000185370
AA Change: S540G

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000139484
Gene: ENSMUSG00000029797
AA Change: S540G

DomainStartEndE-ValueType
TSP1 28 80 1.2e-12 SMART
Pfam:TIL 83 138 3.8e-9 PFAM
VWC 140 196 6e-3 SMART
TSP1 183 233 1.9e-7 SMART
TSP1 277 329 1.5e-14 SMART
TSP1 335 387 1.4e-4 SMART
TSP1 392 443 6.8e-9 SMART
Pfam:TIL 447 502 2e-8 PFAM
Blast:TSP1 549 637 2e-11 BLAST
TSP1 642 690 3.7e-7 SMART
Pfam:TIL 694 750 1.3e-7 PFAM
VWC_def 752 826 2.5e-3 SMART
TSP1 793 843 1.9e-14 SMART
Pfam:TIL 845 899 2.5e-9 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000188970
SMART Domains Protein: ENSMUSP00000140642
Gene: ENSMUSG00000029797

DomainStartEndE-ValueType
Pfam:TSP_1 1 40 9.4e-5 PFAM
TSP1 105 155 1.9e-14 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000212740
AA Change: S4500G

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)
Meta Mutation Damage Score 0.1925 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 95.0%
Validation Efficiency 97% (71/73)
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410004P03Rik T C 12: 17,057,185 (GRCm39) D104G probably damaging Het
2810021J22Rik T C 11: 58,771,750 (GRCm39) S411P probably damaging Het
Adcy2 T C 13: 68,876,024 (GRCm39) R493G probably benign Het
Adcy8 A G 15: 64,609,287 (GRCm39) I874T probably benign Het
Ano2 G T 6: 125,957,087 (GRCm39) E619* probably null Het
Apob A G 12: 8,056,456 (GRCm39) K1613R probably benign Het
Arhgef10 T A 8: 15,006,963 (GRCm39) F476Y probably damaging Het
Bmf G A 2: 118,377,283 (GRCm39) A74V probably damaging Het
Cadps T C 14: 12,467,139 (GRCm38) E925G possibly damaging Het
Ccdc162 T C 10: 41,557,682 (GRCm39) D181G possibly damaging Het
Ccdc85c A T 12: 108,173,434 (GRCm39) C387S probably benign Het
Cntnap5a T C 1: 116,374,410 (GRCm39) V974A possibly damaging Het
Cplx3 T A 9: 57,516,483 (GRCm39) I407F probably damaging Het
Dnah7b T C 1: 46,250,488 (GRCm39) F1703S probably damaging Het
Dsg3 C A 18: 20,672,793 (GRCm39) D821E probably benign Het
Ecel1 G T 1: 87,080,668 (GRCm39) probably null Het
Edn1 A T 13: 42,458,729 (GRCm39) probably null Het
Egfr G A 11: 16,808,980 (GRCm39) C58Y probably damaging Het
Fam184a T C 10: 53,574,596 (GRCm39) N282D probably benign Het
Fhit T A 14: 9,870,091 (GRCm38) Q63L probably damaging Het
Gabarapl2 T C 8: 112,669,150 (GRCm39) V36A probably benign Het
Glis1 T C 4: 107,424,842 (GRCm39) V151A probably benign Het
Gm12695 A G 4: 96,650,217 (GRCm39) S210P probably damaging Het
Gpat4 TAGAAGA TAGA 8: 23,672,865 (GRCm39) probably benign Het
H2-M10.4 G A 17: 36,772,688 (GRCm39) A98V probably benign Het
Hhat C A 1: 192,277,362 (GRCm39) G366C probably damaging Het
Hydin C A 8: 111,189,154 (GRCm39) A1186E probably damaging Het
Itgb2 T A 10: 77,385,937 (GRCm39) probably null Het
Kank1 C T 19: 25,387,398 (GRCm39) A329V possibly damaging Het
Kdm4b T A 17: 56,708,675 (GRCm39) S1070T probably benign Het
Kyat1 A G 2: 30,078,277 (GRCm39) Y101H probably damaging Het
Map4k5 T C 12: 69,858,140 (GRCm39) K679R probably benign Het
Mill1 A T 7: 17,989,853 (GRCm39) D45V probably damaging Het
Myo3a T A 2: 22,412,233 (GRCm39) Y743N probably damaging Het
Nox4 C G 7: 86,946,716 (GRCm39) I137M probably benign Het
Odf4 A G 11: 68,813,665 (GRCm39) probably null Het
Ostf1 A T 19: 18,558,652 (GRCm39) D210E probably damaging Het
Paxip1 A T 5: 27,966,675 (GRCm39) probably null Het
Pitrm1 A G 13: 6,606,578 (GRCm39) T211A probably benign Het
Pla2g4f A G 2: 120,135,496 (GRCm39) S393P probably damaging Het
Plppr3 T C 10: 79,703,359 (GRCm39) T42A probably damaging Het
Plxna4 C A 6: 32,142,779 (GRCm39) G1559W probably damaging Het
Ppp1r13l T C 7: 19,109,308 (GRCm39) probably null Het
Prex1 C T 2: 166,480,252 (GRCm39) V163M probably damaging Het
Prl6a1 A G 13: 27,500,307 (GRCm39) T93A probably benign Het
Psg16 T C 7: 16,824,459 (GRCm39) V81A probably benign Het
Rbm33 A T 5: 28,613,280 (GRCm39) probably benign Het
Rest C T 5: 77,423,090 (GRCm39) P298L possibly damaging Het
Rhobtb3 G A 13: 76,027,051 (GRCm39) R441* probably null Het
Rims4 T A 2: 163,706,914 (GRCm39) K155* probably null Het
Rps6kb1 C T 11: 86,410,713 (GRCm39) probably null Het
Ryr2 T C 13: 11,707,532 (GRCm39) D2835G probably damaging Het
Sc5d C T 9: 42,169,946 (GRCm39) V92I probably benign Het
Sell A T 1: 163,893,829 (GRCm39) I175F probably damaging Het
Serpinb6d A G 13: 33,855,211 (GRCm39) D295G probably damaging Het
Sphk1 A G 11: 116,426,106 (GRCm39) D96G probably damaging Het
Spns3 A T 11: 72,428,096 (GRCm39) V228D probably damaging Het
Syt9 T A 7: 107,035,678 (GRCm39) C232S possibly damaging Het
Terf1 A G 1: 15,889,185 (GRCm39) I176V possibly damaging Het
Tln2 C T 9: 67,209,854 (GRCm39) A428T probably damaging Het
Tmprss7 T C 16: 45,499,711 (GRCm39) N321S probably benign Het
Tomm40 A G 7: 19,435,761 (GRCm39) I323T probably benign Het
Try5 T A 6: 41,288,233 (GRCm39) Q240L possibly damaging Het
Vmn1r213 A T 13: 23,195,800 (GRCm39) I128L probably benign Het
Vmn2r80 T C 10: 79,030,162 (GRCm39) F663L possibly damaging Het
Znfx1 T A 2: 166,880,950 (GRCm39) Y278F probably damaging Het
Zpbp2 A G 11: 98,442,117 (GRCm39) probably benign Het
Other mutations in Sspo
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Sspo APN 6 48,447,387 (GRCm39) missense probably benign 0.02
IGL00339:Sspo APN 6 48,460,680 (GRCm39) splice site probably benign
IGL00391:Sspo APN 6 48,474,320 (GRCm39) missense probably damaging 0.96
IGL00433:Sspo APN 6 48,466,970 (GRCm39) missense probably damaging 1.00
IGL00471:Sspo APN 6 48,475,147 (GRCm39) splice site probably benign
IGL00500:Sspo APN 6 48,474,355 (GRCm39) nonsense probably null
IGL00537:Sspo APN 6 48,475,147 (GRCm39) splice site probably benign
IGL00540:Sspo APN 6 48,475,147 (GRCm39) splice site probably benign
IGL01060:Sspo APN 6 48,426,413 (GRCm39) nonsense probably null
IGL01090:Sspo APN 6 48,467,059 (GRCm39) missense probably benign 0.08
IGL01125:Sspo APN 6 48,469,822 (GRCm39) missense probably damaging 1.00
IGL01447:Sspo APN 6 48,441,600 (GRCm39) splice site probably null
IGL01457:Sspo APN 6 48,475,277 (GRCm39) missense probably benign 0.00
IGL01481:Sspo APN 6 48,425,449 (GRCm39) missense probably benign 0.41
IGL01485:Sspo APN 6 48,455,665 (GRCm39) missense probably damaging 1.00
IGL01544:Sspo APN 6 48,467,953 (GRCm39) missense probably damaging 0.99
IGL01575:Sspo APN 6 48,435,976 (GRCm39) missense probably benign 0.01
IGL01589:Sspo APN 6 48,428,112 (GRCm39) missense probably damaging 1.00
IGL01601:Sspo APN 6 48,463,313 (GRCm39) missense probably benign 0.33
IGL01644:Sspo APN 6 48,429,436 (GRCm39) missense probably benign
IGL01659:Sspo APN 6 48,451,377 (GRCm39) missense probably damaging 1.00
IGL01801:Sspo APN 6 48,434,072 (GRCm39) missense probably damaging 1.00
IGL01872:Sspo APN 6 48,431,623 (GRCm39) missense probably damaging 0.99
IGL01874:Sspo APN 6 48,429,124 (GRCm39) missense probably damaging 1.00
IGL01936:Sspo APN 6 48,452,821 (GRCm39) missense probably damaging 1.00
IGL01941:Sspo APN 6 48,472,116 (GRCm39) missense probably benign 0.19
IGL01986:Sspo APN 6 48,460,237 (GRCm39) missense probably benign 0.05
IGL01987:Sspo APN 6 48,454,558 (GRCm39) splice site probably null
IGL02170:Sspo APN 6 48,444,917 (GRCm39) missense possibly damaging 0.76
IGL02192:Sspo APN 6 48,436,502 (GRCm39) missense possibly damaging 0.86
IGL02210:Sspo APN 6 48,477,426 (GRCm39) missense probably damaging 1.00
IGL02225:Sspo APN 6 48,461,268 (GRCm39) missense probably benign 0.09
IGL02280:Sspo APN 6 48,473,165 (GRCm39) missense probably damaging 1.00
IGL02303:Sspo APN 6 48,461,639 (GRCm39) missense possibly damaging 0.52
IGL02397:Sspo APN 6 48,438,572 (GRCm39) missense probably benign 0.35
IGL02451:Sspo APN 6 48,437,237 (GRCm39) splice site probably benign
IGL02500:Sspo APN 6 48,455,313 (GRCm39) nonsense probably null
IGL02519:Sspo APN 6 48,461,762 (GRCm39) missense probably damaging 1.00
IGL02549:Sspo APN 6 48,428,707 (GRCm39) missense possibly damaging 0.81
IGL02562:Sspo APN 6 48,467,056 (GRCm39) splice site probably null
IGL02673:Sspo APN 6 48,475,709 (GRCm39) critical splice donor site probably null
IGL02673:Sspo APN 6 48,452,794 (GRCm39) missense probably damaging 1.00
IGL02719:Sspo APN 6 48,459,601 (GRCm39) missense probably benign 0.39
IGL02793:Sspo APN 6 48,464,828 (GRCm39) splice site probably benign
IGL03003:Sspo APN 6 48,432,021 (GRCm39) missense probably damaging 0.98
IGL03056:Sspo APN 6 48,447,472 (GRCm39) missense probably benign 0.17
IGL03105:Sspo APN 6 48,450,592 (GRCm39) splice site probably benign
IGL03116:Sspo APN 6 48,471,035 (GRCm39) missense probably benign 0.32
IGL03163:Sspo APN 6 48,461,266 (GRCm39) missense probably benign 0.19
IGL03198:Sspo APN 6 48,454,516 (GRCm39) missense probably benign 0.31
IGL03365:Sspo APN 6 48,436,349 (GRCm39) missense possibly damaging 0.82
Barrier UTSW 6 48,472,146 (GRCm39) missense possibly damaging 0.58
R0312_sspo_280 UTSW 6 48,432,335 (GRCm39) missense possibly damaging 0.52
R3112_Sspo_731 UTSW 6 48,434,534 (GRCm39) missense probably damaging 1.00
R3498_Sspo_650 UTSW 6 48,444,914 (GRCm39) missense possibly damaging 0.58
R4180_Sspo_324 UTSW 6 48,475,329 (GRCm39) critical splice donor site probably null
spotsylvania UTSW 6 48,453,505 (GRCm39) nonsense probably null
ANU74:Sspo UTSW 6 48,437,893 (GRCm39) missense probably damaging 1.00
IGL02984:Sspo UTSW 6 48,472,089 (GRCm39) missense probably benign 0.33
IGL03052:Sspo UTSW 6 48,437,387 (GRCm39) missense probably damaging 1.00
IGL03134:Sspo UTSW 6 48,427,999 (GRCm39) missense probably benign 0.28
PIT4531001:Sspo UTSW 6 48,458,173 (GRCm39) missense probably benign
R0087:Sspo UTSW 6 48,454,719 (GRCm39) missense probably damaging 1.00
R0122:Sspo UTSW 6 48,450,910 (GRCm39) missense possibly damaging 0.95
R0129:Sspo UTSW 6 48,432,352 (GRCm39) missense probably benign 0.00
R0164:Sspo UTSW 6 48,471,128 (GRCm39) splice site probably benign
R0195:Sspo UTSW 6 48,463,570 (GRCm39) missense probably benign
R0200:Sspo UTSW 6 48,463,349 (GRCm39) missense probably null 0.01
R0201:Sspo UTSW 6 48,432,686 (GRCm39) missense possibly damaging 0.64
R0241:Sspo UTSW 6 48,438,429 (GRCm39) missense possibly damaging 0.82
R0241:Sspo UTSW 6 48,438,429 (GRCm39) missense possibly damaging 0.82
R0243:Sspo UTSW 6 48,470,120 (GRCm39) missense probably damaging 1.00
R0268:Sspo UTSW 6 48,442,489 (GRCm39) missense probably benign 0.26
R0312:Sspo UTSW 6 48,432,335 (GRCm39) missense possibly damaging 0.52
R0449:Sspo UTSW 6 48,443,674 (GRCm39) missense probably damaging 1.00
R0523:Sspo UTSW 6 48,428,794 (GRCm39) missense probably benign 0.20
R0576:Sspo UTSW 6 48,441,876 (GRCm39) splice site probably null
R0671:Sspo UTSW 6 48,467,325 (GRCm39) splice site probably benign
R0828:Sspo UTSW 6 48,475,668 (GRCm39) missense probably damaging 1.00
R0880:Sspo UTSW 6 48,452,869 (GRCm39) missense possibly damaging 0.69
R0903:Sspo UTSW 6 48,432,242 (GRCm39) critical splice acceptor site probably null
R1051:Sspo UTSW 6 48,468,389 (GRCm39) nonsense probably null
R1083:Sspo UTSW 6 48,447,933 (GRCm39) missense possibly damaging 0.91
R1109:Sspo UTSW 6 48,474,377 (GRCm39) missense probably damaging 1.00
R1118:Sspo UTSW 6 48,436,352 (GRCm39) missense probably damaging 0.97
R1256:Sspo UTSW 6 48,434,573 (GRCm39) missense probably damaging 1.00
R1342:Sspo UTSW 6 48,438,569 (GRCm39) missense probably benign 0.07
R1355:Sspo UTSW 6 48,425,560 (GRCm39) missense probably benign 0.41
R1370:Sspo UTSW 6 48,425,560 (GRCm39) missense probably benign 0.41
R1469:Sspo UTSW 6 48,467,916 (GRCm39) missense probably damaging 1.00
R1469:Sspo UTSW 6 48,467,916 (GRCm39) missense probably damaging 1.00
R1476:Sspo UTSW 6 48,440,334 (GRCm39) critical splice donor site probably null
R1566:Sspo UTSW 6 48,443,804 (GRCm39) critical splice donor site probably null
R1630:Sspo UTSW 6 48,434,658 (GRCm39) missense probably benign 0.01
R1686:Sspo UTSW 6 48,437,334 (GRCm39) missense probably benign 0.00
R1707:Sspo UTSW 6 48,454,811 (GRCm39) missense probably damaging 0.99
R1727:Sspo UTSW 6 48,471,782 (GRCm39) missense probably damaging 1.00
R1822:Sspo UTSW 6 48,469,820 (GRCm39) missense possibly damaging 0.75
R1831:Sspo UTSW 6 48,466,720 (GRCm39) missense probably damaging 1.00
R1835:Sspo UTSW 6 48,434,274 (GRCm39) missense probably damaging 0.97
R1862:Sspo UTSW 6 48,467,940 (GRCm39) missense probably damaging 0.98
R1878:Sspo UTSW 6 48,436,300 (GRCm39) missense possibly damaging 0.92
R1900:Sspo UTSW 6 48,436,284 (GRCm39) missense probably benign 0.22
R1945:Sspo UTSW 6 48,466,707 (GRCm39) missense possibly damaging 0.93
R1957:Sspo UTSW 6 48,455,207 (GRCm39) missense probably damaging 0.99
R1990:Sspo UTSW 6 48,427,984 (GRCm39) missense probably benign 0.00
R1996:Sspo UTSW 6 48,452,424 (GRCm39) missense possibly damaging 0.50
R2049:Sspo UTSW 6 48,440,465 (GRCm39) missense probably benign 0.36
R2049:Sspo UTSW 6 48,437,697 (GRCm39) splice site probably benign
R2064:Sspo UTSW 6 48,450,596 (GRCm39) missense probably damaging 0.99
R2072:Sspo UTSW 6 48,450,451 (GRCm39) missense probably benign 0.01
R2096:Sspo UTSW 6 48,438,608 (GRCm39) missense probably benign
R2106:Sspo UTSW 6 48,443,250 (GRCm39) missense possibly damaging 0.96
R2230:Sspo UTSW 6 48,477,437 (GRCm39) missense probably benign 0.11
R2230:Sspo UTSW 6 48,425,606 (GRCm39) missense probably damaging 0.97
R2232:Sspo UTSW 6 48,425,606 (GRCm39) missense probably damaging 0.97
R2351:Sspo UTSW 6 48,441,803 (GRCm39) missense probably damaging 1.00
R2423:Sspo UTSW 6 48,430,989 (GRCm39) missense probably benign 0.00
R2508:Sspo UTSW 6 48,441,298 (GRCm39) missense probably damaging 1.00
R3110:Sspo UTSW 6 48,434,534 (GRCm39) missense probably damaging 1.00
R3112:Sspo UTSW 6 48,434,534 (GRCm39) missense probably damaging 1.00
R3413:Sspo UTSW 6 48,457,631 (GRCm39) missense probably damaging 1.00
R3433:Sspo UTSW 6 48,452,885 (GRCm39) splice site probably null
R3498:Sspo UTSW 6 48,444,914 (GRCm39) missense possibly damaging 0.58
R3732:Sspo UTSW 6 48,426,864 (GRCm39) missense probably damaging 1.00
R3816:Sspo UTSW 6 48,458,037 (GRCm39) missense possibly damaging 0.77
R3818:Sspo UTSW 6 48,458,037 (GRCm39) missense possibly damaging 0.77
R3819:Sspo UTSW 6 48,458,037 (GRCm39) missense possibly damaging 0.77
R3838:Sspo UTSW 6 48,457,754 (GRCm39) missense probably damaging 1.00
R3850:Sspo UTSW 6 48,469,424 (GRCm39) missense probably damaging 1.00
R3880:Sspo UTSW 6 48,471,874 (GRCm39) missense probably benign 0.38
R3893:Sspo UTSW 6 48,453,505 (GRCm39) nonsense probably null
R4116:Sspo UTSW 6 48,433,928 (GRCm39) missense probably damaging 0.99
R4179:Sspo UTSW 6 48,475,329 (GRCm39) critical splice donor site probably null
R4180:Sspo UTSW 6 48,475,329 (GRCm39) critical splice donor site probably null
R4207:Sspo UTSW 6 48,455,227 (GRCm39) missense probably benign 0.00
R4210:Sspo UTSW 6 48,441,835 (GRCm39) missense probably benign 0.00
R4223:Sspo UTSW 6 48,428,091 (GRCm39) missense possibly damaging 0.54
R4224:Sspo UTSW 6 48,428,091 (GRCm39) missense possibly damaging 0.54
R4225:Sspo UTSW 6 48,428,091 (GRCm39) missense possibly damaging 0.54
R4229:Sspo UTSW 6 48,467,868 (GRCm39) missense probably benign 0.00
R4230:Sspo UTSW 6 48,467,868 (GRCm39) missense probably benign 0.00
R4363:Sspo UTSW 6 48,475,665 (GRCm39) missense probably damaging 1.00
R4370:Sspo UTSW 6 48,443,282 (GRCm39) missense probably null 0.14
R4407:Sspo UTSW 6 48,437,454 (GRCm39) missense probably damaging 1.00
R4438:Sspo UTSW 6 48,464,287 (GRCm39) missense probably damaging 1.00
R4454:Sspo UTSW 6 48,464,159 (GRCm39) missense probably benign 0.05
R4455:Sspo UTSW 6 48,442,450 (GRCm39) missense probably damaging 1.00
R4561:Sspo UTSW 6 48,452,468 (GRCm39) splice site probably null
R4574:Sspo UTSW 6 48,442,457 (GRCm39) missense probably damaging 1.00
R4578:Sspo UTSW 6 48,440,307 (GRCm39) missense possibly damaging 0.58
R4653:Sspo UTSW 6 48,455,580 (GRCm39) missense probably damaging 1.00
R4656:Sspo UTSW 6 48,431,010 (GRCm39) missense possibly damaging 0.65
R4659:Sspo UTSW 6 48,461,147 (GRCm39) missense probably damaging 1.00
R4664:Sspo UTSW 6 48,450,468 (GRCm39) missense possibly damaging 0.82
R4692:Sspo UTSW 6 48,459,621 (GRCm39) missense probably damaging 1.00
R4703:Sspo UTSW 6 48,477,387 (GRCm39) missense probably damaging 1.00
R4704:Sspo UTSW 6 48,475,638 (GRCm39) missense probably damaging 1.00
R4738:Sspo UTSW 6 48,455,330 (GRCm39) missense possibly damaging 0.78
R4766:Sspo UTSW 6 48,447,514 (GRCm39) missense probably benign 0.04
R4771:Sspo UTSW 6 48,437,813 (GRCm39) missense probably damaging 1.00
R4790:Sspo UTSW 6 48,437,705 (GRCm39) missense probably benign 0.04
R4792:Sspo UTSW 6 48,438,519 (GRCm39) missense probably benign 0.00
R4808:Sspo UTSW 6 48,428,095 (GRCm39) missense probably damaging 1.00
R4812:Sspo UTSW 6 48,467,444 (GRCm39) missense probably benign 0.00
R4883:Sspo UTSW 6 48,437,756 (GRCm39) missense probably benign 0.00
R4906:Sspo UTSW 6 48,442,664 (GRCm39) critical splice acceptor site probably null
R4934:Sspo UTSW 6 48,442,486 (GRCm39) missense probably damaging 1.00
R4945:Sspo UTSW 6 48,444,021 (GRCm39) splice site probably null
R4967:Sspo UTSW 6 48,441,539 (GRCm39) missense probably damaging 0.97
R5016:Sspo UTSW 6 48,429,214 (GRCm39) nonsense probably null
R5018:Sspo UTSW 6 48,432,634 (GRCm39) missense probably damaging 1.00
R5034:Sspo UTSW 6 48,457,757 (GRCm39) missense possibly damaging 0.93
R5044:Sspo UTSW 6 48,443,889 (GRCm39) critical splice acceptor site probably null
R5055:Sspo UTSW 6 48,441,729 (GRCm39) missense probably damaging 1.00
R5087:Sspo UTSW 6 48,465,405 (GRCm39) missense possibly damaging 0.51
R5155:Sspo UTSW 6 48,437,408 (GRCm39) missense probably benign 0.03
R5223:Sspo UTSW 6 48,455,258 (GRCm39) missense probably damaging 1.00
R5249:Sspo UTSW 6 48,470,244 (GRCm39) missense probably damaging 0.98
R5257:Sspo UTSW 6 48,453,428 (GRCm39) missense probably damaging 1.00
R5258:Sspo UTSW 6 48,453,428 (GRCm39) missense probably damaging 1.00
R5276:Sspo UTSW 6 48,467,401 (GRCm39) missense probably damaging 1.00
R5307:Sspo UTSW 6 48,431,784 (GRCm39) missense probably damaging 0.99
R5341:Sspo UTSW 6 48,436,549 (GRCm39) missense probably damaging 1.00
R5361:Sspo UTSW 6 48,443,247 (GRCm39) missense probably benign 0.02
R5385:Sspo UTSW 6 48,439,187 (GRCm39) missense probably benign 0.18
R5394:Sspo UTSW 6 48,472,194 (GRCm39) missense possibly damaging 0.52
R5477:Sspo UTSW 6 48,475,327 (GRCm39) missense possibly damaging 0.60
R5490:Sspo UTSW 6 48,470,214 (GRCm39) missense probably benign 0.33
R5512:Sspo UTSW 6 48,432,605 (GRCm39) missense probably damaging 0.97
R5518:Sspo UTSW 6 48,473,588 (GRCm39) missense possibly damaging 0.92
R5530:Sspo UTSW 6 48,442,517 (GRCm39) missense probably damaging 0.97
R5538:Sspo UTSW 6 48,429,112 (GRCm39) missense probably damaging 0.99
R5590:Sspo UTSW 6 48,451,425 (GRCm39) missense probably damaging 1.00
R5613:Sspo UTSW 6 48,431,978 (GRCm39) missense possibly damaging 0.79
R5638:Sspo UTSW 6 48,469,825 (GRCm39) missense possibly damaging 0.86
R5809:Sspo UTSW 6 48,436,979 (GRCm39) missense possibly damaging 0.59
R5810:Sspo UTSW 6 48,460,832 (GRCm39) missense probably benign 0.02
R5814:Sspo UTSW 6 48,428,818 (GRCm39) missense probably damaging 1.00
R5915:Sspo UTSW 6 48,468,418 (GRCm39) missense possibly damaging 0.83
R5915:Sspo UTSW 6 48,441,530 (GRCm39) missense probably benign 0.00
R5979:Sspo UTSW 6 48,440,627 (GRCm39) missense probably benign 0.20
R5996:Sspo UTSW 6 48,471,110 (GRCm39) missense possibly damaging 0.87
R6012:Sspo UTSW 6 48,428,305 (GRCm39) missense probably benign 0.00
R6025:Sspo UTSW 6 48,463,720 (GRCm39) missense possibly damaging 0.83
R6120:Sspo UTSW 6 48,442,510 (GRCm39) missense probably damaging 1.00
R6150:Sspo UTSW 6 48,463,313 (GRCm39) missense probably benign 0.33
R6221:Sspo UTSW 6 48,440,639 (GRCm39) missense probably damaging 1.00
R6261:Sspo UTSW 6 48,439,125 (GRCm39) missense possibly damaging 0.75
R6312:Sspo UTSW 6 48,434,300 (GRCm39) critical splice donor site probably null
R6372:Sspo UTSW 6 48,449,475 (GRCm39) missense probably damaging 1.00
R6456:Sspo UTSW 6 48,428,740 (GRCm39) missense probably benign 0.08
R6497:Sspo UTSW 6 48,472,142 (GRCm39) missense possibly damaging 0.71
R6501:Sspo UTSW 6 48,472,146 (GRCm39) missense possibly damaging 0.58
R6617:Sspo UTSW 6 48,467,980 (GRCm39) missense possibly damaging 0.93
R6825:Sspo UTSW 6 48,442,459 (GRCm39) missense probably benign 0.04
R6831:Sspo UTSW 6 48,461,767 (GRCm39) missense possibly damaging 0.68
R6861:Sspo UTSW 6 48,464,889 (GRCm39) missense probably benign 0.15
R6961:Sspo UTSW 6 48,440,811 (GRCm39) missense probably benign 0.05
R6967:Sspo UTSW 6 48,466,728 (GRCm39) missense probably benign 0.21
R7016:Sspo UTSW 6 48,426,098 (GRCm39) missense probably damaging 1.00
R7035:Sspo UTSW 6 48,426,147 (GRCm39) splice site probably null
R7058:Sspo UTSW 6 48,425,516 (GRCm39) missense probably damaging 1.00
R7072:Sspo UTSW 6 48,431,913 (GRCm39) missense probably damaging 1.00
R7078:Sspo UTSW 6 48,437,313 (GRCm39) missense probably damaging 1.00
R7082:Sspo UTSW 6 48,455,543 (GRCm39) critical splice acceptor site probably null
R7120:Sspo UTSW 6 48,442,505 (GRCm39) missense probably benign 0.05
R7127:Sspo UTSW 6 48,426,446 (GRCm39) missense probably benign 0.02
R7146:Sspo UTSW 6 48,478,029 (GRCm39) missense probably benign 0.15
R7220:Sspo UTSW 6 48,453,540 (GRCm39) nonsense probably null
R7242:Sspo UTSW 6 48,450,886 (GRCm39) missense probably benign
R7261:Sspo UTSW 6 48,427,011 (GRCm39) missense possibly damaging 0.52
R7313:Sspo UTSW 6 48,450,390 (GRCm39) missense probably benign 0.04
R7313:Sspo UTSW 6 48,431,762 (GRCm39) missense probably damaging 1.00
R7323:Sspo UTSW 6 48,438,581 (GRCm39) missense possibly damaging 0.93
R7330:Sspo UTSW 6 48,452,396 (GRCm39) missense probably benign 0.00
R7351:Sspo UTSW 6 48,441,855 (GRCm39) missense possibly damaging 0.89
R7467:Sspo UTSW 6 48,463,237 (GRCm39) missense probably damaging 1.00
R7475:Sspo UTSW 6 48,432,794 (GRCm39) missense probably benign 0.37
R7489:Sspo UTSW 6 48,450,647 (GRCm39) missense probably damaging 0.99
R7508:Sspo UTSW 6 48,443,633 (GRCm39) missense probably damaging 1.00
R7515:Sspo UTSW 6 48,470,820 (GRCm39) missense probably damaging 1.00
R7564:Sspo UTSW 6 48,426,434 (GRCm39) missense probably benign 0.04
R7607:Sspo UTSW 6 48,466,661 (GRCm39) missense probably damaging 1.00
R7620:Sspo UTSW 6 48,444,020 (GRCm39) critical splice donor site probably null
R7667:Sspo UTSW 6 48,452,305 (GRCm39) nonsense probably null
R7691:Sspo UTSW 6 48,461,163 (GRCm39) missense probably benign 0.12
R7707:Sspo UTSW 6 48,438,461 (GRCm39) missense probably benign 0.01
R7723:Sspo UTSW 6 48,441,572 (GRCm39) missense probably damaging 0.99
R7748:Sspo UTSW 6 48,426,399 (GRCm39) nonsense probably null
R7767:Sspo UTSW 6 48,428,316 (GRCm39) missense probably damaging 0.96
R7792:Sspo UTSW 6 48,431,624 (GRCm39) missense probably damaging 0.98
R7878:Sspo UTSW 6 48,469,460 (GRCm39) missense probably damaging 1.00
R7893:Sspo UTSW 6 48,440,244 (GRCm39) missense probably benign 0.02
R7942:Sspo UTSW 6 48,465,434 (GRCm39) splice site probably null
R7952:Sspo UTSW 6 48,464,263 (GRCm39) missense probably damaging 1.00
R7981:Sspo UTSW 6 48,445,428 (GRCm39) missense probably benign
R7995:Sspo UTSW 6 48,469,823 (GRCm39) missense probably damaging 1.00
R8088:Sspo UTSW 6 48,434,547 (GRCm39) missense probably damaging 1.00
R8129:Sspo UTSW 6 48,443,959 (GRCm39) missense possibly damaging 0.79
R8145:Sspo UTSW 6 48,444,683 (GRCm39) missense possibly damaging 0.49
R8202:Sspo UTSW 6 48,434,534 (GRCm39) missense probably damaging 1.00
R8211:Sspo UTSW 6 48,469,543 (GRCm39) critical splice donor site probably null
R8240:Sspo UTSW 6 48,460,436 (GRCm39) missense possibly damaging 0.84
R8252:Sspo UTSW 6 48,462,386 (GRCm39) missense probably damaging 0.99
R8270:Sspo UTSW 6 48,426,897 (GRCm39) missense probably benign
R8272:Sspo UTSW 6 48,425,453 (GRCm39) missense probably benign 0.03
R8316:Sspo UTSW 6 48,459,622 (GRCm39) missense probably damaging 1.00
R8384:Sspo UTSW 6 48,459,598 (GRCm39) missense probably damaging 1.00
R8390:Sspo UTSW 6 48,444,896 (GRCm39) missense probably benign 0.00
R8770:Sspo UTSW 6 48,451,206 (GRCm39) missense probably null 1.00
R8827:Sspo UTSW 6 48,434,606 (GRCm39) missense possibly damaging 0.59
R8882:Sspo UTSW 6 48,452,390 (GRCm39) missense probably damaging 1.00
R8886:Sspo UTSW 6 48,458,201 (GRCm39) missense possibly damaging 0.92
R8946:Sspo UTSW 6 48,434,071 (GRCm39) missense probably damaging 1.00
R8947:Sspo UTSW 6 48,425,504 (GRCm39) missense probably damaging 1.00
R9028:Sspo UTSW 6 48,473,087 (GRCm39) missense probably benign 0.38
R9043:Sspo UTSW 6 48,470,214 (GRCm39) missense probably benign 0.07
R9056:Sspo UTSW 6 48,450,608 (GRCm39) missense probably damaging 0.97
R9071:Sspo UTSW 6 48,433,982 (GRCm39) missense probably benign 0.00
R9133:Sspo UTSW 6 48,434,747 (GRCm39) missense possibly damaging 0.81
R9187:Sspo UTSW 6 48,472,223 (GRCm39) missense probably damaging 1.00
R9205:Sspo UTSW 6 48,432,806 (GRCm39) missense probably benign 0.03
R9213:Sspo UTSW 6 48,440,869 (GRCm39) missense possibly damaging 0.91
R9214:Sspo UTSW 6 48,440,869 (GRCm39) missense possibly damaging 0.91
R9215:Sspo UTSW 6 48,440,869 (GRCm39) missense possibly damaging 0.91
R9235:Sspo UTSW 6 48,466,718 (GRCm39) missense probably damaging 1.00
R9254:Sspo UTSW 6 48,464,928 (GRCm39) missense probably damaging 1.00
R9291:Sspo UTSW 6 48,473,330 (GRCm39) missense probably damaging 1.00
R9312:Sspo UTSW 6 48,445,396 (GRCm39) missense probably benign 0.00
R9357:Sspo UTSW 6 48,443,989 (GRCm39) missense possibly damaging 0.77
R9480:Sspo UTSW 6 48,470,820 (GRCm39) missense probably damaging 1.00
R9586:Sspo UTSW 6 48,458,039 (GRCm39) missense probably benign 0.03
R9660:Sspo UTSW 6 48,432,707 (GRCm39) missense probably damaging 1.00
R9661:Sspo UTSW 6 48,455,272 (GRCm39) nonsense probably null
R9728:Sspo UTSW 6 48,432,707 (GRCm39) missense probably damaging 1.00
R9776:Sspo UTSW 6 48,439,269 (GRCm39) missense probably benign 0.00
RF009:Sspo UTSW 6 48,436,919 (GRCm39) nonsense probably null
X0060:Sspo UTSW 6 48,457,728 (GRCm39) missense probably damaging 1.00
X0060:Sspo UTSW 6 48,443,228 (GRCm39) missense probably damaging 1.00
X0063:Sspo UTSW 6 48,474,356 (GRCm39) missense probably damaging 0.96
X0065:Sspo UTSW 6 48,438,618 (GRCm39) missense probably benign 0.00
Z1176:Sspo UTSW 6 48,458,227 (GRCm39) missense probably damaging 1.00
Z1177:Sspo UTSW 6 48,467,824 (GRCm39) missense probably damaging 1.00
Z1177:Sspo UTSW 6 48,467,482 (GRCm39) nonsense probably null
Z1177:Sspo UTSW 6 48,450,369 (GRCm39) missense probably damaging 0.99
Z1177:Sspo UTSW 6 48,447,918 (GRCm39) missense probably benign 0.16
Z1177:Sspo UTSW 6 48,441,750 (GRCm39) missense possibly damaging 0.72
Z1177:Sspo UTSW 6 48,433,960 (GRCm39) missense probably benign 0.31
Z1186:Sspo UTSW 6 48,445,441 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- AACCTGAGAGCAAGTGACCC -3'
(R):5'- GCTGACCTCAGGAAATCTTCAAC -3'

Sequencing Primer
(F):5'- CAAGATGCCCAGCTTTAAGC -3'
(R):5'- TTCAACCCAGAAAGCCCAGTGG -3'
Posted On 2015-10-21