Incidental Mutation 'R4604:Csmd3'
ID 345928
Institutional Source Beutler Lab
Gene Symbol Csmd3
Ensembl Gene ENSMUSG00000022311
Gene Name CUB and Sushi multiple domains 3
Synonyms 4930500N14Rik
MMRRC Submission 041816-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4604 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 47444033-48655459 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 47868211 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 770 (S770T)
Ref Sequence ENSEMBL: ENSMUSP00000124775 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100670] [ENSMUST00000160658] [ENSMUST00000162830]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000100670
AA Change: S770T

PolyPhen 2 Score 0.898 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311
AA Change: S770T

DomainStartEndE-ValueType
CUB 65 173 8.79e-30 SMART
CCP 178 235 1.77e-11 SMART
CUB 241 345 2.29e-28 SMART
low complexity region 370 387 N/A INTRINSIC
CCP 486 543 6.9e-14 SMART
CUB 548 659 9.22e-24 SMART
CCP 664 717 1.29e-13 SMART
CUB 721 829 6.87e-32 SMART
CCP 834 891 5.19e-9 SMART
CUB 895 1003 3.23e-37 SMART
CCP 1010 1063 1.82e-13 SMART
CUB 1067 1177 4.87e-23 SMART
CCP 1182 1237 1.82e-13 SMART
CUB 1241 1349 5.02e-25 SMART
CCP 1354 1410 2.5e-11 SMART
CUB 1414 1523 6.27e-26 SMART
CCP 1528 1584 4.41e-12 SMART
CUB 1588 1696 5.37e-34 SMART
CCP 1701 1758 1.18e-12 SMART
CUB 1762 1870 2.27e-23 SMART
CCP 1878 1935 1.84e-9 SMART
CUB 1939 2047 1.8e-35 SMART
CCP 2052 2107 4.48e-13 SMART
CUB 2111 2219 3.95e-32 SMART
CCP 2224 2279 4.02e-15 SMART
CUB 2283 2390 1.74e-33 SMART
CCP 2395 2452 5.82e-12 SMART
CUB 2457 2567 5.3e-24 SMART
CCP 2569 2627 2.11e-9 SMART
CCP 2632 2689 8.23e-12 SMART
CCP 2694 2754 8.56e-10 SMART
CCP 2759 2812 1.14e-14 SMART
CCP 2817 2870 4.76e-17 SMART
CCP 2875 2928 1.85e-14 SMART
CCP 2933 2990 9.9e-15 SMART
CCP 2995 3048 1.79e-12 SMART
CCP 3056 3109 1.72e-14 SMART
CCP 3114 3168 3.17e-13 SMART
CCP 3173 3228 1.25e-11 SMART
CCP 3233 3286 1.25e-11 SMART
CCP 3291 3344 8.23e-12 SMART
CCP 3352 3406 5.6e-14 SMART
CCP 3411 3466 1.89e-11 SMART
transmembrane domain 3630 3652 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000160658
AA Change: S666T

PolyPhen 2 Score 0.606 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311
AA Change: S666T

DomainStartEndE-ValueType
CUB 65 173 8.79e-30 SMART
CCP 178 235 1.77e-11 SMART
CUB 241 345 2.29e-28 SMART
CCP 382 439 6.9e-14 SMART
CUB 444 555 9.22e-24 SMART
CCP 560 613 1.29e-13 SMART
CUB 617 725 6.87e-32 SMART
CCP 730 787 5.19e-9 SMART
CUB 791 899 3.23e-37 SMART
CCP 906 959 1.82e-13 SMART
CUB 963 1073 4.87e-23 SMART
CCP 1078 1133 1.82e-13 SMART
CUB 1137 1245 5.02e-25 SMART
CCP 1250 1306 2.5e-11 SMART
CUB 1310 1419 6.27e-26 SMART
CCP 1424 1480 4.41e-12 SMART
CUB 1484 1592 5.37e-34 SMART
CCP 1597 1654 1.18e-12 SMART
CUB 1658 1766 2.27e-23 SMART
CCP 1774 1831 1.84e-9 SMART
CUB 1835 1943 1.8e-35 SMART
CCP 1948 2003 4.48e-13 SMART
CUB 2007 2115 3.95e-32 SMART
CCP 2120 2175 4.02e-15 SMART
CUB 2179 2286 1.74e-33 SMART
CCP 2291 2348 5.82e-12 SMART
CUB 2353 2463 5.3e-24 SMART
CCP 2465 2523 2.11e-9 SMART
CCP 2528 2585 8.23e-12 SMART
CCP 2590 2643 1.14e-14 SMART
CCP 2648 2701 4.76e-17 SMART
CCP 2706 2759 1.85e-14 SMART
CCP 2764 2821 9.9e-15 SMART
CCP 2826 2879 1.79e-12 SMART
CCP 2887 2940 1.72e-14 SMART
CCP 2945 2999 3.17e-13 SMART
CCP 3004 3059 1.25e-11 SMART
CCP 3064 3117 1.25e-11 SMART
CCP 3122 3175 8.23e-12 SMART
CCP 3183 3237 5.6e-14 SMART
CCP 3242 3297 1.89e-11 SMART
transmembrane domain 3461 3483 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000161653
SMART Domains Protein: ENSMUSP00000124195
Gene: ENSMUSG00000022311

DomainStartEndE-ValueType
CCP 1 51 6.59e-1 SMART
CUB 55 163 3.23e-37 SMART
CCP 170 223 1.82e-13 SMART
CUB 227 337 4.87e-23 SMART
CCP 342 397 1.82e-13 SMART
CUB 401 509 5.02e-25 SMART
CCP 514 570 2.5e-11 SMART
CUB 574 683 6.27e-26 SMART
CCP 688 744 4.41e-12 SMART
CUB 748 856 5.37e-34 SMART
CCP 861 918 1.18e-12 SMART
Pfam:CUB 922 964 9.7e-8 PFAM
CCP 968 1025 1.84e-9 SMART
CUB 1029 1137 1.8e-35 SMART
CCP 1142 1197 4.48e-13 SMART
CUB 1201 1309 3.95e-32 SMART
CCP 1314 1369 4.02e-15 SMART
CUB 1373 1480 1.74e-33 SMART
CCP 1485 1542 5.82e-12 SMART
CUB 1547 1657 5.3e-24 SMART
CCP 1659 1717 2.11e-9 SMART
CCP 1722 1779 8.23e-12 SMART
CCP 1784 1844 8.56e-10 SMART
CCP 1849 1902 1.14e-14 SMART
CCP 1907 1960 4.76e-17 SMART
CCP 1965 2018 1.85e-14 SMART
CCP 2023 2080 9.9e-15 SMART
CCP 2085 2138 1.79e-12 SMART
CCP 2146 2199 1.72e-14 SMART
CCP 2204 2258 3.17e-13 SMART
CCP 2263 2318 1.25e-11 SMART
CCP 2323 2376 1.25e-11 SMART
CCP 2381 2434 8.23e-12 SMART
CCP 2442 2496 5.6e-14 SMART
CCP 2501 2556 1.89e-11 SMART
transmembrane domain 2720 2742 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000162830
AA Change: S770T

PolyPhen 2 Score 0.898 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311
AA Change: S770T

DomainStartEndE-ValueType
CUB 65 173 8.79e-30 SMART
CCP 178 235 1.77e-11 SMART
CUB 241 345 2.29e-28 SMART
low complexity region 370 387 N/A INTRINSIC
CCP 486 543 6.9e-14 SMART
CUB 548 659 9.22e-24 SMART
CCP 664 717 1.29e-13 SMART
CUB 721 829 6.87e-32 SMART
CCP 834 891 5.19e-9 SMART
CUB 895 1003 3.23e-37 SMART
CCP 1010 1063 1.82e-13 SMART
CUB 1067 1177 4.87e-23 SMART
CCP 1182 1237 1.82e-13 SMART
CUB 1241 1349 5.02e-25 SMART
CCP 1354 1410 2.5e-11 SMART
CUB 1414 1523 6.27e-26 SMART
CCP 1528 1584 4.41e-12 SMART
CUB 1588 1696 5.37e-34 SMART
CCP 1701 1758 1.18e-12 SMART
CUB 1762 1870 2.27e-23 SMART
CCP 1878 1935 1.84e-9 SMART
CUB 1939 2047 1.8e-35 SMART
CCP 2052 2107 4.48e-13 SMART
CUB 2111 2219 3.95e-32 SMART
CCP 2224 2279 4.02e-15 SMART
CUB 2283 2390 1.74e-33 SMART
CCP 2395 2452 5.82e-12 SMART
CUB 2457 2567 5.3e-24 SMART
CCP 2569 2627 2.11e-9 SMART
CCP 2632 2689 8.23e-12 SMART
CCP 2694 2754 8.56e-10 SMART
CCP 2759 2812 1.14e-14 SMART
CCP 2817 2870 4.76e-17 SMART
CCP 2875 2928 1.85e-14 SMART
CCP 2933 2990 9.9e-15 SMART
CCP 2995 3048 1.79e-12 SMART
CCP 3056 3109 1.72e-14 SMART
CCP 3114 3168 3.17e-13 SMART
CCP 3173 3228 1.25e-11 SMART
CCP 3233 3286 1.25e-11 SMART
CCP 3291 3344 8.23e-12 SMART
CCP 3352 3406 5.6e-14 SMART
CCP 3411 3466 1.89e-11 SMART
transmembrane domain 3630 3652 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 106 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930518I15Rik C T 2: 156,699,074 (GRCm39) probably benign Het
Abcb6 G A 1: 75,156,521 (GRCm39) T81I probably benign Het
Acp6 A G 3: 97,083,075 (GRCm39) K362R probably benign Het
Adam26a A G 8: 44,023,088 (GRCm39) M134T probably benign Het
Ankrd27 C T 7: 35,327,915 (GRCm39) P812S probably damaging Het
Arl6ip1 AAAATAAATAAATAAATAAATAAATA AAAATAAATAAATAAATAAATAAATAAATA 7: 117,721,122 (GRCm39) probably benign Het
Atp2a1 G A 7: 126,047,795 (GRCm39) R672C probably damaging Het
Atxn2 G T 5: 121,919,406 (GRCm39) W371C probably damaging Het
B3gnt2 T TTCACAAA 11: 22,786,426 (GRCm39) probably null Het
Btnl6 T A 17: 34,727,435 (GRCm39) D365V possibly damaging Het
Ccdc80 T A 16: 44,915,928 (GRCm39) L228Q probably damaging Het
Cdc42bpa A G 1: 179,936,759 (GRCm39) H718R probably benign Het
Cdh18 A G 15: 23,474,454 (GRCm39) K775E probably benign Het
Cdh23 T G 10: 60,173,445 (GRCm39) N1679T possibly damaging Het
Cep192 T A 18: 67,948,993 (GRCm39) D271E possibly damaging Het
Cfap70 G T 14: 20,493,729 (GRCm39) T124K probably benign Het
Ckap5 A T 2: 91,408,476 (GRCm39) E890D probably benign Het
Col22a1 G T 15: 71,824,188 (GRCm39) P569T probably benign Het
Colq A T 14: 31,267,060 (GRCm39) L150Q possibly damaging Het
Csf1 T C 3: 107,664,278 (GRCm39) probably null Het
Cul9 C A 17: 46,841,072 (GRCm39) V733L probably damaging Het
Cyp2c55 A G 19: 39,019,830 (GRCm39) D256G possibly damaging Het
Dclk3 A T 9: 111,298,253 (GRCm39) D599V probably damaging Het
Defb26 T A 2: 152,350,104 (GRCm39) I59F possibly damaging Het
Dnah6 A G 6: 73,106,643 (GRCm39) V1646A possibly damaging Het
Dnm2 T C 9: 21,415,960 (GRCm39) probably null Het
Dock6 A G 9: 21,713,836 (GRCm39) L1867P probably damaging Het
Dock9 G T 14: 121,905,871 (GRCm39) T93K probably damaging Het
Dync2h1 T C 9: 7,140,995 (GRCm39) H1344R probably benign Het
Enam A C 5: 88,652,142 (GRCm39) Q1217P possibly damaging Het
Fbf1 A T 11: 116,049,748 (GRCm39) D91E possibly damaging Het
Fbxo7 T G 10: 85,882,666 (GRCm39) W393G probably damaging Het
Gab2 A G 7: 96,953,420 (GRCm39) T599A probably damaging Het
Gfy T A 7: 44,826,612 (GRCm39) I409F possibly damaging Het
Gm19345 T A 7: 19,591,433 (GRCm39) probably null Het
Gm4787 A G 12: 81,425,987 (GRCm39) M57T probably benign Het
Gper1 A G 5: 139,412,480 (GRCm39) E275G probably damaging Het
Grik4 T C 9: 42,435,882 (GRCm39) E803G probably damaging Het
Gstm3 G A 3: 107,875,513 (GRCm39) P39L possibly damaging Het
Hax1 A T 3: 89,904,767 (GRCm39) V142D probably damaging Het
Hcn3 A T 3: 89,057,747 (GRCm39) I383N probably damaging Het
Hdac10 C A 15: 89,009,600 (GRCm39) probably null Het
Hipk3 A C 2: 104,269,674 (GRCm39) M505R probably damaging Het
Hivep1 C T 13: 42,313,225 (GRCm39) P1822S probably benign Het
Hsd17b13 G T 5: 104,104,124 (GRCm39) H281N unknown Het
Ilrun T C 17: 28,039,289 (GRCm39) D7G probably damaging Het
Irak2 T A 6: 113,649,848 (GRCm39) I222N probably damaging Het
Kalrn G A 16: 34,334,296 (GRCm39) L7F possibly damaging Het
Kcnma1 A G 14: 23,359,106 (GRCm39) probably null Het
Kcnn3 G T 3: 89,427,727 (GRCm39) probably benign Het
Lamb1 A C 12: 31,328,775 (GRCm39) D218A probably damaging Het
Lrrtm1 A T 6: 77,221,127 (GRCm39) N195Y probably damaging Het
Ltf A T 9: 110,851,409 (GRCm39) N72I probably damaging Het
Mcm4 A G 16: 15,447,527 (GRCm39) I479T probably damaging Het
Mfhas1 T C 8: 36,055,764 (GRCm39) S80P probably benign Het
Mknk1 A G 4: 115,735,224 (GRCm39) E364G probably damaging Het
Msh4 C T 3: 153,577,920 (GRCm39) C458Y probably damaging Het
Mtrr A T 13: 68,712,631 (GRCm39) probably null Het
Myo1a T C 10: 127,547,007 (GRCm39) W356R probably damaging Het
Nbea A G 3: 55,631,069 (GRCm39) V2186A probably benign Het
Nfe2l3 T C 6: 51,427,992 (GRCm39) S185P probably damaging Het
Nhsl1 A C 10: 18,407,158 (GRCm39) K1397Q probably damaging Het
Nmbr C T 10: 14,645,908 (GRCm39) R261W probably damaging Het
Npy2r A G 3: 82,448,365 (GRCm39) S137P probably damaging Het
Obscn C T 11: 58,971,031 (GRCm39) G2494D probably damaging Het
Obscn T C 11: 59,013,572 (GRCm39) K1092E probably damaging Het
Oosp2 A C 19: 11,627,047 (GRCm39) I92S probably benign Het
Or5ar1 C T 2: 85,671,526 (GRCm39) C203Y probably damaging Het
Pcdh9 T C 14: 94,124,616 (GRCm39) D518G probably damaging Het
Pde11a G T 2: 76,168,137 (GRCm39) T272K possibly damaging Het
Plekha2 T A 8: 25,549,851 (GRCm39) Q162L probably null Het
Prkag2 T A 5: 25,083,732 (GRCm39) I84F probably damaging Het
Prm2 G T 16: 10,609,613 (GRCm39) probably benign Het
Prpf40a A T 2: 53,032,035 (GRCm39) C800S probably damaging Het
Prr5l A T 2: 101,559,793 (GRCm39) C158S probably benign Het
Prrt3 C A 6: 113,475,198 (GRCm39) C8F possibly damaging Het
Psg25 T C 7: 18,263,728 (GRCm39) T32A probably benign Het
Ruvbl1 T C 6: 88,462,887 (GRCm39) V337A probably benign Het
Sall1 T A 8: 89,756,969 (GRCm39) Q1045L probably damaging Het
Sec22c T C 9: 121,524,708 (GRCm39) Y25C probably damaging Het
Serpina3i A T 12: 104,234,036 (GRCm39) T335S possibly damaging Het
Setd1b TCCACCACCACCACCACCACCACCA TCCACCACCACCACCACCACCA 5: 123,290,137 (GRCm39) probably benign Het
Slc12a8 T A 16: 33,428,529 (GRCm39) I279N probably damaging Het
Slc15a1 G A 14: 121,727,319 (GRCm39) T83I probably damaging Het
Slc22a3 A G 17: 12,678,658 (GRCm39) F222S probably benign Het
Sorcs3 A T 19: 48,682,353 (GRCm39) T463S probably benign Het
Spsb4 C A 9: 96,877,931 (GRCm39) A131S probably benign Het
Sting1 T A 18: 35,871,743 (GRCm39) I170F probably damaging Het
Syne2 A G 12: 76,014,484 (GRCm39) E3225G probably damaging Het
Tchp G A 5: 114,857,634 (GRCm39) probably null Het
Tekt4 T A 17: 25,690,749 (GRCm39) D18E probably benign Het
Timm50 A G 7: 28,010,443 (GRCm39) V37A probably benign Het
Tlx2 A C 6: 83,045,741 (GRCm39) *285G probably null Het
Tshz1 C A 18: 84,031,499 (GRCm39) D970Y probably damaging Het
Ttn A T 2: 76,700,805 (GRCm39) V50E probably damaging Het
Txndc17 T A 11: 72,100,274 (GRCm39) S113T probably benign Het
Tyk2 T C 9: 21,019,305 (GRCm39) Y1039C probably damaging Het
Ubqln3 A G 7: 103,791,698 (GRCm39) S131P probably benign Het
Uncx A T 5: 139,529,837 (GRCm39) H30L possibly damaging Het
Usp25 T A 16: 76,912,303 (GRCm39) D1007E probably damaging Het
Usp47 T C 7: 111,701,038 (GRCm39) V1083A probably damaging Het
Wdr24 T A 17: 26,047,479 (GRCm39) H765Q probably damaging Het
Wrnip1 A G 13: 32,986,330 (GRCm39) D37G probably damaging Het
Xpo6 T C 7: 125,712,924 (GRCm39) T686A possibly damaging Het
Zfp941 G A 7: 140,392,124 (GRCm39) R412C probably damaging Het
Znrf2 T A 6: 54,855,425 (GRCm39) C71* probably null Het
Other mutations in Csmd3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Csmd3 APN 15 48,150,891 (GRCm39) missense possibly damaging 0.61
IGL00591:Csmd3 APN 15 47,868,279 (GRCm39) missense probably damaging 1.00
IGL00668:Csmd3 APN 15 47,777,341 (GRCm39) missense probably damaging 1.00
IGL00753:Csmd3 APN 15 47,507,631 (GRCm39) missense probably damaging 1.00
IGL00773:Csmd3 APN 15 47,454,115 (GRCm39) missense probably damaging 0.96
IGL00926:Csmd3 APN 15 47,574,360 (GRCm39) missense possibly damaging 0.87
IGL00942:Csmd3 APN 15 47,710,502 (GRCm39) critical splice donor site probably null
IGL01080:Csmd3 APN 15 47,744,799 (GRCm39) missense probably benign 0.12
IGL01314:Csmd3 APN 15 47,713,151 (GRCm39) missense probably damaging 1.00
IGL01326:Csmd3 APN 15 47,713,181 (GRCm39) missense probably benign 0.06
IGL01393:Csmd3 APN 15 48,320,995 (GRCm39) missense possibly damaging 0.88
IGL01432:Csmd3 APN 15 47,596,895 (GRCm39) missense probably damaging 1.00
IGL01519:Csmd3 APN 15 47,460,246 (GRCm39) missense probably benign 0.31
IGL01530:Csmd3 APN 15 47,533,013 (GRCm39) missense probably damaging 1.00
IGL01530:Csmd3 APN 15 47,701,833 (GRCm39) missense possibly damaging 0.95
IGL01547:Csmd3 APN 15 47,747,013 (GRCm39) missense probably benign 0.41
IGL01594:Csmd3 APN 15 47,492,635 (GRCm39) missense probably benign 0.01
IGL01618:Csmd3 APN 15 47,874,479 (GRCm39) missense probably benign 0.05
IGL01670:Csmd3 APN 15 47,475,225 (GRCm39) missense probably damaging 1.00
IGL01680:Csmd3 APN 15 47,833,426 (GRCm39) missense probably damaging 1.00
IGL01734:Csmd3 APN 15 48,048,700 (GRCm39) missense probably damaging 1.00
IGL01777:Csmd3 APN 15 47,561,594 (GRCm39) missense probably benign 0.06
IGL01779:Csmd3 APN 15 47,721,290 (GRCm39) missense probably benign 0.10
IGL01820:Csmd3 APN 15 47,470,538 (GRCm39) nonsense probably null
IGL01843:Csmd3 APN 15 47,522,395 (GRCm39) splice site probably benign
IGL01919:Csmd3 APN 15 47,539,168 (GRCm39) missense possibly damaging 0.62
IGL01986:Csmd3 APN 15 47,522,591 (GRCm39) missense possibly damaging 0.82
IGL02049:Csmd3 APN 15 47,864,870 (GRCm39) missense possibly damaging 0.91
IGL02065:Csmd3 APN 15 47,530,024 (GRCm39) missense probably damaging 1.00
IGL02112:Csmd3 APN 15 48,177,265 (GRCm39) missense possibly damaging 0.95
IGL02133:Csmd3 APN 15 47,721,338 (GRCm39) missense possibly damaging 0.86
IGL02203:Csmd3 APN 15 47,713,073 (GRCm39) splice site probably null
IGL02215:Csmd3 APN 15 47,449,084 (GRCm39) missense probably damaging 1.00
IGL02234:Csmd3 APN 15 47,811,512 (GRCm39) missense probably damaging 1.00
IGL02326:Csmd3 APN 15 47,619,359 (GRCm39) splice site probably benign
IGL02478:Csmd3 APN 15 47,701,794 (GRCm39) splice site probably benign
IGL02491:Csmd3 APN 15 47,777,511 (GRCm39) splice site probably benign
IGL02598:Csmd3 APN 15 47,533,086 (GRCm39) missense probably damaging 0.98
IGL02626:Csmd3 APN 15 47,567,503 (GRCm39) splice site probably benign
IGL02696:Csmd3 APN 15 47,533,065 (GRCm39) missense probably benign 0.33
IGL02876:Csmd3 APN 15 47,469,492 (GRCm39) splice site probably benign
IGL02971:Csmd3 APN 15 47,777,325 (GRCm39) splice site probably benign
IGL03068:Csmd3 APN 15 47,710,517 (GRCm39) missense possibly damaging 0.69
IGL03087:Csmd3 APN 15 47,840,429 (GRCm39) missense probably damaging 1.00
IGL03114:Csmd3 APN 15 47,683,847 (GRCm39) missense probably damaging 0.99
IGL03146:Csmd3 APN 15 47,744,873 (GRCm39) missense probably benign 0.25
IGL03193:Csmd3 APN 15 47,492,626 (GRCm39) splice site probably benign
IGL03274:Csmd3 APN 15 47,508,900 (GRCm39) missense probably damaging 1.00
R0040:Csmd3 UTSW 15 47,497,212 (GRCm39) missense probably damaging 1.00
R0071:Csmd3 UTSW 15 47,460,217 (GRCm39) missense probably benign 0.04
R0071:Csmd3 UTSW 15 47,460,217 (GRCm39) missense probably benign 0.04
R0119:Csmd3 UTSW 15 47,710,527 (GRCm39) missense probably benign 0.08
R0124:Csmd3 UTSW 15 47,454,112 (GRCm39) missense probably damaging 1.00
R0127:Csmd3 UTSW 15 47,845,326 (GRCm39) missense probably benign 0.45
R0136:Csmd3 UTSW 15 47,710,527 (GRCm39) missense probably benign 0.08
R0201:Csmd3 UTSW 15 47,483,125 (GRCm39) splice site probably benign
R0240:Csmd3 UTSW 15 47,492,635 (GRCm39) missense probably benign 0.05
R0240:Csmd3 UTSW 15 47,492,635 (GRCm39) missense probably benign 0.05
R0318:Csmd3 UTSW 15 47,522,549 (GRCm39) missense probably damaging 1.00
R0369:Csmd3 UTSW 15 47,833,543 (GRCm39) missense probably damaging 1.00
R0391:Csmd3 UTSW 15 47,520,969 (GRCm39) missense probably damaging 1.00
R0499:Csmd3 UTSW 15 47,710,527 (GRCm39) missense probably benign 0.08
R0506:Csmd3 UTSW 15 48,320,907 (GRCm39) missense probably benign 0.00
R0606:Csmd3 UTSW 15 48,321,058 (GRCm39) missense probably benign
R0639:Csmd3 UTSW 15 47,777,336 (GRCm39) missense probably damaging 1.00
R0658:Csmd3 UTSW 15 47,874,543 (GRCm39) missense possibly damaging 0.66
R0673:Csmd3 UTSW 15 47,777,336 (GRCm39) missense probably damaging 1.00
R0689:Csmd3 UTSW 15 47,619,421 (GRCm39) missense probably benign 0.19
R0696:Csmd3 UTSW 15 47,710,569 (GRCm39) missense probably benign 0.01
R0799:Csmd3 UTSW 15 48,048,780 (GRCm39) splice site probably benign
R0834:Csmd3 UTSW 15 47,747,073 (GRCm39) intron probably benign
R0894:Csmd3 UTSW 15 47,721,316 (GRCm39) missense possibly damaging 0.95
R0926:Csmd3 UTSW 15 47,840,429 (GRCm39) missense probably damaging 1.00
R0943:Csmd3 UTSW 15 47,539,135 (GRCm39) missense probably damaging 0.99
R0944:Csmd3 UTSW 15 47,475,227 (GRCm39) missense probably damaging 1.00
R0967:Csmd3 UTSW 15 47,721,227 (GRCm39) missense probably null 0.89
R0973:Csmd3 UTSW 15 47,522,485 (GRCm39) missense probably damaging 1.00
R1055:Csmd3 UTSW 15 47,744,933 (GRCm39) missense probably damaging 1.00
R1066:Csmd3 UTSW 15 47,777,361 (GRCm39) missense probably damaging 1.00
R1086:Csmd3 UTSW 15 47,559,151 (GRCm39) missense probably damaging 0.99
R1103:Csmd3 UTSW 15 47,811,402 (GRCm39) missense probably damaging 1.00
R1136:Csmd3 UTSW 15 47,539,213 (GRCm39) missense probably damaging 1.00
R1139:Csmd3 UTSW 15 47,559,232 (GRCm39) missense probably damaging 1.00
R1158:Csmd3 UTSW 15 48,156,170 (GRCm39) splice site probably null
R1215:Csmd3 UTSW 15 47,868,227 (GRCm39) splice site probably null
R1233:Csmd3 UTSW 15 48,536,927 (GRCm39) missense probably damaging 1.00
R1271:Csmd3 UTSW 15 47,874,455 (GRCm39) missense probably benign 0.11
R1469:Csmd3 UTSW 15 47,532,598 (GRCm39) nonsense probably null
R1469:Csmd3 UTSW 15 47,532,598 (GRCm39) nonsense probably null
R1479:Csmd3 UTSW 15 47,721,282 (GRCm39) missense probably damaging 1.00
R1480:Csmd3 UTSW 15 47,595,325 (GRCm39) missense possibly damaging 0.90
R1526:Csmd3 UTSW 15 47,449,028 (GRCm39) critical splice donor site probably null
R1527:Csmd3 UTSW 15 47,811,483 (GRCm39) missense probably benign 0.08
R1539:Csmd3 UTSW 15 47,683,794 (GRCm39) missense probably benign 0.24
R1544:Csmd3 UTSW 15 47,475,294 (GRCm39) splice site probably null
R1548:Csmd3 UTSW 15 47,845,371 (GRCm39) missense possibly damaging 0.91
R1574:Csmd3 UTSW 15 47,559,257 (GRCm39) splice site probably null
R1574:Csmd3 UTSW 15 47,559,257 (GRCm39) splice site probably null
R1619:Csmd3 UTSW 15 47,813,346 (GRCm39) missense probably damaging 1.00
R1630:Csmd3 UTSW 15 47,701,918 (GRCm39) missense possibly damaging 0.66
R1665:Csmd3 UTSW 15 47,560,185 (GRCm39) missense probably damaging 1.00
R1680:Csmd3 UTSW 15 47,604,566 (GRCm39) missense probably damaging 1.00
R1725:Csmd3 UTSW 15 47,460,203 (GRCm39) missense probably damaging 1.00
R1743:Csmd3 UTSW 15 48,485,485 (GRCm39) missense probably damaging 1.00
R1749:Csmd3 UTSW 15 47,449,056 (GRCm39) missense probably damaging 1.00
R1752:Csmd3 UTSW 15 47,523,669 (GRCm39) missense probably benign 0.15
R1769:Csmd3 UTSW 15 47,567,505 (GRCm39) splice site probably benign
R1775:Csmd3 UTSW 15 47,763,135 (GRCm39) missense probably damaging 0.99
R1795:Csmd3 UTSW 15 47,721,316 (GRCm39) missense possibly damaging 0.95
R1819:Csmd3 UTSW 15 47,617,131 (GRCm39) missense possibly damaging 0.56
R1840:Csmd3 UTSW 15 47,470,560 (GRCm39) missense probably damaging 1.00
R1860:Csmd3 UTSW 15 47,522,588 (GRCm39) missense probably damaging 1.00
R1861:Csmd3 UTSW 15 47,522,588 (GRCm39) missense probably damaging 1.00
R1879:Csmd3 UTSW 15 47,520,915 (GRCm39) missense possibly damaging 0.90
R1958:Csmd3 UTSW 15 47,868,035 (GRCm39) critical splice donor site probably null
R1965:Csmd3 UTSW 15 47,713,144 (GRCm39) missense probably benign 0.15
R1970:Csmd3 UTSW 15 48,536,927 (GRCm39) missense probably damaging 1.00
R2029:Csmd3 UTSW 15 47,701,975 (GRCm39) missense probably damaging 1.00
R2051:Csmd3 UTSW 15 48,485,389 (GRCm39) critical splice donor site probably null
R2108:Csmd3 UTSW 15 47,868,257 (GRCm39) missense possibly damaging 0.81
R2132:Csmd3 UTSW 15 48,320,899 (GRCm39) missense probably benign 0.06
R2146:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2147:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2148:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2157:Csmd3 UTSW 15 47,559,183 (GRCm39) missense probably damaging 0.99
R2159:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2160:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2161:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2162:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2164:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2213:Csmd3 UTSW 15 47,683,843 (GRCm39) missense possibly damaging 0.92
R2301:Csmd3 UTSW 15 47,595,394 (GRCm39) missense probably damaging 1.00
R2302:Csmd3 UTSW 15 48,177,447 (GRCm39) missense probably benign
R2355:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2497:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2509:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2566:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2567:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2568:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2570:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2571:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R2870:Csmd3 UTSW 15 47,721,320 (GRCm39) missense probably damaging 1.00
R2870:Csmd3 UTSW 15 47,721,320 (GRCm39) missense probably damaging 1.00
R2907:Csmd3 UTSW 15 47,874,449 (GRCm39) missense probably damaging 0.99
R3116:Csmd3 UTSW 15 47,520,995 (GRCm39) missense probably damaging 1.00
R3423:Csmd3 UTSW 15 47,710,648 (GRCm39) missense probably damaging 0.98
R3425:Csmd3 UTSW 15 47,710,648 (GRCm39) missense probably damaging 0.98
R3508:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R3746:Csmd3 UTSW 15 47,713,162 (GRCm39) missense probably benign 0.04
R3813:Csmd3 UTSW 15 48,655,209 (GRCm39) missense possibly damaging 0.82
R3832:Csmd3 UTSW 15 47,604,632 (GRCm39) frame shift probably null
R3959:Csmd3 UTSW 15 47,507,585 (GRCm39) missense probably benign 0.18
R4042:Csmd3 UTSW 15 47,477,480 (GRCm39) missense probably damaging 1.00
R4043:Csmd3 UTSW 15 47,619,362 (GRCm39) critical splice donor site probably null
R4191:Csmd3 UTSW 15 47,710,667 (GRCm39) missense probably damaging 0.99
R4192:Csmd3 UTSW 15 47,710,667 (GRCm39) missense probably damaging 0.99
R4419:Csmd3 UTSW 15 47,567,707 (GRCm39) missense probably damaging 1.00
R4426:Csmd3 UTSW 15 47,532,581 (GRCm39) missense possibly damaging 0.51
R4434:Csmd3 UTSW 15 47,763,191 (GRCm39) missense possibly damaging 0.68
R4438:Csmd3 UTSW 15 47,763,191 (GRCm39) missense possibly damaging 0.68
R4490:Csmd3 UTSW 15 48,177,429 (GRCm39) missense possibly damaging 0.83
R4562:Csmd3 UTSW 15 47,763,240 (GRCm39) missense probably benign 0.32
R4620:Csmd3 UTSW 15 47,449,149 (GRCm39) missense probably benign 0.09
R4632:Csmd3 UTSW 15 47,874,605 (GRCm39) missense probably damaging 0.99
R4679:Csmd3 UTSW 15 48,024,479 (GRCm39) nonsense probably null
R4696:Csmd3 UTSW 15 47,777,364 (GRCm39) missense probably benign 0.24
R4718:Csmd3 UTSW 15 47,561,546 (GRCm39) nonsense probably null
R4723:Csmd3 UTSW 15 47,532,556 (GRCm39) missense probably benign 0.29
R4801:Csmd3 UTSW 15 47,484,688 (GRCm39) missense probably damaging 1.00
R4802:Csmd3 UTSW 15 47,484,688 (GRCm39) missense probably damaging 1.00
R4806:Csmd3 UTSW 15 48,177,464 (GRCm39) missense probably benign
R4816:Csmd3 UTSW 15 47,721,330 (GRCm39) missense possibly damaging 0.68
R4935:Csmd3 UTSW 15 48,024,480 (GRCm39) missense probably damaging 1.00
R4955:Csmd3 UTSW 15 48,536,914 (GRCm39) missense probably damaging 0.99
R4991:Csmd3 UTSW 15 47,864,874 (GRCm39) missense probably damaging 1.00
R5031:Csmd3 UTSW 15 47,522,588 (GRCm39) missense probably damaging 1.00
R5034:Csmd3 UTSW 15 47,492,683 (GRCm39) missense possibly damaging 0.94
R5035:Csmd3 UTSW 15 47,454,175 (GRCm39) missense probably damaging 1.00
R5120:Csmd3 UTSW 15 48,536,891 (GRCm39) nonsense probably null
R5224:Csmd3 UTSW 15 47,752,080 (GRCm39) missense possibly damaging 0.91
R5235:Csmd3 UTSW 15 47,492,674 (GRCm39) missense probably benign 0.20
R5279:Csmd3 UTSW 15 48,655,340 (GRCm39) splice site probably null
R5360:Csmd3 UTSW 15 47,532,599 (GRCm39) missense probably damaging 0.99
R5365:Csmd3 UTSW 15 47,868,145 (GRCm39) missense possibly damaging 0.68
R5379:Csmd3 UTSW 15 47,499,846 (GRCm39) nonsense probably null
R5381:Csmd3 UTSW 15 47,604,611 (GRCm39) missense probably benign 0.21
R5393:Csmd3 UTSW 15 47,497,099 (GRCm39) missense probably damaging 1.00
R5413:Csmd3 UTSW 15 47,701,831 (GRCm39) missense probably damaging 1.00
R5549:Csmd3 UTSW 15 48,048,753 (GRCm39) missense probably damaging 0.98
R5550:Csmd3 UTSW 15 48,048,753 (GRCm39) missense probably damaging 0.98
R5551:Csmd3 UTSW 15 48,177,492 (GRCm39) missense probably benign 0.13
R5567:Csmd3 UTSW 15 47,508,864 (GRCm39) missense possibly damaging 0.92
R5621:Csmd3 UTSW 15 48,177,374 (GRCm39) missense possibly damaging 0.84
R5668:Csmd3 UTSW 15 47,559,151 (GRCm39) missense possibly damaging 0.48
R5677:Csmd3 UTSW 15 48,485,447 (GRCm39) missense probably damaging 0.98
R5701:Csmd3 UTSW 15 48,403,729 (GRCm39) missense probably damaging 0.99
R5701:Csmd3 UTSW 15 47,513,617 (GRCm39) missense probably damaging 1.00
R5871:Csmd3 UTSW 15 47,752,112 (GRCm39) missense probably damaging 0.98
R5872:Csmd3 UTSW 15 47,445,923 (GRCm39) missense probably damaging 1.00
R5874:Csmd3 UTSW 15 47,507,666 (GRCm39) missense probably damaging 1.00
R5952:Csmd3 UTSW 15 47,596,901 (GRCm39) missense probably damaging 0.98
R5956:Csmd3 UTSW 15 48,655,278 (GRCm39) missense possibly damaging 0.84
R5966:Csmd3 UTSW 15 47,713,135 (GRCm39) missense probably damaging 0.96
R5969:Csmd3 UTSW 15 47,811,386 (GRCm39) missense probably damaging 1.00
R5989:Csmd3 UTSW 15 47,454,160 (GRCm39) missense possibly damaging 0.69
R6017:Csmd3 UTSW 15 48,177,408 (GRCm39) missense possibly damaging 0.95
R6057:Csmd3 UTSW 15 47,618,787 (GRCm39) missense probably damaging 1.00
R6127:Csmd3 UTSW 15 47,513,624 (GRCm39) missense probably damaging 1.00
R6178:Csmd3 UTSW 15 48,536,854 (GRCm39) missense probably damaging 1.00
R6198:Csmd3 UTSW 15 48,177,273 (GRCm39) missense probably benign 0.28
R6213:Csmd3 UTSW 15 47,492,656 (GRCm39) missense probably damaging 1.00
R6256:Csmd3 UTSW 15 47,533,125 (GRCm39) missense probably damaging 1.00
R6274:Csmd3 UTSW 15 47,484,833 (GRCm39) missense probably benign
R6327:Csmd3 UTSW 15 47,744,783 (GRCm39) missense probably damaging 1.00
R6354:Csmd3 UTSW 15 47,744,885 (GRCm39) missense probably damaging 1.00
R6405:Csmd3 UTSW 15 47,683,767 (GRCm39) missense probably damaging 0.99
R6410:Csmd3 UTSW 15 48,536,803 (GRCm39) missense probably damaging 1.00
R6416:Csmd3 UTSW 15 48,536,956 (GRCm39) missense probably damaging 1.00
R6463:Csmd3 UTSW 15 47,539,875 (GRCm39) missense probably damaging 1.00
R6536:Csmd3 UTSW 15 47,701,863 (GRCm39) missense probably damaging 1.00
R6625:Csmd3 UTSW 15 47,470,471 (GRCm39) missense probably benign 0.02
R6695:Csmd3 UTSW 15 47,721,230 (GRCm39) missense probably damaging 0.99
R6895:Csmd3 UTSW 15 47,529,910 (GRCm39) splice site probably null
R6906:Csmd3 UTSW 15 47,710,569 (GRCm39) missense probably benign 0.01
R6914:Csmd3 UTSW 15 47,874,534 (GRCm39) missense possibly damaging 0.53
R6920:Csmd3 UTSW 15 47,507,601 (GRCm39) missense probably damaging 1.00
R7024:Csmd3 UTSW 15 47,574,387 (GRCm39) missense probably damaging 1.00
R7178:Csmd3 UTSW 15 47,454,170 (GRCm39) missense
R7192:Csmd3 UTSW 15 47,567,633 (GRCm39) missense
R7220:Csmd3 UTSW 15 48,320,994 (GRCm39) missense probably damaging 0.99
R7362:Csmd3 UTSW 15 47,619,388 (GRCm39) missense possibly damaging 0.65
R7380:Csmd3 UTSW 15 47,450,361 (GRCm39) missense
R7397:Csmd3 UTSW 15 47,559,130 (GRCm39) missense
R7467:Csmd3 UTSW 15 47,492,640 (GRCm39) missense
R7585:Csmd3 UTSW 15 48,485,471 (GRCm39) missense possibly damaging 0.76
R7623:Csmd3 UTSW 15 47,813,334 (GRCm39) missense
R7649:Csmd3 UTSW 15 47,532,539 (GRCm39) missense
R7691:Csmd3 UTSW 15 47,604,569 (GRCm39) missense
R7695:Csmd3 UTSW 15 47,683,777 (GRCm39) missense
R7759:Csmd3 UTSW 15 47,561,569 (GRCm39) missense
R7817:Csmd3 UTSW 15 47,721,356 (GRCm39) missense probably damaging 0.99
R8052:Csmd3 UTSW 15 47,569,783 (GRCm39) missense
R8089:Csmd3 UTSW 15 47,532,603 (GRCm39) missense
R8110:Csmd3 UTSW 15 47,507,666 (GRCm39) missense probably damaging 1.00
R8152:Csmd3 UTSW 15 47,532,860 (GRCm39) splice site probably null
R8323:Csmd3 UTSW 15 47,561,547 (GRCm39) missense
R8341:Csmd3 UTSW 15 47,561,547 (GRCm39) missense
R8353:Csmd3 UTSW 15 47,813,349 (GRCm39) missense probably damaging 1.00
R8364:Csmd3 UTSW 15 48,536,837 (GRCm39) missense probably damaging 1.00
R8405:Csmd3 UTSW 15 47,619,379 (GRCm39) missense probably damaging 1.00
R8412:Csmd3 UTSW 15 47,499,794 (GRCm39) missense
R8436:Csmd3 UTSW 15 47,868,218 (GRCm39) missense probably damaging 0.97
R8516:Csmd3 UTSW 15 47,492,761 (GRCm39) nonsense probably null
R8553:Csmd3 UTSW 15 47,484,724 (GRCm39) missense possibly damaging 0.52
R8554:Csmd3 UTSW 15 47,507,538 (GRCm39) missense probably benign 0.32
R8678:Csmd3 UTSW 15 47,499,849 (GRCm39) missense
R8751:Csmd3 UTSW 15 47,845,402 (GRCm39) missense
R8758:Csmd3 UTSW 15 47,469,593 (GRCm39) missense
R8768:Csmd3 UTSW 15 47,561,572 (GRCm39) missense
R8785:Csmd3 UTSW 15 48,177,482 (GRCm39) missense probably benign 0.00
R8788:Csmd3 UTSW 15 47,470,513 (GRCm39) missense
R8798:Csmd3 UTSW 15 47,595,382 (GRCm39) missense
R8801:Csmd3 UTSW 15 48,321,024 (GRCm39) missense possibly damaging 0.70
R8811:Csmd3 UTSW 15 47,560,139 (GRCm39) missense
R8844:Csmd3 UTSW 15 48,536,815 (GRCm39) missense probably damaging 0.98
R8844:Csmd3 UTSW 15 47,604,590 (GRCm39) missense probably damaging 0.96
R8892:Csmd3 UTSW 15 47,604,634 (GRCm39) missense
R8897:Csmd3 UTSW 15 48,222,739 (GRCm39) missense probably benign 0.06
R9001:Csmd3 UTSW 15 47,596,901 (GRCm39) missense
R9007:Csmd3 UTSW 15 47,751,892 (GRCm39) intron probably benign
R9016:Csmd3 UTSW 15 47,522,438 (GRCm39) missense
R9039:Csmd3 UTSW 15 47,483,308 (GRCm39) splice site probably benign
R9109:Csmd3 UTSW 15 47,617,187 (GRCm39) missense
R9121:Csmd3 UTSW 15 47,683,774 (GRCm39) missense
R9155:Csmd3 UTSW 15 47,449,051 (GRCm39) missense
R9176:Csmd3 UTSW 15 47,864,937 (GRCm39) missense
R9281:Csmd3 UTSW 15 47,460,272 (GRCm39) missense
R9298:Csmd3 UTSW 15 47,617,187 (GRCm39) missense
R9304:Csmd3 UTSW 15 47,569,805 (GRCm39) missense
R9343:Csmd3 UTSW 15 48,015,001 (GRCm39) missense probably damaging 1.00
R9367:Csmd3 UTSW 15 47,567,564 (GRCm39) missense
R9405:Csmd3 UTSW 15 47,539,187 (GRCm39) missense
R9448:Csmd3 UTSW 15 47,460,315 (GRCm39) missense
R9460:Csmd3 UTSW 15 47,617,130 (GRCm39) missense
R9481:Csmd3 UTSW 15 47,470,459 (GRCm39) missense
R9520:Csmd3 UTSW 15 47,561,608 (GRCm39) missense
R9551:Csmd3 UTSW 15 48,655,356 (GRCm39) start gained probably benign
R9552:Csmd3 UTSW 15 48,655,356 (GRCm39) start gained probably benign
R9568:Csmd3 UTSW 15 48,150,942 (GRCm39) missense probably damaging 0.97
R9571:Csmd3 UTSW 15 48,655,398 (GRCm39) start gained probably benign
R9607:Csmd3 UTSW 15 47,618,811 (GRCm39) missense probably damaging 0.98
R9621:Csmd3 UTSW 15 47,713,116 (GRCm39) missense
R9671:Csmd3 UTSW 15 47,845,299 (GRCm39) missense
R9718:Csmd3 UTSW 15 47,560,083 (GRCm39) missense
U24488:Csmd3 UTSW 15 47,573,795 (GRCm39) missense probably damaging 1.00
V8831:Csmd3 UTSW 15 48,321,092 (GRCm39) missense probably damaging 0.96
X0021:Csmd3 UTSW 15 47,833,489 (GRCm39) nonsense probably null
Z1088:Csmd3 UTSW 15 47,710,677 (GRCm39) missense probably damaging 0.98
Z1088:Csmd3 UTSW 15 47,499,789 (GRCm39) missense probably damaging 1.00
Z1177:Csmd3 UTSW 15 47,596,813 (GRCm39) missense
Z1177:Csmd3 UTSW 15 47,539,130 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- TGTGATGTTGAAGCCACGC -3'
(R):5'- TCCTGAATTCACTCTTCAGCAAAGG -3'

Sequencing Primer
(F):5'- CCCTGACATAGAGTGGTCAGCTTG -3'
(R):5'- TTCACTCTTCAGCAAAGGAAAAAC -3'
Posted On 2015-09-25