Incidental Mutation 'R0201:Csmd3'
ID 23673
Institutional Source Beutler Lab
Gene Symbol Csmd3
Ensembl Gene ENSMUSG00000022311
Gene Name CUB and Sushi multiple domains 3
Synonyms 4930500N14Rik
MMRRC Submission 038458-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0201 (G1)
Quality Score 225
Status Validated
Chromosome 15
Chromosomal Location 47580637-48792063 bp(-) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 47619729 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124775 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100670] [ENSMUST00000160658] [ENSMUST00000162830]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000100670
SMART Domains Protein: ENSMUSP00000098235
Gene: ENSMUSG00000022311

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 probably benign
Transcript: ENSMUST00000160658
SMART Domains Protein: ENSMUSP00000124753
Gene: ENSMUSG00000022311

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 noncoding transcript
Transcript: ENSMUST00000162006
Predicted Effect probably benign
Transcript: ENSMUST00000162830
SMART Domains Protein: ENSMUSP00000124775
Gene: ENSMUSG00000022311

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: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 94.2%
Validation Efficiency 97% (91/94)
Allele List at MGI
Other mutations in this stock
Total: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamdec1 A G 14: 68,581,957 (GRCm38) probably null Het
Adamts16 T A 13: 70,779,644 (GRCm38) Q492L possibly damaging Het
Aplnr A G 2: 85,137,177 (GRCm38) D182G probably damaging Het
Arnt2 G T 7: 84,361,659 (GRCm38) S3* probably null Het
Asxl3 T C 18: 22,523,154 (GRCm38) V1407A probably benign Het
Atg13 A T 2: 91,684,762 (GRCm38) probably null Het
Atm A T 9: 53,454,279 (GRCm38) probably benign Het
Birc6 T G 17: 74,609,327 (GRCm38) V1746G possibly damaging Het
Cbln1 G T 8: 87,472,113 (GRCm38) T43K probably benign Het
Cbx5 T C 15: 103,199,700 (GRCm38) T173A probably damaging Het
Cc2d2a A G 5: 43,737,512 (GRCm38) Y1437C probably damaging Het
Ccdc78 C A 17: 25,789,236 (GRCm38) probably benign Het
Cd2bp2 A G 7: 127,193,828 (GRCm38) Y341H probably damaging Het
Cdhr5 T A 7: 141,276,378 (GRCm38) D88V probably damaging Het
Ces1f T A 8: 93,267,329 (GRCm38) T275S probably null Het
Clca4a T C 3: 144,960,717 (GRCm38) N458S probably benign Het
Cog5 A G 12: 31,839,841 (GRCm38) K521R probably damaging Het
Csf2ra T A 19: 61,225,568 (GRCm38) T305S probably benign Het
Cts6 T A 13: 61,201,499 (GRCm38) R132* probably null Het
D5Ertd579e G T 5: 36,616,465 (GRCm38) N195K probably damaging Het
Ddx1 A G 12: 13,223,808 (GRCm38) V606A probably damaging Het
Dip2b G A 15: 100,186,147 (GRCm38) D884N probably damaging Het
Ehhadh A G 16: 21,773,493 (GRCm38) probably null Het
Enpp1 T A 10: 24,653,917 (GRCm38) T608S probably benign Het
Fancm T C 12: 65,101,632 (GRCm38) Y674H probably damaging Het
Fat4 T A 3: 38,891,596 (GRCm38) V1546D probably damaging Het
Fsd1 G A 17: 55,990,522 (GRCm38) A158T probably benign Het
Fzd2 T A 11: 102,606,122 (GRCm38) M464K probably damaging Het
Gjc2 A G 11: 59,177,590 (GRCm38) F22S possibly damaging Het
Gm13101 T C 4: 143,964,890 (GRCm38) E421G probably damaging Het
Gria2 T C 3: 80,707,838 (GRCm38) Y445C probably damaging Het
Hsdl1 T A 8: 119,566,256 (GRCm38) I147F possibly damaging Het
Ifi44 T C 3: 151,745,636 (GRCm38) Y226C probably damaging Het
Il16 A G 7: 83,722,308 (GRCm38) C97R probably damaging Het
Impg1 A T 9: 80,345,561 (GRCm38) S369T probably damaging Het
Jmjd1c A G 10: 67,219,109 (GRCm38) T390A unknown Het
Lgi1 A G 19: 38,301,293 (GRCm38) E269G possibly damaging Het
Lrp6 G T 6: 134,450,897 (GRCm38) Y1577* probably null Het
Lrrc74a G T 12: 86,761,773 (GRCm38) probably benign Het
Man1c1 A T 4: 134,640,398 (GRCm38) probably null Het
Map1lc3b A C 8: 121,590,550 (GRCm38) Q9P possibly damaging Het
Mboat1 G A 13: 30,202,375 (GRCm38) R124H probably benign Het
Mcu A G 10: 59,456,677 (GRCm38) L60P probably damaging Het
Mrs2 G T 13: 25,018,534 (GRCm38) Q75K probably benign Het
Muc2 CGTG CGTGTG 7: 141,699,185 (GRCm38) probably null Het
Neb G A 2: 52,206,878 (GRCm38) probably benign Het
Nlrp2 C T 7: 5,328,329 (GRCm38) G356D probably benign Het
Notch3 A G 17: 32,156,148 (GRCm38) probably benign Het
Npr2 A C 4: 43,641,617 (GRCm38) S474R probably damaging Het
Nupl1 A G 14: 60,244,616 (GRCm38) F100L probably benign Het
Osbpl6 A C 2: 76,546,042 (GRCm38) D87A possibly damaging Het
Pabpc2 A T 18: 39,775,307 (GRCm38) M542L probably benign Het
Papln A G 12: 83,783,027 (GRCm38) probably benign Het
Parpbp T C 10: 88,092,896 (GRCm38) I561V possibly damaging Het
Pcdhb13 C T 18: 37,442,581 (GRCm38) A4V probably benign Het
Pelp1 T C 11: 70,395,704 (GRCm38) T533A possibly damaging Het
Poldip3 T A 15: 83,135,296 (GRCm38) M182L probably benign Het
Por T C 5: 135,731,178 (GRCm38) S240P possibly damaging Het
Pramef20 A T 4: 144,377,273 (GRCm38) probably benign Het
Prss22 A T 17: 23,996,301 (GRCm38) V167D probably damaging Het
Prss37 A C 6: 40,516,349 (GRCm38) L61R probably damaging Het
Psmd1 C T 1: 86,118,616 (GRCm38) T702M probably benign Het
Pxdn G T 12: 30,002,431 (GRCm38) G869V possibly damaging Het
Rabgap1l A G 1: 160,453,745 (GRCm38) probably benign Het
Rapgef6 T C 11: 54,619,941 (GRCm38) V228A probably damaging Het
Rnf169 T C 7: 99,926,003 (GRCm38) R462G possibly damaging Het
Rnft2 A G 5: 118,194,680 (GRCm38) probably benign Het
Sgo2b T C 8: 63,926,636 (GRCm38) D1054G probably benign Het
Sh3bgr T C 16: 96,228,517 (GRCm38) probably benign Het
Slc12a4 A G 8: 105,945,350 (GRCm38) V910A possibly damaging Het
Slc6a12 A T 6: 121,355,372 (GRCm38) I222F probably benign Het
Spty2d1 G A 7: 46,997,901 (GRCm38) R427* probably null Het
Ssc5d A G 7: 4,944,663 (GRCm38) T1339A probably benign Het
Sspo A C 6: 48,455,752 (GRCm38) E854A possibly damaging Het
Stx7 A G 10: 24,185,079 (GRCm38) probably benign Het
Styk1 A T 6: 131,301,730 (GRCm38) probably benign Het
Tex33 T A 15: 78,378,828 (GRCm38) M209L probably damaging Het
Tmem163 T G 1: 127,668,637 (GRCm38) probably benign Het
Tmppe C CT 9: 114,404,639 (GRCm38) probably null Het
Tmx2 A G 2: 84,673,082 (GRCm38) V229A probably benign Het
Top2b T C 14: 16,383,174 (GRCm38) L54P probably damaging Het
Trim62 A T 4: 128,902,550 (GRCm38) Y280F probably benign Het
Tssk4 A T 14: 55,651,559 (GRCm38) K181* probably null Het
Tssk4 A T 14: 55,651,560 (GRCm38) K181M probably damaging Het
Ubn1 A G 16: 5,064,614 (GRCm38) D313G probably damaging Het
Ugt1a10 C T 1: 88,215,123 (GRCm38) P113L probably damaging Het
Ugt1a10 C T 1: 88,218,249 (GRCm38) P473L probably damaging Het
Other mutations in Csmd3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Csmd3 APN 15 48,287,495 (GRCm38) missense possibly damaging 0.61
IGL00591:Csmd3 APN 15 48,004,883 (GRCm38) missense probably damaging 1.00
IGL00668:Csmd3 APN 15 47,913,945 (GRCm38) missense probably damaging 1.00
IGL00753:Csmd3 APN 15 47,644,235 (GRCm38) missense probably damaging 1.00
IGL00773:Csmd3 APN 15 47,590,719 (GRCm38) missense probably damaging 0.96
IGL00926:Csmd3 APN 15 47,710,964 (GRCm38) missense possibly damaging 0.87
IGL00942:Csmd3 APN 15 47,847,106 (GRCm38) critical splice donor site probably null
IGL01080:Csmd3 APN 15 47,881,403 (GRCm38) missense probably benign 0.12
IGL01314:Csmd3 APN 15 47,849,755 (GRCm38) missense probably damaging 1.00
IGL01326:Csmd3 APN 15 47,849,785 (GRCm38) missense probably benign 0.06
IGL01393:Csmd3 APN 15 48,457,599 (GRCm38) missense possibly damaging 0.88
IGL01432:Csmd3 APN 15 47,733,499 (GRCm38) missense probably damaging 1.00
IGL01519:Csmd3 APN 15 47,596,850 (GRCm38) missense probably benign 0.31
IGL01530:Csmd3 APN 15 47,669,617 (GRCm38) missense probably damaging 1.00
IGL01530:Csmd3 APN 15 47,838,437 (GRCm38) missense possibly damaging 0.95
IGL01547:Csmd3 APN 15 47,883,617 (GRCm38) missense probably benign 0.41
IGL01594:Csmd3 APN 15 47,629,239 (GRCm38) missense probably benign 0.01
IGL01618:Csmd3 APN 15 48,011,083 (GRCm38) missense probably benign 0.05
IGL01670:Csmd3 APN 15 47,611,829 (GRCm38) missense probably damaging 1.00
IGL01680:Csmd3 APN 15 47,970,030 (GRCm38) missense probably damaging 1.00
IGL01734:Csmd3 APN 15 48,185,304 (GRCm38) missense probably damaging 1.00
IGL01777:Csmd3 APN 15 47,698,198 (GRCm38) missense probably benign 0.06
IGL01779:Csmd3 APN 15 47,857,894 (GRCm38) missense probably benign 0.10
IGL01820:Csmd3 APN 15 47,607,142 (GRCm38) nonsense probably null
IGL01843:Csmd3 APN 15 47,658,999 (GRCm38) splice site probably benign
IGL01919:Csmd3 APN 15 47,675,772 (GRCm38) missense possibly damaging 0.62
IGL01986:Csmd3 APN 15 47,659,195 (GRCm38) missense possibly damaging 0.82
IGL02049:Csmd3 APN 15 48,001,474 (GRCm38) missense possibly damaging 0.91
IGL02065:Csmd3 APN 15 47,666,628 (GRCm38) missense probably damaging 1.00
IGL02112:Csmd3 APN 15 48,313,869 (GRCm38) missense possibly damaging 0.95
IGL02133:Csmd3 APN 15 47,857,942 (GRCm38) missense possibly damaging 0.86
IGL02203:Csmd3 APN 15 47,849,677 (GRCm38) splice site probably null
IGL02215:Csmd3 APN 15 47,585,688 (GRCm38) missense probably damaging 1.00
IGL02234:Csmd3 APN 15 47,948,116 (GRCm38) missense probably damaging 1.00
IGL02326:Csmd3 APN 15 47,755,963 (GRCm38) splice site probably benign
IGL02478:Csmd3 APN 15 47,838,398 (GRCm38) splice site probably benign
IGL02491:Csmd3 APN 15 47,914,115 (GRCm38) splice site probably benign
IGL02598:Csmd3 APN 15 47,669,690 (GRCm38) missense probably damaging 0.98
IGL02626:Csmd3 APN 15 47,704,107 (GRCm38) splice site probably benign
IGL02696:Csmd3 APN 15 47,669,669 (GRCm38) missense probably benign 0.33
IGL02876:Csmd3 APN 15 47,606,096 (GRCm38) splice site probably benign
IGL02971:Csmd3 APN 15 47,913,929 (GRCm38) splice site probably benign
IGL03068:Csmd3 APN 15 47,847,121 (GRCm38) missense possibly damaging 0.69
IGL03087:Csmd3 APN 15 47,977,033 (GRCm38) missense probably damaging 1.00
IGL03114:Csmd3 APN 15 47,820,451 (GRCm38) missense probably damaging 0.99
IGL03146:Csmd3 APN 15 47,881,477 (GRCm38) missense probably benign 0.25
IGL03193:Csmd3 APN 15 47,629,230 (GRCm38) splice site probably benign
IGL03274:Csmd3 APN 15 47,645,504 (GRCm38) missense probably damaging 1.00
R0040:Csmd3 UTSW 15 47,633,816 (GRCm38) missense probably damaging 1.00
R0071:Csmd3 UTSW 15 47,596,821 (GRCm38) missense probably benign 0.04
R0071:Csmd3 UTSW 15 47,596,821 (GRCm38) missense probably benign 0.04
R0119:Csmd3 UTSW 15 47,847,131 (GRCm38) missense probably benign 0.08
R0124:Csmd3 UTSW 15 47,590,716 (GRCm38) missense probably damaging 1.00
R0127:Csmd3 UTSW 15 47,981,930 (GRCm38) missense probably benign 0.45
R0136:Csmd3 UTSW 15 47,847,131 (GRCm38) missense probably benign 0.08
R0240:Csmd3 UTSW 15 47,629,239 (GRCm38) missense probably benign 0.05
R0240:Csmd3 UTSW 15 47,629,239 (GRCm38) missense probably benign 0.05
R0318:Csmd3 UTSW 15 47,659,153 (GRCm38) missense probably damaging 1.00
R0369:Csmd3 UTSW 15 47,970,147 (GRCm38) missense probably damaging 1.00
R0391:Csmd3 UTSW 15 47,657,573 (GRCm38) missense probably damaging 1.00
R0499:Csmd3 UTSW 15 47,847,131 (GRCm38) missense probably benign 0.08
R0506:Csmd3 UTSW 15 48,457,511 (GRCm38) missense probably benign 0.00
R0606:Csmd3 UTSW 15 48,457,662 (GRCm38) missense probably benign
R0639:Csmd3 UTSW 15 47,913,940 (GRCm38) missense probably damaging 1.00
R0658:Csmd3 UTSW 15 48,011,147 (GRCm38) missense possibly damaging 0.66
R0673:Csmd3 UTSW 15 47,913,940 (GRCm38) missense probably damaging 1.00
R0689:Csmd3 UTSW 15 47,756,025 (GRCm38) missense probably benign 0.19
R0696:Csmd3 UTSW 15 47,847,173 (GRCm38) missense probably benign 0.01
R0799:Csmd3 UTSW 15 48,185,384 (GRCm38) splice site probably benign
R0834:Csmd3 UTSW 15 47,883,677 (GRCm38) intron probably benign
R0894:Csmd3 UTSW 15 47,857,920 (GRCm38) missense possibly damaging 0.95
R0926:Csmd3 UTSW 15 47,977,033 (GRCm38) missense probably damaging 1.00
R0943:Csmd3 UTSW 15 47,675,739 (GRCm38) missense probably damaging 0.99
R0944:Csmd3 UTSW 15 47,611,831 (GRCm38) missense probably damaging 1.00
R0967:Csmd3 UTSW 15 47,857,831 (GRCm38) missense probably null 0.89
R0973:Csmd3 UTSW 15 47,659,089 (GRCm38) missense probably damaging 1.00
R1055:Csmd3 UTSW 15 47,881,537 (GRCm38) missense probably damaging 1.00
R1066:Csmd3 UTSW 15 47,913,965 (GRCm38) missense probably damaging 1.00
R1086:Csmd3 UTSW 15 47,695,755 (GRCm38) missense probably damaging 0.99
R1103:Csmd3 UTSW 15 47,948,006 (GRCm38) missense probably damaging 1.00
R1136:Csmd3 UTSW 15 47,675,817 (GRCm38) missense probably damaging 1.00
R1139:Csmd3 UTSW 15 47,695,836 (GRCm38) missense probably damaging 1.00
R1158:Csmd3 UTSW 15 48,292,774 (GRCm38) splice site probably null
R1215:Csmd3 UTSW 15 48,004,831 (GRCm38) splice site probably null
R1233:Csmd3 UTSW 15 48,673,531 (GRCm38) missense probably damaging 1.00
R1271:Csmd3 UTSW 15 48,011,059 (GRCm38) missense probably benign 0.11
R1469:Csmd3 UTSW 15 47,669,202 (GRCm38) nonsense probably null
R1469:Csmd3 UTSW 15 47,669,202 (GRCm38) nonsense probably null
R1479:Csmd3 UTSW 15 47,857,886 (GRCm38) missense probably damaging 1.00
R1480:Csmd3 UTSW 15 47,731,929 (GRCm38) missense possibly damaging 0.90
R1526:Csmd3 UTSW 15 47,585,632 (GRCm38) critical splice donor site probably null
R1527:Csmd3 UTSW 15 47,948,087 (GRCm38) missense probably benign 0.08
R1539:Csmd3 UTSW 15 47,820,398 (GRCm38) missense probably benign 0.24
R1544:Csmd3 UTSW 15 47,611,898 (GRCm38) splice site probably null
R1548:Csmd3 UTSW 15 47,981,975 (GRCm38) missense possibly damaging 0.91
R1574:Csmd3 UTSW 15 47,695,861 (GRCm38) splice site probably null
R1574:Csmd3 UTSW 15 47,695,861 (GRCm38) splice site probably null
R1619:Csmd3 UTSW 15 47,949,950 (GRCm38) missense probably damaging 1.00
R1630:Csmd3 UTSW 15 47,838,522 (GRCm38) missense possibly damaging 0.66
R1665:Csmd3 UTSW 15 47,696,789 (GRCm38) missense probably damaging 1.00
R1680:Csmd3 UTSW 15 47,741,170 (GRCm38) missense probably damaging 1.00
R1725:Csmd3 UTSW 15 47,596,807 (GRCm38) missense probably damaging 1.00
R1743:Csmd3 UTSW 15 48,622,089 (GRCm38) missense probably damaging 1.00
R1749:Csmd3 UTSW 15 47,585,660 (GRCm38) missense probably damaging 1.00
R1752:Csmd3 UTSW 15 47,660,273 (GRCm38) missense probably benign 0.15
R1769:Csmd3 UTSW 15 47,704,109 (GRCm38) splice site probably benign
R1775:Csmd3 UTSW 15 47,899,739 (GRCm38) missense probably damaging 0.99
R1795:Csmd3 UTSW 15 47,857,920 (GRCm38) missense possibly damaging 0.95
R1819:Csmd3 UTSW 15 47,753,735 (GRCm38) missense possibly damaging 0.56
R1840:Csmd3 UTSW 15 47,607,164 (GRCm38) missense probably damaging 1.00
R1860:Csmd3 UTSW 15 47,659,192 (GRCm38) missense probably damaging 1.00
R1861:Csmd3 UTSW 15 47,659,192 (GRCm38) missense probably damaging 1.00
R1879:Csmd3 UTSW 15 47,657,519 (GRCm38) missense possibly damaging 0.90
R1958:Csmd3 UTSW 15 48,004,639 (GRCm38) critical splice donor site probably null
R1965:Csmd3 UTSW 15 47,849,748 (GRCm38) missense probably benign 0.15
R1970:Csmd3 UTSW 15 48,673,531 (GRCm38) missense probably damaging 1.00
R2029:Csmd3 UTSW 15 47,838,579 (GRCm38) missense probably damaging 1.00
R2051:Csmd3 UTSW 15 48,621,993 (GRCm38) critical splice donor site probably null
R2108:Csmd3 UTSW 15 48,004,861 (GRCm38) missense possibly damaging 0.81
R2132:Csmd3 UTSW 15 48,457,503 (GRCm38) missense probably benign 0.06
R2146:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2147:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2148:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2157:Csmd3 UTSW 15 47,695,787 (GRCm38) missense probably damaging 0.99
R2159:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2160:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2161:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2162:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2164:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2213:Csmd3 UTSW 15 47,820,447 (GRCm38) missense possibly damaging 0.92
R2301:Csmd3 UTSW 15 47,731,998 (GRCm38) missense probably damaging 1.00
R2302:Csmd3 UTSW 15 48,314,051 (GRCm38) missense probably benign
R2355:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2497:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2509:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2566:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2567:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2568:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2570:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2571:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R2870:Csmd3 UTSW 15 47,857,924 (GRCm38) missense probably damaging 1.00
R2870:Csmd3 UTSW 15 47,857,924 (GRCm38) missense probably damaging 1.00
R2907:Csmd3 UTSW 15 48,011,053 (GRCm38) missense probably damaging 0.99
R3116:Csmd3 UTSW 15 47,657,599 (GRCm38) missense probably damaging 1.00
R3423:Csmd3 UTSW 15 47,847,252 (GRCm38) missense probably damaging 0.98
R3425:Csmd3 UTSW 15 47,847,252 (GRCm38) missense probably damaging 0.98
R3508:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R3746:Csmd3 UTSW 15 47,849,766 (GRCm38) missense probably benign 0.04
R3813:Csmd3 UTSW 15 48,791,813 (GRCm38) missense possibly damaging 0.82
R3832:Csmd3 UTSW 15 47,741,236 (GRCm38) frame shift probably null
R3959:Csmd3 UTSW 15 47,644,189 (GRCm38) missense probably benign 0.18
R4042:Csmd3 UTSW 15 47,614,084 (GRCm38) missense probably damaging 1.00
R4043:Csmd3 UTSW 15 47,755,966 (GRCm38) critical splice donor site probably null
R4191:Csmd3 UTSW 15 47,847,271 (GRCm38) missense probably damaging 0.99
R4192:Csmd3 UTSW 15 47,847,271 (GRCm38) missense probably damaging 0.99
R4419:Csmd3 UTSW 15 47,704,311 (GRCm38) missense probably damaging 1.00
R4426:Csmd3 UTSW 15 47,669,185 (GRCm38) missense possibly damaging 0.51
R4434:Csmd3 UTSW 15 47,899,795 (GRCm38) missense possibly damaging 0.68
R4438:Csmd3 UTSW 15 47,899,795 (GRCm38) missense possibly damaging 0.68
R4490:Csmd3 UTSW 15 48,314,033 (GRCm38) missense possibly damaging 0.83
R4562:Csmd3 UTSW 15 47,899,844 (GRCm38) missense probably benign 0.32
R4604:Csmd3 UTSW 15 48,004,815 (GRCm38) missense possibly damaging 0.90
R4620:Csmd3 UTSW 15 47,585,753 (GRCm38) missense probably benign 0.09
R4632:Csmd3 UTSW 15 48,011,209 (GRCm38) missense probably damaging 0.99
R4679:Csmd3 UTSW 15 48,161,083 (GRCm38) nonsense probably null
R4696:Csmd3 UTSW 15 47,913,968 (GRCm38) missense probably benign 0.24
R4718:Csmd3 UTSW 15 47,698,150 (GRCm38) nonsense probably null
R4723:Csmd3 UTSW 15 47,669,160 (GRCm38) missense probably benign 0.29
R4801:Csmd3 UTSW 15 47,621,292 (GRCm38) missense probably damaging 1.00
R4802:Csmd3 UTSW 15 47,621,292 (GRCm38) missense probably damaging 1.00
R4806:Csmd3 UTSW 15 48,314,068 (GRCm38) missense probably benign
R4816:Csmd3 UTSW 15 47,857,934 (GRCm38) missense possibly damaging 0.68
R4935:Csmd3 UTSW 15 48,161,084 (GRCm38) missense probably damaging 1.00
R4955:Csmd3 UTSW 15 48,673,518 (GRCm38) missense probably damaging 0.99
R4991:Csmd3 UTSW 15 48,001,478 (GRCm38) missense probably damaging 1.00
R5031:Csmd3 UTSW 15 47,659,192 (GRCm38) missense probably damaging 1.00
R5034:Csmd3 UTSW 15 47,629,287 (GRCm38) missense possibly damaging 0.94
R5035:Csmd3 UTSW 15 47,590,779 (GRCm38) missense probably damaging 1.00
R5120:Csmd3 UTSW 15 48,673,495 (GRCm38) nonsense probably null
R5224:Csmd3 UTSW 15 47,888,684 (GRCm38) missense possibly damaging 0.91
R5235:Csmd3 UTSW 15 47,629,278 (GRCm38) missense probably benign 0.20
R5279:Csmd3 UTSW 15 48,791,944 (GRCm38) splice site probably null
R5360:Csmd3 UTSW 15 47,669,203 (GRCm38) missense probably damaging 0.99
R5365:Csmd3 UTSW 15 48,004,749 (GRCm38) missense possibly damaging 0.68
R5379:Csmd3 UTSW 15 47,636,450 (GRCm38) nonsense probably null
R5381:Csmd3 UTSW 15 47,741,215 (GRCm38) missense probably benign 0.21
R5393:Csmd3 UTSW 15 47,633,703 (GRCm38) missense probably damaging 1.00
R5413:Csmd3 UTSW 15 47,838,435 (GRCm38) missense probably damaging 1.00
R5549:Csmd3 UTSW 15 48,185,357 (GRCm38) missense probably damaging 0.98
R5550:Csmd3 UTSW 15 48,185,357 (GRCm38) missense probably damaging 0.98
R5551:Csmd3 UTSW 15 48,314,096 (GRCm38) missense probably benign 0.13
R5567:Csmd3 UTSW 15 47,645,468 (GRCm38) missense possibly damaging 0.92
R5621:Csmd3 UTSW 15 48,313,978 (GRCm38) missense possibly damaging 0.84
R5668:Csmd3 UTSW 15 47,695,755 (GRCm38) missense possibly damaging 0.48
R5677:Csmd3 UTSW 15 48,622,051 (GRCm38) missense probably damaging 0.98
R5701:Csmd3 UTSW 15 48,540,333 (GRCm38) missense probably damaging 0.99
R5701:Csmd3 UTSW 15 47,650,221 (GRCm38) missense probably damaging 1.00
R5871:Csmd3 UTSW 15 47,888,716 (GRCm38) missense probably damaging 0.98
R5872:Csmd3 UTSW 15 47,582,527 (GRCm38) missense probably damaging 1.00
R5874:Csmd3 UTSW 15 47,644,270 (GRCm38) missense probably damaging 1.00
R5952:Csmd3 UTSW 15 47,733,505 (GRCm38) missense probably damaging 0.98
R5956:Csmd3 UTSW 15 48,791,882 (GRCm38) missense possibly damaging 0.84
R5966:Csmd3 UTSW 15 47,849,739 (GRCm38) missense probably damaging 0.96
R5969:Csmd3 UTSW 15 47,947,990 (GRCm38) missense probably damaging 1.00
R5989:Csmd3 UTSW 15 47,590,764 (GRCm38) missense possibly damaging 0.69
R6017:Csmd3 UTSW 15 48,314,012 (GRCm38) missense possibly damaging 0.95
R6057:Csmd3 UTSW 15 47,755,391 (GRCm38) missense probably damaging 1.00
R6127:Csmd3 UTSW 15 47,650,228 (GRCm38) missense probably damaging 1.00
R6178:Csmd3 UTSW 15 48,673,458 (GRCm38) missense probably damaging 1.00
R6198:Csmd3 UTSW 15 48,313,877 (GRCm38) missense probably benign 0.28
R6213:Csmd3 UTSW 15 47,629,260 (GRCm38) missense probably damaging 1.00
R6256:Csmd3 UTSW 15 47,669,729 (GRCm38) missense probably damaging 1.00
R6274:Csmd3 UTSW 15 47,621,437 (GRCm38) missense probably benign
R6327:Csmd3 UTSW 15 47,881,387 (GRCm38) missense probably damaging 1.00
R6354:Csmd3 UTSW 15 47,881,489 (GRCm38) missense probably damaging 1.00
R6405:Csmd3 UTSW 15 47,820,371 (GRCm38) missense probably damaging 0.99
R6410:Csmd3 UTSW 15 48,673,407 (GRCm38) missense probably damaging 1.00
R6416:Csmd3 UTSW 15 48,673,560 (GRCm38) missense probably damaging 1.00
R6463:Csmd3 UTSW 15 47,676,479 (GRCm38) missense probably damaging 1.00
R6536:Csmd3 UTSW 15 47,838,467 (GRCm38) missense probably damaging 1.00
R6625:Csmd3 UTSW 15 47,607,075 (GRCm38) missense probably benign 0.02
R6695:Csmd3 UTSW 15 47,857,834 (GRCm38) missense probably damaging 0.99
R6895:Csmd3 UTSW 15 47,666,514 (GRCm38) splice site probably null
R6906:Csmd3 UTSW 15 47,847,173 (GRCm38) missense probably benign 0.01
R6914:Csmd3 UTSW 15 48,011,138 (GRCm38) missense possibly damaging 0.53
R6920:Csmd3 UTSW 15 47,644,205 (GRCm38) missense probably damaging 1.00
R7024:Csmd3 UTSW 15 47,710,991 (GRCm38) missense probably damaging 1.00
R7178:Csmd3 UTSW 15 47,590,774 (GRCm38) missense
R7192:Csmd3 UTSW 15 47,704,237 (GRCm38) missense
R7220:Csmd3 UTSW 15 48,457,598 (GRCm38) missense probably damaging 0.99
R7362:Csmd3 UTSW 15 47,755,992 (GRCm38) missense possibly damaging 0.65
R7380:Csmd3 UTSW 15 47,586,965 (GRCm38) missense
R7397:Csmd3 UTSW 15 47,695,734 (GRCm38) missense
R7467:Csmd3 UTSW 15 47,629,244 (GRCm38) missense
R7585:Csmd3 UTSW 15 48,622,075 (GRCm38) missense possibly damaging 0.76
R7623:Csmd3 UTSW 15 47,949,938 (GRCm38) missense
R7649:Csmd3 UTSW 15 47,669,143 (GRCm38) missense
R7691:Csmd3 UTSW 15 47,741,173 (GRCm38) missense
R7695:Csmd3 UTSW 15 47,820,381 (GRCm38) missense
R7759:Csmd3 UTSW 15 47,698,173 (GRCm38) missense
R7817:Csmd3 UTSW 15 47,857,960 (GRCm38) missense probably damaging 0.99
R8052:Csmd3 UTSW 15 47,706,387 (GRCm38) missense
R8089:Csmd3 UTSW 15 47,669,207 (GRCm38) missense
R8110:Csmd3 UTSW 15 47,644,270 (GRCm38) missense probably damaging 1.00
R8152:Csmd3 UTSW 15 47,669,464 (GRCm38) splice site probably null
R8323:Csmd3 UTSW 15 47,698,151 (GRCm38) missense
R8341:Csmd3 UTSW 15 47,698,151 (GRCm38) missense
R8353:Csmd3 UTSW 15 47,949,953 (GRCm38) missense probably damaging 1.00
R8364:Csmd3 UTSW 15 48,673,441 (GRCm38) missense probably damaging 1.00
R8405:Csmd3 UTSW 15 47,755,983 (GRCm38) missense probably damaging 1.00
R8412:Csmd3 UTSW 15 47,636,398 (GRCm38) missense
R8436:Csmd3 UTSW 15 48,004,822 (GRCm38) missense probably damaging 0.97
R8516:Csmd3 UTSW 15 47,629,365 (GRCm38) nonsense probably null
R8553:Csmd3 UTSW 15 47,621,328 (GRCm38) missense possibly damaging 0.52
R8554:Csmd3 UTSW 15 47,644,142 (GRCm38) missense probably benign 0.32
R8678:Csmd3 UTSW 15 47,636,453 (GRCm38) missense
R8751:Csmd3 UTSW 15 47,982,006 (GRCm38) missense
R8758:Csmd3 UTSW 15 47,606,197 (GRCm38) missense
R8768:Csmd3 UTSW 15 47,698,176 (GRCm38) missense
R8785:Csmd3 UTSW 15 48,314,086 (GRCm38) missense probably benign 0.00
R8788:Csmd3 UTSW 15 47,607,117 (GRCm38) missense
R8798:Csmd3 UTSW 15 47,731,986 (GRCm38) missense
R8801:Csmd3 UTSW 15 48,457,628 (GRCm38) missense possibly damaging 0.70
R8811:Csmd3 UTSW 15 47,696,743 (GRCm38) missense
R8844:Csmd3 UTSW 15 48,673,419 (GRCm38) missense probably damaging 0.98
R8844:Csmd3 UTSW 15 47,741,194 (GRCm38) missense probably damaging 0.96
R8892:Csmd3 UTSW 15 47,741,238 (GRCm38) missense
R8897:Csmd3 UTSW 15 48,359,343 (GRCm38) missense probably benign 0.06
R9001:Csmd3 UTSW 15 47,733,505 (GRCm38) missense
R9007:Csmd3 UTSW 15 47,888,496 (GRCm38) intron probably benign
R9016:Csmd3 UTSW 15 47,659,042 (GRCm38) missense
R9039:Csmd3 UTSW 15 47,619,912 (GRCm38) splice site probably benign
R9109:Csmd3 UTSW 15 47,753,791 (GRCm38) missense
R9121:Csmd3 UTSW 15 47,820,378 (GRCm38) missense
R9155:Csmd3 UTSW 15 47,585,655 (GRCm38) missense
R9176:Csmd3 UTSW 15 48,001,541 (GRCm38) missense
R9281:Csmd3 UTSW 15 47,596,876 (GRCm38) missense
R9298:Csmd3 UTSW 15 47,753,791 (GRCm38) missense
R9304:Csmd3 UTSW 15 47,706,409 (GRCm38) missense
R9343:Csmd3 UTSW 15 48,151,605 (GRCm38) missense probably damaging 1.00
R9367:Csmd3 UTSW 15 47,704,168 (GRCm38) missense
R9405:Csmd3 UTSW 15 47,675,791 (GRCm38) missense
R9448:Csmd3 UTSW 15 47,596,919 (GRCm38) missense
R9460:Csmd3 UTSW 15 47,753,734 (GRCm38) missense
R9481:Csmd3 UTSW 15 47,607,063 (GRCm38) missense
R9520:Csmd3 UTSW 15 47,698,212 (GRCm38) missense
R9551:Csmd3 UTSW 15 48,791,960 (GRCm38) start gained probably benign
R9552:Csmd3 UTSW 15 48,791,960 (GRCm38) start gained probably benign
R9568:Csmd3 UTSW 15 48,287,546 (GRCm38) missense probably damaging 0.97
R9571:Csmd3 UTSW 15 48,792,002 (GRCm38) start gained probably benign
R9607:Csmd3 UTSW 15 47,755,415 (GRCm38) missense probably damaging 0.98
R9621:Csmd3 UTSW 15 47,849,720 (GRCm38) missense
R9671:Csmd3 UTSW 15 47,981,903 (GRCm38) missense
R9718:Csmd3 UTSW 15 47,696,687 (GRCm38) missense
U24488:Csmd3 UTSW 15 47,710,399 (GRCm38) missense probably damaging 1.00
V8831:Csmd3 UTSW 15 48,457,696 (GRCm38) missense probably damaging 0.96
X0021:Csmd3 UTSW 15 47,970,093 (GRCm38) nonsense probably null
Z1088:Csmd3 UTSW 15 47,847,281 (GRCm38) missense probably damaging 0.98
Z1088:Csmd3 UTSW 15 47,636,393 (GRCm38) missense probably damaging 1.00
Z1177:Csmd3 UTSW 15 47,733,417 (GRCm38) missense
Z1177:Csmd3 UTSW 15 47,675,734 (GRCm38) missense
Predicted Primers PCR Primer
(F):5'- TGAGACAAAGTGGCACCTACTCAGG -3'
(R):5'- TCCCCAGATCTCTAATGGAAGGCTG -3'

Sequencing Primer
(F):5'- CTTCTATCAACACTGAGGTGGAC -3'
(R):5'- CTGGAAGGAACAAATTTCGACTG -3'
Posted On 2013-04-16