Incidental Mutation 'R7271:Csmd1'
ID 565294
Institutional Source Beutler Lab
Gene Symbol Csmd1
Ensembl Gene ENSMUSG00000060924
Gene Name CUB and Sushi multiple domains 1
Synonyms
MMRRC Submission 045356-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7271 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 15942537-17585602 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 17077295 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Arginine at position 121 (W121R)
Ref Sequence ENSEMBL: ENSMUSP00000080751 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000082104]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000082104
AA Change: W121R

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000080751
Gene: ENSMUSG00000060924
AA Change: W121R

DomainStartEndE-ValueType
signal peptide 1 29 N/A INTRINSIC
CUB 32 140 1.46e-26 SMART
CCP 145 202 1.01e-11 SMART
CUB 208 312 1.05e-27 SMART
CCP 349 406 1.28e-8 SMART
CUB 411 522 2.34e-25 SMART
CCP 527 580 1.22e-14 SMART
CUB 584 692 1.61e-37 SMART
CCP 697 754 4.41e-12 SMART
CUB 758 866 6.55e-38 SMART
CCP 873 926 2.53e-12 SMART
CUB 930 1040 8.94e-22 SMART
CCP 1045 1100 7.06e-11 SMART
CUB 1104 1212 3.14e-26 SMART
CCP 1217 1273 1.18e-12 SMART
CUB 1277 1386 9.72e-32 SMART
CCP 1391 1447 2.06e-12 SMART
CUB 1451 1559 1.68e-35 SMART
CCP 1564 1621 2.53e-12 SMART
CUB 1625 1733 4.24e-14 SMART
CCP 1741 1798 9.46e-12 SMART
CUB 1802 1910 4.23e-32 SMART
CCP 1915 1970 8.23e-12 SMART
CUB 1974 2082 8.59e-33 SMART
CCP 2087 2142 6.09e-15 SMART
CUB 2146 2253 2.36e-30 SMART
CCP 2258 2315 1.1e-12 SMART
CUB 2320 2430 4.3e-24 SMART
CCP 2432 2490 2.94e-8 SMART
CCP 2495 2552 2.03e-11 SMART
CCP 2557 2617 1.22e-5 SMART
CCP 2622 2675 2.72e-12 SMART
CCP 2680 2733 5.86e-17 SMART
CCP 2738 2791 6.09e-15 SMART
CCP 2796 2854 9.1e-14 SMART
CCP 2859 2912 3.96e-14 SMART
CCP 2920 2973 4.41e-12 SMART
CCP 2978 3032 2.94e-8 SMART
CCP 3037 3092 6.59e-11 SMART
CCP 3097 3150 4.12e-12 SMART
CCP 3155 3208 7.92e-14 SMART
CCP 3216 3270 2.8e-14 SMART
CCP 3275 3330 3.78e-11 SMART
transmembrane domain 3487 3509 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (58/58)
MGI Phenotype PHENOTYPE: Mice exhibit normal pre-pulse inhibition, social interaction, sucrose preference and d-amphetamine sensitivity. [provided by MGI curators]
Allele List at MGI

All alleles(1) : Targeted, knock-out(1)

Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afg1l C T 10: 42,291,544 (GRCm39) probably null Het
Ahnak2 A T 12: 112,780,802 (GRCm38) V70E Het
Alpk3 A G 7: 80,728,202 (GRCm39) E444G possibly damaging Het
Amer2 T A 14: 60,617,123 (GRCm39) D439E possibly damaging Het
Ano6 A G 15: 95,811,781 (GRCm39) Y222C probably damaging Het
Atp4a A C 7: 30,421,944 (GRCm39) K827Q probably benign Het
Atp9a G A 2: 168,576,047 (GRCm39) Het
Casp7 T A 19: 56,424,793 (GRCm39) C171S probably damaging Het
Ccdc9b T A 2: 118,591,164 (GRCm39) probably null Het
Ccng2 C G 5: 93,421,202 (GRCm39) S237R probably benign Het
Cdkl1 A G 12: 69,795,585 (GRCm39) L315S probably benign Het
Cfap91 A G 16: 38,148,708 (GRCm39) I240T probably damaging Het
Crybg1 G T 10: 43,873,619 (GRCm39) S1163* probably null Het
Cyyr1 A T 16: 85,262,493 (GRCm39) M88K possibly damaging Het
Dlc1 T C 8: 37,049,954 (GRCm39) Q587R probably damaging Het
Dock2 T C 11: 34,223,750 (GRCm39) E1128G possibly damaging Het
Dynap T A 18: 70,374,320 (GRCm39) T69S possibly damaging Het
Esr1 T C 10: 4,733,874 (GRCm39) C225R probably damaging Het
Fbxo31 C T 8: 122,305,503 (GRCm39) probably benign Het
Fndc11 G A 2: 180,863,893 (GRCm39) V233I possibly damaging Het
Fto T C 8: 92,211,818 (GRCm39) F381S probably damaging Het
Gtf2ird1 A G 5: 134,433,758 (GRCm39) L223P probably benign Het
Ifi214 A T 1: 173,357,042 (GRCm39) H20Q probably damaging Het
Impa2 T A 18: 67,439,806 (GRCm39) I101N probably damaging Het
Kidins220 A T 12: 25,061,570 (GRCm39) T854S probably benign Het
Lamb1 T A 12: 31,337,423 (GRCm39) C385S probably damaging Het
Lrrc8c A G 5: 105,755,853 (GRCm39) S543G probably benign Het
Manba A T 3: 135,248,137 (GRCm39) Y342F probably damaging Het
Map3k1 T C 13: 111,893,231 (GRCm39) D758G probably benign Het
Mtor G T 4: 148,630,942 (GRCm39) A2300S possibly damaging Het
Musk T A 4: 58,373,409 (GRCm39) M793K probably damaging Het
Nup133 A C 8: 124,649,153 (GRCm39) I563S probably benign Het
Or10ab4 G A 7: 107,654,423 (GRCm39) R78Q probably damaging Het
Or10ag55-ps1 T A 2: 87,114,725 (GRCm39) N30K probably benign Het
Or4k77 A G 2: 111,199,693 (GRCm39) T239A probably damaging Het
Or8g21 A T 9: 38,905,953 (GRCm39) Y259* probably null Het
Pcdh12 C A 18: 38,416,100 (GRCm39) V342F probably damaging Het
Pcdhb4 T A 18: 37,441,222 (GRCm39) H177Q possibly damaging Het
Pcnx2 G A 8: 126,613,690 (GRCm39) A587V probably benign Het
Phkb C T 8: 86,770,418 (GRCm39) P896S probably damaging Het
Prss36 A G 7: 127,543,877 (GRCm39) S165P probably benign Het
Prss43 A G 9: 110,657,671 (GRCm39) D190G probably damaging Het
Psmd14 T C 2: 61,591,356 (GRCm39) V53A probably damaging Het
Sel1l3 T G 5: 53,273,704 (GRCm39) H1054P probably damaging Het
Selenoh T C 2: 84,500,631 (GRCm39) R70G probably damaging Het
Serpinb9d A G 13: 33,378,617 (GRCm39) Q21R probably benign Het
Slc29a1 T C 17: 45,899,288 (GRCm39) E262G probably benign Het
Slc7a14 A G 3: 31,278,384 (GRCm39) L407P probably damaging Het
Smyd4 T C 11: 75,281,325 (GRCm39) V266A possibly damaging Het
Spata31d1a T A 13: 59,849,913 (GRCm39) R738S probably benign Het
Speer4a2 G A 5: 26,292,993 (GRCm39) T67I probably benign Het
Srcin1 C T 11: 97,442,715 (GRCm39) G38S probably damaging Het
Stab2 A T 10: 86,838,972 (GRCm39) probably null Het
Syde2 A G 3: 145,726,031 (GRCm39) N1308D possibly damaging Het
Trip11 A T 12: 101,850,611 (GRCm39) M1151K probably damaging Het
Ttll4 A T 1: 74,727,820 (GRCm39) I861F possibly damaging Het
Zfp319 G A 8: 96,058,471 (GRCm39) probably benign Het
Zfp518b T C 5: 38,831,907 (GRCm39) N33D probably benign Het
Zfp874a T A 13: 67,591,415 (GRCm39) I90F probably benign Het
Zmiz2 G T 11: 6,349,593 (GRCm39) V412L probably damaging Het
Other mutations in Csmd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00095:Csmd1 APN 8 16,059,297 (GRCm39) splice site probably benign
IGL00433:Csmd1 APN 8 16,281,387 (GRCm39) missense probably damaging 1.00
IGL00500:Csmd1 APN 8 15,971,139 (GRCm39) missense probably damaging 1.00
IGL00666:Csmd1 APN 8 16,240,004 (GRCm39) missense probably damaging 1.00
IGL00913:Csmd1 APN 8 16,121,301 (GRCm39) missense probably benign 0.00
IGL01012:Csmd1 APN 8 15,967,341 (GRCm39) missense probably benign 0.00
IGL01123:Csmd1 APN 8 17,584,944 (GRCm39) missense possibly damaging 0.96
IGL01348:Csmd1 APN 8 15,960,596 (GRCm39) missense probably damaging 0.99
IGL01444:Csmd1 APN 8 16,250,069 (GRCm39) missense probably benign 0.00
IGL01530:Csmd1 APN 8 15,953,195 (GRCm39) missense probably damaging 0.99
IGL01548:Csmd1 APN 8 16,338,660 (GRCm39) nonsense probably null
IGL01814:Csmd1 APN 8 16,551,389 (GRCm39) missense probably damaging 1.00
IGL01889:Csmd1 APN 8 16,048,857 (GRCm39) missense probably damaging 1.00
IGL02055:Csmd1 APN 8 16,119,015 (GRCm39) missense probably damaging 0.99
IGL02066:Csmd1 APN 8 15,976,594 (GRCm39) missense probably damaging 1.00
IGL02097:Csmd1 APN 8 16,261,773 (GRCm39) missense probably null 0.17
IGL02112:Csmd1 APN 8 16,131,719 (GRCm39) missense probably benign 0.18
IGL02161:Csmd1 APN 8 16,408,426 (GRCm39) missense probably damaging 0.97
IGL02189:Csmd1 APN 8 16,321,620 (GRCm39) missense probably damaging 0.99
IGL02272:Csmd1 APN 8 16,249,907 (GRCm39) missense probably damaging 0.99
IGL02292:Csmd1 APN 8 16,261,884 (GRCm39) missense probably damaging 1.00
IGL02385:Csmd1 APN 8 15,953,275 (GRCm39) missense probably benign 0.08
IGL02424:Csmd1 APN 8 16,142,340 (GRCm39) missense probably benign 0.22
IGL02492:Csmd1 APN 8 16,052,597 (GRCm39) missense probably benign 0.13
IGL02507:Csmd1 APN 8 17,584,992 (GRCm39) utr 5 prime probably benign
IGL02513:Csmd1 APN 8 16,049,869 (GRCm39) splice site probably benign
IGL02727:Csmd1 APN 8 16,281,341 (GRCm39) missense probably damaging 1.00
IGL02728:Csmd1 APN 8 16,049,779 (GRCm39) critical splice donor site probably null
IGL02852:Csmd1 APN 8 15,945,728 (GRCm39) missense probably damaging 0.99
IGL02935:Csmd1 APN 8 16,273,348 (GRCm39) missense probably damaging 1.00
IGL02945:Csmd1 APN 8 16,321,584 (GRCm39) missense possibly damaging 0.92
IGL02959:Csmd1 APN 8 15,960,465 (GRCm39) missense probably damaging 0.99
IGL03113:Csmd1 APN 8 16,078,712 (GRCm39) missense probably benign
IGL03129:Csmd1 APN 8 16,011,521 (GRCm39) missense probably damaging 0.99
IGL03131:Csmd1 APN 8 16,138,231 (GRCm39) missense probably damaging 1.00
IGL03275:Csmd1 APN 8 16,207,106 (GRCm39) missense probably benign 0.00
IGL03297:Csmd1 APN 8 16,059,432 (GRCm39) nonsense probably null
ikura UTSW 8 16,281,285 (GRCm39) missense probably damaging 1.00
I2289:Csmd1 UTSW 8 15,962,381 (GRCm39) missense probably benign 0.10
IGL03055:Csmd1 UTSW 8 16,145,515 (GRCm39) missense probably damaging 1.00
IGL03097:Csmd1 UTSW 8 15,995,127 (GRCm39) missense probably damaging 1.00
PIT4260001:Csmd1 UTSW 8 16,120,327 (GRCm39) missense probably damaging 1.00
PIT4378001:Csmd1 UTSW 8 15,945,728 (GRCm39) missense probably damaging 0.99
PIT4520001:Csmd1 UTSW 8 15,956,023 (GRCm39) missense probably benign 0.01
R0037:Csmd1 UTSW 8 15,967,248 (GRCm39) missense probably damaging 0.97
R0095:Csmd1 UTSW 8 16,283,065 (GRCm39) missense probably damaging 1.00
R0113:Csmd1 UTSW 8 16,034,849 (GRCm39) missense probably damaging 1.00
R0129:Csmd1 UTSW 8 16,129,956 (GRCm39) missense possibly damaging 0.95
R0144:Csmd1 UTSW 8 16,441,838 (GRCm39) missense probably benign 0.16
R0166:Csmd1 UTSW 8 16,283,036 (GRCm39) missense probably benign 0.29
R0227:Csmd1 UTSW 8 16,441,836 (GRCm39) missense probably benign 0.05
R0279:Csmd1 UTSW 8 16,273,249 (GRCm39) missense probably damaging 0.99
R0280:Csmd1 UTSW 8 16,321,616 (GRCm39) missense probably damaging 1.00
R0312:Csmd1 UTSW 8 16,034,760 (GRCm39) missense probably damaging 1.00
R0355:Csmd1 UTSW 8 15,968,330 (GRCm39) missense probably damaging 0.97
R0367:Csmd1 UTSW 8 15,967,270 (GRCm39) missense probably damaging 1.00
R0395:Csmd1 UTSW 8 16,396,652 (GRCm39) missense probably damaging 0.99
R0413:Csmd1 UTSW 8 16,760,530 (GRCm39) missense probably damaging 0.97
R0457:Csmd1 UTSW 8 16,551,407 (GRCm39) critical splice acceptor site probably null
R0463:Csmd1 UTSW 8 15,971,759 (GRCm39) missense probably damaging 0.99
R0482:Csmd1 UTSW 8 16,283,115 (GRCm39) missense probably damaging 1.00
R0501:Csmd1 UTSW 8 17,077,339 (GRCm39) missense probably damaging 0.97
R0505:Csmd1 UTSW 8 16,042,758 (GRCm39) missense probably damaging 1.00
R0507:Csmd1 UTSW 8 16,235,358 (GRCm39) splice site probably benign
R0511:Csmd1 UTSW 8 15,982,529 (GRCm39) missense possibly damaging 0.80
R0555:Csmd1 UTSW 8 16,235,287 (GRCm39) missense probably benign
R0580:Csmd1 UTSW 8 15,960,528 (GRCm39) missense probably damaging 1.00
R0610:Csmd1 UTSW 8 15,968,208 (GRCm39) missense possibly damaging 0.95
R0634:Csmd1 UTSW 8 16,276,405 (GRCm39) missense probably damaging 1.00
R0666:Csmd1 UTSW 8 16,119,063 (GRCm39) missense possibly damaging 0.88
R0674:Csmd1 UTSW 8 16,050,550 (GRCm39) missense probably benign 0.03
R0675:Csmd1 UTSW 8 16,208,145 (GRCm39) missense probably benign 0.01
R0763:Csmd1 UTSW 8 17,077,300 (GRCm39) missense possibly damaging 0.67
R0781:Csmd1 UTSW 8 15,971,174 (GRCm39) missense probably benign 0.35
R0862:Csmd1 UTSW 8 16,240,040 (GRCm39) missense probably damaging 0.99
R0864:Csmd1 UTSW 8 16,240,040 (GRCm39) missense probably damaging 0.99
R0925:Csmd1 UTSW 8 16,760,634 (GRCm39) missense probably benign 0.29
R0926:Csmd1 UTSW 8 16,083,590 (GRCm39) splice site probably null
R1005:Csmd1 UTSW 8 16,338,707 (GRCm39) missense probably damaging 0.99
R1073:Csmd1 UTSW 8 16,408,477 (GRCm39) splice site probably benign
R1185:Csmd1 UTSW 8 16,408,362 (GRCm39) missense probably damaging 0.96
R1185:Csmd1 UTSW 8 16,408,362 (GRCm39) missense probably damaging 0.96
R1185:Csmd1 UTSW 8 16,408,362 (GRCm39) missense probably damaging 0.96
R1256:Csmd1 UTSW 8 16,129,978 (GRCm39) missense probably damaging 1.00
R1294:Csmd1 UTSW 8 16,748,052 (GRCm39) missense probably damaging 0.99
R1375:Csmd1 UTSW 8 16,513,095 (GRCm39) splice site probably null
R1447:Csmd1 UTSW 8 15,975,306 (GRCm39) nonsense probably null
R1450:Csmd1 UTSW 8 15,995,180 (GRCm39) critical splice acceptor site probably null
R1470:Csmd1 UTSW 8 16,207,218 (GRCm39) splice site probably benign
R1580:Csmd1 UTSW 8 15,975,299 (GRCm39) missense probably damaging 1.00
R1591:Csmd1 UTSW 8 15,950,710 (GRCm39) missense probably damaging 0.99
R1658:Csmd1 UTSW 8 16,131,739 (GRCm39) missense possibly damaging 0.69
R1678:Csmd1 UTSW 8 15,968,252 (GRCm39) missense possibly damaging 0.58
R1717:Csmd1 UTSW 8 17,266,708 (GRCm39) missense possibly damaging 0.58
R1735:Csmd1 UTSW 8 15,982,610 (GRCm39) missense probably damaging 0.99
R1750:Csmd1 UTSW 8 15,967,303 (GRCm39) missense probably damaging 0.99
R1753:Csmd1 UTSW 8 16,207,134 (GRCm39) nonsense probably null
R1822:Csmd1 UTSW 8 16,273,340 (GRCm39) missense probably damaging 1.00
R1875:Csmd1 UTSW 8 15,979,101 (GRCm39) missense probably damaging 0.99
R1909:Csmd1 UTSW 8 15,956,116 (GRCm39) missense probably damaging 1.00
R1912:Csmd1 UTSW 8 16,284,012 (GRCm39) critical splice donor site probably null
R1993:Csmd1 UTSW 8 16,396,698 (GRCm39) missense probably damaging 0.99
R2067:Csmd1 UTSW 8 15,950,782 (GRCm39) missense probably benign
R2094:Csmd1 UTSW 8 16,129,992 (GRCm39) missense probably damaging 0.99
R2119:Csmd1 UTSW 8 17,266,749 (GRCm39) missense probably damaging 0.98
R2127:Csmd1 UTSW 8 15,967,392 (GRCm39) missense probably damaging 1.00
R2138:Csmd1 UTSW 8 15,979,088 (GRCm39) missense probably damaging 0.96
R2216:Csmd1 UTSW 8 17,077,355 (GRCm39) critical splice acceptor site probably null
R2220:Csmd1 UTSW 8 16,042,641 (GRCm39) missense possibly damaging 0.94
R2380:Csmd1 UTSW 8 16,240,101 (GRCm39) missense probably damaging 1.00
R2471:Csmd1 UTSW 8 16,261,776 (GRCm39) missense probably damaging 1.00
R2984:Csmd1 UTSW 8 16,003,782 (GRCm39) missense probably damaging 1.00
R3001:Csmd1 UTSW 8 16,246,184 (GRCm39) missense probably damaging 0.98
R3002:Csmd1 UTSW 8 16,246,184 (GRCm39) missense probably damaging 0.98
R3003:Csmd1 UTSW 8 16,246,184 (GRCm39) missense probably damaging 0.98
R3103:Csmd1 UTSW 8 15,967,405 (GRCm39) missense probably damaging 1.00
R3104:Csmd1 UTSW 8 17,077,247 (GRCm39) missense probably damaging 1.00
R3620:Csmd1 UTSW 8 16,042,684 (GRCm39) missense probably benign 0.29
R3621:Csmd1 UTSW 8 16,042,684 (GRCm39) missense probably benign 0.29
R3748:Csmd1 UTSW 8 15,956,071 (GRCm39) missense probably damaging 0.99
R3780:Csmd1 UTSW 8 16,252,000 (GRCm39) missense probably damaging 1.00
R3815:Csmd1 UTSW 8 16,052,522 (GRCm39) missense probably damaging 1.00
R3816:Csmd1 UTSW 8 16,052,522 (GRCm39) missense probably damaging 1.00
R3818:Csmd1 UTSW 8 16,052,522 (GRCm39) missense probably damaging 1.00
R3819:Csmd1 UTSW 8 16,052,522 (GRCm39) missense probably damaging 1.00
R3850:Csmd1 UTSW 8 16,129,936 (GRCm39) missense probably benign 0.00
R3945:Csmd1 UTSW 8 15,960,619 (GRCm39) splice site probably null
R3980:Csmd1 UTSW 8 15,956,056 (GRCm39) nonsense probably null
R4061:Csmd1 UTSW 8 15,995,158 (GRCm39) missense probably benign 0.00
R4086:Csmd1 UTSW 8 16,042,738 (GRCm39) missense probably damaging 0.99
R4087:Csmd1 UTSW 8 16,042,738 (GRCm39) missense probably damaging 0.99
R4089:Csmd1 UTSW 8 16,042,738 (GRCm39) missense probably damaging 0.99
R4183:Csmd1 UTSW 8 15,960,464 (GRCm39) missense probably damaging 0.99
R4226:Csmd1 UTSW 8 16,050,490 (GRCm39) missense probably damaging 0.99
R4454:Csmd1 UTSW 8 15,995,011 (GRCm39) missense probably damaging 0.99
R4533:Csmd1 UTSW 8 15,981,037 (GRCm39) splice site probably null
R4544:Csmd1 UTSW 8 16,760,652 (GRCm39) missense possibly damaging 0.93
R4547:Csmd1 UTSW 8 16,441,811 (GRCm39) missense possibly damaging 0.48
R4612:Csmd1 UTSW 8 15,971,908 (GRCm39) splice site probably null
R4620:Csmd1 UTSW 8 16,052,694 (GRCm39) critical splice acceptor site probably null
R4627:Csmd1 UTSW 8 16,747,933 (GRCm39) missense probably benign 0.00
R4633:Csmd1 UTSW 8 16,052,620 (GRCm39) missense probably damaging 0.99
R4646:Csmd1 UTSW 8 15,982,511 (GRCm39) missense possibly damaging 0.87
R4648:Csmd1 UTSW 8 16,048,788 (GRCm39) nonsense probably null
R4668:Csmd1 UTSW 8 16,073,905 (GRCm39) missense possibly damaging 0.50
R4709:Csmd1 UTSW 8 16,760,522 (GRCm39) critical splice donor site probably null
R4709:Csmd1 UTSW 8 16,073,905 (GRCm39) missense possibly damaging 0.96
R4741:Csmd1 UTSW 8 15,960,447 (GRCm39) missense probably damaging 0.99
R4774:Csmd1 UTSW 8 16,059,369 (GRCm39) missense probably benign 0.11
R4793:Csmd1 UTSW 8 16,138,277 (GRCm39) missense probably damaging 1.00
R4829:Csmd1 UTSW 8 16,177,310 (GRCm39) missense probably damaging 1.00
R4888:Csmd1 UTSW 8 15,945,674 (GRCm39) utr 3 prime probably benign
R4896:Csmd1 UTSW 8 16,059,439 (GRCm39) missense probably benign 0.00
R4932:Csmd1 UTSW 8 16,073,779 (GRCm39) missense probably damaging 0.99
R4944:Csmd1 UTSW 8 16,048,772 (GRCm39) missense probably damaging 1.00
R4953:Csmd1 UTSW 8 16,249,931 (GRCm39) missense probably damaging 0.99
R4996:Csmd1 UTSW 8 15,960,452 (GRCm39) missense probably damaging 0.97
R5028:Csmd1 UTSW 8 16,039,090 (GRCm39) missense probably damaging 1.00
R5146:Csmd1 UTSW 8 16,246,204 (GRCm39) missense probably damaging 1.00
R5272:Csmd1 UTSW 8 16,249,958 (GRCm39) missense probably damaging 0.99
R5327:Csmd1 UTSW 8 17,266,728 (GRCm39) missense possibly damaging 0.94
R5399:Csmd1 UTSW 8 16,760,613 (GRCm39) missense probably damaging 1.00
R5411:Csmd1 UTSW 8 15,960,471 (GRCm39) missense probably damaging 1.00
R5462:Csmd1 UTSW 8 16,011,486 (GRCm39) missense probably benign 0.12
R5463:Csmd1 UTSW 8 16,034,860 (GRCm39) missense probably benign 0.34
R5497:Csmd1 UTSW 8 16,135,195 (GRCm39) missense probably benign 0.20
R5536:Csmd1 UTSW 8 16,338,674 (GRCm39) missense probably damaging 0.99
R5711:Csmd1 UTSW 8 16,003,703 (GRCm39) missense probably damaging 1.00
R5730:Csmd1 UTSW 8 16,235,206 (GRCm39) nonsense probably null
R5788:Csmd1 UTSW 8 16,251,980 (GRCm39) missense probably damaging 1.00
R5941:Csmd1 UTSW 8 15,982,471 (GRCm39) missense probably damaging 0.99
R5960:Csmd1 UTSW 8 16,121,430 (GRCm39) missense possibly damaging 0.68
R5961:Csmd1 UTSW 8 16,120,366 (GRCm39) missense probably damaging 0.99
R5969:Csmd1 UTSW 8 16,121,367 (GRCm39) missense probably benign 0.00
R5998:Csmd1 UTSW 8 15,960,443 (GRCm39) missense probably damaging 1.00
R6062:Csmd1 UTSW 8 16,142,319 (GRCm39) missense possibly damaging 0.68
R6109:Csmd1 UTSW 8 16,249,874 (GRCm39) missense possibly damaging 0.93
R6116:Csmd1 UTSW 8 16,261,864 (GRCm39) missense probably damaging 1.00
R6143:Csmd1 UTSW 8 16,138,315 (GRCm39) missense probably damaging 1.00
R6155:Csmd1 UTSW 8 15,953,231 (GRCm39) missense probably benign 0.01
R6197:Csmd1 UTSW 8 15,976,611 (GRCm39) missense probably benign 0.32
R6247:Csmd1 UTSW 8 16,246,249 (GRCm39) missense possibly damaging 0.91
R6304:Csmd1 UTSW 8 16,108,688 (GRCm39) missense probably damaging 1.00
R6317:Csmd1 UTSW 8 16,760,658 (GRCm39) missense possibly damaging 0.89
R6318:Csmd1 UTSW 8 15,953,212 (GRCm39) missense probably damaging 1.00
R6338:Csmd1 UTSW 8 15,982,492 (GRCm39) missense possibly damaging 0.75
R6369:Csmd1 UTSW 8 17,585,020 (GRCm39) start gained probably benign
R6447:Csmd1 UTSW 8 15,960,527 (GRCm39) missense probably damaging 1.00
R6454:Csmd1 UTSW 8 15,971,150 (GRCm39) missense probably damaging 0.99
R6494:Csmd1 UTSW 8 16,261,709 (GRCm39) splice site probably null
R6614:Csmd1 UTSW 8 17,266,803 (GRCm39) missense probably damaging 1.00
R6736:Csmd1 UTSW 8 16,052,626 (GRCm39) missense probably damaging 0.99
R6769:Csmd1 UTSW 8 16,121,408 (GRCm39) missense possibly damaging 0.80
R6771:Csmd1 UTSW 8 16,121,408 (GRCm39) missense possibly damaging 0.80
R6804:Csmd1 UTSW 8 16,087,260 (GRCm39) missense probably damaging 1.00
R6818:Csmd1 UTSW 8 16,235,341 (GRCm39) missense probably damaging 1.00
R6863:Csmd1 UTSW 8 17,584,929 (GRCm39) missense possibly damaging 0.85
R6930:Csmd1 UTSW 8 16,142,409 (GRCm39) missense probably damaging 0.97
R6969:Csmd1 UTSW 8 17,266,805 (GRCm39) missense possibly damaging 0.94
R7112:Csmd1 UTSW 8 16,151,142 (GRCm39) missense probably damaging 1.00
R7124:Csmd1 UTSW 8 15,953,202 (GRCm39) missense probably damaging 1.00
R7167:Csmd1 UTSW 8 15,976,524 (GRCm39) missense probably benign
R7243:Csmd1 UTSW 8 15,965,357 (GRCm39) missense probably damaging 1.00
R7260:Csmd1 UTSW 8 16,050,574 (GRCm39) missense probably damaging 1.00
R7324:Csmd1 UTSW 8 16,108,721 (GRCm39) missense probably damaging 1.00
R7325:Csmd1 UTSW 8 16,108,721 (GRCm39) missense probably damaging 1.00
R7327:Csmd1 UTSW 8 16,108,721 (GRCm39) missense probably damaging 1.00
R7373:Csmd1 UTSW 8 16,042,713 (GRCm39) missense probably damaging 1.00
R7406:Csmd1 UTSW 8 16,338,707 (GRCm39) missense probably damaging 0.99
R7427:Csmd1 UTSW 8 16,073,864 (GRCm39) missense possibly damaging 0.91
R7428:Csmd1 UTSW 8 16,073,864 (GRCm39) missense possibly damaging 0.91
R7445:Csmd1 UTSW 8 16,208,268 (GRCm39) missense possibly damaging 0.61
R7458:Csmd1 UTSW 8 16,003,738 (GRCm39) missense probably damaging 1.00
R7476:Csmd1 UTSW 8 15,945,731 (GRCm39) missense probably damaging 1.00
R7527:Csmd1 UTSW 8 16,261,732 (GRCm39) missense probably damaging 1.00
R7544:Csmd1 UTSW 8 16,142,310 (GRCm39) missense probably damaging 1.00
R7583:Csmd1 UTSW 8 16,048,833 (GRCm39) missense probably damaging 0.96
R7603:Csmd1 UTSW 8 16,338,696 (GRCm39) missense probably damaging 1.00
R7607:Csmd1 UTSW 8 15,968,331 (GRCm39) missense possibly damaging 0.94
R7642:Csmd1 UTSW 8 16,135,192 (GRCm39) missense probably damaging 0.99
R7669:Csmd1 UTSW 8 15,967,273 (GRCm39) missense probably damaging 1.00
R7720:Csmd1 UTSW 8 15,981,108 (GRCm39) missense probably damaging 1.00
R7728:Csmd1 UTSW 8 16,281,285 (GRCm39) missense probably damaging 1.00
R7738:Csmd1 UTSW 8 16,151,004 (GRCm39) missense probably damaging 1.00
R7745:Csmd1 UTSW 8 15,982,461 (GRCm39) critical splice donor site probably null
R7879:Csmd1 UTSW 8 16,441,820 (GRCm39) missense probably benign 0.28
R7884:Csmd1 UTSW 8 16,011,418 (GRCm39) missense probably damaging 1.00
R7897:Csmd1 UTSW 8 17,584,935 (GRCm39) missense possibly damaging 0.96
R8111:Csmd1 UTSW 8 15,967,306 (GRCm39) missense probably benign
R8119:Csmd1 UTSW 8 17,077,310 (GRCm39) missense probably damaging 0.99
R8134:Csmd1 UTSW 8 15,982,550 (GRCm39) missense probably damaging 0.99
R8187:Csmd1 UTSW 8 16,177,188 (GRCm39) missense probably damaging 0.99
R8196:Csmd1 UTSW 8 16,059,468 (GRCm39) missense probably benign 0.18
R8231:Csmd1 UTSW 8 16,747,939 (GRCm39) missense possibly damaging 0.82
R8242:Csmd1 UTSW 8 16,760,670 (GRCm39) missense probably benign 0.42
R8274:Csmd1 UTSW 8 15,960,453 (GRCm39) missense possibly damaging 0.93
R8286:Csmd1 UTSW 8 16,039,188 (GRCm39) missense probably benign 0.18
R8289:Csmd1 UTSW 8 16,108,716 (GRCm39) missense probably damaging 0.99
R8314:Csmd1 UTSW 8 16,208,258 (GRCm39) missense probably benign
R8323:Csmd1 UTSW 8 17,266,751 (GRCm39) nonsense probably null
R8387:Csmd1 UTSW 8 16,050,484 (GRCm39) missense possibly damaging 0.94
R8413:Csmd1 UTSW 8 15,950,676 (GRCm39) missense probably damaging 0.98
R8672:Csmd1 UTSW 8 15,976,598 (GRCm39) missense probably benign 0.01
R8765:Csmd1 UTSW 8 16,760,627 (GRCm39) nonsense probably null
R8789:Csmd1 UTSW 8 17,266,722 (GRCm39) missense probably damaging 0.99
R8828:Csmd1 UTSW 8 16,048,794 (GRCm39) missense probably benign 0.00
R8858:Csmd1 UTSW 8 16,120,318 (GRCm39) missense probably benign 0.10
R8878:Csmd1 UTSW 8 15,960,528 (GRCm39) missense probably damaging 1.00
R8911:Csmd1 UTSW 8 16,748,019 (GRCm39) missense probably damaging 0.99
R8966:Csmd1 UTSW 8 16,250,059 (GRCm39) missense probably damaging 1.00
R8978:Csmd1 UTSW 8 15,971,056 (GRCm39) missense probably benign 0.37
R8996:Csmd1 UTSW 8 15,971,105 (GRCm39) missense possibly damaging 0.54
R9045:Csmd1 UTSW 8 16,284,088 (GRCm39) missense probably damaging 0.99
R9084:Csmd1 UTSW 8 16,138,325 (GRCm39) missense probably benign
R9124:Csmd1 UTSW 8 16,034,806 (GRCm39) missense probably damaging 0.99
R9127:Csmd1 UTSW 8 16,273,286 (GRCm39) missense probably benign 0.31
R9146:Csmd1 UTSW 8 16,048,832 (GRCm39) missense probably benign 0.00
R9198:Csmd1 UTSW 8 15,962,430 (GRCm39) missense probably damaging 1.00
R9285:Csmd1 UTSW 8 15,956,088 (GRCm39) missense probably damaging 1.00
R9303:Csmd1 UTSW 8 16,011,532 (GRCm39) missense probably benign 0.31
R9305:Csmd1 UTSW 8 16,011,532 (GRCm39) missense probably benign 0.31
R9326:Csmd1 UTSW 8 16,049,803 (GRCm39) missense probably benign 0.21
R9356:Csmd1 UTSW 8 16,252,069 (GRCm39) missense probably damaging 1.00
R9385:Csmd1 UTSW 8 16,034,756 (GRCm39) missense probably benign 0.19
R9444:Csmd1 UTSW 8 16,208,250 (GRCm39) missense probably benign 0.30
R9476:Csmd1 UTSW 8 15,981,215 (GRCm39) critical splice acceptor site probably null
R9506:Csmd1 UTSW 8 16,250,023 (GRCm39) missense probably damaging 1.00
R9614:Csmd1 UTSW 8 16,208,239 (GRCm39) missense probably benign 0.00
R9668:Csmd1 UTSW 8 16,261,772 (GRCm39) missense probably benign 0.00
X0011:Csmd1 UTSW 8 16,246,277 (GRCm39) missense probably damaging 1.00
X0021:Csmd1 UTSW 8 16,235,270 (GRCm39) missense probably damaging 1.00
X0024:Csmd1 UTSW 8 16,087,232 (GRCm39) missense probably damaging 0.99
X0028:Csmd1 UTSW 8 15,965,333 (GRCm39) missense possibly damaging 0.79
Z1088:Csmd1 UTSW 8 16,239,992 (GRCm39) missense possibly damaging 0.50
Z1088:Csmd1 UTSW 8 16,142,272 (GRCm39) missense probably damaging 1.00
Z1088:Csmd1 UTSW 8 15,971,875 (GRCm39) missense possibly damaging 0.91
Z1088:Csmd1 UTSW 8 16,396,631 (GRCm39) missense probably damaging 0.99
Z1088:Csmd1 UTSW 8 16,250,072 (GRCm39) missense probably damaging 0.97
Z1176:Csmd1 UTSW 8 16,087,212 (GRCm39) missense probably damaging 1.00
Z1176:Csmd1 UTSW 8 16,048,814 (GRCm39) missense probably damaging 1.00
Z1177:Csmd1 UTSW 8 16,250,033 (GRCm39) missense probably damaging 1.00
Z1177:Csmd1 UTSW 8 16,034,708 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAAGACAATGTTGTATCTGCTTGAC -3'
(R):5'- ATGGCTACCTAAGTCTTTGATGATGTC -3'

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