Incidental Mutation 'R7243:Csmd1'
ID 563359
Institutional Source Beutler Lab
Gene Symbol Csmd1
Ensembl Gene ENSMUSG00000060924
Gene Name CUB and Sushi multiple domains 1
Synonyms
MMRRC Submission 045307-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7243 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 15942537-17585602 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 15965357 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 3218 (D3218V)
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: D3218V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000080751
Gene: ENSMUSG00000060924
AA Change: D3218V

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: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 99% (73/74)
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: 75 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acap1 G A 11: 69,781,297 (GRCm39) H103Y probably benign Het
Adamdec1 A G 14: 68,809,203 (GRCm39) M253T probably benign Het
Alox15 C A 11: 70,241,540 (GRCm39) G114C probably null Het
Aox3 G T 1: 58,177,466 (GRCm39) G227V unknown Het
Atp8a2 A T 14: 59,885,291 (GRCm39) N1144K probably benign Het
Cacna1c C T 6: 118,614,690 (GRCm39) probably null Het
Cog6 A T 3: 52,909,736 (GRCm39) W314R probably damaging Het
Col5a2 A G 1: 45,415,320 (GRCm39) I1473T probably benign Het
Cyp3a11 A G 5: 145,795,613 (GRCm39) M446T probably damaging Het
Dhps A G 8: 85,801,567 (GRCm39) Y340C probably benign Het
Dnah7b A G 1: 46,122,914 (GRCm39) N108S probably benign Het
Dnajb1 C T 8: 84,337,393 (GRCm39) P323L probably damaging Het
Dspp TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG 5: 104,326,227 (GRCm39) probably benign Het
Dync2h1 G T 9: 7,102,405 (GRCm39) T2665K possibly damaging Het
Etv1 C T 12: 38,907,045 (GRCm39) S349L probably benign Het
Fam171a1 A T 2: 3,119,653 (GRCm39) T21S probably benign Het
Fbh1 T A 2: 11,756,336 (GRCm39) T749S probably benign Het
Fcho2 T C 13: 98,891,724 (GRCm39) D346G possibly damaging Het
Fcrl5 A G 3: 87,349,552 (GRCm39) H109R probably benign Het
Fstl1 A G 16: 37,647,088 (GRCm39) S153G probably benign Het
Fyb1 T C 15: 6,673,180 (GRCm39) F605L probably benign Het
Gcat T A 15: 78,921,063 (GRCm39) M363K possibly damaging Het
Gm10604 T C 4: 11,980,113 (GRCm39) T64A unknown Het
Grin2d A G 7: 45,515,552 (GRCm39) L147P probably damaging Het
Ift88 A T 14: 57,667,993 (GRCm39) probably null Het
Ighg1 A T 12: 113,294,066 (GRCm39) C26S Het
Ing2 A G 8: 48,127,574 (GRCm39) S48P probably damaging Het
Kat6a C T 8: 23,428,791 (GRCm39) T1382I probably benign Het
Kdm1a A G 4: 136,279,265 (GRCm39) V765A probably damaging Het
Klk1b26 T C 7: 43,665,691 (GRCm39) S168P not run Het
Klk1b26 A G 7: 43,666,337 (GRCm39) N260S probably damaging Het
Lama3 G A 18: 12,552,902 (GRCm39) G438D probably damaging Het
Larp6 T A 9: 60,620,569 (GRCm39) D27E probably benign Het
Lrba T A 3: 86,658,823 (GRCm39) probably null Het
Lrig2 A T 3: 104,404,883 (GRCm39) probably null Het
Megf9 T C 4: 70,353,708 (GRCm39) E366G probably benign Het
Mob1b T A 5: 88,891,304 (GRCm39) D52E probably damaging Het
Ndufb3 A T 1: 58,630,282 (GRCm39) H11L unknown Het
Odc1 T G 12: 17,600,058 (GRCm39) Y407* probably null Het
Ogfr GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG 2: 180,237,059 (GRCm39) probably benign Het
Opa1 A G 16: 29,405,814 (GRCm39) I126M probably benign Het
Or2t47 T C 11: 58,442,227 (GRCm39) I279M probably damaging Het
Or3a1b T A 11: 74,012,559 (GRCm39) V148E probably damaging Het
Or51a10 A G 7: 103,698,962 (GRCm39) Y200H probably damaging Het
Or51f5 A T 7: 102,430,865 (GRCm39) T61S probably benign Het
Pcca A G 14: 123,114,186 (GRCm39) H633R probably benign Het
Pcdhb22 A G 18: 37,653,685 (GRCm39) R461G probably benign Het
Pcf11 A T 7: 92,309,268 (GRCm39) D647E probably damaging Het
Plscr1l1 A G 9: 92,225,726 (GRCm39) Y16C probably damaging Het
Plxnd1 T A 6: 115,949,468 (GRCm39) I773F probably benign Het
Prl8a1 A T 13: 27,766,086 (GRCm39) L3Q probably damaging Het
Psg17 C A 7: 18,552,640 (GRCm39) G212C probably damaging Het
Ptbp2 G T 3: 119,546,761 (GRCm39) N40K possibly damaging Het
Ptprj T C 2: 90,276,765 (GRCm39) H1102R probably damaging Het
Rbfox3 T C 11: 118,404,100 (GRCm39) Y33C probably damaging Het
Ros1 T A 10: 51,999,477 (GRCm39) N1158Y probably damaging Het
Rpgrip1l T C 8: 91,996,751 (GRCm39) I710V probably benign Het
Scn9a A G 2: 66,370,874 (GRCm39) F569L probably damaging Het
Slc12a4 A T 8: 106,680,552 (GRCm39) M190K probably damaging Het
Slc22a20 G A 19: 6,021,599 (GRCm39) R468C probably damaging Het
Slc45a2 T A 15: 11,023,436 (GRCm39) Y347N possibly damaging Het
Slc4a10 A G 2: 62,134,206 (GRCm39) Y974C probably damaging Het
Snap47 A G 11: 59,319,548 (GRCm39) S197P probably benign Het
Snph T C 2: 151,436,173 (GRCm39) S252G probably damaging Het
Spns2 A T 11: 72,347,686 (GRCm39) W335R probably damaging Het
Thnsl1 A G 2: 21,217,658 (GRCm39) I471V probably damaging Het
Tmprss11f C A 5: 86,677,975 (GRCm39) G265C probably damaging Het
Tnn C T 1: 159,934,687 (GRCm39) R1242H probably benign Het
Tsc2 T C 17: 24,818,604 (GRCm39) R1412G probably benign Het
Tsc22d2 G T 3: 58,323,884 (GRCm39) V259F unknown Het
Ttll13 A C 7: 79,903,911 (GRCm39) K280Q probably damaging Het
Wls A T 3: 159,615,402 (GRCm39) I306F possibly damaging Het
Zfp566 A G 7: 29,777,701 (GRCm39) V160A probably benign Het
Zfyve28 T C 5: 34,356,219 (GRCm39) T761A probably damaging Het
Zswim8 G A 14: 20,764,436 (GRCm39) R602Q 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
R7260:Csmd1 UTSW 8 16,050,574 (GRCm39) missense probably damaging 1.00
R7271:Csmd1 UTSW 8 17,077,295 (GRCm39) missense probably damaging 0.99
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'- TCTTGGATAAATGGATTTCCTGTGC -3'
(R):5'- AATCCAAGATGCCCAAGGAG -3'

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