Incidental Mutation 'R7603:Csmd1'
ID 588117
Institutional Source Beutler Lab
Gene Symbol Csmd1
Ensembl Gene ENSMUSG00000060924
Gene Name CUB and Sushi multiple domains 1
Synonyms
MMRRC Submission 045713-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7603 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 15892537-17535586 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 16288682 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 470 (D470E)
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: D470E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000080751
Gene: ENSMUSG00000060924
AA Change: D470E

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: 98.9%
Validation Efficiency 98% (47/48)
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: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610010F05Rik T C 11: 23,566,191 (GRCm38) T709A probably benign Het
Abca6 T C 11: 110,180,258 (GRCm38) K1536E possibly damaging Het
Abhd16a T A 17: 35,101,960 (GRCm38) probably null Het
Actrt3 C T 3: 30,598,547 (GRCm38) A133T probably benign Het
Adcy10 C T 1: 165,564,237 (GRCm38) R1329W probably damaging Het
Apol7b T C 15: 77,423,456 (GRCm38) M280V possibly damaging Het
Canx A T 11: 50,311,628 (GRCm38) D50E probably benign Het
Cyp2c23 C T 19: 44,014,930 (GRCm38) D269N probably damaging Het
Ddah1 T C 3: 145,759,019 (GRCm38) V53A probably benign Het
Epha7 C T 4: 28,871,937 (GRCm38) S422L probably benign Het
Fastkd5 A G 2: 130,615,041 (GRCm38) V543A possibly damaging Het
Fggy G A 4: 95,769,506 (GRCm38) G295R probably damaging Het
Frs2 T C 10: 117,074,063 (GRCm38) T465A probably benign Het
Glipr1 A T 10: 111,988,832 (GRCm38) N156K probably benign Het
Gnpnat1 C T 14: 45,384,617 (GRCm38) V40I probably benign Het
H2-Q7 T C 17: 35,439,963 (GRCm38) L130P probably damaging Het
Herc1 T A 9: 66,451,383 (GRCm38) L86* probably null Het
Hspg2 T C 4: 137,548,368 (GRCm38) L2778P probably damaging Het
Hspg2 T A 4: 137,557,192 (GRCm38) I3487N possibly damaging Het
Htra4 T G 8: 25,025,700 (GRCm38) I441L probably benign Het
Ints7 A T 1: 191,596,224 (GRCm38) H203L probably damaging Het
Lama2 T C 10: 27,266,680 (GRCm38) T601A possibly damaging Het
Lin7b T C 7: 45,368,432 (GRCm38) probably benign Het
Lmbr1l G A 15: 98,908,691 (GRCm38) Q280* probably null Het
Lpin3 G T 2: 160,903,754 (GRCm38) probably null Het
Map1lc3b A T 8: 121,593,529 (GRCm38) H27L possibly damaging Het
Mfsd14a C A 3: 116,633,883 (GRCm38) V369F probably damaging Het
Ndufa12 C T 10: 94,220,779 (GRCm38) A123V probably benign Het
Nek9 A G 12: 85,303,514 (GRCm38) F929L probably benign Het
Nup210 A T 6: 91,076,697 (GRCm38) D279E probably benign Het
Olfr553 A G 7: 102,614,938 (GRCm38) V17A probably benign Het
Parp1 T C 1: 180,600,212 (GRCm38) probably null Het
Phc3 T C 3: 30,907,452 (GRCm38) I944V probably damaging Het
Phf20 C T 2: 156,302,851 (GRCm38) A793V probably benign Het
Phf21a A C 2: 92,357,007 (GRCm38) R540S probably benign Het
Pogk A G 1: 166,401,911 (GRCm38) C124R probably benign Het
Rif1 C T 2: 52,076,175 (GRCm38) S93L probably damaging Het
Sele A G 1: 164,049,515 (GRCm38) E120G probably damaging Het
Slc4a1ap T C 5: 31,546,195 (GRCm38) L49P Het
Snap47 T C 11: 59,428,547 (GRCm38) D255G probably damaging Het
Tcstv3 T C 13: 120,317,610 (GRCm38) V15A probably damaging Het
Tmcc1 A T 6: 116,043,131 (GRCm38) Y453* probably null Het
Tpsg1 G T 17: 25,373,210 (GRCm38) G86V probably damaging Het
Urb1 CACTTAC CAC 16: 90,772,573 (GRCm38) probably benign Het
Usp20 T A 2: 31,011,474 (GRCm38) V459E probably damaging Het
Vmn1r202 A T 13: 22,501,620 (GRCm38) L209Q probably damaging Het
Vps13b T C 15: 35,576,439 (GRCm38) S998P probably damaging Het
Other mutations in Csmd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00095:Csmd1 APN 8 16,009,297 (GRCm38) splice site probably benign
IGL00433:Csmd1 APN 8 16,231,373 (GRCm38) missense probably damaging 1.00
IGL00500:Csmd1 APN 8 15,921,139 (GRCm38) missense probably damaging 1.00
IGL00666:Csmd1 APN 8 16,189,990 (GRCm38) missense probably damaging 1.00
IGL00913:Csmd1 APN 8 16,071,287 (GRCm38) missense probably benign 0.00
IGL01012:Csmd1 APN 8 15,917,341 (GRCm38) missense probably benign 0.00
IGL01123:Csmd1 APN 8 17,534,928 (GRCm38) missense possibly damaging 0.96
IGL01348:Csmd1 APN 8 15,910,596 (GRCm38) missense probably damaging 0.99
IGL01444:Csmd1 APN 8 16,200,055 (GRCm38) missense probably benign 0.00
IGL01530:Csmd1 APN 8 15,903,195 (GRCm38) missense probably damaging 0.99
IGL01548:Csmd1 APN 8 16,288,646 (GRCm38) nonsense probably null
IGL01814:Csmd1 APN 8 16,501,375 (GRCm38) missense probably damaging 1.00
IGL01889:Csmd1 APN 8 15,998,857 (GRCm38) missense probably damaging 1.00
IGL02055:Csmd1 APN 8 16,069,001 (GRCm38) missense probably damaging 0.99
IGL02066:Csmd1 APN 8 15,926,594 (GRCm38) missense probably damaging 1.00
IGL02097:Csmd1 APN 8 16,211,759 (GRCm38) missense probably null 0.17
IGL02112:Csmd1 APN 8 16,081,705 (GRCm38) missense probably benign 0.18
IGL02161:Csmd1 APN 8 16,358,412 (GRCm38) missense probably damaging 0.97
IGL02189:Csmd1 APN 8 16,271,606 (GRCm38) missense probably damaging 0.99
IGL02272:Csmd1 APN 8 16,199,893 (GRCm38) missense probably damaging 0.99
IGL02292:Csmd1 APN 8 16,211,870 (GRCm38) missense probably damaging 1.00
IGL02385:Csmd1 APN 8 15,903,275 (GRCm38) missense probably benign 0.08
IGL02424:Csmd1 APN 8 16,092,326 (GRCm38) missense probably benign 0.22
IGL02492:Csmd1 APN 8 16,002,597 (GRCm38) missense probably benign 0.13
IGL02507:Csmd1 APN 8 17,534,976 (GRCm38) utr 5 prime probably benign
IGL02513:Csmd1 APN 8 15,999,869 (GRCm38) splice site probably benign
IGL02727:Csmd1 APN 8 16,231,327 (GRCm38) missense probably damaging 1.00
IGL02728:Csmd1 APN 8 15,999,779 (GRCm38) critical splice donor site probably null
IGL02852:Csmd1 APN 8 15,895,728 (GRCm38) missense probably damaging 0.99
IGL02935:Csmd1 APN 8 16,223,334 (GRCm38) missense probably damaging 1.00
IGL02945:Csmd1 APN 8 16,271,570 (GRCm38) missense possibly damaging 0.92
IGL02959:Csmd1 APN 8 15,910,465 (GRCm38) missense probably damaging 0.99
IGL03113:Csmd1 APN 8 16,028,698 (GRCm38) missense probably benign
IGL03129:Csmd1 APN 8 15,961,521 (GRCm38) missense probably damaging 0.99
IGL03131:Csmd1 APN 8 16,088,217 (GRCm38) missense probably damaging 1.00
IGL03275:Csmd1 APN 8 16,157,092 (GRCm38) missense probably benign 0.00
IGL03297:Csmd1 APN 8 16,009,432 (GRCm38) nonsense probably null
ikura UTSW 8 16,231,271 (GRCm38) missense probably damaging 1.00
I2289:Csmd1 UTSW 8 15,912,381 (GRCm38) missense probably benign 0.10
IGL03055:Csmd1 UTSW 8 16,095,501 (GRCm38) missense probably damaging 1.00
IGL03097:Csmd1 UTSW 8 15,945,127 (GRCm38) missense probably damaging 1.00
PIT4260001:Csmd1 UTSW 8 16,070,313 (GRCm38) missense probably damaging 1.00
PIT4378001:Csmd1 UTSW 8 15,895,728 (GRCm38) missense probably damaging 0.99
PIT4520001:Csmd1 UTSW 8 15,906,023 (GRCm38) missense probably benign 0.01
R0037:Csmd1 UTSW 8 15,917,248 (GRCm38) missense probably damaging 0.97
R0095:Csmd1 UTSW 8 16,233,051 (GRCm38) missense probably damaging 1.00
R0113:Csmd1 UTSW 8 15,984,849 (GRCm38) missense probably damaging 1.00
R0129:Csmd1 UTSW 8 16,079,942 (GRCm38) missense possibly damaging 0.95
R0144:Csmd1 UTSW 8 16,391,824 (GRCm38) missense probably benign 0.16
R0166:Csmd1 UTSW 8 16,233,022 (GRCm38) missense probably benign 0.29
R0227:Csmd1 UTSW 8 16,391,822 (GRCm38) missense probably benign 0.05
R0279:Csmd1 UTSW 8 16,223,235 (GRCm38) missense probably damaging 0.99
R0280:Csmd1 UTSW 8 16,271,602 (GRCm38) missense probably damaging 1.00
R0312:Csmd1 UTSW 8 15,984,760 (GRCm38) missense probably damaging 1.00
R0355:Csmd1 UTSW 8 15,918,330 (GRCm38) missense probably damaging 0.97
R0367:Csmd1 UTSW 8 15,917,270 (GRCm38) missense probably damaging 1.00
R0395:Csmd1 UTSW 8 16,346,638 (GRCm38) missense probably damaging 0.99
R0413:Csmd1 UTSW 8 16,710,514 (GRCm38) missense probably damaging 0.97
R0457:Csmd1 UTSW 8 16,501,393 (GRCm38) critical splice acceptor site probably null
R0463:Csmd1 UTSW 8 15,921,759 (GRCm38) missense probably damaging 0.99
R0482:Csmd1 UTSW 8 16,233,101 (GRCm38) missense probably damaging 1.00
R0501:Csmd1 UTSW 8 17,027,323 (GRCm38) missense probably damaging 0.97
R0505:Csmd1 UTSW 8 15,992,758 (GRCm38) missense probably damaging 1.00
R0507:Csmd1 UTSW 8 16,185,344 (GRCm38) splice site probably benign
R0511:Csmd1 UTSW 8 15,932,529 (GRCm38) missense possibly damaging 0.80
R0555:Csmd1 UTSW 8 16,185,273 (GRCm38) missense probably benign
R0580:Csmd1 UTSW 8 15,910,528 (GRCm38) missense probably damaging 1.00
R0610:Csmd1 UTSW 8 15,918,208 (GRCm38) missense possibly damaging 0.95
R0634:Csmd1 UTSW 8 16,226,391 (GRCm38) missense probably damaging 1.00
R0666:Csmd1 UTSW 8 16,069,049 (GRCm38) missense possibly damaging 0.88
R0674:Csmd1 UTSW 8 16,000,550 (GRCm38) missense probably benign 0.03
R0675:Csmd1 UTSW 8 16,158,131 (GRCm38) missense probably benign 0.01
R0763:Csmd1 UTSW 8 17,027,284 (GRCm38) missense possibly damaging 0.67
R0781:Csmd1 UTSW 8 15,921,174 (GRCm38) missense probably benign 0.35
R0862:Csmd1 UTSW 8 16,190,026 (GRCm38) missense probably damaging 0.99
R0864:Csmd1 UTSW 8 16,190,026 (GRCm38) missense probably damaging 0.99
R0925:Csmd1 UTSW 8 16,710,618 (GRCm38) missense probably benign 0.29
R0926:Csmd1 UTSW 8 16,033,576 (GRCm38) splice site probably null
R1005:Csmd1 UTSW 8 16,288,693 (GRCm38) missense probably damaging 0.99
R1073:Csmd1 UTSW 8 16,358,463 (GRCm38) splice site probably benign
R1185:Csmd1 UTSW 8 16,358,348 (GRCm38) missense probably damaging 0.96
R1185:Csmd1 UTSW 8 16,358,348 (GRCm38) missense probably damaging 0.96
R1185:Csmd1 UTSW 8 16,358,348 (GRCm38) missense probably damaging 0.96
R1256:Csmd1 UTSW 8 16,079,964 (GRCm38) missense probably damaging 1.00
R1294:Csmd1 UTSW 8 16,698,036 (GRCm38) missense probably damaging 0.99
R1375:Csmd1 UTSW 8 16,463,081 (GRCm38) splice site probably null
R1447:Csmd1 UTSW 8 15,925,306 (GRCm38) nonsense probably null
R1450:Csmd1 UTSW 8 15,945,180 (GRCm38) critical splice acceptor site probably null
R1470:Csmd1 UTSW 8 16,157,204 (GRCm38) splice site probably benign
R1580:Csmd1 UTSW 8 15,925,299 (GRCm38) missense probably damaging 1.00
R1591:Csmd1 UTSW 8 15,900,710 (GRCm38) missense probably damaging 0.99
R1658:Csmd1 UTSW 8 16,081,725 (GRCm38) missense possibly damaging 0.69
R1678:Csmd1 UTSW 8 15,918,252 (GRCm38) missense possibly damaging 0.58
R1717:Csmd1 UTSW 8 17,216,692 (GRCm38) missense possibly damaging 0.58
R1735:Csmd1 UTSW 8 15,932,610 (GRCm38) missense probably damaging 0.99
R1750:Csmd1 UTSW 8 15,917,303 (GRCm38) missense probably damaging 0.99
R1753:Csmd1 UTSW 8 16,157,120 (GRCm38) nonsense probably null
R1822:Csmd1 UTSW 8 16,223,326 (GRCm38) missense probably damaging 1.00
R1875:Csmd1 UTSW 8 15,929,101 (GRCm38) missense probably damaging 0.99
R1909:Csmd1 UTSW 8 15,906,116 (GRCm38) missense probably damaging 1.00
R1912:Csmd1 UTSW 8 16,233,998 (GRCm38) critical splice donor site probably null
R1993:Csmd1 UTSW 8 16,346,684 (GRCm38) missense probably damaging 0.99
R2067:Csmd1 UTSW 8 15,900,782 (GRCm38) missense probably benign
R2094:Csmd1 UTSW 8 16,079,978 (GRCm38) missense probably damaging 0.99
R2119:Csmd1 UTSW 8 17,216,733 (GRCm38) missense probably damaging 0.98
R2127:Csmd1 UTSW 8 15,917,392 (GRCm38) missense probably damaging 1.00
R2138:Csmd1 UTSW 8 15,929,088 (GRCm38) missense probably damaging 0.96
R2216:Csmd1 UTSW 8 17,027,339 (GRCm38) critical splice acceptor site probably null
R2220:Csmd1 UTSW 8 15,992,641 (GRCm38) missense possibly damaging 0.94
R2380:Csmd1 UTSW 8 16,190,087 (GRCm38) missense probably damaging 1.00
R2471:Csmd1 UTSW 8 16,211,762 (GRCm38) missense probably damaging 1.00
R2984:Csmd1 UTSW 8 15,953,782 (GRCm38) missense probably damaging 1.00
R3001:Csmd1 UTSW 8 16,196,170 (GRCm38) missense probably damaging 0.98
R3002:Csmd1 UTSW 8 16,196,170 (GRCm38) missense probably damaging 0.98
R3003:Csmd1 UTSW 8 16,196,170 (GRCm38) missense probably damaging 0.98
R3103:Csmd1 UTSW 8 15,917,405 (GRCm38) missense probably damaging 1.00
R3104:Csmd1 UTSW 8 17,027,231 (GRCm38) missense probably damaging 1.00
R3620:Csmd1 UTSW 8 15,992,684 (GRCm38) missense probably benign 0.29
R3621:Csmd1 UTSW 8 15,992,684 (GRCm38) missense probably benign 0.29
R3748:Csmd1 UTSW 8 15,906,071 (GRCm38) missense probably damaging 0.99
R3780:Csmd1 UTSW 8 16,201,986 (GRCm38) missense probably damaging 1.00
R3815:Csmd1 UTSW 8 16,002,522 (GRCm38) missense probably damaging 1.00
R3816:Csmd1 UTSW 8 16,002,522 (GRCm38) missense probably damaging 1.00
R3818:Csmd1 UTSW 8 16,002,522 (GRCm38) missense probably damaging 1.00
R3819:Csmd1 UTSW 8 16,002,522 (GRCm38) missense probably damaging 1.00
R3850:Csmd1 UTSW 8 16,079,922 (GRCm38) missense probably benign 0.00
R3945:Csmd1 UTSW 8 15,910,619 (GRCm38) splice site probably null
R3980:Csmd1 UTSW 8 15,906,056 (GRCm38) nonsense probably null
R4061:Csmd1 UTSW 8 15,945,158 (GRCm38) missense probably benign 0.00
R4086:Csmd1 UTSW 8 15,992,738 (GRCm38) missense probably damaging 0.99
R4087:Csmd1 UTSW 8 15,992,738 (GRCm38) missense probably damaging 0.99
R4089:Csmd1 UTSW 8 15,992,738 (GRCm38) missense probably damaging 0.99
R4183:Csmd1 UTSW 8 15,910,464 (GRCm38) missense probably damaging 0.99
R4226:Csmd1 UTSW 8 16,000,490 (GRCm38) missense probably damaging 0.99
R4454:Csmd1 UTSW 8 15,945,011 (GRCm38) missense probably damaging 0.99
R4533:Csmd1 UTSW 8 15,931,037 (GRCm38) splice site probably null
R4544:Csmd1 UTSW 8 16,710,636 (GRCm38) missense possibly damaging 0.93
R4547:Csmd1 UTSW 8 16,391,797 (GRCm38) missense possibly damaging 0.48
R4612:Csmd1 UTSW 8 15,921,908 (GRCm38) splice site probably null
R4620:Csmd1 UTSW 8 16,002,694 (GRCm38) critical splice acceptor site probably null
R4627:Csmd1 UTSW 8 16,697,917 (GRCm38) missense probably benign 0.00
R4633:Csmd1 UTSW 8 16,002,620 (GRCm38) missense probably damaging 0.99
R4646:Csmd1 UTSW 8 15,932,511 (GRCm38) missense possibly damaging 0.87
R4648:Csmd1 UTSW 8 15,998,788 (GRCm38) nonsense probably null
R4668:Csmd1 UTSW 8 16,023,891 (GRCm38) missense possibly damaging 0.50
R4709:Csmd1 UTSW 8 16,710,506 (GRCm38) critical splice donor site probably null
R4709:Csmd1 UTSW 8 16,023,891 (GRCm38) missense possibly damaging 0.96
R4741:Csmd1 UTSW 8 15,910,447 (GRCm38) missense probably damaging 0.99
R4774:Csmd1 UTSW 8 16,009,369 (GRCm38) missense probably benign 0.11
R4793:Csmd1 UTSW 8 16,088,263 (GRCm38) missense probably damaging 1.00
R4829:Csmd1 UTSW 8 16,127,296 (GRCm38) missense probably damaging 1.00
R4888:Csmd1 UTSW 8 15,895,674 (GRCm38) utr 3 prime probably benign
R4896:Csmd1 UTSW 8 16,009,439 (GRCm38) missense probably benign 0.00
R4932:Csmd1 UTSW 8 16,023,765 (GRCm38) missense probably damaging 0.99
R4944:Csmd1 UTSW 8 15,998,772 (GRCm38) missense probably damaging 1.00
R4953:Csmd1 UTSW 8 16,199,917 (GRCm38) missense probably damaging 0.99
R4996:Csmd1 UTSW 8 15,910,452 (GRCm38) missense probably damaging 0.97
R5028:Csmd1 UTSW 8 15,989,090 (GRCm38) missense probably damaging 1.00
R5146:Csmd1 UTSW 8 16,196,190 (GRCm38) missense probably damaging 1.00
R5272:Csmd1 UTSW 8 16,199,944 (GRCm38) missense probably damaging 0.99
R5327:Csmd1 UTSW 8 17,216,712 (GRCm38) missense possibly damaging 0.94
R5399:Csmd1 UTSW 8 16,710,597 (GRCm38) missense probably damaging 1.00
R5411:Csmd1 UTSW 8 15,910,471 (GRCm38) missense probably damaging 1.00
R5462:Csmd1 UTSW 8 15,961,486 (GRCm38) missense probably benign 0.12
R5463:Csmd1 UTSW 8 15,984,860 (GRCm38) missense probably benign 0.34
R5497:Csmd1 UTSW 8 16,085,181 (GRCm38) missense probably benign 0.20
R5536:Csmd1 UTSW 8 16,288,660 (GRCm38) missense probably damaging 0.99
R5711:Csmd1 UTSW 8 15,953,703 (GRCm38) missense probably damaging 1.00
R5730:Csmd1 UTSW 8 16,185,192 (GRCm38) nonsense probably null
R5788:Csmd1 UTSW 8 16,201,966 (GRCm38) missense probably damaging 1.00
R5941:Csmd1 UTSW 8 15,932,471 (GRCm38) missense probably damaging 0.99
R5960:Csmd1 UTSW 8 16,071,416 (GRCm38) missense possibly damaging 0.68
R5961:Csmd1 UTSW 8 16,070,352 (GRCm38) missense probably damaging 0.99
R5969:Csmd1 UTSW 8 16,071,353 (GRCm38) missense probably benign 0.00
R5998:Csmd1 UTSW 8 15,910,443 (GRCm38) missense probably damaging 1.00
R6062:Csmd1 UTSW 8 16,092,305 (GRCm38) missense possibly damaging 0.68
R6109:Csmd1 UTSW 8 16,199,860 (GRCm38) missense possibly damaging 0.93
R6116:Csmd1 UTSW 8 16,211,850 (GRCm38) missense probably damaging 1.00
R6143:Csmd1 UTSW 8 16,088,301 (GRCm38) missense probably damaging 1.00
R6155:Csmd1 UTSW 8 15,903,231 (GRCm38) missense probably benign 0.01
R6197:Csmd1 UTSW 8 15,926,611 (GRCm38) missense probably benign 0.32
R6247:Csmd1 UTSW 8 16,196,235 (GRCm38) missense possibly damaging 0.91
R6304:Csmd1 UTSW 8 16,058,674 (GRCm38) missense probably damaging 1.00
R6317:Csmd1 UTSW 8 16,710,642 (GRCm38) missense possibly damaging 0.89
R6318:Csmd1 UTSW 8 15,903,212 (GRCm38) missense probably damaging 1.00
R6338:Csmd1 UTSW 8 15,932,492 (GRCm38) missense possibly damaging 0.75
R6369:Csmd1 UTSW 8 17,535,004 (GRCm38) start gained probably benign
R6447:Csmd1 UTSW 8 15,910,527 (GRCm38) missense probably damaging 1.00
R6454:Csmd1 UTSW 8 15,921,150 (GRCm38) missense probably damaging 0.99
R6494:Csmd1 UTSW 8 16,211,695 (GRCm38) splice site probably null
R6614:Csmd1 UTSW 8 17,216,787 (GRCm38) missense probably damaging 1.00
R6736:Csmd1 UTSW 8 16,002,626 (GRCm38) missense probably damaging 0.99
R6769:Csmd1 UTSW 8 16,071,394 (GRCm38) missense possibly damaging 0.80
R6771:Csmd1 UTSW 8 16,071,394 (GRCm38) missense possibly damaging 0.80
R6804:Csmd1 UTSW 8 16,037,246 (GRCm38) missense probably damaging 1.00
R6818:Csmd1 UTSW 8 16,185,327 (GRCm38) missense probably damaging 1.00
R6863:Csmd1 UTSW 8 17,534,913 (GRCm38) missense possibly damaging 0.85
R6930:Csmd1 UTSW 8 16,092,395 (GRCm38) missense probably damaging 0.97
R6969:Csmd1 UTSW 8 17,216,789 (GRCm38) missense possibly damaging 0.94
R7112:Csmd1 UTSW 8 16,101,128 (GRCm38) missense probably damaging 1.00
R7124:Csmd1 UTSW 8 15,903,202 (GRCm38) missense probably damaging 1.00
R7167:Csmd1 UTSW 8 15,926,524 (GRCm38) missense probably benign
R7243:Csmd1 UTSW 8 15,915,357 (GRCm38) missense probably damaging 1.00
R7260:Csmd1 UTSW 8 16,000,574 (GRCm38) missense probably damaging 1.00
R7271:Csmd1 UTSW 8 17,027,279 (GRCm38) missense probably damaging 0.99
R7324:Csmd1 UTSW 8 16,058,707 (GRCm38) missense probably damaging 1.00
R7325:Csmd1 UTSW 8 16,058,707 (GRCm38) missense probably damaging 1.00
R7327:Csmd1 UTSW 8 16,058,707 (GRCm38) missense probably damaging 1.00
R7373:Csmd1 UTSW 8 15,992,713 (GRCm38) missense probably damaging 1.00
R7406:Csmd1 UTSW 8 16,288,693 (GRCm38) missense probably damaging 0.99
R7427:Csmd1 UTSW 8 16,023,850 (GRCm38) missense possibly damaging 0.91
R7428:Csmd1 UTSW 8 16,023,850 (GRCm38) missense possibly damaging 0.91
R7445:Csmd1 UTSW 8 16,158,254 (GRCm38) missense possibly damaging 0.61
R7458:Csmd1 UTSW 8 15,953,738 (GRCm38) missense probably damaging 1.00
R7476:Csmd1 UTSW 8 15,895,731 (GRCm38) missense probably damaging 1.00
R7527:Csmd1 UTSW 8 16,211,718 (GRCm38) missense probably damaging 1.00
R7544:Csmd1 UTSW 8 16,092,296 (GRCm38) missense probably damaging 1.00
R7583:Csmd1 UTSW 8 15,998,833 (GRCm38) missense probably damaging 0.96
R7607:Csmd1 UTSW 8 15,918,331 (GRCm38) missense possibly damaging 0.94
R7642:Csmd1 UTSW 8 16,085,178 (GRCm38) missense probably damaging 0.99
R7669:Csmd1 UTSW 8 15,917,273 (GRCm38) missense probably damaging 1.00
R7720:Csmd1 UTSW 8 15,931,108 (GRCm38) missense probably damaging 1.00
R7728:Csmd1 UTSW 8 16,231,271 (GRCm38) missense probably damaging 1.00
R7738:Csmd1 UTSW 8 16,100,990 (GRCm38) missense probably damaging 1.00
R7745:Csmd1 UTSW 8 15,932,461 (GRCm38) critical splice donor site probably null
R7879:Csmd1 UTSW 8 16,391,806 (GRCm38) missense probably benign 0.28
R7884:Csmd1 UTSW 8 15,961,418 (GRCm38) missense probably damaging 1.00
R7897:Csmd1 UTSW 8 17,534,919 (GRCm38) missense possibly damaging 0.96
R8111:Csmd1 UTSW 8 15,917,306 (GRCm38) missense probably benign
R8119:Csmd1 UTSW 8 17,027,294 (GRCm38) missense probably damaging 0.99
R8134:Csmd1 UTSW 8 15,932,550 (GRCm38) missense probably damaging 0.99
R8187:Csmd1 UTSW 8 16,127,174 (GRCm38) missense probably damaging 0.99
R8196:Csmd1 UTSW 8 16,009,468 (GRCm38) missense probably benign 0.18
R8231:Csmd1 UTSW 8 16,697,923 (GRCm38) missense possibly damaging 0.82
R8242:Csmd1 UTSW 8 16,710,654 (GRCm38) missense probably benign 0.42
R8274:Csmd1 UTSW 8 15,910,453 (GRCm38) missense possibly damaging 0.93
R8286:Csmd1 UTSW 8 15,989,188 (GRCm38) missense probably benign 0.18
R8289:Csmd1 UTSW 8 16,058,702 (GRCm38) missense probably damaging 0.99
R8314:Csmd1 UTSW 8 16,158,244 (GRCm38) missense probably benign
R8323:Csmd1 UTSW 8 17,216,735 (GRCm38) nonsense probably null
R8387:Csmd1 UTSW 8 16,000,484 (GRCm38) missense possibly damaging 0.94
R8413:Csmd1 UTSW 8 15,900,676 (GRCm38) missense probably damaging 0.98
R8672:Csmd1 UTSW 8 15,926,598 (GRCm38) missense probably benign 0.01
R8765:Csmd1 UTSW 8 16,710,611 (GRCm38) nonsense probably null
R8789:Csmd1 UTSW 8 17,216,706 (GRCm38) missense probably damaging 0.99
R8828:Csmd1 UTSW 8 15,998,794 (GRCm38) missense probably benign 0.00
R8858:Csmd1 UTSW 8 16,070,304 (GRCm38) missense probably benign 0.10
R8878:Csmd1 UTSW 8 15,910,528 (GRCm38) missense probably damaging 1.00
R8911:Csmd1 UTSW 8 16,698,003 (GRCm38) missense probably damaging 0.99
R8966:Csmd1 UTSW 8 16,200,045 (GRCm38) missense probably damaging 1.00
R8978:Csmd1 UTSW 8 15,921,056 (GRCm38) missense probably benign 0.37
R8996:Csmd1 UTSW 8 15,921,105 (GRCm38) missense possibly damaging 0.54
R9045:Csmd1 UTSW 8 16,234,074 (GRCm38) missense probably damaging 0.99
R9084:Csmd1 UTSW 8 16,088,311 (GRCm38) missense probably benign
R9124:Csmd1 UTSW 8 15,984,806 (GRCm38) missense probably damaging 0.99
R9127:Csmd1 UTSW 8 16,223,272 (GRCm38) missense probably benign 0.31
R9146:Csmd1 UTSW 8 15,998,832 (GRCm38) missense probably benign 0.00
R9198:Csmd1 UTSW 8 15,912,430 (GRCm38) missense probably damaging 1.00
R9285:Csmd1 UTSW 8 15,906,088 (GRCm38) missense probably damaging 1.00
R9303:Csmd1 UTSW 8 15,961,532 (GRCm38) missense probably benign 0.31
R9305:Csmd1 UTSW 8 15,961,532 (GRCm38) missense probably benign 0.31
R9326:Csmd1 UTSW 8 15,999,803 (GRCm38) missense probably benign 0.21
R9356:Csmd1 UTSW 8 16,202,055 (GRCm38) missense probably damaging 1.00
R9385:Csmd1 UTSW 8 15,984,756 (GRCm38) missense probably benign 0.19
R9444:Csmd1 UTSW 8 16,158,236 (GRCm38) missense probably benign 0.30
R9476:Csmd1 UTSW 8 15,931,215 (GRCm38) critical splice acceptor site probably null
R9506:Csmd1 UTSW 8 16,200,009 (GRCm38) missense probably damaging 1.00
R9614:Csmd1 UTSW 8 16,158,225 (GRCm38) missense probably benign 0.00
R9668:Csmd1 UTSW 8 16,211,758 (GRCm38) missense probably benign 0.00
X0011:Csmd1 UTSW 8 16,196,263 (GRCm38) missense probably damaging 1.00
X0021:Csmd1 UTSW 8 16,185,256 (GRCm38) missense probably damaging 1.00
X0024:Csmd1 UTSW 8 16,037,218 (GRCm38) missense probably damaging 0.99
X0028:Csmd1 UTSW 8 15,915,333 (GRCm38) missense possibly damaging 0.79
Z1088:Csmd1 UTSW 8 16,189,978 (GRCm38) missense possibly damaging 0.50
Z1088:Csmd1 UTSW 8 16,092,258 (GRCm38) missense probably damaging 1.00
Z1088:Csmd1 UTSW 8 15,921,875 (GRCm38) missense possibly damaging 0.91
Z1088:Csmd1 UTSW 8 16,346,617 (GRCm38) missense probably damaging 0.99
Z1088:Csmd1 UTSW 8 16,200,058 (GRCm38) missense probably damaging 0.97
Z1176:Csmd1 UTSW 8 16,037,198 (GRCm38) missense probably damaging 1.00
Z1176:Csmd1 UTSW 8 15,998,814 (GRCm38) missense probably damaging 1.00
Z1177:Csmd1 UTSW 8 16,200,019 (GRCm38) missense probably damaging 1.00
Z1177:Csmd1 UTSW 8 15,984,708 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCAGTTAGTCCTCATGCAAATCAG -3'
(R):5'- TTCAACCAAACCTTGACTACTCATG -3'

Sequencing Primer
(F):5'- GTCCTCATGCAAATCAGAGTGGTC -3'
(R):5'- CTCATGTAGTGACTAGAAGCAGCTTG -3'
Posted On 2019-10-24