Incidental Mutation 'R6031:Ccdc125'
ID 482101
Institutional Source Beutler Lab
Gene Symbol Ccdc125
Ensembl Gene ENSMUSG00000048924
Gene Name coiled-coil domain containing 125
Synonyms 5830436D01Rik
MMRRC Submission 044203-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6031 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 100806225-100833748 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 100820877 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130107 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057325] [ENSMUST00000170347]
AlphaFold Q5U465
Predicted Effect probably null
Transcript: ENSMUST00000057325
SMART Domains Protein: ENSMUSP00000058484
Gene: ENSMUSG00000048924

DomainStartEndE-ValueType
coiled coil region 101 193 N/A INTRINSIC
coiled coil region 286 308 N/A INTRINSIC
Blast:ETS 362 447 1e-35 BLAST
Predicted Effect probably null
Transcript: ENSMUST00000170347
SMART Domains Protein: ENSMUSP00000130107
Gene: ENSMUSG00000048924

DomainStartEndE-ValueType
coiled coil region 101 151 N/A INTRINSIC
coiled coil region 260 282 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 96.7%
  • 20x: 88.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700010I14Rik T C 17: 9,214,084 (GRCm39) Y304H possibly damaging Het
Add2 A G 6: 86,075,655 (GRCm39) E268G probably damaging Het
Akr1b1 A C 6: 34,289,609 (GRCm39) V67G probably benign Het
Alms1 A T 6: 85,599,937 (GRCm39) N1588Y probably damaging Het
Arhgap23 A T 11: 97,366,965 (GRCm39) D1082V probably damaging Het
Asb6 A G 2: 30,714,207 (GRCm39) V301A probably benign Het
Ascc3 C T 10: 50,718,279 (GRCm39) R1991* probably null Het
Atg7 T A 6: 114,648,194 (GRCm39) C31S probably benign Het
Camsap2 A T 1: 136,208,176 (GRCm39) N1105K possibly damaging Het
Ccdc63 T C 5: 122,267,799 (GRCm39) I56V possibly damaging Het
Cpd T C 11: 76,681,714 (GRCm39) E1143G probably benign Het
Cpt1a T A 19: 3,421,556 (GRCm39) probably null Het
Creb3l2 A T 6: 37,311,369 (GRCm39) D473E probably benign Het
Crocc A T 4: 140,761,668 (GRCm39) probably null Het
Ctsd A T 7: 141,930,451 (GRCm39) C364S probably damaging Het
Disp2 G T 2: 118,620,275 (GRCm39) V336L probably benign Het
Efr3b A G 12: 4,017,106 (GRCm39) I782T possibly damaging Het
Fam98a A G 17: 75,846,427 (GRCm39) V230A probably damaging Het
Fat3 T A 9: 15,899,788 (GRCm39) T3082S probably benign Het
Frmd3 T C 4: 74,105,688 (GRCm39) Y445H probably damaging Het
Galt G A 4: 41,757,202 (GRCm39) R185Q probably benign Het
Gatb T C 3: 85,520,818 (GRCm39) I309T possibly damaging Het
Gfi1b G A 2: 28,503,820 (GRCm39) Q127* probably null Het
Gfpt1 C A 6: 87,063,302 (GRCm39) T563N probably damaging Het
Gria1 A G 11: 57,108,608 (GRCm39) D237G probably damaging Het
Hspbp1 A T 7: 4,666,465 (GRCm39) V305D probably benign Het
Hyls1 G A 9: 35,472,480 (GRCm39) S312F probably benign Het
Iars1 T C 13: 49,859,307 (GRCm39) V9A probably damaging Het
Ipo4 G A 14: 55,869,596 (GRCm39) P355S probably damaging Het
Jade2 G T 11: 51,717,413 (GRCm39) C314* probably null Het
Kri1 T C 9: 21,186,565 (GRCm39) E597G probably benign Het
Mcub A G 3: 129,720,038 (GRCm39) Y152H probably damaging Het
Med23 C T 10: 24,779,646 (GRCm39) R542* probably null Het
Ndc80 T C 17: 71,818,483 (GRCm39) N291S probably benign Het
Nop2 T C 6: 125,110,529 (GRCm39) probably null Het
Nrxn1 T C 17: 90,896,218 (GRCm39) N984S probably damaging Het
Ntm A C 9: 28,920,671 (GRCm39) L86R probably damaging Het
Numa1 T A 7: 101,661,219 (GRCm39) D1847E possibly damaging Het
Odf2l A G 3: 144,845,624 (GRCm39) Q334R probably damaging Het
Or10ak11 A T 4: 118,687,588 (GRCm39) probably null Het
Or2ag2 C T 7: 106,485,134 (GRCm39) V297I possibly damaging Het
Or4a39 T A 2: 89,237,316 (GRCm39) T36S probably damaging Het
Or5ac17 T C 16: 59,036,296 (GRCm39) R227G probably benign Het
Or6ae1 A T 7: 139,742,722 (GRCm39) V47E possibly damaging Het
Or6c203 A G 10: 129,010,224 (GRCm39) V222A probably benign Het
Pacc1 A G 1: 191,073,037 (GRCm39) R153G probably benign Het
Pcdhb19 A T 18: 37,630,776 (GRCm39) K190N probably damaging Het
Pdik1l A G 4: 134,006,352 (GRCm39) F197L probably damaging Het
Rnf113a2 T C 12: 84,464,764 (GRCm39) F219L probably damaging Het
Rnf208 A C 2: 25,133,776 (GRCm39) T157P probably damaging Het
Scn8a A T 15: 100,881,865 (GRCm39) D644V probably damaging Het
Thbs3 T A 3: 89,125,401 (GRCm39) C204S probably damaging Het
Tlr3 A G 8: 45,851,565 (GRCm39) I444T probably damaging Het
Trpm8 A T 1: 88,282,191 (GRCm39) I696F possibly damaging Het
Ttn A T 2: 76,660,941 (GRCm39) V7422D possibly damaging Het
Ufl1 A G 4: 25,278,038 (GRCm39) V139A probably benign Het
Uggt2 A T 14: 119,308,238 (GRCm39) V381D probably benign Het
Vgll3 T A 16: 65,636,367 (GRCm39) Y173N probably damaging Het
Vmn1r9 A G 6: 57,048,158 (GRCm39) T78A probably benign Het
Vps13b T A 15: 35,472,114 (GRCm39) L806M probably damaging Het
Vps13d A C 4: 144,895,079 (GRCm39) H394Q probably benign Het
Wdr53 T A 16: 32,075,536 (GRCm39) V247D probably damaging Het
Wdr81 A T 11: 75,338,695 (GRCm39) L1488Q probably damaging Het
Zc3h6 A G 2: 128,809,732 (GRCm39) D3G possibly damaging Het
Zfp93 G T 7: 23,975,725 (GRCm39) C570F probably damaging Het
Zfp943 C T 17: 22,212,357 (GRCm39) T481I probably benign Het
Other mutations in Ccdc125
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01888:Ccdc125 APN 13 100,823,610 (GRCm39) splice site probably benign
IGL02867:Ccdc125 APN 13 100,820,790 (GRCm39) splice site probably benign
R0002:Ccdc125 UTSW 13 100,830,114 (GRCm39) nonsense probably null
R0014:Ccdc125 UTSW 13 100,820,846 (GRCm39) missense possibly damaging 0.82
R0717:Ccdc125 UTSW 13 100,826,866 (GRCm39) missense probably damaging 0.99
R1661:Ccdc125 UTSW 13 100,830,081 (GRCm39) missense probably benign 0.37
R1665:Ccdc125 UTSW 13 100,830,081 (GRCm39) missense probably benign 0.37
R3118:Ccdc125 UTSW 13 100,826,827 (GRCm39) missense possibly damaging 0.46
R3751:Ccdc125 UTSW 13 100,814,459 (GRCm39) missense possibly damaging 0.90
R4415:Ccdc125 UTSW 13 100,832,817 (GRCm39) missense possibly damaging 0.83
R4838:Ccdc125 UTSW 13 100,814,453 (GRCm39) missense possibly damaging 0.52
R5734:Ccdc125 UTSW 13 100,823,622 (GRCm39) missense possibly damaging 0.66
R5812:Ccdc125 UTSW 13 100,820,812 (GRCm39) missense probably damaging 1.00
R6031:Ccdc125 UTSW 13 100,820,877 (GRCm39) splice site probably null
R6419:Ccdc125 UTSW 13 100,826,834 (GRCm39) missense probably damaging 1.00
R6456:Ccdc125 UTSW 13 100,832,817 (GRCm39) missense possibly damaging 0.83
R6733:Ccdc125 UTSW 13 100,830,995 (GRCm39) missense probably benign 0.04
R7183:Ccdc125 UTSW 13 100,826,866 (GRCm39) missense possibly damaging 0.90
R7354:Ccdc125 UTSW 13 100,814,382 (GRCm39) splice site probably null
R7644:Ccdc125 UTSW 13 100,814,884 (GRCm39) splice site probably null
R7910:Ccdc125 UTSW 13 100,819,327 (GRCm39) missense possibly damaging 0.83
R7948:Ccdc125 UTSW 13 100,832,910 (GRCm39) missense probably benign 0.00
R7973:Ccdc125 UTSW 13 100,806,331 (GRCm39) start gained probably benign
R8669:Ccdc125 UTSW 13 100,832,683 (GRCm39) missense probably damaging 0.97
R8695:Ccdc125 UTSW 13 100,814,552 (GRCm39) missense probably benign
R8736:Ccdc125 UTSW 13 100,815,833 (GRCm39) missense possibly damaging 0.83
R9297:Ccdc125 UTSW 13 100,832,920 (GRCm39) missense probably damaging 0.97
R9318:Ccdc125 UTSW 13 100,832,920 (GRCm39) missense probably damaging 0.97
R9424:Ccdc125 UTSW 13 100,820,876 (GRCm39) missense possibly damaging 0.90
R9513:Ccdc125 UTSW 13 100,826,875 (GRCm39) missense probably benign 0.15
X0027:Ccdc125 UTSW 13 100,818,353 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2017-06-27