Incidental Mutation 'R6886:Ccdc181'
ID 536930
Institutional Source Beutler Lab
Gene Symbol Ccdc181
Ensembl Gene ENSMUSG00000026578
Gene Name coiled-coil domain containing 181
Synonyms 4930455F23Rik
MMRRC Submission 044980-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6886 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 164103154-164115416 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 164107665 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 116 (E116G)
Ref Sequence ENSEMBL: ENSMUSP00000027867 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000027867]
AlphaFold Q80ZU5
Predicted Effect probably damaging
Transcript: ENSMUST00000027867
AA Change: E116G

PolyPhen 2 Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000027867
Gene: ENSMUSG00000026578
AA Change: E116G

DomainStartEndE-ValueType
low complexity region 116 122 N/A INTRINSIC
coiled coil region 334 378 N/A INTRINSIC
low complexity region 474 485 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp7b A T 8: 22,518,706 (GRCm39) M44K probably benign Het
Bad T C 19: 6,928,702 (GRCm39) probably benign Het
Bbs12 A G 3: 37,373,390 (GRCm39) D61G probably damaging Het
Bcr C T 10: 74,989,769 (GRCm39) R722C probably damaging Het
Carf C A 1: 60,175,413 (GRCm39) probably null Het
Celsr1 A G 15: 85,915,855 (GRCm39) V706A probably benign Het
Col9a1 T A 1: 24,224,426 (GRCm39) S203T unknown Het
Ctsl T C 13: 64,512,961 (GRCm39) probably null Het
Exosc7 A T 9: 122,965,023 (GRCm39) E277D probably benign Het
Fam20b A T 1: 156,518,081 (GRCm39) W238R probably damaging Het
Fanci A T 7: 79,070,090 (GRCm39) H430L possibly damaging Het
Fstl4 A G 11: 53,077,277 (GRCm39) D678G probably damaging Het
Gm10801 TC TCGGC 2: 98,494,151 (GRCm39) probably benign Het
Gm11569 T A 11: 99,689,247 (GRCm39) probably benign Het
Igfn1 G A 1: 135,901,198 (GRCm39) R306W probably damaging Het
Il6 C T 5: 30,223,201 (GRCm39) probably benign Het
Khdc1c T C 1: 21,439,749 (GRCm39) L100P possibly damaging Het
Kif18a G A 2: 109,127,008 (GRCm39) R314H probably damaging Het
Kif26b A C 1: 178,701,703 (GRCm39) K694T probably damaging Het
Kndc1 A G 7: 139,493,485 (GRCm39) T484A probably benign Het
Lonrf1 T C 8: 36,696,191 (GRCm39) probably null Het
Man1a2 C T 3: 100,563,387 (GRCm39) G169D probably benign Het
Med6 G T 12: 81,638,159 (GRCm39) D17E probably damaging Het
Neb T C 2: 52,110,236 (GRCm39) K204R probably damaging Het
Nhlrc1 T A 13: 47,167,252 (GRCm39) N335I possibly damaging Het
Nlrp12 T C 7: 3,289,313 (GRCm39) M400V probably benign Het
Or7e173 G T 9: 19,938,428 (GRCm39) H269N probably benign Het
Or8k22 A T 2: 86,163,408 (GRCm39) C97* probably null Het
Pkhd1 C T 1: 20,417,504 (GRCm39) S2549N probably benign Het
Pramel26 A G 4: 143,539,332 (GRCm39) F54L probably benign Het
Rab4b A C 7: 26,872,381 (GRCm39) L145R probably damaging Het
Rad50 T C 11: 53,577,011 (GRCm39) I526V probably benign Het
Rel T C 11: 23,694,304 (GRCm39) H309R probably benign Het
Rnf2 G T 1: 151,349,017 (GRCm39) N34K possibly damaging Het
Serpina3m G T 12: 104,355,386 (GRCm39) V18F possibly damaging Het
Serpinb9c T C 13: 33,334,310 (GRCm39) K244R probably benign Het
Setbp1 T A 18: 78,900,715 (GRCm39) Y984F probably damaging Het
Slc12a5 T A 2: 164,824,825 (GRCm39) M410K probably benign Het
Smarca4 C T 9: 21,570,127 (GRCm39) A710V probably damaging Het
Snx19 C A 9: 30,340,231 (GRCm39) D456E probably damaging Het
Ssrp1 T A 2: 84,870,280 (GRCm39) D101E probably benign Het
Tax1bp1 A T 6: 52,710,208 (GRCm39) E162D probably benign Het
Tenm4 T A 7: 96,446,599 (GRCm39) M823K possibly damaging Het
Tesk1 A G 4: 43,443,592 (GRCm39) D53G possibly damaging Het
Tnrc6a T A 7: 122,786,668 (GRCm39) S1577T probably benign Het
Tpr A G 1: 150,299,716 (GRCm39) I1270V probably benign Het
Trp53bp2 T C 1: 182,256,608 (GRCm39) probably null Het
Ube4a A T 9: 44,860,141 (GRCm39) I307N probably damaging Het
Unc13b A G 4: 43,170,156 (GRCm39) probably benign Het
Vmn2r3 T C 3: 64,166,927 (GRCm39) K735E probably damaging Het
Vmn2r54 A G 7: 12,366,080 (GRCm39) F285L probably benign Het
Vmn2r81 T G 10: 79,103,988 (GRCm39) S204A possibly damaging Het
Washc1 A G 17: 66,426,061 (GRCm39) D453G probably damaging Het
Zfp329 T A 7: 12,544,025 (GRCm39) I500L probably benign Het
Zfp516 A G 18: 82,975,125 (GRCm39) D441G probably benign Het
Zfp644 T C 5: 106,785,777 (GRCm39) T257A possibly damaging Het
Other mutations in Ccdc181
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01631:Ccdc181 APN 1 164,107,713 (GRCm39) missense possibly damaging 0.75
IGL02634:Ccdc181 APN 1 164,107,514 (GRCm39) missense probably benign 0.00
IGL02902:Ccdc181 APN 1 164,107,470 (GRCm39) missense probably benign
IGL03201:Ccdc181 APN 1 164,108,213 (GRCm39) missense probably benign 0.13
R1228:Ccdc181 UTSW 1 164,113,960 (GRCm39) nonsense probably null
R1371:Ccdc181 UTSW 1 164,108,172 (GRCm39) missense probably benign 0.34
R1819:Ccdc181 UTSW 1 164,110,047 (GRCm39) nonsense probably null
R2240:Ccdc181 UTSW 1 164,107,596 (GRCm39) missense probably damaging 1.00
R3160:Ccdc181 UTSW 1 164,107,865 (GRCm39) missense probably damaging 0.97
R3162:Ccdc181 UTSW 1 164,107,865 (GRCm39) missense probably damaging 0.97
R4678:Ccdc181 UTSW 1 164,105,846 (GRCm39) missense probably damaging 1.00
R5286:Ccdc181 UTSW 1 164,105,810 (GRCm39) missense probably damaging 1.00
R6179:Ccdc181 UTSW 1 164,107,487 (GRCm39) missense probably benign 0.21
R7517:Ccdc181 UTSW 1 164,107,989 (GRCm39) missense probably damaging 1.00
R7528:Ccdc181 UTSW 1 164,107,527 (GRCm39) missense probably benign
R9012:Ccdc181 UTSW 1 164,110,062 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CAGAACTTGGCCAACAGCTC -3'
(R):5'- GTCACCAGAAATACATAACTGGGAC -3'

Sequencing Primer
(F):5'- GGCCAACAGCTCTCTGATC -3'
(R):5'- GGACAGTTTCCCAGACATATTGGTC -3'
Posted On 2018-10-18