Incidental Mutation 'R6405:Ccdc110'
ID 516257
Institutional Source Beutler Lab
Gene Symbol Ccdc110
Ensembl Gene ENSMUSG00000071104
Gene Name coiled-coil domain containing 110
Synonyms LOC212392
MMRRC Submission 044550-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # R6405 (G1)
Quality Score 225.009
Status Not validated
Chromosome 8
Chromosomal Location 46387656-46397182 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 46394734 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 208 (Y208*)
Ref Sequence ENSEMBL: ENSMUSP00000092964 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095326] [ENSMUST00000174815]
AlphaFold Q3V125
Predicted Effect probably null
Transcript: ENSMUST00000095326
AA Change: Y208*
SMART Domains Protein: ENSMUSP00000092964
Gene: ENSMUSG00000071104
AA Change: Y208*

DomainStartEndE-ValueType
coiled coil region 442 794 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000174815
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930562C15Rik T C 16: 4,669,742 (GRCm39) V769A probably damaging Het
Abca4 A G 3: 121,967,311 (GRCm39) probably null Het
Ahnak2 A T 12: 112,739,771 (GRCm39) S628T probably damaging Het
Ano8 T C 8: 71,935,674 (GRCm39) T315A probably damaging Het
Arhgap32 T A 9: 32,159,784 (GRCm39) V267E probably benign Het
Asnsd1 A T 1: 53,387,154 (GRCm39) S158T probably damaging Het
Asxl2 T A 12: 3,543,758 (GRCm39) V309E probably damaging Het
Bhlhe40 TG TGG 6: 108,641,818 (GRCm39) 254 probably null Het
Cfap157 G T 2: 32,671,408 (GRCm39) Q133K probably damaging Het
Cfap53 A G 18: 74,492,677 (GRCm39) E467G probably damaging Het
Csmd3 T C 15: 47,683,767 (GRCm39) I1688M probably damaging Het
Cyp3a11 A T 5: 145,799,230 (GRCm39) L319Q probably damaging Het
Dchs2 A G 3: 83,261,570 (GRCm39) I2613V probably benign Het
Dhx35 T A 2: 158,636,839 (GRCm39) W11R probably damaging Het
Dscam C T 16: 96,479,625 (GRCm39) G1174D probably damaging Het
Fan1 T A 7: 64,022,234 (GRCm39) N340Y probably damaging Het
Fsip2 A G 2: 82,820,430 (GRCm39) T5388A possibly damaging Het
Gm10549 C A 18: 33,597,358 (GRCm39) probably benign Het
Greb1l T A 18: 10,501,076 (GRCm39) I402K probably benign Het
Hectd3 A T 4: 116,857,821 (GRCm39) M585L probably benign Het
Inpp5k T C 11: 75,524,004 (GRCm39) probably null Het
Lalba T G 15: 98,378,632 (GRCm39) probably null Het
Lgals9 C A 11: 78,862,211 (GRCm39) V125L probably benign Het
Ncbp2 CGTCTGGATG CG 16: 31,775,161 (GRCm39) probably null Het
Or2g25 A G 17: 37,971,014 (GRCm39) I70T possibly damaging Het
Peg10 C CTCG 6: 4,756,453 (GRCm39) probably benign Het
Rab4b T A 7: 26,872,379 (GRCm39) D94V probably damaging Het
Rhpn2 A G 7: 35,071,864 (GRCm39) E243G probably benign Het
Rp1 T C 1: 4,415,994 (GRCm39) D1706G probably damaging Het
Slc29a3 A T 10: 60,551,805 (GRCm39) I413N probably damaging Het
Slc7a9 T C 7: 35,154,064 (GRCm39) L229P probably damaging Het
Tenm2 T C 11: 36,755,686 (GRCm39) H104R probably benign Het
Tmem87a A G 2: 120,210,231 (GRCm39) Y241H probably damaging Het
Trpv5 G T 6: 41,651,602 (GRCm39) T192K probably damaging Het
Unc79 T C 12: 103,134,595 (GRCm39) V2189A probably damaging Het
Vmn2r106 A C 17: 20,499,361 (GRCm39) S183R probably benign Het
Vmn2r112 G T 17: 22,837,216 (GRCm39) C559F probably damaging Het
Wdhd1 T C 14: 47,481,324 (GRCm39) D1031G possibly damaging Het
Wnt5b T C 6: 119,410,457 (GRCm39) S328G probably benign Het
Zcchc7 T C 4: 44,926,032 (GRCm39) Y344H probably damaging Het
Other mutations in Ccdc110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01898:Ccdc110 APN 8 46,395,161 (GRCm39) missense possibly damaging 0.76
IGL02175:Ccdc110 APN 8 46,393,660 (GRCm39) missense probably benign 0.07
IGL02471:Ccdc110 APN 8 46,394,793 (GRCm39) missense probably benign 0.14
IGL02524:Ccdc110 APN 8 46,394,979 (GRCm39) missense probably benign
IGL02887:Ccdc110 APN 8 46,396,221 (GRCm39) missense probably benign 0.01
IGL03227:Ccdc110 APN 8 46,394,586 (GRCm39) missense probably damaging 1.00
IGL03238:Ccdc110 APN 8 46,394,859 (GRCm39) missense probably benign 0.00
droll UTSW 8 46,395,864 (GRCm39) missense probably benign 0.10
humorless UTSW 8 46,396,487 (GRCm39) missense probably benign 0.03
R0049:Ccdc110 UTSW 8 46,395,663 (GRCm39) missense probably damaging 1.00
R0049:Ccdc110 UTSW 8 46,395,663 (GRCm39) missense probably damaging 1.00
R0110:Ccdc110 UTSW 8 46,388,194 (GRCm39) missense probably benign 0.00
R0189:Ccdc110 UTSW 8 46,388,119 (GRCm39) missense probably damaging 0.98
R0218:Ccdc110 UTSW 8 46,387,761 (GRCm39) splice site probably benign
R0280:Ccdc110 UTSW 8 46,396,487 (GRCm39) missense probably benign 0.03
R0332:Ccdc110 UTSW 8 46,396,001 (GRCm39) nonsense probably null
R0371:Ccdc110 UTSW 8 46,395,843 (GRCm39) missense possibly damaging 0.86
R0469:Ccdc110 UTSW 8 46,388,194 (GRCm39) missense probably benign 0.00
R0502:Ccdc110 UTSW 8 46,387,761 (GRCm39) splice site probably benign
R0510:Ccdc110 UTSW 8 46,388,194 (GRCm39) missense probably benign 0.00
R0534:Ccdc110 UTSW 8 46,388,175 (GRCm39) missense possibly damaging 0.73
R0647:Ccdc110 UTSW 8 46,396,425 (GRCm39) missense probably damaging 0.99
R0714:Ccdc110 UTSW 8 46,396,047 (GRCm39) missense possibly damaging 0.71
R0721:Ccdc110 UTSW 8 46,395,026 (GRCm39) missense probably benign
R1029:Ccdc110 UTSW 8 46,394,817 (GRCm39) missense probably damaging 0.98
R1147:Ccdc110 UTSW 8 46,397,121 (GRCm39) missense possibly damaging 0.64
R1147:Ccdc110 UTSW 8 46,397,121 (GRCm39) missense possibly damaging 0.64
R1170:Ccdc110 UTSW 8 46,394,922 (GRCm39) missense probably benign 0.22
R1340:Ccdc110 UTSW 8 46,395,218 (GRCm39) missense probably benign 0.02
R1540:Ccdc110 UTSW 8 46,395,362 (GRCm39) nonsense probably null
R1587:Ccdc110 UTSW 8 46,394,783 (GRCm39) missense probably benign 0.01
R1602:Ccdc110 UTSW 8 46,391,955 (GRCm39) missense probably benign 0.12
R1629:Ccdc110 UTSW 8 46,395,164 (GRCm39) missense probably benign 0.08
R1842:Ccdc110 UTSW 8 46,393,605 (GRCm39) missense probably damaging 1.00
R1933:Ccdc110 UTSW 8 46,396,287 (GRCm39) missense probably damaging 1.00
R1934:Ccdc110 UTSW 8 46,396,287 (GRCm39) missense probably damaging 1.00
R2006:Ccdc110 UTSW 8 46,396,349 (GRCm39) missense probably damaging 1.00
R2043:Ccdc110 UTSW 8 46,395,864 (GRCm39) missense probably benign 0.10
R2093:Ccdc110 UTSW 8 46,395,114 (GRCm39) missense probably damaging 1.00
R2165:Ccdc110 UTSW 8 46,395,876 (GRCm39) missense probably benign 0.00
R3613:Ccdc110 UTSW 8 46,395,843 (GRCm39) missense possibly damaging 0.86
R3923:Ccdc110 UTSW 8 46,395,426 (GRCm39) missense probably damaging 1.00
R4648:Ccdc110 UTSW 8 46,395,705 (GRCm39) missense possibly damaging 0.95
R4773:Ccdc110 UTSW 8 46,396,245 (GRCm39) missense probably damaging 1.00
R4901:Ccdc110 UTSW 8 46,396,437 (GRCm39) missense probably benign 0.35
R4911:Ccdc110 UTSW 8 46,395,944 (GRCm39) missense probably benign 0.00
R4923:Ccdc110 UTSW 8 46,396,460 (GRCm39) missense probably benign 0.29
R5104:Ccdc110 UTSW 8 46,395,729 (GRCm39) missense probably damaging 0.99
R5561:Ccdc110 UTSW 8 46,393,646 (GRCm39) missense probably benign 0.02
R5966:Ccdc110 UTSW 8 46,395,573 (GRCm39) missense probably damaging 1.00
R5976:Ccdc110 UTSW 8 46,396,536 (GRCm39) missense possibly damaging 0.71
R6141:Ccdc110 UTSW 8 46,394,807 (GRCm39) missense possibly damaging 0.89
R6326:Ccdc110 UTSW 8 46,395,078 (GRCm39) missense probably damaging 1.00
R6366:Ccdc110 UTSW 8 46,396,425 (GRCm39) missense probably damaging 0.99
R6482:Ccdc110 UTSW 8 46,395,825 (GRCm39) missense probably benign 0.00
R6815:Ccdc110 UTSW 8 46,395,024 (GRCm39) missense probably benign 0.19
R7387:Ccdc110 UTSW 8 46,395,233 (GRCm39) missense probably benign 0.00
R7680:Ccdc110 UTSW 8 46,394,688 (GRCm39) missense possibly damaging 0.64
R8099:Ccdc110 UTSW 8 46,395,130 (GRCm39) missense probably damaging 1.00
R8114:Ccdc110 UTSW 8 46,396,140 (GRCm39) missense probably damaging 1.00
R8151:Ccdc110 UTSW 8 46,395,830 (GRCm39) missense probably damaging 1.00
R8295:Ccdc110 UTSW 8 46,396,416 (GRCm39) missense probably damaging 0.97
R8532:Ccdc110 UTSW 8 46,396,032 (GRCm39) missense probably damaging 1.00
R9072:Ccdc110 UTSW 8 46,395,875 (GRCm39) missense probably benign 0.00
R9073:Ccdc110 UTSW 8 46,395,875 (GRCm39) missense probably benign 0.00
R9088:Ccdc110 UTSW 8 46,394,882 (GRCm39) missense probably damaging 0.99
R9803:Ccdc110 UTSW 8 46,395,626 (GRCm39) missense probably benign
X0053:Ccdc110 UTSW 8 46,395,998 (GRCm39) missense possibly damaging 0.56
X0054:Ccdc110 UTSW 8 46,394,880 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCAGTAGTAACAGTGACACTGGTC -3'
(R):5'- ACCTTGAGTACTCGCGTCTG -3'

Sequencing Primer
(F):5'- AGTGACACTGGTCTCCCTCAG -3'
(R):5'- ACTTGTGAGTGCCAGCTC -3'
Posted On 2018-05-04