Incidental Mutation 'R4183:Ccdc27'
ID 319813
Institutional Source Beutler Lab
Gene Symbol Ccdc27
Ensembl Gene ENSMUSG00000039492
Gene Name coiled-coil domain containing 27
Synonyms LOC381580
MMRRC Submission 041019-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # R4183 (G1)
Quality Score 148
Status Not validated
Chromosome 4
Chromosomal Location 154111096-154127134 bp(-) (GRCm39)
Type of Mutation small deletion (1 aa in frame mutation)
DNA Base Change (assembly) TTCCTCCTCCTCCTCCTCCTC to TTCCTCCTCCTCCTCCTC at 154120763 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000039642 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047207]
AlphaFold Q3V036
Predicted Effect probably benign
Transcript: ENSMUST00000047207
SMART Domains Protein: ENSMUSP00000039642
Gene: ENSMUSG00000039492

DomainStartEndE-ValueType
low complexity region 39 53 N/A INTRINSIC
coiled coil region 203 243 N/A INTRINSIC
low complexity region 305 320 N/A INTRINSIC
low complexity region 329 358 N/A INTRINSIC
coiled coil region 390 575 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd11 T C 8: 123,626,415 (GRCm39) I198V possibly damaging Het
Arhgap12 T C 18: 6,111,734 (GRCm39) D210G probably damaging Het
Arpc2 T A 1: 74,287,322 (GRCm39) N31K probably damaging Het
Atp11a T A 8: 12,866,990 (GRCm39) V139D possibly damaging Het
Bicral T C 17: 47,124,955 (GRCm39) K615E probably damaging Het
Chrnb1 T C 11: 69,677,922 (GRCm39) M277V possibly damaging Het
Csmd1 C T 8: 15,960,464 (GRCm39) C3317Y probably damaging Het
Ddx1 A T 12: 13,281,504 (GRCm39) L353* probably null Het
Degs2 T C 12: 108,658,358 (GRCm39) K207R probably damaging Het
Fam167a T C 14: 63,689,769 (GRCm39) V22A probably benign Het
Fam186a G A 15: 99,831,566 (GRCm39) probably benign Het
Gprc5b T C 7: 118,583,749 (GRCm39) D40G probably benign Het
Grsf1 G A 5: 88,812,015 (GRCm39) P271S probably benign Het
Inpp5j A G 11: 3,451,134 (GRCm39) I505T probably damaging Het
Lurap1l G A 4: 80,872,095 (GRCm39) S196N probably benign Het
Mapk8 T C 14: 33,104,177 (GRCm39) D413G probably damaging Het
Mapkbp1 A G 2: 119,848,346 (GRCm39) D632G probably damaging Het
Mcidas A G 13: 113,130,906 (GRCm39) D77G probably damaging Het
Mdga1 A G 17: 30,188,964 (GRCm39) V33A unknown Het
Me3 A G 7: 89,501,038 (GRCm39) D583G probably benign Het
Mndal T A 1: 173,703,337 (GRCm39) T23S possibly damaging Het
Myh13 T C 11: 67,240,436 (GRCm39) M780T possibly damaging Het
Nat10 A G 2: 103,570,158 (GRCm39) L395P probably damaging Het
Naxd T C 8: 11,552,757 (GRCm39) V59A probably damaging Het
Nbeal2 A T 9: 110,465,743 (GRCm39) V876E probably benign Het
Or11h4b C G 14: 50,918,507 (GRCm39) E195Q probably benign Het
Or1o2 T G 17: 37,542,739 (GRCm39) H174P possibly damaging Het
Or4a39 T C 2: 89,236,935 (GRCm39) T163A probably benign Het
Or51v8 T C 7: 103,320,178 (GRCm39) Y20C possibly damaging Het
Or8g50 A G 9: 39,648,344 (GRCm39) T78A probably benign Het
Pcdhgb8 G C 18: 37,896,594 (GRCm39) D555H probably damaging Het
Pcsk4 C T 10: 80,160,845 (GRCm39) R327Q probably benign Het
Pkhd1 C T 1: 20,188,031 (GRCm39) V3426I probably benign Het
Ranbp2 T C 10: 58,301,488 (GRCm39) F687L possibly damaging Het
Rb1 A G 14: 73,435,966 (GRCm39) probably null Het
Tfpi2 C A 6: 3,963,926 (GRCm39) V51L probably damaging Het
Tnn T C 1: 159,924,925 (GRCm39) D1143G probably damaging Het
Ttn A G 2: 76,541,586 (GRCm39) M25473T probably benign Het
Vmn1r201 A G 13: 22,659,022 (GRCm39) I79V probably benign Het
Vmn2r79 A G 7: 86,651,099 (GRCm39) H166R possibly damaging Het
Wdr25 T A 12: 108,993,257 (GRCm39) F491Y probably benign Het
Zfp972 G A 2: 177,563,250 (GRCm39) Q56* probably null Het
Zfp982 A G 4: 147,597,150 (GRCm39) K169R probably benign Het
Other mutations in Ccdc27
AlleleSourceChrCoordTypePredicted EffectPPH Score
PIT4466001:Ccdc27 UTSW 4 154,126,184 (GRCm39) missense unknown
PIT4472001:Ccdc27 UTSW 4 154,126,184 (GRCm39) missense unknown
R0078:Ccdc27 UTSW 4 154,120,195 (GRCm39) splice site probably benign
R0883:Ccdc27 UTSW 4 154,120,941 (GRCm39) missense unknown
R1389:Ccdc27 UTSW 4 154,126,226 (GRCm39) missense unknown
R1773:Ccdc27 UTSW 4 154,126,222 (GRCm39) missense unknown
R1869:Ccdc27 UTSW 4 154,111,220 (GRCm39) splice site probably null
R2020:Ccdc27 UTSW 4 154,117,770 (GRCm39) missense probably null 0.05
R2070:Ccdc27 UTSW 4 154,126,270 (GRCm39) missense unknown
R2131:Ccdc27 UTSW 4 154,120,763 (GRCm39) small deletion probably benign
R3825:Ccdc27 UTSW 4 154,120,742 (GRCm39) missense unknown
R4254:Ccdc27 UTSW 4 154,123,976 (GRCm39) missense unknown
R5932:Ccdc27 UTSW 4 154,111,231 (GRCm39) missense probably benign 0.22
R6269:Ccdc27 UTSW 4 154,122,179 (GRCm39) missense unknown
R6324:Ccdc27 UTSW 4 154,120,648 (GRCm39) missense probably benign 0.02
R6761:Ccdc27 UTSW 4 154,122,155 (GRCm39) missense unknown
R7090:Ccdc27 UTSW 4 154,112,523 (GRCm39) missense probably benign 0.03
R7163:Ccdc27 UTSW 4 154,117,282 (GRCm39) missense not run
R7488:Ccdc27 UTSW 4 154,117,424 (GRCm39) missense probably benign 0.22
R7555:Ccdc27 UTSW 4 154,126,274 (GRCm39) missense unknown
R7651:Ccdc27 UTSW 4 154,112,556 (GRCm39) missense probably damaging 1.00
R7826:Ccdc27 UTSW 4 154,123,958 (GRCm39) critical splice donor site probably null
R8250:Ccdc27 UTSW 4 154,126,245 (GRCm39) missense unknown
R8815:Ccdc27 UTSW 4 154,111,205 (GRCm39) missense probably benign 0.02
R8835:Ccdc27 UTSW 4 154,127,023 (GRCm39) missense unknown
R9019:Ccdc27 UTSW 4 154,124,014 (GRCm39) missense unknown
R9224:Ccdc27 UTSW 4 154,122,174 (GRCm39) missense unknown
R9252:Ccdc27 UTSW 4 154,125,507 (GRCm39) missense unknown
R9267:Ccdc27 UTSW 4 154,117,441 (GRCm39) missense probably damaging 1.00
RF016:Ccdc27 UTSW 4 154,120,567 (GRCm39) missense probably benign 0.04
Z1177:Ccdc27 UTSW 4 154,120,928 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ATACTCCTCCAGCTGAGCCATC -3'
(R):5'- ACGAACTGGGTTGCTTCCTAG -3'

Sequencing Primer
(F):5'- TCAGCTCCTCCTCAAAGGACTC -3'
(R):5'- AGAGTTGGTACCTCCCCC -3'
Posted On 2015-06-10