Incidental Mutation 'R2876:Ccdc152'
ID260572
Institutional Source Beutler Lab
Gene Symbol Ccdc152
Ensembl Gene ENSMUSG00000091119
Gene Namecoiled-coil domain containing 152
SynonymsENSMUSG00000071814
MMRRC Submission 040464-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.115) question?
Stock #R2876 (G1)
Quality Score225
Status Validated
Chromosome15
Chromosomal Location3280070-3303526 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 3298181 bp
ZygosityHeterozygous
Amino Acid Change Asparagine to Serine at position 38 (N38S)
Ref Sequence ENSEMBL: ENSMUSP00000153730 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165386] [ENSMUST00000226261] [ENSMUST00000228405]
Predicted Effect probably damaging
Transcript: ENSMUST00000165386
AA Change: N38S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129305
Gene: ENSMUSG00000091119
AA Change: N38S

DomainStartEndE-ValueType
coiled coil region 76 186 N/A INTRINSIC
coiled coil region 211 250 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000226261
AA Change: N38S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000228405
AA Change: N38S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Meta Mutation Damage Score 0.0784 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 95% (42/44)
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730507C01Rik C A 12: 18,533,643 Q235K possibly damaging Het
Abcc1 A T 16: 14,457,960 H906L probably benign Het
Acot6 T G 12: 84,101,262 D97E possibly damaging Het
Acvr2a T A 2: 48,892,178 M241K probably damaging Het
Adamts9 T C 6: 92,795,910 probably benign Het
Adgb T G 10: 10,422,719 T422P probably damaging Het
Adrm1 A G 2: 180,175,618 T293A probably damaging Het
Ankfn1 A G 11: 89,391,636 V395A possibly damaging Het
Atp2b1 A G 10: 98,999,745 M451V probably damaging Het
Cdh23 A T 10: 60,307,496 N3017K probably damaging Het
Cenpf A G 1: 189,658,644 M997T probably benign Het
Gcc2 A G 10: 58,290,302 E1344G probably damaging Het
Gen1 A C 12: 11,242,068 S573R probably benign Het
Gm38394 C T 1: 133,656,860 C913Y probably damaging Het
Ilvbl C A 10: 78,583,056 Q410K probably benign Het
Ints11 C A 4: 155,887,425 probably benign Het
Itfg1 T C 8: 85,780,510 probably benign Het
Lrrc27 C T 7: 139,228,684 probably benign Het
Maml3 G A 3: 51,690,059 A422V possibly damaging Het
Masp2 T A 4: 148,608,001 I317K probably benign Het
Olfr154 A G 2: 85,663,690 V248A probably damaging Het
Olfr700 C G 7: 106,805,997 S155T probably benign Het
Olfr702 A T 7: 106,824,457 V23E probably benign Het
Papln T A 12: 83,778,927 S661T probably damaging Het
Pi4ka A G 16: 17,367,550 S229P possibly damaging Het
Piezo2 A G 18: 63,053,035 S1688P probably damaging Het
Pzp T C 6: 128,491,550 T1005A probably damaging Het
Rad1 T C 15: 10,490,331 V128A probably benign Het
Rhbdd1 A G 1: 82,368,369 D215G probably benign Het
Rnft2 G A 5: 118,193,621 R417C probably damaging Het
Scn2a A C 2: 65,715,897 I935L possibly damaging Het
Sdc4 T C 2: 164,431,291 D33G possibly damaging Het
Slco1c1 T C 6: 141,559,856 S454P probably damaging Het
Spidr A T 16: 15,912,589 probably null Het
Srp72 T A 5: 76,995,920 probably benign Het
Ttll4 A G 1: 74,686,438 probably null Het
Ttn C T 2: 76,920,340 S3455N probably damaging Het
Vcan T A 13: 89,704,237 E868V probably damaging Het
Vmn2r89 G T 14: 51,455,084 G115C possibly damaging Het
Zscan29 T C 2: 121,164,100 Y468C probably damaging Het
Other mutations in Ccdc152
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01466:Ccdc152 APN 15 3293847 splice site probably benign
IGL01543:Ccdc152 APN 15 3298124 missense possibly damaging 0.91
R0622:Ccdc152 UTSW 15 3298178 missense probably damaging 0.96
R1605:Ccdc152 UTSW 15 3298121 missense probably damaging 0.99
R2875:Ccdc152 UTSW 15 3298181 missense probably damaging 1.00
R4990:Ccdc152 UTSW 15 3301157 missense probably benign 0.00
R5114:Ccdc152 UTSW 15 3282837 missense probably damaging 0.99
R5732:Ccdc152 UTSW 15 3292378 critical splice donor site probably null
R6336:Ccdc152 UTSW 15 3301129 missense probably damaging 1.00
R6704:Ccdc152 UTSW 15 3280713 missense probably damaging 1.00
R7593:Ccdc152 UTSW 15 3280655 missense probably damaging 1.00
R8300:Ccdc152 UTSW 15 3298152 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGCTATGAGACAACACTCTGG -3'
(R):5'- TTGAAGGCTCAATACAGTACGG -3'

Sequencing Primer
(F):5'- CACTCTGGAACATTCTATATGCACG -3'
(R):5'- GGCTCAATACAGTACGGTTTATTTG -3'
Posted On2015-01-23