Incidental Mutation 'R3910:Cimip3'
ID 309355
Institutional Source Beutler Lab
Gene Symbol Cimip3
Ensembl Gene ENSMUSG00000047150
Gene Name ciliary microtubule inner protein 3
Synonyms 1700001C19Rik
MMRRC Submission 040815-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.048) question?
Stock # R3910 (G1)
Quality Score 217
Status Validated
Chromosome 17
Chromosomal Location 47723659-47748301 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) AC to A at 47744348 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000120133 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037701] [ENSMUST00000061885] [ENSMUST00000150819]
AlphaFold Q8K168
Predicted Effect probably benign
Transcript: ENSMUST00000037701
SMART Domains Protein: ENSMUSP00000045345
Gene: ENSMUSG00000034382

DomainStartEndE-ValueType
low complexity region 140 151 N/A INTRINSIC
low complexity region 157 180 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000061885
SMART Domains Protein: ENSMUSP00000050873
Gene: ENSMUSG00000047150

DomainStartEndE-ValueType
low complexity region 74 86 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000150819
SMART Domains Protein: ENSMUSP00000120133
Gene: ENSMUSG00000034382

DomainStartEndE-ValueType
low complexity region 140 151 N/A INTRINSIC
low complexity region 157 237 N/A INTRINSIC
low complexity region 294 312 N/A INTRINSIC
low complexity region 314 325 N/A INTRINSIC
low complexity region 354 364 N/A INTRINSIC
low complexity region 384 423 N/A INTRINSIC
low complexity region 429 444 N/A INTRINSIC
low complexity region 522 535 N/A INTRINSIC
low complexity region 612 627 N/A INTRINSIC
internal_repeat_1 628 654 6.24e-9 PROSPERO
low complexity region 656 671 N/A INTRINSIC
internal_repeat_1 688 714 6.24e-9 PROSPERO
low complexity region 853 863 N/A INTRINSIC
low complexity region 976 1016 N/A INTRINSIC
low complexity region 1147 1154 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160678
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 97% (36/37)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bod1l T C 5: 41,974,441 (GRCm39) E2291G probably damaging Het
Cchcr1 T C 17: 35,836,233 (GRCm39) V341A probably damaging Het
Dsg1c T C 18: 20,399,253 (GRCm39) V119A possibly damaging Het
Fap A G 2: 62,386,448 (GRCm39) S58P probably damaging Het
Flnc A T 6: 29,459,426 (GRCm39) T2509S probably damaging Het
Fnip2 A T 3: 79,386,812 (GRCm39) D971E possibly damaging Het
Gab2 A G 7: 96,948,280 (GRCm39) Y290C probably damaging Het
Gm7104 C T 12: 88,251,364 (GRCm39) noncoding transcript Het
Ints10 T A 8: 69,266,272 (GRCm39) S478T probably damaging Het
Iqca1l A T 5: 24,750,440 (GRCm39) probably benign Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Krt90 G A 15: 101,471,218 (GRCm39) R15W probably damaging Het
Lgr5 A G 10: 115,423,368 (GRCm39) S11P possibly damaging Het
Mycn T A 12: 12,987,281 (GRCm39) N372I probably damaging Het
Or2ag18 A T 7: 106,405,072 (GRCm39) V199D probably damaging Het
Or9a2 A G 6: 41,749,083 (GRCm39) V50A probably benign Het
Paxbp1 T A 16: 90,839,569 (GRCm39) E117V probably damaging Het
Phc2 T C 4: 128,637,351 (GRCm39) probably null Het
Prr5 T A 15: 84,587,345 (GRCm39) V365E probably benign Het
Rev3l A G 10: 39,696,552 (GRCm39) I521M probably damaging Het
Robo3 A T 9: 37,330,591 (GRCm39) Y1002N probably damaging Het
Svep1 A T 4: 58,145,156 (GRCm39) probably null Het
Thsd7a A G 6: 12,331,548 (GRCm39) V1342A probably damaging Het
Tmtc3 A C 10: 100,284,888 (GRCm39) N582K probably damaging Het
Tnfrsf11b G A 15: 54,119,578 (GRCm39) probably benign Het
Trim30a A G 7: 104,060,348 (GRCm39) V476A probably damaging Het
Ugt1a8 A G 1: 88,015,770 (GRCm39) E61G possibly damaging Het
Vmn1r75 A T 7: 11,614,757 (GRCm39) N163I possibly damaging Het
Vps35l A G 7: 118,345,613 (GRCm39) T49A possibly damaging Het
Zfp119a G A 17: 56,173,520 (GRCm39) L108F probably benign Het
Other mutations in Cimip3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0675:Cimip3 UTSW 17 47,724,701 (GRCm39) missense probably benign 0.25
R1529:Cimip3 UTSW 17 47,724,815 (GRCm39) missense probably benign 0.11
R2256:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R2257:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R2512:Cimip3 UTSW 17 47,724,651 (GRCm39) missense probably benign
R2883:Cimip3 UTSW 17 47,747,650 (GRCm39) missense probably damaging 0.99
R3498:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R3499:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R3834:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R3835:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R3901:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R3911:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R3913:Cimip3 UTSW 17 47,744,348 (GRCm39) unclassified probably benign
R4191:Cimip3 UTSW 17 47,747,562 (GRCm39) missense probably damaging 0.99
R4280:Cimip3 UTSW 17 47,724,780 (GRCm39) missense probably benign 0.02
R7054:Cimip3 UTSW 17 47,748,114 (GRCm39) critical splice donor site probably null
R8008:Cimip3 UTSW 17 47,747,661 (GRCm39) missense probably damaging 0.98
Z1176:Cimip3 UTSW 17 47,724,659 (GRCm39) missense probably benign 0.44
Predicted Primers PCR Primer
(F):5'- GGATTGTCTTTTAGAACAACCCTCC -3'
(R):5'- AGTTATCATGCAGTAGCCCC -3'

Sequencing Primer
(F):5'- ACTGTAGCTCCGTGTAGAACC -3'
(R):5'- GTAGCCCCCGTCCCTATTAAAATAG -3'
Posted On 2015-04-17