Incidental Mutation 'R0399:Cep68'
ID 38072
Institutional Source Beutler Lab
Gene Symbol Cep68
Ensembl Gene ENSMUSG00000044066
Gene Name centrosomal protein 68
Synonyms 6030463E10Rik
MMRRC Submission 038604-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.140) question?
Stock # R0399 (G1)
Quality Score 194
Status Validated
Chromosome 11
Chromosomal Location 20177037-20199424 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 20180571 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 687 (I687L)
Ref Sequence ENSEMBL: ENSMUSP00000054943 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020358] [ENSMUST00000050611] [ENSMUST00000109602] [ENSMUST00000163483]
AlphaFold Q8C0D9
Predicted Effect probably benign
Transcript: ENSMUST00000020358
SMART Domains Protein: ENSMUSP00000020358
Gene: ENSMUSG00000020149

DomainStartEndE-ValueType
RAB 9 172 2.9e-107 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000050611
AA Change: I687L

PolyPhen 2 Score 0.102 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000054943
Gene: ENSMUSG00000044066
AA Change: I687L

DomainStartEndE-ValueType
low complexity region 178 190 N/A INTRINSIC
low complexity region 311 325 N/A INTRINSIC
SPEC 605 706 1.28e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000109602
SMART Domains Protein: ENSMUSP00000105231
Gene: ENSMUSG00000020149

DomainStartEndE-ValueType
Pfam:Ras 10 31 7.6e-6 PFAM
Pfam:Ras 29 107 8e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000163483
SMART Domains Protein: ENSMUSP00000127330
Gene: ENSMUSG00000020149

DomainStartEndE-ValueType
RAB 12 175 2.9e-107 SMART
Meta Mutation Damage Score 0.1804 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.4%
Validation Efficiency 99% (71/72)
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6030452D12Rik T C 8: 107,231,174 (GRCm39) M120T unknown Het
Actr1a A T 19: 46,373,450 (GRCm39) probably null Het
Anapc5 A T 5: 122,929,816 (GRCm39) V555D probably damaging Het
Aox1 A G 1: 58,108,008 (GRCm39) probably null Het
Arhgap30 A G 1: 171,232,384 (GRCm39) E343G probably damaging Het
Asap2 C T 12: 21,267,998 (GRCm39) T291I possibly damaging Het
Atp5f1a T A 18: 77,869,536 (GRCm39) Y439* probably null Het
Auts2 A T 5: 131,469,362 (GRCm39) S428T probably benign Het
B3gnt7 T A 1: 86,233,433 (GRCm39) C109* probably null Het
C4b C A 17: 34,947,843 (GRCm39) Q1657H probably damaging Het
Cadm2 A T 16: 66,544,225 (GRCm39) L268* probably null Het
Cep290 G A 10: 100,390,262 (GRCm39) probably benign Het
Chd6 T A 2: 160,894,608 (GRCm39) D84V probably damaging Het
Clpx A G 9: 65,230,051 (GRCm39) T514A probably benign Het
Cox18 A T 5: 90,362,887 (GRCm39) C324S probably benign Het
Cryzl2 T C 1: 157,289,586 (GRCm39) Y75H probably damaging Het
Cxcr6 C T 9: 123,640,016 (GRCm39) A339V possibly damaging Het
Dock1 T C 7: 134,765,171 (GRCm39) L1721P probably benign Het
Dstyk T C 1: 132,380,818 (GRCm39) probably benign Het
Ecpas T C 4: 58,827,047 (GRCm39) T1029A possibly damaging Het
Ehf A G 2: 103,097,215 (GRCm39) Y246H probably damaging Het
Epas1 T C 17: 87,112,621 (GRCm39) V73A probably benign Het
Filip1 A G 9: 79,725,592 (GRCm39) I1009T possibly damaging Het
Glis3 A T 19: 28,276,168 (GRCm39) probably benign Het
Gm17333 A T 16: 77,649,678 (GRCm39) noncoding transcript Het
Gpc1 G A 1: 92,785,031 (GRCm39) R358H possibly damaging Het
Gpr155 A T 2: 73,200,346 (GRCm39) I387N possibly damaging Het
Gria1 A G 11: 57,076,853 (GRCm39) D83G probably damaging Het
Grid2 A G 6: 64,643,036 (GRCm39) I933V probably benign Het
Hhatl C T 9: 121,617,828 (GRCm39) A254T probably benign Het
Hook2 A G 8: 85,720,196 (GRCm39) probably benign Het
Ift140 T A 17: 25,269,314 (GRCm39) S656R possibly damaging Het
Il11ra1 A T 4: 41,766,185 (GRCm39) T241S probably benign Het
Kank1 A G 19: 25,388,606 (GRCm39) I760V probably benign Het
Kansl1 T C 11: 104,314,958 (GRCm39) E360G possibly damaging Het
Klf9 A T 19: 23,119,446 (GRCm39) S110C probably damaging Het
Klhl31 A G 9: 77,557,935 (GRCm39) N217S probably benign Het
Lct T C 1: 128,228,262 (GRCm39) Y1077C probably damaging Het
Lrrc49 A T 9: 60,517,529 (GRCm39) probably benign Het
Lrrn1 T A 6: 107,546,081 (GRCm39) H626Q probably benign Het
Mmp28 A T 11: 83,342,558 (GRCm39) L40Q probably damaging Het
Mroh1 C T 15: 76,336,299 (GRCm39) A1530V probably benign Het
Myo1e A G 9: 70,209,075 (GRCm39) probably benign Het
Naa25 A T 5: 121,573,553 (GRCm39) M761L probably benign Het
Ncln G A 10: 81,324,131 (GRCm39) A465V probably damaging Het
Nktr A G 9: 121,560,550 (GRCm39) N98S probably damaging Het
Or52h9 T A 7: 104,202,576 (GRCm39) V150E probably benign Het
Or5a1 G C 19: 12,097,734 (GRCm39) A114G possibly damaging Het
Or6d15 C A 6: 116,559,742 (GRCm39) S55I probably benign Het
Or8b4 G T 9: 37,830,849 (GRCm39) A304S possibly damaging Het
Or9g3 T C 2: 85,590,248 (GRCm39) I157M possibly damaging Het
Pacsin2 T C 15: 83,270,983 (GRCm39) Y222C probably damaging Het
Pcdhb15 C T 18: 37,607,221 (GRCm39) T151M possibly damaging Het
Plcz1 C A 6: 139,968,956 (GRCm39) V161L possibly damaging Het
Ppp6c G A 2: 39,090,136 (GRCm39) probably benign Het
Relch A G 1: 105,678,684 (GRCm39) probably benign Het
Rhbdf2 T A 11: 116,494,818 (GRCm39) Y286F probably benign Het
Rtn3 A T 19: 7,435,241 (GRCm39) D231E probably damaging Het
Slc35c2 A C 2: 165,122,815 (GRCm39) Y156* probably null Het
Spata46 A G 1: 170,139,106 (GRCm39) D35G probably damaging Het
Tmed3 A G 9: 89,584,926 (GRCm39) F110L possibly damaging Het
Tmem104 T G 11: 115,092,134 (GRCm39) probably benign Het
Tpbg T A 9: 85,726,991 (GRCm39) V320E possibly damaging Het
Trib2 T C 12: 15,843,664 (GRCm39) D190G probably damaging Het
Tspan2 A G 3: 102,666,701 (GRCm39) T26A probably damaging Het
Usp17lb A C 7: 104,490,358 (GRCm39) Y190D possibly damaging Het
Utp18 C T 11: 93,770,973 (GRCm39) probably benign Het
Utp20 A T 10: 88,656,841 (GRCm39) D121E probably damaging Het
Vmn1r80 T A 7: 11,927,244 (GRCm39) M118K possibly damaging Het
Vmn1r84 T C 7: 12,095,794 (GRCm39) S300G probably benign Het
Other mutations in Cep68
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01617:Cep68 APN 11 20,189,510 (GRCm39) missense probably benign 0.14
IGL02404:Cep68 APN 11 20,190,004 (GRCm39) missense possibly damaging 0.89
IGL02441:Cep68 APN 11 20,189,186 (GRCm39) missense probably benign 0.01
IGL02554:Cep68 APN 11 20,190,096 (GRCm39) missense possibly damaging 0.61
IGL02732:Cep68 APN 11 20,186,109 (GRCm39) unclassified probably benign
PIT4366001:Cep68 UTSW 11 20,190,007 (GRCm39) missense probably benign 0.21
PIT4418001:Cep68 UTSW 11 20,189,731 (GRCm39) missense probably benign
R0792:Cep68 UTSW 11 20,190,652 (GRCm39) missense possibly damaging 0.76
R0882:Cep68 UTSW 11 20,189,393 (GRCm39) missense probably benign
R1163:Cep68 UTSW 11 20,190,539 (GRCm39) missense probably damaging 0.99
R1869:Cep68 UTSW 11 20,190,217 (GRCm39) missense probably damaging 1.00
R2023:Cep68 UTSW 11 20,189,888 (GRCm39) missense probably benign
R2901:Cep68 UTSW 11 20,190,187 (GRCm39) missense probably damaging 0.99
R2902:Cep68 UTSW 11 20,190,187 (GRCm39) missense probably damaging 0.99
R4292:Cep68 UTSW 11 20,190,079 (GRCm39) missense probably damaging 0.99
R4393:Cep68 UTSW 11 20,188,544 (GRCm39) missense probably benign 0.01
R4557:Cep68 UTSW 11 20,189,113 (GRCm39) intron probably benign
R4581:Cep68 UTSW 11 20,189,333 (GRCm39) missense probably benign 0.02
R4647:Cep68 UTSW 11 20,189,349 (GRCm39) missense probably benign 0.00
R4887:Cep68 UTSW 11 20,189,239 (GRCm39) missense probably benign 0.15
R5081:Cep68 UTSW 11 20,188,477 (GRCm39) missense probably damaging 0.98
R5658:Cep68 UTSW 11 20,191,885 (GRCm39) critical splice donor site probably null
R6380:Cep68 UTSW 11 20,180,498 (GRCm39) missense probably benign
R7444:Cep68 UTSW 11 20,189,438 (GRCm39) missense probably benign 0.01
R7455:Cep68 UTSW 11 20,180,571 (GRCm39) missense probably damaging 0.99
R7486:Cep68 UTSW 11 20,192,166 (GRCm39) missense probably benign 0.05
R8075:Cep68 UTSW 11 20,189,335 (GRCm39) missense probably benign 0.01
R8388:Cep68 UTSW 11 20,180,582 (GRCm39) missense probably damaging 1.00
R8407:Cep68 UTSW 11 20,190,446 (GRCm39) missense possibly damaging 0.62
R8501:Cep68 UTSW 11 20,189,132 (GRCm39) missense unknown
R8830:Cep68 UTSW 11 20,180,418 (GRCm39) unclassified probably benign
R8980:Cep68 UTSW 11 20,190,390 (GRCm39) missense probably benign
R9354:Cep68 UTSW 11 20,188,569 (GRCm39) missense probably damaging 1.00
R9534:Cep68 UTSW 11 20,190,686 (GRCm39) missense probably benign 0.00
R9597:Cep68 UTSW 11 20,188,506 (GRCm39) missense probably benign 0.00
R9780:Cep68 UTSW 11 20,192,142 (GRCm39) missense probably benign 0.09
Predicted Primers PCR Primer
(F):5'- TTTACTGGGACAGCCTTGTGCC -3'
(R):5'- AGCTCTGGAACCTTTGGAACATCAC -3'

Sequencing Primer
(F):5'- CAGTGGTTGGACAGTAAGTCCTC -3'
(R):5'- ggagaaatggttcagtgggtaag -3'
Posted On 2013-05-23