Incidental Mutation 'IGL02732:Cep68'
ID 305527
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cep68
Ensembl Gene ENSMUSG00000044066
Gene Name centrosomal protein 68
Synonyms 6030463E10Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.140) question?
Stock # IGL02732
Quality Score
Status
Chromosome 11
Chromosomal Location 20177037-20199424 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 20186109 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000125113 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050611] [ENSMUST00000109596] [ENSMUST00000162811]
AlphaFold Q8C0D9
Predicted Effect probably benign
Transcript: ENSMUST00000050611
SMART Domains Protein: ENSMUSP00000054943
Gene: ENSMUSG00000044066

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: ENSMUST00000109596
SMART Domains Protein: ENSMUSP00000105225
Gene: ENSMUSG00000044066

DomainStartEndE-ValueType
low complexity region 178 190 N/A INTRINSIC
low complexity region 311 325 N/A INTRINSIC
SCOP:d1quua1 594 648 1e-2 SMART
Blast:SPEC 605 646 6e-21 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000162811
SMART Domains Protein: ENSMUSP00000125113
Gene: ENSMUSG00000044066

DomainStartEndE-ValueType
low complexity region 178 190 N/A INTRINSIC
low complexity region 311 325 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Apoo-ps C A 13: 107,551,123 (GRCm39) noncoding transcript Het
Ash1l T A 3: 88,873,535 (GRCm39) V106E probably damaging Het
Baz2a A G 10: 127,961,044 (GRCm39) T1618A possibly damaging Het
Brca1 A G 11: 101,383,045 (GRCm39) S1732P probably benign Het
Cdh1 T A 8: 107,392,955 (GRCm39) I813N probably damaging Het
Cdk5rap2 G A 4: 70,184,902 (GRCm39) R1183* probably null Het
Cep170 C T 1: 176,564,440 (GRCm39) E1479K probably damaging Het
Cog7 C T 7: 121,522,590 (GRCm39) V750I probably benign Het
Cplane1 A G 15: 8,209,375 (GRCm39) T271A probably benign Het
Cyb5d1 A C 11: 69,284,635 (GRCm39) probably null Het
Dlgap4 A G 2: 156,591,243 (GRCm39) K120E probably benign Het
Dmtf1 T C 5: 9,186,098 (GRCm39) I75V possibly damaging Het
Fnip2 T C 3: 79,373,004 (GRCm39) T995A probably damaging Het
Hecw2 G A 1: 53,965,847 (GRCm39) probably benign Het
Il17rd T A 14: 26,809,376 (GRCm39) F111I probably damaging Het
Itgb8 A C 12: 119,127,088 (GRCm39) M722R probably benign Het
Maip1 A G 1: 57,449,114 (GRCm39) D165G probably damaging Het
Mcm6 A T 1: 128,287,227 (GRCm39) C26S probably benign Het
Mdp1 T C 14: 55,896,678 (GRCm39) I128V possibly damaging Het
Myof A T 19: 37,966,164 (GRCm39) F385L possibly damaging Het
Nebl C T 2: 17,457,295 (GRCm39) probably benign Het
Nusap1 A G 2: 119,466,061 (GRCm39) E227G probably damaging Het
Or4b13 A G 2: 90,082,652 (GRCm39) S227P probably damaging Het
Or51m1 T G 7: 103,578,336 (GRCm39) M102R probably damaging Het
Or52e3 A C 7: 102,869,447 (GRCm39) N174T probably benign Het
Pamr1 A T 2: 102,472,486 (GRCm39) H595L probably benign Het
Pate5 C T 9: 35,750,345 (GRCm39) G109D probably damaging Het
Pdgfc G A 3: 80,944,864 (GRCm39) probably benign Het
Pierce1 T C 2: 28,355,192 (GRCm39) N91S probably damaging Het
Ptpn22 A T 3: 103,793,349 (GRCm39) E500V probably damaging Het
Ptprg G T 14: 12,225,617 (GRCm38) probably null Het
R3hdm2 T C 10: 127,319,929 (GRCm39) F513L probably benign Het
Ramac T C 7: 81,417,473 (GRCm39) probably null Het
Rhobtb3 C A 13: 76,059,056 (GRCm39) L247F probably damaging Het
Scfd1 T C 12: 51,469,756 (GRCm39) S434P probably benign Het
Serpinb3d T A 1: 107,010,526 (GRCm39) probably null Het
Sin3b T C 8: 73,460,081 (GRCm39) F223L possibly damaging Het
Slc9c1 T C 16: 45,370,548 (GRCm39) V263A possibly damaging Het
Sntb1 A G 15: 55,655,596 (GRCm39) S207P possibly damaging Het
Sqor A T 2: 122,641,682 (GRCm39) T1S possibly damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Ssh2 A G 11: 77,328,602 (GRCm39) probably null Het
Tasor2 A G 13: 3,623,626 (GRCm39) V2108A probably benign Het
Tmod2 A G 9: 75,493,454 (GRCm39) V167A possibly damaging Het
Trak2 G A 1: 58,949,222 (GRCm39) T526M probably benign Het
Trdn G A 10: 33,344,195 (GRCm39) probably null Het
Trim5 T A 7: 103,927,672 (GRCm39) E156V probably benign Het
Twf1 A G 15: 94,478,890 (GRCm39) S273P probably damaging Het
Xylt1 T C 7: 117,191,164 (GRCm39) V320A possibly damaging Het
Zfp518a G A 19: 40,903,061 (GRCm39) G997R probably damaging 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
PIT4366001:Cep68 UTSW 11 20,190,007 (GRCm39) missense probably benign 0.21
PIT4418001:Cep68 UTSW 11 20,189,731 (GRCm39) missense probably benign
R0399:Cep68 UTSW 11 20,180,571 (GRCm39) missense probably benign 0.10
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
Posted On 2015-04-16