Incidental Mutation 'IGL02816:Ttc27'
ID 360816
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ttc27
Ensembl Gene ENSMUSG00000024078
Gene Name tetratricopeptide repeat domain 27
Synonyms 2610511O17Rik
Accession Numbers
Essential gene? Probably essential (E-score: 0.957) question?
Stock # IGL02816
Quality Score
Status
Chromosome 17
Chromosomal Location 75024730-75170565 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 75054769 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000024882 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000024882]
AlphaFold Q8CD92
Predicted Effect probably benign
Transcript: ENSMUST00000024882
SMART Domains Protein: ENSMUSP00000024882
Gene: ENSMUSG00000024078

DomainStartEndE-ValueType
TPR 531 564 7.34e-3 SMART
TPR 565 598 5.56e-3 SMART
TPR 599 632 3.81e-1 SMART
Blast:TPR 633 666 7e-15 BLAST
coiled coil region 817 847 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Caskin1 C A 17: 24,721,144 (GRCm39) P495T probably benign Het
Clcn4 A G 7: 7,298,087 (GRCm39) C41R probably damaging Het
Etfdh G A 3: 79,530,112 (GRCm39) T52M probably damaging Het
Fam227a T C 15: 79,510,497 (GRCm39) T386A possibly damaging Het
Gabrr3 T C 16: 59,260,830 (GRCm39) probably benign Het
Krt25 G T 11: 99,208,977 (GRCm39) D284E probably benign Het
Map1b T C 13: 99,578,263 (GRCm39) D130G probably damaging Het
Nlrp3 T A 11: 59,446,608 (GRCm39) F785I probably benign Het
Nrn1 C A 13: 36,914,080 (GRCm39) probably null Het
Numa1 T A 7: 101,645,307 (GRCm39) I311N probably damaging Het
Pkd1 T C 17: 24,813,489 (GRCm39) C4010R probably benign Het
Prph A G 15: 98,955,301 (GRCm39) M423V probably damaging Het
Rb1cc1 T A 1: 6,333,052 (GRCm39) probably benign Het
Ribc2 T G 15: 85,017,106 (GRCm39) V48G probably damaging Het
Scyl1 A T 19: 5,820,410 (GRCm39) N141K probably damaging Het
Sec23a T A 12: 59,025,331 (GRCm39) M497L probably benign Het
Strada C T 11: 106,055,251 (GRCm39) probably benign Het
Tas2r144 A T 6: 42,192,539 (GRCm39) Y93F probably benign Het
Tmem94 T A 11: 115,679,530 (GRCm39) probably null Het
Trpc3 A G 3: 36,705,851 (GRCm39) F448S probably damaging Het
Ttc13 A G 8: 125,439,415 (GRCm39) I113T possibly damaging Het
Ttll13 G T 7: 79,902,842 (GRCm39) C170F possibly damaging Het
Yes1 C T 5: 32,802,451 (GRCm39) T122M probably damaging Het
Other mutations in Ttc27
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00422:Ttc27 APN 17 75,087,811 (GRCm39) missense probably damaging 1.00
IGL01508:Ttc27 APN 17 75,142,352 (GRCm39) missense probably damaging 0.98
IGL02010:Ttc27 APN 17 75,087,906 (GRCm39) splice site probably benign
IGL02189:Ttc27 APN 17 75,036,894 (GRCm39) missense probably damaging 0.99
IGL02487:Ttc27 APN 17 75,163,549 (GRCm39) missense probably damaging 1.00
IGL02745:Ttc27 APN 17 75,046,728 (GRCm39) missense probably benign 0.37
IGL03389:Ttc27 APN 17 75,165,028 (GRCm39) missense probably benign 0.00
R0024:Ttc27 UTSW 17 75,077,259 (GRCm39) missense possibly damaging 0.79
R0511:Ttc27 UTSW 17 75,025,710 (GRCm39) missense probably benign 0.22
R0518:Ttc27 UTSW 17 75,163,544 (GRCm39) missense possibly damaging 0.80
R0521:Ttc27 UTSW 17 75,163,544 (GRCm39) missense possibly damaging 0.80
R0633:Ttc27 UTSW 17 75,036,972 (GRCm39) missense probably benign 0.02
R1415:Ttc27 UTSW 17 75,046,667 (GRCm39) missense probably benign
R1597:Ttc27 UTSW 17 75,170,402 (GRCm39) missense possibly damaging 0.95
R1961:Ttc27 UTSW 17 75,087,851 (GRCm39) missense probably damaging 0.99
R2038:Ttc27 UTSW 17 75,163,497 (GRCm39) missense probably benign 0.00
R3012:Ttc27 UTSW 17 75,147,454 (GRCm39) missense probably benign 0.17
R3619:Ttc27 UTSW 17 75,058,123 (GRCm39) splice site probably null
R4155:Ttc27 UTSW 17 75,147,455 (GRCm39) missense probably benign 0.09
R4272:Ttc27 UTSW 17 75,147,355 (GRCm39) missense probably damaging 1.00
R4291:Ttc27 UTSW 17 75,163,474 (GRCm39) missense probably damaging 1.00
R4557:Ttc27 UTSW 17 75,136,544 (GRCm39) missense probably benign 0.00
R5068:Ttc27 UTSW 17 75,106,337 (GRCm39) missense probably damaging 1.00
R5069:Ttc27 UTSW 17 75,106,337 (GRCm39) missense probably damaging 1.00
R5070:Ttc27 UTSW 17 75,106,337 (GRCm39) missense probably damaging 1.00
R5074:Ttc27 UTSW 17 75,054,750 (GRCm39) missense probably damaging 1.00
R5169:Ttc27 UTSW 17 75,054,690 (GRCm39) nonsense probably null
R5203:Ttc27 UTSW 17 75,084,649 (GRCm39) missense probably damaging 1.00
R5272:Ttc27 UTSW 17 75,049,972 (GRCm39) missense probably damaging 1.00
R6260:Ttc27 UTSW 17 75,165,086 (GRCm39) missense probably damaging 0.99
R6797:Ttc27 UTSW 17 75,036,883 (GRCm39) missense probably benign 0.28
R6830:Ttc27 UTSW 17 75,163,550 (GRCm39) nonsense probably null
R6987:Ttc27 UTSW 17 75,084,736 (GRCm39) critical splice donor site probably null
R7121:Ttc27 UTSW 17 75,054,710 (GRCm39) missense probably benign 0.04
R7393:Ttc27 UTSW 17 75,077,259 (GRCm39) missense possibly damaging 0.79
R7543:Ttc27 UTSW 17 75,024,745 (GRCm39) start gained probably benign
R7635:Ttc27 UTSW 17 75,025,710 (GRCm39) missense probably benign 0.22
R8231:Ttc27 UTSW 17 75,024,959 (GRCm39) missense probably benign 0.19
R8365:Ttc27 UTSW 17 75,054,669 (GRCm39) missense probably damaging 1.00
R8464:Ttc27 UTSW 17 75,024,925 (GRCm39) missense probably benign
R8493:Ttc27 UTSW 17 75,050,047 (GRCm39) critical splice donor site probably null
R8687:Ttc27 UTSW 17 75,046,679 (GRCm39) missense probably benign 0.00
X0026:Ttc27 UTSW 17 75,163,432 (GRCm39) missense probably benign 0.19
Posted On 2015-12-18