Incidental Mutation 'IGL00949:Plet1'
ID 28205
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Plet1
Ensembl Gene ENSMUSG00000032068
Gene Name placenta expressed transcript 1
Synonyms PLET1, 0610037B23Rik, 1600029D21Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00949
Quality Score
Status
Chromosome 9
Chromosomal Location 50405825-50416782 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 50410523 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 105 (T105A)
Ref Sequence ENSEMBL: ENSMUSP00000139422 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114474] [ENSMUST00000188047]
AlphaFold Q8VEN2
Predicted Effect possibly damaging
Transcript: ENSMUST00000114474
AA Change: T105A

PolyPhen 2 Score 0.617 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000110118
Gene: ENSMUSG00000032068
AA Change: T105A

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
low complexity region 163 209 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000188047
AA Change: T105A

PolyPhen 2 Score 0.617 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000139422
Gene: ENSMUSG00000032068
AA Change: T105A

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188703
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190941
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl4 A G X: 141,126,325 (GRCm39) C303R probably damaging Het
Als2 C T 1: 59,254,731 (GRCm39) G209S probably damaging Het
Ankrd11 T C 8: 123,635,467 (GRCm39) T56A possibly damaging Het
Arnt T A 3: 95,394,579 (GRCm39) I381N probably damaging Het
Atp13a1 T C 8: 70,252,653 (GRCm39) probably benign Het
Cd180 A T 13: 102,830,268 (GRCm39) T21S possibly damaging Het
Cdc27 T C 11: 104,420,229 (GRCm39) Y138C probably damaging Het
Dhx16 A G 17: 36,198,826 (GRCm39) T753A probably benign Het
Dnah1 A G 14: 31,029,047 (GRCm39) M561T probably benign Het
Dsc3 C A 18: 20,118,688 (GRCm39) G259C probably null Het
Enox2 A T X: 48,129,484 (GRCm39) D346E probably benign Het
Exoc3l T C 8: 106,017,130 (GRCm39) E619G probably benign Het
Exosc9 T C 3: 36,617,415 (GRCm39) probably benign Het
Gmpr2 C T 14: 55,914,207 (GRCm39) probably benign Het
Golga1 T C 2: 38,931,267 (GRCm39) E289G probably damaging Het
H3c1 G A 13: 23,946,014 (GRCm39) T108I probably damaging Het
Jmy A G 13: 93,590,510 (GRCm39) V531A probably damaging Het
Lamp2 T C X: 37,524,350 (GRCm39) N156S probably benign Het
Lrrn1 C A 6: 107,546,261 (GRCm39) N686K probably benign Het
Lyst T C 13: 13,810,070 (GRCm39) V580A possibly damaging Het
Ms4a8a C A 19: 11,056,808 (GRCm39) L91F probably benign Het
Naip2 A G 13: 100,298,099 (GRCm39) F646L probably damaging Het
Npat T C 9: 53,474,662 (GRCm39) V818A probably benign Het
Or2w4 A T 13: 21,795,521 (GRCm39) I206N probably damaging Het
Padi3 C A 4: 140,516,254 (GRCm39) R542L possibly damaging Het
Pid1 A G 1: 84,016,227 (GRCm39) V46A probably damaging Het
Pld5 A T 1: 175,803,039 (GRCm39) C409S probably damaging Het
Polrmt T C 10: 79,573,431 (GRCm39) probably null Het
Pp2d1 T C 17: 53,822,667 (GRCm39) N133S probably benign Het
Prpf40b G T 15: 99,204,419 (GRCm39) V228L probably benign Het
Ptgfrn A T 3: 100,980,161 (GRCm39) M393K probably benign Het
Slc9a1 C T 4: 133,143,762 (GRCm39) T416I probably benign Het
Slc9c1 T C 16: 45,413,721 (GRCm39) S950P probably benign Het
Slitrk1 A T 14: 109,149,241 (GRCm39) V490D probably damaging Het
Th T C 7: 142,450,763 (GRCm39) Y131C probably benign Het
Tlr6 A G 5: 65,110,855 (GRCm39) L684P probably damaging Het
Tpm3 A G 3: 89,997,165 (GRCm39) E234G probably damaging Het
Tti1 A G 2: 157,824,319 (GRCm39) Y1045H probably benign Het
Txnl4b T A 8: 110,295,707 (GRCm39) V37D probably benign Het
Ufl1 A T 4: 25,275,822 (GRCm39) F194I probably damaging Het
Usp13 G A 3: 32,940,726 (GRCm39) E412K possibly damaging Het
Usp46 A T 5: 74,163,903 (GRCm39) L251Q possibly damaging Het
Other mutations in Plet1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01458:Plet1 APN 9 50,406,017 (GRCm39) missense probably benign 0.21
IGL02108:Plet1 APN 9 50,410,387 (GRCm39) splice site probably benign
IGL03063:Plet1 APN 9 50,415,722 (GRCm39) missense probably benign 0.00
R0012:Plet1 UTSW 9 50,410,430 (GRCm39) missense probably benign 0.02
R1895:Plet1 UTSW 9 50,415,652 (GRCm39) splice site probably null
R1946:Plet1 UTSW 9 50,415,652 (GRCm39) splice site probably null
R5127:Plet1 UTSW 9 50,415,595 (GRCm39) missense probably benign 0.16
R6352:Plet1 UTSW 9 50,412,407 (GRCm39) missense probably damaging 0.99
Posted On 2013-04-17