Incidental Mutation 'IGL02615:Platr26'
ID 300638
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Platr26
Ensembl Gene ENSMUSG00000064263
Gene Name pluripotency associated transcript 26
Synonyms Gm1631, LOC381371
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.311) question?
Stock # IGL02615
Quality Score
Status
Chromosome 2
Chromosomal Location 71549761-71561310 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 71560770 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000079720
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430033K04Rik G T 5: 138,644,402 (GRCm39) E96* probably null Het
Adck5 C T 15: 76,473,367 (GRCm39) S72L possibly damaging Het
Afdn A G 17: 14,046,238 (GRCm39) H404R probably benign Het
Aph1c A T 9: 66,726,688 (GRCm39) V222E possibly damaging Het
Armc8 T C 9: 99,409,122 (GRCm39) probably benign Het
Bcl2l13 A T 6: 120,839,828 (GRCm39) D42V probably damaging Het
Bhlhe22 C T 3: 18,109,064 (GRCm39) T38I possibly damaging Het
Ccdc51 A T 9: 108,918,503 (GRCm39) T31S probably benign Het
Ctbp2 A G 7: 132,597,076 (GRCm39) I669T probably benign Het
Dennd4c A G 4: 86,739,704 (GRCm39) T998A probably benign Het
Dpp4 T C 2: 62,189,672 (GRCm39) Y410C probably damaging Het
Gli2 T A 1: 118,772,128 (GRCm39) N526Y probably damaging Het
Ighv1-64 A G 12: 115,471,307 (GRCm39) I70T possibly damaging Het
Mphosph10 A T 7: 64,030,793 (GRCm39) probably benign Het
Mrps34 A G 17: 25,114,767 (GRCm39) probably null Het
Myo1f A T 17: 33,823,630 (GRCm39) I1053L probably benign Het
Nckap5l G A 15: 99,327,263 (GRCm39) P142L possibly damaging Het
Rag2 T A 2: 101,459,913 (GRCm39) Y74* probably null Het
Rnf213 A T 11: 119,331,615 (GRCm39) M2275L probably damaging Het
Rsbn1 T A 3: 103,861,068 (GRCm39) L498Q probably damaging Het
Scp2 A G 4: 107,964,828 (GRCm39) V62A probably benign Het
Spag17 A G 3: 99,979,401 (GRCm39) I1421V probably benign Het
Spata31f1e C T 4: 42,793,027 (GRCm39) M368I probably benign Het
St6galnac4 A G 2: 32,484,216 (GRCm39) H138R probably benign Het
Syne2 T A 12: 76,143,768 (GRCm39) M1045K probably damaging Het
Tbxas1 C T 6: 39,004,800 (GRCm39) T349M probably damaging Het
U2surp T G 9: 95,375,284 (GRCm39) D146A probably benign Het
Usp38 T C 8: 81,711,780 (GRCm39) M752V probably benign Het
Other mutations in Platr26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01467:Platr26 APN 2 71,553,656 (GRCm39) exon noncoding transcript
R0988:Platr26 UTSW 2 71,553,631 (GRCm39) splice site noncoding transcript
R3962:Platr26 UTSW 2 71,549,849 (GRCm39) exon noncoding transcript
R4998:Platr26 UTSW 2 71,561,214 (GRCm39) exon noncoding transcript
Posted On 2015-04-16