Incidental Mutation 'IGL02881:1700029H14Rik'
ID 362821
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700029H14Rik
Ensembl Gene ENSMUSG00000031452
Gene Name RIKEN cDNA 1700029H14 gene
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02881
Quality Score
Status
Chromosome 8
Chromosomal Location 13600733-13612461 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 13605999 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147812 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033830] [ENSMUST00000134023] [ENSMUST00000151400] [ENSMUST00000187391] [ENSMUST00000209207]
AlphaFold E9PY36
Predicted Effect probably benign
Transcript: ENSMUST00000033830
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132787
Predicted Effect probably benign
Transcript: ENSMUST00000134023
Predicted Effect probably benign
Transcript: ENSMUST00000151400
Predicted Effect probably benign
Transcript: ENSMUST00000187391
Predicted Effect probably benign
Transcript: ENSMUST00000209207
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aatf A G 11: 84,362,115 (GRCm39) probably benign Het
Asap3 A T 4: 135,966,548 (GRCm39) H542L probably benign Het
Cyp4v3 A T 8: 45,761,753 (GRCm39) L389H probably damaging Het
Dnah17 C T 11: 117,932,944 (GRCm39) E3605K probably damaging Het
Fry C T 5: 150,282,516 (GRCm39) T347M probably damaging Het
Glul C A 1: 153,782,862 (GRCm39) T191K probably benign Het
Grsf1 A T 5: 88,821,689 (GRCm39) L125Q probably damaging Het
Hfm1 A G 5: 107,022,118 (GRCm39) I976T probably damaging Het
Itgb5 A G 16: 33,740,275 (GRCm39) T462A probably benign Het
Lmna G T 3: 88,410,233 (GRCm39) R60S possibly damaging Het
Mrpl10 T A 11: 96,937,899 (GRCm39) V89D probably damaging Het
Muc5b C T 7: 141,411,449 (GRCm39) T1465I unknown Het
Myh15 A C 16: 48,937,628 (GRCm39) D743A possibly damaging Het
Noxo1 C A 17: 24,918,409 (GRCm39) L190I probably damaging Het
Noxo1 T A 17: 24,918,410 (GRCm39) L190Q probably damaging Het
Nrn1 C A 13: 36,914,080 (GRCm39) probably null Het
Or2aj5 A T 16: 19,425,050 (GRCm39) Y123N probably damaging Het
Or4c121 T A 2: 89,023,985 (GRCm39) Y131F probably damaging Het
Or5m13 A G 2: 85,748,460 (GRCm39) S64G probably benign Het
Or8h8 A G 2: 86,753,057 (GRCm39) V273A possibly damaging Het
Pfkfb4 A G 9: 108,836,364 (GRCm39) T131A probably null Het
Phf20l1 T C 15: 66,466,829 (GRCm39) probably null Het
Pnliprp2 A G 19: 58,759,878 (GRCm39) D363G probably benign Het
Prpf6 C T 2: 181,273,864 (GRCm39) T336I probably benign Het
Rcc1 C T 4: 132,065,067 (GRCm39) R139H probably benign Het
Sae1 T G 7: 16,093,043 (GRCm39) K221N probably damaging Het
Slc45a1 T C 4: 150,722,987 (GRCm39) K299R probably benign Het
Slco1a8 T C 6: 141,917,969 (GRCm39) R636G probably benign Het
Smad2 C A 18: 76,432,851 (GRCm39) probably null Het
Tmem117 T C 15: 94,777,306 (GRCm39) F152S probably damaging Het
Tmem232 C T 17: 65,757,365 (GRCm39) C276Y probably damaging Het
Tor1b A T 2: 30,843,865 (GRCm39) K47* probably null Het
Ttn A G 2: 76,740,147 (GRCm39) V3464A probably benign Het
Ube3b A G 5: 114,550,945 (GRCm39) T870A possibly damaging Het
Zscan25 T G 5: 145,227,296 (GRCm39) L320R probably benign Het
Other mutations in 1700029H14Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03069:1700029H14Rik APN 8 13,607,704 (GRCm39) critical splice acceptor site probably null
R0242:1700029H14Rik UTSW 8 13,601,676 (GRCm39) missense probably benign
R0242:1700029H14Rik UTSW 8 13,601,676 (GRCm39) missense probably benign
R0243:1700029H14Rik UTSW 8 13,604,715 (GRCm39) missense possibly damaging 0.46
R0419:1700029H14Rik UTSW 8 13,601,842 (GRCm39) splice site probably benign
R1747:1700029H14Rik UTSW 8 13,608,814 (GRCm39) missense probably damaging 0.96
R1758:1700029H14Rik UTSW 8 13,612,237 (GRCm39) missense possibly damaging 0.66
R3890:1700029H14Rik UTSW 8 13,604,700 (GRCm39) missense probably damaging 0.97
R5004:1700029H14Rik UTSW 8 13,605,927 (GRCm39) missense possibly damaging 0.81
R8067:1700029H14Rik UTSW 8 13,608,643 (GRCm39) missense possibly damaging 0.78
R9412:1700029H14Rik UTSW 8 13,604,695 (GRCm39) missense possibly damaging 0.66
Posted On 2015-12-18