Incidental Mutation 'IGL02881:1700029H14Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700029H14Rik
Ensembl Gene ENSMUSG00000031452
Gene NameRIKEN cDNA 1700029H14 gene
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL02881
Quality Score
Chromosomal Location13550733-13562461 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to A at 13555999 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147812 (fasta)
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: 84,471,289 probably benign Het
Asap3 A T 4: 136,239,237 H542L probably benign Het
Cyp4v3 A T 8: 45,308,716 L389H probably damaging Het
Dnah17 C T 11: 118,042,118 E3605K probably damaging Het
Fry C T 5: 150,359,051 T347M probably damaging Het
Glul C A 1: 153,907,116 T191K probably benign Het
Gm6614 T C 6: 141,972,243 R636G probably benign Het
Grsf1 A T 5: 88,673,830 L125Q probably damaging Het
Hfm1 A G 5: 106,874,252 I976T probably damaging Het
Itgb5 A G 16: 33,919,905 T462A probably benign Het
Lmna G T 3: 88,502,926 R60S possibly damaging Het
Mrpl10 T A 11: 97,047,073 V89D probably damaging Het
Muc5b C T 7: 141,857,712 T1465I unknown Het
Myh15 A C 16: 49,117,265 D743A possibly damaging Het
Noxo1 C A 17: 24,699,435 L190I probably damaging Het
Noxo1 T A 17: 24,699,436 L190Q probably damaging Het
Nrn1 C A 13: 36,730,106 probably null Het
Olfr1025-ps1 A G 2: 85,918,116 S64G probably benign Het
Olfr1098 A G 2: 86,922,713 V273A possibly damaging Het
Olfr1226 T A 2: 89,193,641 Y131F probably damaging Het
Olfr170 A T 16: 19,606,300 Y123N probably damaging Het
Pfkfb4 A G 9: 109,007,296 T131A probably null Het
Phf20l1 T C 15: 66,594,980 probably null Het
Pnliprp2 A G 19: 58,771,446 D363G probably benign Het
Prpf6 C T 2: 181,632,071 T336I probably benign Het
Rcc1 C T 4: 132,337,756 R139H probably benign Het
Sae1 T G 7: 16,359,118 K221N probably damaging Het
Slc45a1 T C 4: 150,638,530 K299R probably benign Het
Smad2 C A 18: 76,299,780 probably null Het
Tmem117 T C 15: 94,879,425 F152S probably damaging Het
Tmem232 C T 17: 65,450,370 C276Y probably damaging Het
Tor1b A T 2: 30,953,853 K47* probably null Het
Ttn A G 2: 76,909,803 V3464A probably benign Het
Ube3b A G 5: 114,412,884 T870A possibly damaging Het
Zscan25 T G 5: 145,290,486 L320R probably benign Het
Other mutations in 1700029H14Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03069:1700029H14Rik APN 8 13557704 critical splice acceptor site probably null
R0242:1700029H14Rik UTSW 8 13551676 missense probably benign
R0242:1700029H14Rik UTSW 8 13551676 missense probably benign
R0243:1700029H14Rik UTSW 8 13554715 missense possibly damaging 0.46
R0419:1700029H14Rik UTSW 8 13551842 splice site probably benign
R1747:1700029H14Rik UTSW 8 13558814 missense probably damaging 0.96
R1758:1700029H14Rik UTSW 8 13562237 missense possibly damaging 0.66
R3890:1700029H14Rik UTSW 8 13554700 missense probably damaging 0.97
R5004:1700029H14Rik UTSW 8 13555927 missense possibly damaging 0.81
R8067:1700029H14Rik UTSW 8 13558643 missense possibly damaging 0.78
Posted On2015-12-18