Incidental Mutation 'IGL02881:1700029H14Rik'
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ID362821
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700029H14Rik
Ensembl Gene ENSMUSG00000031452
Gene NameRIKEN cDNA 1700029H14 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.026) question?
Stock #IGL02881
Quality Score
Status
Chromosome8
Chromosomal Location13550733-13562461 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to A at 13555999 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147812 (fasta)
Gene Model
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 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
Posted On2015-12-18