Incidental Mutation 'IGL02301:Gm9513'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9513
Ensembl Gene ENSMUSG00000090710
Gene Namepredicted gene 9513
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.054) question?
Stock #IGL02301
Quality Score
Chromosomal Location36475638-36477186 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 36477187 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000129404 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165591]
Predicted Effect probably benign
Transcript: ENSMUST00000165591
SMART Domains Protein: ENSMUSP00000129404
Gene: ENSMUSG00000090710

signal peptide 1 21 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap8l A G 17: 32,332,926 probably benign Het
Alk T C 17: 71,874,176 Q1373R probably damaging Het
Atf7ip2 T G 16: 10,211,047 S148A probably benign Het
Bpi C T 2: 158,274,814 S377F probably damaging Het
Ccni A T 5: 93,188,175 C122S possibly damaging Het
Cd5l A G 3: 87,365,993 R90G probably benign Het
Ceacam3 C T 7: 17,163,101 S664F probably damaging Het
Clca3a2 A T 3: 144,806,372 D534E probably damaging Het
Ep400 A T 5: 110,674,960 S2524R probably damaging Het
Fhdc1 G A 3: 84,444,735 A1061V possibly damaging Het
Gart A G 16: 91,621,837 probably benign Het
Gsdmc4 A G 15: 63,895,264 V219A probably benign Het
Hus1 T C 11: 8,996,915 T261A probably benign Het
Lman2l A G 1: 36,443,543 I84T probably damaging Het
Megf8 G A 7: 25,337,900 V742M probably damaging Het
Myo1d A G 11: 80,676,853 V267A probably benign Het
Notch2 A G 3: 98,141,554 T1803A probably benign Het
Olfr1278 T A 2: 111,292,697 M143K probably benign Het
Olfr23 T A 11: 73,941,068 M274K possibly damaging Het
Olfr814 A G 10: 129,874,079 F226S probably damaging Het
Pde5a G A 3: 122,760,885 R208Q probably damaging Het
Pla2r1 T C 2: 60,452,436 N745S probably benign Het
Ptgdr2 T A 19: 10,940,209 I30N possibly damaging Het
Rap1gap2 G A 11: 74,407,369 T415I probably damaging Het
Slc6a6 T C 6: 91,726,056 Y137H probably benign Het
Sptbn1 A T 11: 30,142,129 D532E probably damaging Het
Stk39 T C 2: 68,211,962 D543G probably damaging Het
Trpc4 G A 3: 54,291,232 V526M probably damaging Het
Trrap A G 5: 144,777,917 I100V probably benign Het
Vmn1r-ps123 A C 13: 22,996,357 noncoding transcript Het
Vwa5b2 G A 16: 20,604,790 G1151D probably damaging Het
Zfp358 T A 8: 3,496,858 I480N probably benign Het
Zfp423 T C 8: 87,781,574 D714G probably damaging Het
Other mutations in Gm9513
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0448:Gm9513 UTSW 9 36477116 missense probably benign
R5341:Gm9513 UTSW 9 36477061 nonsense probably null
R7411:Gm9513 UTSW 9 36475684 missense possibly damaging 0.90
RF005:Gm9513 UTSW 9 36475674 missense possibly damaging 0.61
Z1176:Gm9513 UTSW 9 36476511 missense probably damaging 0.98
Posted On2015-04-16