Incidental Mutation 'IGL01898:F830104G03Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol F830104G03Rik
Ensembl Gene ENSMUSG00000074592
Gene NameRIKEN cDNA F830104G03 gene
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01898
Quality Score
Chromosomal Location56889978-56890593 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to A at 56890216 bp
Amino Acid Change Glutamine to Stop codon at position 97 (Q97*)
Gene Model predicted gene model for transcript(s):
Predicted Effect probably null
Transcript: ENSMUST00000099093
AA Change: Q97*
SMART Domains Protein: ENSMUSP00000096691
Gene: ENSMUSG00000074592
AA Change: Q97*

coiled coil region 28 56 N/A INTRINSIC
low complexity region 73 84 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl10 A T 2: 154,552,713 D195V probably damaging Het
Aqp11 A G 7: 97,726,663 W260R probably benign Het
Atp8a2 T C 14: 60,023,513 T390A probably damaging Het
Atp8b4 T C 2: 126,389,361 N431S probably benign Het
C130026I21Rik A G 1: 85,254,186 probably benign Het
Ccdc110 T G 8: 45,942,124 S351A possibly damaging Het
Cntnap4 T C 8: 112,856,307 F1006L possibly damaging Het
Ddr2 A G 1: 169,998,156 F292L possibly damaging Het
Fam171a2 T C 11: 102,439,756 T267A possibly damaging Het
Gm10718 A T 9: 3,025,118 Y194F probably benign Het
Gm21738 G A 14: 19,416,979 S144L probably benign Het
Igkv5-45 T A 6: 69,775,892 K69* probably null Het
Mios T C 6: 8,222,668 I534T probably benign Het
Nus1 A G 10: 52,430,067 D185G probably benign Het
Proc A G 18: 32,133,145 probably null Het
Psma3 T A 12: 70,984,674 H36Q probably benign Het
Sh3rf3 G T 10: 59,049,530 A412S probably damaging Het
Smgc A T 15: 91,844,524 probably null Het
Spta1 T A 1: 174,213,862 S1297R probably benign Het
Steap3 T C 1: 120,241,574 D293G probably benign Het
Tbx18 A T 9: 87,707,859 M342K possibly damaging Het
Trip11 T C 12: 101,885,676 M425V probably benign Het
Vmn2r-ps159 C T 4: 156,338,254 noncoding transcript Het
Other mutations in F830104G03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1669:F830104G03Rik UTSW 3 56890577 missense unknown
R4479:F830104G03Rik UTSW 3 56890213 missense unknown
R4877:F830104G03Rik UTSW 3 56890496 missense unknown
Posted On2014-05-07