Incidental Mutation 'IGL01898:F830104G03Rik'
ID179455
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol F830104G03Rik
Ensembl Gene ENSMUSG00000074592
Gene NameRIKEN cDNA F830104G03 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01898
Quality Score
Status
Chromosome3
Chromosomal Location56889978-56890593 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to A at 56890216 bp
ZygosityHeterozygous
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*

DomainStartEndE-ValueType
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