Incidental Mutation 'R4479:F830104G03Rik'
ID 331390
Institutional Source Beutler Lab
Gene Symbol F830104G03Rik
Ensembl Gene ENSMUSG00000074592
Gene Name RIKEN cDNA F830104G03 gene
Synonyms
MMRRC Submission 041736-MU
Accession Numbers
Essential gene? Not available question?
Stock # R4479 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 56795483-56798749 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 56797634 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 98 (S98P)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000099093
AA Change: S98P
SMART Domains Protein: ENSMUSP00000096691
Gene: ENSMUSG00000074592
AA Change: S98P

DomainStartEndE-ValueType
coiled coil region 28 56 N/A INTRINSIC
low complexity region 73 84 N/A INTRINSIC
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.6%
Validation Efficiency 95% (36/38)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc6 T C 7: 45,654,663 (GRCm39) T553A possibly damaging Het
Adamts20 C T 15: 94,301,326 (GRCm39) R66H probably damaging Het
Anks1b A G 10: 89,885,754 (GRCm39) E150G probably damaging Het
Chp2 A G 7: 121,820,141 (GRCm39) D97G probably benign Het
Cnbd2 T C 2: 156,175,573 (GRCm39) probably benign Het
D130040H23Rik C A 8: 69,755,155 (GRCm39) H187N possibly damaging Het
Dusp15 A G 2: 152,786,102 (GRCm39) L135P probably damaging Het
Eif4g1 G T 16: 20,497,593 (GRCm39) probably benign Het
Erlin2 G T 8: 27,515,127 (GRCm39) V10L probably benign Het
Fat3 G A 9: 15,909,567 (GRCm39) S2145F probably damaging Het
Gm3159 T C 14: 4,398,584 (GRCm38) Y92H probably damaging Het
Ighv1-22 G T 12: 114,710,283 (GRCm39) A15E possibly damaging Het
Ints4 T C 7: 97,134,178 (GRCm39) S37P probably damaging Het
Irs1 G A 1: 82,265,015 (GRCm39) T1067I probably damaging Het
Lrrc28 C T 7: 67,181,362 (GRCm39) probably null Het
Or10v1 A G 19: 11,873,922 (GRCm39) Y179C probably damaging Het
Or4a71 A G 2: 89,358,514 (GRCm39) I80T possibly damaging Het
Or5ac24 G A 16: 59,165,230 (GRCm39) T278I probably damaging Het
Psg18 C T 7: 18,084,787 (GRCm39) S103N probably benign Het
Psma3 T C 12: 71,031,555 (GRCm39) probably benign Het
Slc7a11 T C 3: 50,372,412 (GRCm39) probably benign Het
Tas2r115 T C 6: 132,714,495 (GRCm39) D152G probably damaging Het
Tti1 A T 2: 157,850,315 (GRCm39) L308Q possibly damaging Het
Unc93b1 G A 19: 3,985,236 (GRCm39) A15T probably benign Het
Usp43 G A 11: 67,747,233 (GRCm39) R820C possibly damaging Het
Vmn2r68 TCC TC 7: 84,870,758 (GRCm39) probably null Het
Vps8 A T 16: 21,363,986 (GRCm39) probably benign Het
Wdr73 T C 7: 80,542,969 (GRCm39) E213G probably benign Het
Zfp286 C G 11: 62,671,030 (GRCm39) G348R probably damaging Het
Zkscan5 T C 5: 145,147,984 (GRCm39) probably benign Het
Other mutations in F830104G03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01898:F830104G03Rik APN 3 56,797,637 (GRCm39) nonsense probably null 0.00
R1669:F830104G03Rik UTSW 3 56,797,998 (GRCm39) missense unknown
R4877:F830104G03Rik UTSW 3 56,797,917 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GCTTTATCTTTACAGCACTGACTTG -3'
(R):5'- TTTAAGACTGAGCAGGGTGG -3'

Sequencing Primer
(F):5'- CAGCACTGACTTGGTTACAATTG -3'
(R):5'- TGAGCAGGGTGGCCTGG -3'
Posted On 2015-07-21