Incidental Mutation 'R4479:F830104G03Rik'
ID331390
Institutional Source Beutler Lab
Gene Symbol F830104G03Rik
Ensembl Gene ENSMUSG00000074592
Gene NameRIKEN cDNA F830104G03 gene
Synonyms
MMRRC Submission 041736-MU
Accession Numbers
Is this an essential gene? Not available question?
Stock #R4479 (G1)
Quality Score225
Status Validated
Chromosome3
Chromosomal Location56889978-56890593 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 56890213 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 98 (S98P)
Gene Model predicted gene model for transcript(s):
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: 46,005,239 T553A possibly damaging Het
Adamts20 C T 15: 94,403,445 R66H probably damaging Het
Anks1b A G 10: 90,049,892 E150G probably damaging Het
Chp2 A G 7: 122,220,918 D97G probably benign Het
Cnbd2 T C 2: 156,333,653 probably benign Het
D130040H23Rik C A 8: 69,302,503 H187N possibly damaging Het
Dusp15 A G 2: 152,944,182 L135P probably damaging Het
Eif4g1 G T 16: 20,678,843 probably benign Het
Erlin2 G T 8: 27,025,099 V10L probably benign Het
Fat3 G A 9: 15,998,271 S2145F probably damaging Het
Gm3159 T C 14: 4,398,584 Y92H probably damaging Het
Ighv1-22 G T 12: 114,746,663 A15E possibly damaging Het
Ints4 T C 7: 97,484,971 S37P probably damaging Het
Irs1 G A 1: 82,287,294 T1067I probably damaging Het
Lrrc28 C T 7: 67,531,614 probably null Het
Olfr1243 A G 2: 89,528,170 I80T possibly damaging Het
Olfr1420 A G 19: 11,896,558 Y179C probably damaging Het
Olfr206 G A 16: 59,344,867 T278I probably damaging Het
Psg18 C T 7: 18,350,862 S103N probably benign Het
Psma3 T C 12: 70,984,781 probably benign Het
Slc7a11 T C 3: 50,417,963 probably benign Het
Tas2r115 T C 6: 132,737,532 D152G probably damaging Het
Tti1 A T 2: 158,008,395 L308Q possibly damaging Het
Unc93b1 G A 19: 3,935,236 A15T probably benign Het
Usp43 G A 11: 67,856,407 R820C possibly damaging Het
Vmn2r68 TCC TC 7: 85,221,550 probably null Het
Vps8 A T 16: 21,545,236 probably benign Het
Wdr73 T C 7: 80,893,221 E213G probably benign Het
Zfp286 C G 11: 62,780,204 G348R probably damaging Het
Zkscan5 T C 5: 145,211,174 probably benign Het
Other mutations in F830104G03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01898:F830104G03Rik APN 3 56890216 nonsense probably null 0.00
R1669:F830104G03Rik UTSW 3 56890577 missense unknown
R4877:F830104G03Rik UTSW 3 56890496 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 On2015-07-21