Incidental Mutation 'R3888:B930094E09Rik'
Institutional Source Beutler Lab
Gene Symbol B930094E09Rik
Ensembl Gene ENSMUSG00000092124
Gene NameRIKEN cDNA B930094E09 gene
MMRRC Submission 040800-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.156) question?
Stock #R3888 (G1)
Quality Score220
Status Not validated
Chromosomal Location31609512-31610751 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 31609689 bp
Amino Acid Change Serine to Asparagine at position 59 (S59N)
Ref Sequence ENSEMBL: ENSMUSP00000128772 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000060396] [ENSMUST00000164667]
Predicted Effect silent
Transcript: ENSMUST00000060396
SMART Domains Protein: ENSMUSP00000053325
Gene: ENSMUSG00000024259

low complexity region 74 95 N/A INTRINSIC
transmembrane domain 268 290 N/A INTRINSIC
Pfam:Mito_carr 311 417 2.7e-12 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000164667
AA Change: S59N
SMART Domains Protein: ENSMUSP00000128772
Gene: ENSMUSG00000092124
AA Change: S59N

low complexity region 10 28 N/A INTRINSIC
low complexity region 43 64 N/A INTRINSIC
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933407L21Rik T A 1: 85,940,551 probably null Het
Acbd6 A G 1: 155,624,897 D201G probably damaging Het
Adam17 G A 12: 21,325,587 R744C probably damaging Het
Adss A G 1: 177,767,769 Y402H probably damaging Het
Ano3 T A 2: 110,885,000 K31I probably damaging Het
Cmya5 T G 13: 93,093,656 R1641S probably benign Het
Cps1 C A 1: 67,165,500 T493K possibly damaging Het
Dmxl1 T A 18: 49,878,259 M1161K probably damaging Het
Etl4 C T 2: 20,529,961 Q76* probably null Het
Fn1 T C 1: 71,640,306 Y511C probably damaging Het
Foxd2 T C 4: 114,908,286 H179R unknown Het
Frem1 T C 4: 82,913,607 R1991G probably benign Het
Gimap7 G A 6: 48,723,845 E122K probably benign Het
Hps3 A G 3: 20,003,223 probably null Het
Kctd2 A T 11: 115,427,519 K209N probably damaging Het
Lcor T A 19: 41,558,356 S126R probably damaging Het
Lct T C 1: 128,304,226 M629V probably damaging Het
Lrp5 G A 19: 3,612,330 R173C probably damaging Het
Muc5ac T C 7: 141,791,224 V144A possibly damaging Het
Mypn T C 10: 63,192,510 Y258C probably damaging Het
Ntf3 T C 6: 126,102,442 M21V probably benign Het
Olfr1243 T A 2: 89,527,732 H226L possibly damaging Het
Olfr1447 A T 19: 12,901,133 C216S probably benign Het
Olfr802 A T 10: 129,682,219 D173E probably benign Het
Olfr802 G A 10: 129,682,218 H174Y possibly damaging Het
Ptpro T A 6: 137,443,594 V1007D probably damaging Het
Rbm45 A G 2: 76,375,424 S207G probably benign Het
Robo3 G A 9: 37,422,181 Q723* probably null Het
Rreb1 G T 13: 37,893,965 R51L probably damaging Het
Slc12a6 T A 2: 112,267,030 L70Q possibly damaging Het
Slc15a2 A G 16: 36,782,304 F65S probably damaging Het
Slitrk5 T A 14: 111,679,797 C284* probably null Het
Smim17 G T 7: 6,429,280 G74C probably damaging Het
Snapc4 G A 2: 26,365,498 Q1005* probably null Het
Suv39h2 G A 2: 3,464,808 T170I probably benign Het
Thrb A G 14: 18,033,551 K424R probably damaging Het
Tm4sf4 C T 3: 57,437,745 Q191* probably null Het
Trak1 G T 9: 121,442,797 probably null Het
Ttn A G 2: 76,710,274 S25796P probably damaging Het
Ugp2 T C 11: 21,353,366 R80G probably benign Het
Utp15 C T 13: 98,259,166 V103I probably benign Het
Wdr3 A T 3: 100,153,906 S249T probably benign Het
Zeb1 T A 18: 5,748,743 D86E probably damaging Het
Other mutations in B930094E09Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3885:B930094E09Rik UTSW 18 31609689 missense unknown
R3889:B930094E09Rik UTSW 18 31609689 missense unknown
R3893:B930094E09Rik UTSW 18 31609689 missense unknown
R6179:B930094E09Rik UTSW 18 31609858 utr 5 prime probably benign
Predicted Primers PCR Primer

Sequencing Primer
Posted On2015-04-30