Incidental Mutation 'R6514:4933414I15Rik'
ID 520522
Institutional Source Beutler Lab
Gene Symbol 4933414I15Rik
Ensembl Gene ENSMUSG00000072983
Gene Name RIKEN cDNA 4933414I15 gene
Synonyms ENSMUSG00000051192
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R6514 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 50940711-50943765 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to A at 50942742 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Alanine to Valine at position 11 (A11V)
Ref Sequence ENSEMBL: ENSMUSP00000104751 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109123]
AlphaFold Q9D4D5
Predicted Effect unknown
Transcript: ENSMUST00000109123
AA Change: A11V
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156329
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.2%
Validation Efficiency 95% (35/37)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Add1 T A 5: 34,605,973 H168Q probably damaging Het
Apol7b C T 15: 77,423,926 R123Q probably benign Het
Arrdc3 A G 13: 80,889,190 E155G probably damaging Het
Capn7 T G 14: 31,344,554 D108E probably benign Het
Cdc6 A G 11: 98,919,292 T476A probably benign Het
Cntnap5c A G 17: 58,330,170 E1014G probably damaging Het
Crybg1 A T 10: 43,997,215 L1299H probably damaging Het
Duoxa1 A G 2: 122,304,713 S184P probably benign Het
Ech1 A G 7: 28,826,015 H65R possibly damaging Het
Egr3 T C 14: 70,078,917 L59P probably damaging Het
Eif4enif1 T A 11: 3,240,996 D724E probably null Het
Erbb2 A G 11: 98,420,146 D44G probably benign Het
Fer1l5 A G 1: 36,403,616 I739V probably benign Het
Gfm1 T C 3: 67,473,546 F665L probably benign Het
Gm10801 T A 2: 98,663,869 W119R probably benign Het
H2-M11 A T 17: 36,548,947 E277D probably damaging Het
Ighv1-66 T C 12: 115,593,120 Y114C possibly damaging Het
Irf1 C G 11: 53,771,322 L12V probably damaging Het
Itpr3 C T 17: 27,091,370 A403V probably benign Het
Ly6g C T 15: 75,156,732 P14S probably benign Het
Mfsd13a T C 19: 46,374,625 probably null Het
Mme T A 3: 63,364,844 C621* probably null Het
Mmp16 T C 4: 18,116,123 C576R probably damaging Het
Ngp A T 9: 110,419,949 I30F probably damaging Het
Olfr450 T A 6: 42,817,996 I175N probably damaging Het
Pdcd6ip G A 9: 113,689,694 T166I probably benign Het
Pgd C T 4: 149,160,752 probably null Het
Plcb4 T A 2: 135,954,996 H440Q probably benign Het
Ppl A G 16: 5,087,317 S1705P probably damaging Het
Ryr1 A G 7: 29,046,841 F3831S probably damaging Het
Serpine2 A C 1: 79,821,570 probably null Het
Skor2 T A 18: 76,862,694 W906R probably damaging Het
Tle6 G A 10: 81,591,976 H482Y probably damaging Het
Ufl1 T A 4: 25,262,238 D336V probably damaging Het
Vav1 T C 17: 57,327,660 F832L probably damaging Het
Other mutations in 4933414I15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02269:4933414I15Rik APN 11 50942598 missense unknown
IGL02598:4933414I15Rik APN 11 50943621 start codon destroyed probably null
BB010:4933414I15Rik UTSW 11 50942400 missense unknown
BB020:4933414I15Rik UTSW 11 50942400 missense unknown
R2384:4933414I15Rik UTSW 11 50942506 missense unknown
R5226:4933414I15Rik UTSW 11 50942589 missense unknown
R7933:4933414I15Rik UTSW 11 50942400 missense unknown
R8219:4933414I15Rik UTSW 11 50942536 missense unknown
R8700:4933414I15Rik UTSW 11 50942517 missense unknown
Predicted Primers PCR Primer
(F):5'- TGGTTTCACTGGCCAGCATC -3'
(R):5'- ATGTATCGATGTACCGGGGC -3'

Sequencing Primer
(F):5'- CCAGCATCCAGTGGACAGATG -3'
(R):5'- TATCGATGTACCGGGGCCAATC -3'
Posted On 2018-06-06