Incidental Mutation 'R0815:Rbm11'
ID 78592
Institutional Source Beutler Lab
Gene Symbol Rbm11
Ensembl Gene ENSMUSG00000032940
Gene Name RNA binding motif protein 11
Synonyms
MMRRC Submission 038995-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R0815 (G1)
Quality Score 225
Status Validated
Chromosome 16
Chromosomal Location 75389796-75399706 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 75393525 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 74 (R74C)
Ref Sequence ENSEMBL: ENSMUSP00000109891 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046378] [ENSMUST00000114249] [ENSMUST00000114253]
AlphaFold Q80YT9
Predicted Effect probably damaging
Transcript: ENSMUST00000046378
AA Change: R74C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000038956
Gene: ENSMUSG00000032940
AA Change: R74C

DomainStartEndE-ValueType
RRM 11 83 3.25e-23 SMART
low complexity region 210 217 N/A INTRINSIC
low complexity region 228 237 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000114249
AA Change: R74C

PolyPhen 2 Score 0.915 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000109887
Gene: ENSMUSG00000032940
AA Change: R74C

DomainStartEndE-ValueType
RRM 11 83 3.25e-23 SMART
low complexity region 210 217 N/A INTRINSIC
low complexity region 228 237 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000114253
AA Change: R74C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000109891
Gene: ENSMUSG00000032940
AA Change: R74C

DomainStartEndE-ValueType
RRM 11 83 3.25e-23 SMART
low complexity region 210 217 N/A INTRINSIC
low complexity region 228 237 N/A INTRINSIC
Meta Mutation Damage Score 0.2092 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 96.5%
  • 20x: 91.3%
Validation Efficiency 97% (58/60)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 A G 12: 118,865,184 (GRCm39) probably benign Het
Abcf2 A T 5: 24,772,268 (GRCm39) Y487N probably damaging Het
Adcy4 T C 14: 56,021,056 (GRCm39) Y27C probably damaging Het
Atp2a2 T C 5: 122,609,299 (GRCm39) I188V probably benign Het
Cacna1s A T 1: 136,040,695 (GRCm39) I1231F possibly damaging Het
Capn7 T A 14: 31,091,714 (GRCm39) C704S possibly damaging Het
Celsr2 G T 3: 108,308,617 (GRCm39) T1770K possibly damaging Het
Chmp7 C T 14: 69,956,899 (GRCm39) M336I probably benign Het
Cul9 T C 17: 46,848,748 (GRCm39) probably null Het
Dpp10 A G 1: 123,360,658 (GRCm39) probably null Het
Dscaml1 A G 9: 45,656,372 (GRCm39) I1571V probably benign Het
Eif3j2 T A 18: 43,610,036 (GRCm39) Y259F probably benign Het
Erc2 A C 14: 27,747,105 (GRCm39) N345T probably benign Het
Fbxo21 T C 5: 118,133,573 (GRCm39) probably benign Het
Frmd8 A T 19: 5,915,084 (GRCm39) probably benign Het
Gfm1 T C 3: 67,381,928 (GRCm39) S705P probably damaging Het
Gucy1b2 T C 14: 62,656,511 (GRCm39) D282G probably benign Het
H2-Ab1 T C 17: 34,486,328 (GRCm39) I129T probably damaging Het
H2-M10.3 T A 17: 36,677,582 (GRCm39) Y232F probably damaging Het
Lipm A T 19: 34,096,161 (GRCm39) T326S probably benign Het
Lrrc8c T C 5: 105,756,400 (GRCm39) L725P probably damaging Het
Map3k19 A G 1: 127,762,375 (GRCm39) probably benign Het
Med31 T A 11: 72,104,657 (GRCm39) N50I probably damaging Het
Myo15b T G 11: 115,757,162 (GRCm39) probably benign Het
Nemp1 T C 10: 127,528,893 (GRCm39) L199S probably damaging Het
Nod2 G A 8: 89,399,290 (GRCm39) probably benign Het
Oga C T 19: 45,771,425 (GRCm39) A49T probably benign Het
Or2ak6 A G 11: 58,593,435 (GRCm39) R303G possibly damaging Het
Or5b21 A G 19: 12,840,008 (GRCm39) I290V probably benign Het
Parva G A 7: 112,167,071 (GRCm39) V215M probably damaging Het
Phf1 T C 17: 27,156,114 (GRCm39) probably benign Het
Plscr1l1 A T 9: 92,233,140 (GRCm39) I88L possibly damaging Het
Ppp1r12c G T 7: 4,489,365 (GRCm39) Q240K probably damaging Het
Ralgapa1 A T 12: 55,809,466 (GRCm39) Y436* probably null Het
Ralgapa1 C A 12: 55,829,562 (GRCm39) probably benign Het
Robo3 A G 9: 37,333,479 (GRCm39) V744A probably damaging Het
Rsbn1 T G 3: 103,861,469 (GRCm39) S522A probably damaging Het
Scel T A 14: 103,823,916 (GRCm39) S381R possibly damaging Het
Sec31b G A 19: 44,506,612 (GRCm39) Q909* probably null Het
Slc38a11 T A 2: 65,184,124 (GRCm39) I176L possibly damaging Het
Slc39a4 C T 15: 76,496,839 (GRCm39) D574N probably damaging Het
Slc44a1 T G 4: 53,536,421 (GRCm39) V199G possibly damaging Het
Sltm A G 9: 70,469,190 (GRCm39) T150A probably benign Het
Son C A 16: 91,452,372 (GRCm39) A373D probably damaging Het
Sp140 C T 1: 85,547,772 (GRCm39) probably benign Het
Speg A G 1: 75,392,036 (GRCm39) Y1606C probably damaging Het
Srgap1 A T 10: 121,621,379 (GRCm39) V1061D probably damaging Het
Stat5a A G 11: 100,765,908 (GRCm39) probably null Het
Supt4a T A 11: 87,628,409 (GRCm39) probably benign Het
Teddm1b A G 1: 153,750,638 (GRCm39) K149R possibly damaging Het
Thnsl2 A T 6: 71,111,208 (GRCm39) L220* probably null Het
Tinf2 G A 14: 55,917,566 (GRCm39) P308S probably benign Het
Tmem131l A G 3: 83,847,879 (GRCm39) S329P probably benign Het
Tnf T C 17: 35,420,120 (GRCm39) probably benign Het
Upp2 A G 2: 58,661,568 (GRCm39) T144A probably benign Het
Vmn2r94 T G 17: 18,477,973 (GRCm39) Q146P probably damaging Het
Zfhx4 T A 3: 5,310,375 (GRCm39) S919R possibly damaging Het
Other mutations in Rbm11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01732:Rbm11 APN 16 75,397,510 (GRCm39) missense probably benign 0.01
IGL02245:Rbm11 APN 16 75,389,896 (GRCm39) missense possibly damaging 0.74
IGL03350:Rbm11 APN 16 75,397,696 (GRCm39) missense probably benign 0.31
R0060:Rbm11 UTSW 16 75,395,667 (GRCm39) missense probably damaging 0.98
R1351:Rbm11 UTSW 16 75,393,531 (GRCm39) missense possibly damaging 0.91
R1562:Rbm11 UTSW 16 75,393,423 (GRCm39) missense probably damaging 1.00
R1793:Rbm11 UTSW 16 75,397,685 (GRCm39) missense probably damaging 1.00
R1891:Rbm11 UTSW 16 75,397,675 (GRCm39) missense possibly damaging 0.87
R1965:Rbm11 UTSW 16 75,395,656 (GRCm39) splice site probably null
R3757:Rbm11 UTSW 16 75,393,469 (GRCm39) missense probably damaging 1.00
R3928:Rbm11 UTSW 16 75,389,932 (GRCm39) critical splice donor site probably null
R4513:Rbm11 UTSW 16 75,393,475 (GRCm39) missense probably damaging 1.00
R5314:Rbm11 UTSW 16 75,393,474 (GRCm39) missense probably damaging 1.00
R5418:Rbm11 UTSW 16 75,393,423 (GRCm39) missense probably damaging 1.00
R5530:Rbm11 UTSW 16 75,389,861 (GRCm39) missense possibly damaging 0.66
R5891:Rbm11 UTSW 16 75,395,725 (GRCm39) missense possibly damaging 0.55
R6293:Rbm11 UTSW 16 75,393,655 (GRCm39) splice site probably null
R7853:Rbm11 UTSW 16 75,389,923 (GRCm39) missense probably damaging 1.00
R8167:Rbm11 UTSW 16 75,395,673 (GRCm39) missense probably benign 0.01
R8356:Rbm11 UTSW 16 75,397,694 (GRCm39) missense probably benign
R9571:Rbm11 UTSW 16 75,397,543 (GRCm39) missense possibly damaging 0.73
Predicted Primers PCR Primer
(F):5'- TGCGTTATTTGTGGAGCTATTAACGACT -3'
(R):5'- GCTTGGTAATATGGTAGACACTGCCAAT -3'

Sequencing Primer
(F):5'- AGTCAAACTTGAATCTTTGATTTGTC -3'
(R):5'- agcaagattacagttatgaagtacc -3'
Posted On 2013-10-16