Incidental Mutation 'R6285:Nol11'
ID508197
Institutional Source Beutler Lab
Gene Symbol Nol11
Ensembl Gene ENSMUSG00000018433
Gene Namenucleolar protein 11
Synonyms1500002M01Rik
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.935) question?
Stock #R6285 (G1)
Quality Score225.009
Status Validated
Chromosome11
Chromosomal Location107166663-107189381 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to G at 107181034 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Serine at position 244 (R244S)
Ref Sequence ENSEMBL: ENSMUSP00000102368 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018577] [ENSMUST00000106757]
Predicted Effect probably benign
Transcript: ENSMUST00000018577
AA Change: R244S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000018577
Gene: ENSMUSG00000018433
AA Change: R244S

DomainStartEndE-ValueType
SCOP:d1jmxb_ 32 176 3e-3 SMART
Pfam:NUC205 200 243 3.7e-26 PFAM
low complexity region 619 629 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106757
AA Change: R244S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000102368
Gene: ENSMUSG00000018433
AA Change: R244S

DomainStartEndE-ValueType
SCOP:d1jmxb_ 32 176 3e-3 SMART
Pfam:NUC205 200 243 7.3e-29 PFAM
low complexity region 599 609 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136917
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 98.8%
  • 20x: 96.9%
Validation Efficiency 100% (68/68)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A730017C20Rik A G 18: 59,072,224 K28R probably benign Het
Acad9 A T 3: 36,082,175 M370L probably benign Het
Aimp1 A G 3: 132,667,504 M225T possibly damaging Het
Atp8a1 T C 5: 67,667,607 I809V possibly damaging Het
Bbs10 A G 10: 111,299,761 Y245C probably damaging Het
Cabin1 A T 10: 75,684,323 F1572Y probably damaging Het
Cd79a A G 7: 24,899,347 N107S possibly damaging Het
Cdc7 G A 5: 106,983,059 A428T probably benign Het
Cep290 A G 10: 100,523,329 T974A probably benign Het
Cep350 A T 1: 155,953,374 N261K possibly damaging Het
Cfap46 T A 7: 139,661,085 D8V probably damaging Het
Col6a4 T C 9: 106,074,986 D571G probably damaging Het
Cpe A C 8: 64,617,611 V200G probably benign Het
Ctnnd1 C T 2: 84,613,887 probably null Het
D5Ertd579e A C 5: 36,615,577 C491W probably damaging Het
Dek A G 13: 47,099,380 I183T probably damaging Het
Dennd1a A T 2: 37,852,441 H437Q possibly damaging Het
Dido1 C T 2: 180,661,147 A1655T probably benign Het
Eva1b A G 4: 126,149,485 D106G probably damaging Het
Evc2 G T 5: 37,424,579 S1189I possibly damaging Het
Faap100 A T 11: 120,376,732 L405Q probably damaging Het
Fbxw15 T A 9: 109,557,166 M249L probably benign Het
Gbp10 A T 5: 105,218,460 L526Q probably damaging Het
Gm13084 A G 4: 143,816,039 C4R probably damaging Het
Gm14025 T G 2: 129,037,799 T736P possibly damaging Het
Gm19402 A C 10: 77,690,520 probably benign Het
Gm2244 A G 14: 19,540,797 Y141H probably damaging Het
Gm4181 A T 14: 51,633,209 N98K probably damaging Het
Gm765 T C 6: 98,238,173 D163G probably damaging Het
Golga4 C T 9: 118,558,627 R616* probably null Het
Gpank1 T A 17: 35,124,290 S226T probably damaging Het
Hipk3 T C 2: 104,471,425 M141V probably damaging Het
Hoxc11 T C 15: 102,954,743 V73A probably benign Het
Igf1r T G 7: 68,004,137 I141S possibly damaging Het
Jak2 T A 19: 29,295,659 F628I probably benign Het
Kcp C A 6: 29,502,365 V227L probably benign Het
Knl1 T G 2: 119,071,941 C1374W probably damaging Het
Larp6 A T 9: 60,737,760 R394S probably benign Het
Lilra5 G A 7: 4,242,115 G253R probably damaging Het
Map3k4 A G 17: 12,264,058 S591P probably damaging Het
Mrpl16 T A 19: 11,772,968 I72K probably damaging Het
Nr2f1 T C 13: 78,195,663 T161A probably benign Het
Nrd1 G T 4: 109,038,006 V476F probably damaging Het
Olfr1406 G T 1: 173,183,910 H175N probably damaging Het
Olfr419 A T 1: 174,250,829 S33T possibly damaging Het
Olfr451-ps1 A T 6: 42,800,909 H56L probably benign Het
Olfr535 T A 7: 140,492,713 L25Q possibly damaging Het
P2rx1 A G 11: 73,008,148 I62V probably benign Het
Pcdhgc5 A T 18: 37,820,621 Y316F probably benign Het
Pecam1 T C 11: 106,685,239 D490G probably benign Het
Pfkfb2 A T 1: 130,707,562 Y87* probably null Het
Poldip2 A G 11: 78,517,632 probably null Het
Ppp2r5b T A 19: 6,230,536 Q304L probably benign Het
Psg26 A G 7: 18,482,828 F29L probably benign Het
Ptk6 A T 2: 181,197,093 L289Q probably null Het
Ptprt A T 2: 161,901,497 I508N possibly damaging Het
Rasgrp4 T C 7: 29,148,383 F406S probably damaging Het
Rspo3 A G 10: 29,499,930 probably null Het
Sept8 G T 11: 53,534,767 probably null Het
Sirt2 A C 7: 28,788,046 T345P probably benign Het
Slc6a20b T C 9: 123,609,096 E205G possibly damaging Het
Sqstm1 G A 11: 50,202,591 Q327* probably null Het
Susd3 T A 13: 49,237,521 S98C probably damaging Het
Tada2b G A 5: 36,476,842 R56W probably damaging Het
Tbc1d2 A T 4: 46,615,045 V546E possibly damaging Het
Tbx6 A G 7: 126,781,568 Q21R possibly damaging Het
Usp24 T G 4: 106,374,100 probably null Het
Vmn2r103 A G 17: 19,812,144 T727A probably benign Het
Wdr48 C T 9: 119,920,610 T531M probably damaging Het
Other mutations in Nol11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00646:Nol11 APN 11 107173460 missense probably benign
IGL01656:Nol11 APN 11 107189172 missense probably benign 0.00
IGL01687:Nol11 APN 11 107186869 missense probably damaging 0.97
IGL02179:Nol11 APN 11 107189256 start codon destroyed probably null 1.00
IGL02538:Nol11 APN 11 107173373 missense probably benign 0.02
IGL03395:Nol11 APN 11 107175722 missense probably benign 0.06
R0526:Nol11 UTSW 11 107184771 nonsense probably null
R1734:Nol11 UTSW 11 107175623 missense possibly damaging 0.80
R2143:Nol11 UTSW 11 107181055 missense probably benign 0.03
R2385:Nol11 UTSW 11 107189206 missense probably benign 0.40
R3036:Nol11 UTSW 11 107173244 missense possibly damaging 0.87
R3522:Nol11 UTSW 11 107173628 missense possibly damaging 0.94
R3895:Nol11 UTSW 11 107168347 missense probably damaging 1.00
R4404:Nol11 UTSW 11 107173725 missense probably damaging 1.00
R4664:Nol11 UTSW 11 107181000 missense possibly damaging 0.89
R4705:Nol11 UTSW 11 107184718 intron probably benign
R5704:Nol11 UTSW 11 107173369 missense probably benign 0.43
R5991:Nol11 UTSW 11 107171145 missense probably benign 0.02
R6221:Nol11 UTSW 11 107171616 missense possibly damaging 0.50
R6222:Nol11 UTSW 11 107171616 missense possibly damaging 0.50
R6223:Nol11 UTSW 11 107171616 missense possibly damaging 0.50
R6467:Nol11 UTSW 11 107181086 missense possibly damaging 0.95
R7080:Nol11 UTSW 11 107180052 missense probably damaging 1.00
R7679:Nol11 UTSW 11 107173316 missense probably benign 0.00
R7767:Nol11 UTSW 11 107179082 missense possibly damaging 0.67
Predicted Primers PCR Primer
(F):5'- ACAGATGGAGTTCGTGTACTGG -3'
(R):5'- TGGACTTGTAGTCTTAGAAACCTTC -3'

Sequencing Primer
(F):5'- TACACACTGCGGTCCTAGTG -3'
(R):5'- CCTTCAAATACATTTTTAGAAACCCC -3'
Posted On2018-03-15