Incidental Mutation 'IGL01325:Nol4l'
ID74245
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nol4l
Ensembl Gene ENSMUSG00000061411
Gene Namenucleolar protein 4-like
SynonymsLOC381396, 8430427H17Rik
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.896) question?
Stock #IGL01325
Quality Score
Status
Chromosome2
Chromosomal Location153407462-153529971 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to G at 153436351 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000105407 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035346] [ENSMUST00000109784]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000035346
SMART Domains Protein: ENSMUSP00000036571
Gene: ENSMUSG00000061411

DomainStartEndE-ValueType
low complexity region 58 71 N/A INTRINSIC
low complexity region 277 305 N/A INTRINSIC
low complexity region 405 422 N/A INTRINSIC
low complexity region 619 639 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000109784
SMART Domains Protein: ENSMUSP00000105407
Gene: ENSMUSG00000061411

DomainStartEndE-ValueType
low complexity region 33 61 N/A INTRINSIC
SCOP:d1sig__ 161 246 1e-2 SMART
low complexity region 375 395 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132770
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930486L24Rik T C 13: 60,853,533 T127A probably damaging Het
Acrv1 T A 9: 36,698,514 M227K probably benign Het
Adam22 T C 5: 8,127,333 N592S probably benign Het
Adamts15 T A 9: 30,921,688 I184F possibly damaging Het
Adcy1 T C 11: 7,064,102 V168A possibly damaging Het
Arl6ip5 T C 6: 97,232,540 F179L probably benign Het
Asxl2 G T 12: 3,427,172 R6L probably damaging Het
Btaf1 T A 19: 37,004,649 probably benign Het
Ccdc136 T C 6: 29,412,950 F445L probably benign Het
Cpne3 T C 4: 19,535,229 S268G probably benign Het
Crtc3 C T 7: 80,677,368 R70Q probably damaging Het
Fam169a C A 13: 97,122,699 A421E probably benign Het
Fhod1 A T 8: 105,331,649 M825K probably benign Het
Gjb2 T C 14: 57,100,221 T177A probably benign Het
Gm6576 A G 15: 27,025,884 noncoding transcript Het
Herpud2 A G 9: 25,113,911 V175A probably benign Het
Hmgxb3 T C 18: 61,134,006 D1052G probably damaging Het
Itpr1 T A 6: 108,381,208 F578L probably benign Het
Kdm7a T G 6: 39,158,309 probably benign Het
Krt76 A T 15: 101,884,888 S572T unknown Het
Lrrcc1 T C 3: 14,536,541 probably null Het
March9 A C 10: 127,057,590 V183G probably damaging Het
Mkl2 T C 16: 13,401,224 V578A probably damaging Het
Ndufaf6 A T 4: 11,070,251 D123E probably benign Het
Nhlh2 T G 3: 102,013,026 Y125D probably damaging Het
Npas1 C T 7: 16,463,322 G206D probably benign Het
Olfr651 T C 7: 104,553,689 F257L probably damaging Het
Olfr994 C A 2: 85,430,295 C178F possibly damaging Het
Pcdhb4 T A 18: 37,309,623 V662E probably damaging Het
Plxna3 G A X: 74,335,794 G758S probably damaging Het
Prdm15 T A 16: 97,806,517 N709Y probably damaging Het
Pygo2 C T 3: 89,432,446 probably benign Het
Ranbp2 T A 10: 58,476,298 S947T probably damaging Het
Rasgrp1 T A 2: 117,298,529 H203L probably damaging Het
Rbbp6 G A 7: 122,988,618 G270R probably damaging Het
Rcl1 A G 19: 29,121,262 probably null Het
Rpl23a-ps1 T C 1: 45,981,633 noncoding transcript Het
Serpinb7 T G 1: 107,435,380 H91Q probably damaging Het
Shd C T 17: 55,972,839 P111S possibly damaging Het
Slc35e1 G T 8: 72,483,758 probably benign Het
Srgap3 C T 6: 112,775,686 R279H probably damaging Het
Sstr4 G A 2: 148,395,552 E28K probably benign Het
Stip1 T C 19: 7,021,096 probably benign Het
Syne2 A G 12: 75,926,514 E1097G probably benign Het
Tbcd T A 11: 121,540,993 V489E probably damaging Het
Tnks2 T A 19: 36,871,633 S516R probably benign Het
Trmt44 T A 5: 35,568,803 R343S possibly damaging Het
Trps1 A G 15: 50,846,814 S47P probably benign Het
Ubr3 A C 2: 69,917,097 K235Q possibly damaging Het
Uckl1 G A 2: 181,574,961 Q48* probably null Het
Vat1 T C 11: 101,465,715 D140G probably benign Het
Vmn2r80 A G 10: 79,194,247 T636A possibly damaging Het
Zfp423 A T 8: 87,781,611 probably null Het
Zfp667 C A 7: 6,290,546 T15N probably damaging Het
Other mutations in Nol4l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00933:Nol4l APN 2 153477936 missense probably damaging 0.96
IGL02608:Nol4l APN 2 153436293 missense possibly damaging 0.50
IGL02886:Nol4l APN 2 153529537 missense probably benign 0.27
IGL03210:Nol4l APN 2 153529458 missense probably benign 0.03
IGL03055:Nol4l UTSW 2 153436270 synonymous silent
R0285:Nol4l UTSW 2 153483853 splice site probably benign
R0345:Nol4l UTSW 2 153411752 missense probably benign 0.00
R0555:Nol4l UTSW 2 153417684 splice site probably null
R1966:Nol4l UTSW 2 153529455 missense probably benign 0.01
R2044:Nol4l UTSW 2 153529521 missense possibly damaging 0.66
R2368:Nol4l UTSW 2 153418039 missense probably damaging 1.00
R4855:Nol4l UTSW 2 153411806 missense probably benign 0.06
R5696:Nol4l UTSW 2 153418106 missense probably damaging 0.99
R5776:Nol4l UTSW 2 153417821 missense probably damaging 1.00
R6807:Nol4l UTSW 2 153483826 nonsense probably null
R6845:Nol4l UTSW 2 153416662 missense probably benign 0.00
R6872:Nol4l UTSW 2 153483817 missense probably damaging 0.98
R6940:Nol4l UTSW 2 153411764 missense probably benign 0.00
R8165:Nol4l UTSW 2 153420553 nonsense probably null
R8263:Nol4l UTSW 2 153417417 missense probably damaging 0.99
R8500:Nol4l UTSW 2 153436346 missense probably damaging 0.99
R8938:Nol4l UTSW 2 153420731 missense probably damaging 1.00
R9097:Nol4l UTSW 2 153470710 missense probably damaging 0.96
R9098:Nol4l UTSW 2 153470710 missense probably damaging 0.96
R9099:Nol4l UTSW 2 153470710 missense probably damaging 0.96
R9115:Nol4l UTSW 2 153411718 missense probably damaging 1.00
Posted On2013-10-07