Incidental Mutation 'IGL03144:Nop2'
ID410845
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nop2
Ensembl Gene ENSMUSG00000038279
Gene NameNOP2 nucleolar protein
Synonyms120kDa, Nol1
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.967) question?
Stock #IGL03144
Quality Score
Status
Chromosome6
Chromosomal Location125131909-125144753 bp(+) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to A at 125137512 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000047123 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044200] [ENSMUST00000204185]
Predicted Effect probably null
Transcript: ENSMUST00000044200
SMART Domains Protein: ENSMUSP00000047123
Gene: ENSMUSG00000038279

DomainStartEndE-ValueType
low complexity region 41 57 N/A INTRINSIC
low complexity region 97 109 N/A INTRINSIC
low complexity region 166 176 N/A INTRINSIC
Pfam:Methyltr_RsmF_N 268 359 2.9e-12 PFAM
Pfam:Nol1_Nop2_Fmu 362 570 2e-86 PFAM
Pfam:P120R 609 630 2.7e-11 PFAM
Pfam:P120R 663 685 1.1e-12 PFAM
low complexity region 729 745 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000204185
SMART Domains Protein: ENSMUSP00000145333
Gene: ENSMUSG00000038279

DomainStartEndE-ValueType
low complexity region 41 57 N/A INTRINSIC
low complexity region 97 109 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a gene trapped allele exhibit complete prenatal lethality. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 C A 17: 24,381,964 Q451K probably benign Het
Acly A T 11: 100,515,083 D294E possibly damaging Het
Arid3a C T 10: 79,946,482 probably benign Het
Ascc3 T C 10: 50,767,443 V1830A probably benign Het
Atp6v1b1 T C 6: 83,758,351 V467A probably benign Het
Ccdc171 A T 4: 83,818,090 I1233L probably damaging Het
Ccdc74a C A 16: 17,648,866 Q146K possibly damaging Het
Cdh26 A G 2: 178,468,174 D420G probably damaging Het
Ceacam20 T C 7: 19,971,519 V145A possibly damaging Het
Cmya5 C A 13: 93,090,868 A2571S probably damaging Het
Cog2 T C 8: 124,541,024 S360P probably damaging Het
Col26a1 G T 5: 136,765,348 T132N probably damaging Het
Col6a2 T A 10: 76,614,425 H224L probably benign Het
Cpm C T 10: 117,683,414 S409L probably benign Het
Dock4 G T 12: 40,692,907 probably benign Het
Dpy19l2 T A 9: 24,646,307 N391Y possibly damaging Het
Exosc9 G A 3: 36,554,135 G126D probably damaging Het
Eya3 T C 4: 132,693,142 S256P probably benign Het
Fat3 T C 9: 16,375,245 D994G probably damaging Het
Fat4 A G 3: 38,956,859 Q2036R possibly damaging Het
Fryl T C 5: 73,101,455 Q662R probably null Het
Gm13271 A G 4: 88,755,399 R178G probably benign Het
Gpr165 T A X: 96,716,954 L279Q probably damaging Het
Htr1b A G 9: 81,631,945 L203P probably damaging Het
Kcnb2 T C 1: 15,709,888 L328P probably damaging Het
Klhl26 C T 8: 70,452,564 R198H probably damaging Het
Nhsl2 A G X: 102,079,509 R973G possibly damaging Het
Nmi A T 2: 51,952,534 F182Y probably damaging Het
Nrn1 C A 13: 36,730,106 probably null Het
Olfr50 A G 2: 36,794,081 T282A probably benign Het
Ooep G T 9: 78,378,007 A109E possibly damaging Het
Pan3 T C 5: 147,450,781 probably benign Het
Pcdhb6 A G 18: 37,334,406 N127D probably damaging Het
Rabgap1 G A 2: 37,540,532 R695H probably damaging Het
Rxrg G A 1: 167,598,758 G3R possibly damaging Het
Slc17a3 T C 13: 23,846,440 M178T probably benign Het
Slc39a8 A G 3: 135,884,210 E287G probably benign Het
Slc44a5 G T 3: 154,243,540 D217Y possibly damaging Het
Slc4a10 G T 2: 62,250,466 V346L probably benign Het
Slc9a4 T C 1: 40,612,202 Y547H probably damaging Het
St6galnac3 A C 3: 153,205,527 Y266D probably damaging Het
Stard6 A T 18: 70,476,111 Y3F possibly damaging Het
Stk25 C A 1: 93,629,136 L53F probably damaging Het
Tep1 A T 14: 50,844,017 probably benign Het
Tmem151a T A 19: 5,085,372 M1L probably benign Het
Trim10 T C 17: 36,876,848 S319P probably damaging Het
Trmt44 G T 5: 35,564,422 P466T probably benign Het
Unc79 T C 12: 103,042,142 I256T probably damaging Het
Vmn2r125 G T 4: 156,350,019 L33F possibly damaging Het
Other mutations in Nop2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00787:Nop2 APN 6 125133546 missense probably damaging 1.00
IGL00913:Nop2 APN 6 125139821 missense probably damaging 1.00
IGL02568:Nop2 APN 6 125140850 missense probably damaging 1.00
IGL02850:Nop2 APN 6 125144085 missense possibly damaging 0.67
IGL02850:Nop2 APN 6 125144070 missense probably benign 0.01
IGL02851:Nop2 APN 6 125144085 missense possibly damaging 0.67
IGL02851:Nop2 APN 6 125144070 missense probably benign 0.01
IGL03338:Nop2 APN 6 125139732 splice site probably null
R0211:Nop2 UTSW 6 125141344 missense probably damaging 1.00
R0211:Nop2 UTSW 6 125141344 missense probably damaging 1.00
R0486:Nop2 UTSW 6 125140673 missense probably null 0.14
R0627:Nop2 UTSW 6 125139704 missense possibly damaging 0.90
R1022:Nop2 UTSW 6 125137186 missense probably benign 0.02
R1024:Nop2 UTSW 6 125137186 missense probably benign 0.02
R1068:Nop2 UTSW 6 125132279 missense probably damaging 0.99
R1750:Nop2 UTSW 6 125137638 missense probably benign 0.00
R1847:Nop2 UTSW 6 125137079 unclassified probably benign
R1940:Nop2 UTSW 6 125134634 missense probably benign 0.43
R1972:Nop2 UTSW 6 125134639 missense probably benign 0.02
R2059:Nop2 UTSW 6 125139860 missense probably null 0.95
R2100:Nop2 UTSW 6 125140822 missense probably damaging 1.00
R3123:Nop2 UTSW 6 125132201 utr 5 prime probably benign
R3124:Nop2 UTSW 6 125132201 utr 5 prime probably benign
R3160:Nop2 UTSW 6 125134592 missense probably benign 0.00
R3162:Nop2 UTSW 6 125134592 missense probably benign 0.00
R4521:Nop2 UTSW 6 125133552 missense probably damaging 1.00
R4522:Nop2 UTSW 6 125133552 missense probably damaging 1.00
R4523:Nop2 UTSW 6 125133552 missense probably damaging 1.00
R4524:Nop2 UTSW 6 125133552 missense probably damaging 1.00
R4571:Nop2 UTSW 6 125140881 critical splice donor site probably null
R4695:Nop2 UTSW 6 125144556 missense probably benign 0.00
R4747:Nop2 UTSW 6 125137094 missense probably benign
R5010:Nop2 UTSW 6 125133763 missense probably benign 0.00
R5385:Nop2 UTSW 6 125144361 missense probably benign
R5455:Nop2 UTSW 6 125140643 missense probably benign 0.19
R5567:Nop2 UTSW 6 125133763 missense probably benign 0.00
R5914:Nop2 UTSW 6 125134728 missense probably benign 0.01
R5993:Nop2 UTSW 6 125144019 missense probably benign 0.00
R6031:Nop2 UTSW 6 125133566 critical splice donor site probably null
R6031:Nop2 UTSW 6 125133566 critical splice donor site probably null
R6065:Nop2 UTSW 6 125144565 missense probably benign
R6352:Nop2 UTSW 6 125137207 missense probably benign
R6436:Nop2 UTSW 6 125137311 missense probably benign 0.01
R7393:Nop2 UTSW 6 125133546 nonsense probably null
Posted On2016-08-02