Incidental Mutation 'IGL01155:Naa16'
ID 52745
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Naa16
Ensembl Gene ENSMUSG00000022020
Gene Name N(alpha)-acetyltransferase 16, NatA auxiliary subunit
Synonyms Narg1l, 1300019C06Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # IGL01155
Quality Score
Status
Chromosome 14
Chromosomal Location 79325269-79390778 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 79384715 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 27 (K27N)
Ref Sequence ENSEMBL: ENSMUSP00000131268 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022597] [ENSMUST00000163486] [ENSMUST00000169500]
AlphaFold Q9DBB4
Predicted Effect possibly damaging
Transcript: ENSMUST00000022597
AA Change: K61N

PolyPhen 2 Score 0.714 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000022597
Gene: ENSMUSG00000022020
AA Change: K61N

DomainStartEndE-ValueType
TPR 46 79 2.99e1 SMART
TPR 80 113 2.98e-3 SMART
Blast:TPR 224 257 1e-10 BLAST
TPR 374 407 9.96e0 SMART
TPR 408 441 7.47e0 SMART
low complexity region 616 633 N/A INTRINSIC
Blast:TPR 672 705 3e-12 BLAST
low complexity region 830 841 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000163486
AA Change: K27N

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000131268
Gene: ENSMUSG00000022020
AA Change: K27N

DomainStartEndE-ValueType
TPR 12 45 2.99e1 SMART
TPR 46 79 2.98e-3 SMART
Blast:TPR 190 223 3e-10 BLAST
TPR 340 373 9.96e0 SMART
TPR 374 407 7.47e0 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165337
Predicted Effect probably benign
Transcript: ENSMUST00000169500
SMART Domains Protein: ENSMUSP00000127298
Gene: ENSMUSG00000022020

DomainStartEndE-ValueType
PDB:4KVO|D 1 46 1e-6 PDB
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,950,275 (GRCm38) V124I probably damaging Het
Adgrl3 T A 5: 81,560,893 (GRCm38) I409N probably benign Het
Akap13 A G 7: 75,569,936 (GRCm38) D29G probably damaging Het
Ap4e1 C A 2: 127,043,445 (GRCm38) T322K probably damaging Het
Arfgef1 G A 1: 10,198,982 (GRCm38) probably benign Het
Asic5 A G 3: 82,008,588 (GRCm38) T282A probably benign Het
Bptf T C 11: 107,080,727 (GRCm38) T985A probably damaging Het
Btnl9 A G 11: 49,175,691 (GRCm38) F349L probably damaging Het
Bves T A 10: 45,353,859 (GRCm38) I253K probably damaging Het
Cars T A 7: 143,569,849 (GRCm38) Y455F probably benign Het
Cfap206 C T 4: 34,721,562 (GRCm38) S162N probably damaging Het
Cuedc2 C A 19: 46,332,649 (GRCm38) V15F probably damaging Het
Defa22 T A 8: 21,163,037 (GRCm38) probably null Het
Fat1 G A 8: 45,023,949 (GRCm38) A2011T probably damaging Het
Fyb2 C T 4: 104,999,386 (GRCm38) T533I probably benign Het
Gm1043 T C 5: 37,187,089 (GRCm38) L182P probably damaging Het
Ice1 A T 13: 70,604,082 (GRCm38) V1295E possibly damaging Het
Il12b T A 11: 44,404,088 (GRCm38) S18T probably benign Het
Iqcg A G 16: 33,040,875 (GRCm38) V157A probably damaging Het
Itgax T A 7: 128,145,035 (GRCm38) M937K probably benign Het
Large1 T C 8: 73,131,989 (GRCm38) S84G probably benign Het
Lrp1b T C 2: 41,770,935 (GRCm38) T54A probably benign Het
Mfn1 A G 3: 32,542,836 (GRCm38) M148V probably damaging Het
Mobp C A 9: 120,168,234 (GRCm38) T73K probably benign Het
Ms4a3 T C 19: 11,629,655 (GRCm38) probably benign Het
Muc5ac C T 7: 141,806,943 (GRCm38) probably benign Het
Mzt2 A C 16: 15,862,410 (GRCm38) S104A possibly damaging Het
Nos1 T A 5: 117,945,926 (GRCm38) I1267N probably damaging Het
Olfr16 T A 1: 172,956,924 (GRCm38) I43N probably benign Het
Rara A G 11: 98,968,184 (GRCm38) E153G possibly damaging Het
Scn2a T G 2: 65,717,748 (GRCm38) S66A probably damaging Het
Slc6a1 A T 6: 114,314,465 (GRCm38) probably null Het
Sorbs3 A G 14: 70,199,341 (GRCm38) V136A probably damaging Het
Spink5 T A 18: 43,981,147 (GRCm38) H143Q probably benign Het
Susd2 G A 10: 75,640,892 (GRCm38) T99I possibly damaging Het
T C T 17: 8,441,745 (GRCm38) probably null Het
Tac2 G A 10: 127,726,134 (GRCm38) probably null Het
Tfap4 G T 16: 4,547,359 (GRCm38) P180T probably damaging Het
Trap1 G A 16: 4,043,978 (GRCm38) Q641* probably null Het
Unc119 A G 11: 78,348,609 (GRCm38) N252S probably damaging Het
Other mutations in Naa16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00551:Naa16 APN 14 79,355,729 (GRCm38) missense probably damaging 1.00
IGL01025:Naa16 APN 14 79,384,756 (GRCm38) missense probably damaging 1.00
IGL01335:Naa16 APN 14 79,345,116 (GRCm38) splice site probably benign
IGL01981:Naa16 APN 14 79,381,516 (GRCm38) missense probably benign 0.05
IGL02230:Naa16 APN 14 79,377,361 (GRCm38) splice site probably benign
IGL02313:Naa16 APN 14 79,384,668 (GRCm38) missense probably damaging 1.00
IGL02418:Naa16 APN 14 79,383,366 (GRCm38) missense probably damaging 1.00
IGL02544:Naa16 APN 14 79,335,820 (GRCm38) missense probably damaging 1.00
IGL03051:Naa16 APN 14 79,369,082 (GRCm38) missense probably benign 0.01
IGL03064:Naa16 APN 14 79,339,628 (GRCm38) missense probably damaging 0.98
IGL03205:Naa16 APN 14 79,356,512 (GRCm38) missense possibly damaging 0.89
PIT4508001:Naa16 UTSW 14 79,369,087 (GRCm38) missense probably benign 0.15
R0651:Naa16 UTSW 14 79,351,392 (GRCm38) missense probably damaging 1.00
R1429:Naa16 UTSW 14 79,359,527 (GRCm38) missense probably benign 0.01
R1674:Naa16 UTSW 14 79,387,057 (GRCm38) start codon destroyed probably null 0.65
R1693:Naa16 UTSW 14 79,351,456 (GRCm38) missense probably damaging 1.00
R1874:Naa16 UTSW 14 79,355,743 (GRCm38) missense possibly damaging 0.62
R1992:Naa16 UTSW 14 79,356,491 (GRCm38) missense probably damaging 1.00
R2015:Naa16 UTSW 14 79,345,059 (GRCm38) missense probably damaging 1.00
R2391:Naa16 UTSW 14 79,370,049 (GRCm38) missense probably benign 0.16
R2847:Naa16 UTSW 14 79,335,883 (GRCm38) missense probably damaging 1.00
R2848:Naa16 UTSW 14 79,335,883 (GRCm38) missense probably damaging 1.00
R2877:Naa16 UTSW 14 79,343,298 (GRCm38) missense probably benign 0.00
R3884:Naa16 UTSW 14 79,343,262 (GRCm38) missense probably damaging 0.98
R4001:Naa16 UTSW 14 79,343,121 (GRCm38) splice site probably null
R4199:Naa16 UTSW 14 79,355,871 (GRCm38) missense probably damaging 1.00
R4638:Naa16 UTSW 14 79,340,033 (GRCm38) splice site probably null
R4676:Naa16 UTSW 14 79,336,348 (GRCm38) unclassified probably benign
R4690:Naa16 UTSW 14 79,345,057 (GRCm38) missense probably damaging 1.00
R4952:Naa16 UTSW 14 79,345,085 (GRCm38) missense probably damaging 1.00
R5087:Naa16 UTSW 14 79,377,415 (GRCm38) missense possibly damaging 0.68
R5104:Naa16 UTSW 14 79,384,700 (GRCm38) nonsense probably null
R5729:Naa16 UTSW 14 79,355,780 (GRCm38) missense probably damaging 1.00
R6178:Naa16 UTSW 14 79,383,340 (GRCm38) missense possibly damaging 0.93
R6960:Naa16 UTSW 14 79,359,471 (GRCm38) missense possibly damaging 0.65
R7794:Naa16 UTSW 14 79,377,494 (GRCm38) missense probably damaging 1.00
R7936:Naa16 UTSW 14 79,341,046 (GRCm38) missense possibly damaging 0.47
R8356:Naa16 UTSW 14 79,359,475 (GRCm38) missense probably benign 0.00
R8456:Naa16 UTSW 14 79,359,475 (GRCm38) missense probably benign 0.00
R8892:Naa16 UTSW 14 79,390,576 (GRCm38) missense probably benign 0.32
R8931:Naa16 UTSW 14 79,344,955 (GRCm38) missense probably damaging 1.00
R9010:Naa16 UTSW 14 79,370,042 (GRCm38) missense probably benign 0.01
R9068:Naa16 UTSW 14 79,374,849 (GRCm38) missense probably benign 0.18
R9360:Naa16 UTSW 14 79,356,503 (GRCm38) missense probably benign 0.05
R9688:Naa16 UTSW 14 79,335,869 (GRCm38) nonsense probably null
X0064:Naa16 UTSW 14 79,351,389 (GRCm38) missense probably damaging 1.00
Z1177:Naa16 UTSW 14 79,344,979 (GRCm38) missense probably damaging 1.00
Posted On 2013-06-21