Incidental Mutation 'R5714:Nat8f2'
ID 451044
Institutional Source Beutler Lab
Gene Symbol Nat8f2
Ensembl Gene ENSMUSG00000033634
Gene Name N-acetyltransferase 8 (GCN5-related) family member 2
Synonyms Cml2
MMRRC Submission 043186-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5714 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 85842404-85846119 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 85844891 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 157 (V157A)
Ref Sequence ENSEMBL: ENSMUSP00000044587 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045008]
AlphaFold Q8CHQ9
Predicted Effect probably benign
Transcript: ENSMUST00000045008
AA Change: V157A

PolyPhen 2 Score 0.431 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000044587
Gene: ENSMUSG00000033634
AA Change: V157A

DomainStartEndE-ValueType
transmembrane domain 37 56 N/A INTRINSIC
Pfam:Acetyltransf_10 77 192 4.9e-14 PFAM
Pfam:Acetyltransf_9 79 195 1.1e-9 PFAM
Pfam:Acetyltransf_4 84 205 1.1e-9 PFAM
Pfam:Acetyltransf_8 86 205 6.9e-12 PFAM
Pfam:Acetyltransf_7 104 194 2e-14 PFAM
Pfam:Acetyltransf_1 111 193 1e-17 PFAM
Pfam:FR47 130 200 5.1e-8 PFAM
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alpk2 G T 18: 65,438,532 (GRCm39) Q1421K possibly damaging Het
Ankub1 G A 3: 57,580,258 (GRCm39) T133M probably benign Het
Bcar3 G A 3: 122,248,736 (GRCm39) V112M possibly damaging Het
Cacna1s A G 1: 136,039,804 (GRCm39) K1476R probably benign Het
Cdc42ep1 C A 15: 78,733,977 (GRCm39) A359E possibly damaging Het
Cemip T A 7: 83,624,387 (GRCm39) D483V probably damaging Het
Cyp4f39 G A 17: 32,700,799 (GRCm39) R156H probably damaging Het
Dpys T A 15: 39,720,553 (GRCm39) H69L probably damaging Het
Fbxl21 A G 13: 56,674,885 (GRCm39) I79V probably benign Het
Fgf9 T C 14: 58,347,022 (GRCm39) L205P probably damaging Het
Fkbp14 A G 6: 54,562,835 (GRCm39) F144L probably damaging Het
Flnb A C 14: 7,929,073 (GRCm38) D1934A probably damaging Het
Garre1 G A 7: 33,939,941 (GRCm39) Q717* probably null Het
Glul T C 1: 153,782,243 (GRCm39) probably benign Het
Helz T A 11: 107,517,347 (GRCm39) probably null Het
Kap A G 6: 133,828,956 (GRCm39) Y42H probably benign Het
Kcnh8 T C 17: 53,285,150 (GRCm39) V1040A probably benign Het
Kptn A G 7: 15,854,683 (GRCm39) probably null Het
Lypd3 A G 7: 24,338,494 (GRCm39) T182A possibly damaging Het
Mcm5 A C 8: 75,847,538 (GRCm39) D445A probably damaging Het
Mios T A 6: 8,215,434 (GRCm39) I210K probably damaging Het
Or1e16 T A 11: 73,286,187 (GRCm39) probably null Het
Pard3b C A 1: 62,677,075 (GRCm39) A1140E probably null Het
Pcnt A T 10: 76,256,325 (GRCm39) D638E probably damaging Het
Pdgfra T C 5: 75,346,673 (GRCm39) I834T probably damaging Het
Phyhd1 T A 2: 30,169,994 (GRCm39) L162H probably damaging Het
Polg C A 7: 79,101,739 (GRCm39) A1026S possibly damaging Het
Prl7c1 A T 13: 27,962,949 (GRCm39) L18* probably null Het
Rars2 T A 4: 34,645,779 (GRCm39) M232K probably benign Het
Rtl1 A G 12: 109,560,114 (GRCm39) V575A probably damaging Het
Slc18b1 A T 10: 23,674,664 (GRCm39) T40S probably benign Het
Slc22a19 T C 19: 7,688,387 (GRCm39) T58A probably damaging Het
Slc27a6 A T 18: 58,731,625 (GRCm39) E325V probably damaging Het
Slc35e2 C T 4: 155,694,483 (GRCm39) P10L probably benign Het
Srd5a3 T A 5: 76,301,413 (GRCm39) F214Y probably benign Het
Tgfbr2 A T 9: 116,004,092 (GRCm39) L5Q probably damaging Het
Tmem94 C A 11: 115,684,016 (GRCm39) Q779K probably benign Het
Ttn G A 2: 76,652,837 (GRCm39) P216S probably benign Het
Ush2a A T 1: 188,132,454 (GRCm39) Q892L probably benign Het
Vgll4 A T 6: 114,867,737 (GRCm39) M38K possibly damaging Het
Vmn2r109 A G 17: 20,773,121 (GRCm39) I500T probably damaging Het
Vps33a T C 5: 123,707,563 (GRCm39) I135V probably benign Het
Wscd1 T C 11: 71,675,261 (GRCm39) probably null Het
Zfp457 C A 13: 67,444,490 (GRCm39) M4I possibly damaging Het
Zfp532 G A 18: 65,756,606 (GRCm39) G180R possibly damaging Het
Zfp97 A G 17: 17,365,871 (GRCm39) T457A possibly damaging Het
Other mutations in Nat8f2
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4449:Nat8f2 UTSW 6 85,844,668 (GRCm39) missense possibly damaging 0.84
FR4737:Nat8f2 UTSW 6 85,844,668 (GRCm39) missense possibly damaging 0.84
R0063:Nat8f2 UTSW 6 85,844,815 (GRCm39) missense possibly damaging 0.50
R0063:Nat8f2 UTSW 6 85,844,815 (GRCm39) missense possibly damaging 0.50
R0384:Nat8f2 UTSW 6 85,845,350 (GRCm39) missense possibly damaging 0.63
R0532:Nat8f2 UTSW 6 85,844,784 (GRCm39) missense probably benign 0.01
R2143:Nat8f2 UTSW 6 85,845,239 (GRCm39) missense probably benign 0.00
R3698:Nat8f2 UTSW 6 85,844,778 (GRCm39) missense probably benign 0.16
R4335:Nat8f2 UTSW 6 85,845,233 (GRCm39) missense probably damaging 1.00
R5369:Nat8f2 UTSW 6 85,844,854 (GRCm39) nonsense probably null
R5484:Nat8f2 UTSW 6 85,844,994 (GRCm39) missense possibly damaging 0.76
R6737:Nat8f2 UTSW 6 85,845,194 (GRCm39) missense probably benign 0.00
R7676:Nat8f2 UTSW 6 85,845,194 (GRCm39) missense probably benign 0.00
R8054:Nat8f2 UTSW 6 85,844,754 (GRCm39) missense probably benign 0.00
R8415:Nat8f2 UTSW 6 85,845,024 (GRCm39) missense probably damaging 0.99
R9598:Nat8f2 UTSW 6 85,844,848 (GRCm39) missense probably benign 0.01
R9710:Nat8f2 UTSW 6 85,844,683 (GRCm39) nonsense probably null
Z1176:Nat8f2 UTSW 6 85,845,026 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCCTGGTCCTGAAGCAAAAG -3'
(R):5'- CAGATCTTGCTGACATCACCAAGTC -3'

Sequencing Primer
(F):5'- TGGTCCTGAAGCAAAAGGGAGAG -3'
(R):5'- AGTCTTACCTGAATGCACATGGC -3'
Posted On 2017-01-03