Incidental Mutation 'R7134:Nap1l1'
ID 552927
Institutional Source Beutler Lab
Gene Symbol Nap1l1
Ensembl Gene ENSMUSG00000058799
Gene Name nucleosome assembly protein 1-like 1
Synonyms D10Ertd68e
MMRRC Submission 045219-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.333) question?
Stock # R7134 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 111309084-111334011 bp(+) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) G to A at 111330655 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000070068 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000065917] [ENSMUST00000217908] [ENSMUST00000218828] [ENSMUST00000219143] [ENSMUST00000219961]
AlphaFold P28656
Predicted Effect probably null
Transcript: ENSMUST00000065917
SMART Domains Protein: ENSMUSP00000070068
Gene: ENSMUSG00000058799

DomainStartEndE-ValueType
coiled coil region 6 31 N/A INTRINSIC
Pfam:NAP 75 346 1.5e-96 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000217908
Predicted Effect probably null
Transcript: ENSMUST00000218828
Predicted Effect probably null
Transcript: ENSMUST00000219143
Predicted Effect probably null
Transcript: ENSMUST00000219961
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 99% (84/85)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the nucleosome assembly protein (NAP) family. This protein participates in DNA replication and may play a role in modulating chromatin formation and contribute to the regulation of cell proliferation. Alternative splicing results in multiple transcript variants encoding different isoforms; however, not all have been fully described. [provided by RefSeq, Apr 2015]
Allele List at MGI
Other mutations in this stock
Total: 86 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 A G 17: 36,270,144 (GRCm39) F638S possibly damaging Het
Actl6b T A 5: 137,562,762 (GRCm39) N159K probably damaging Het
Adam6a T G 12: 113,508,655 (GRCm39) S343A probably benign Het
Ankrd17 G A 5: 90,380,173 (GRCm39) T2505I probably damaging Het
Ankrd17 T C 5: 90,433,382 (GRCm39) T728A probably benign Het
Asap2 G T 12: 21,315,964 (GRCm39) E919* probably null Het
Atp10b A T 11: 43,136,291 (GRCm39) I1140F probably damaging Het
Cep126 A T 9: 8,103,383 (GRCm39) V209E probably damaging Het
Cfap65 C T 1: 74,965,792 (GRCm39) R406Q probably benign Het
Cldn1 T C 16: 26,190,376 (GRCm39) M1V probably null Het
Cryl1 C T 14: 57,512,956 (GRCm39) D304N probably benign Het
D3Ertd751e T C 3: 41,708,212 (GRCm39) probably null Het
D630044L22Rik A T 17: 26,181,090 (GRCm39) M156L probably benign Het
Ddx21 T C 10: 62,427,634 (GRCm39) D423G possibly damaging Het
Dock2 T A 11: 34,260,363 (GRCm39) M993L probably benign Het
Dusp29 A T 14: 21,727,129 (GRCm39) I173N probably damaging Het
Eif4g1 C T 16: 20,500,252 (GRCm39) A675V probably damaging Het
Eml1 C T 12: 108,472,810 (GRCm39) S206L probably benign Het
Farp2 A C 1: 93,531,181 (GRCm39) I560L probably benign Het
Fbn1 A T 2: 125,223,969 (GRCm39) D593E probably benign Het
Fetub A G 16: 22,748,007 (GRCm39) D61G possibly damaging Het
Fpgs T C 2: 32,576,641 (GRCm39) K329E probably benign Het
Fpgt T C 3: 154,797,120 (GRCm39) Y45C probably damaging Het
Gas2l1 A T 11: 5,011,106 (GRCm39) C574* probably null Het
Gm9747 G T 1: 82,211,837 (GRCm39) C12F unknown Het
H2-T23 T C 17: 36,342,709 (GRCm39) Y143C probably damaging Het
Hhip A T 8: 80,719,142 (GRCm39) S462T probably benign Het
Hnf1a C T 5: 115,091,446 (GRCm39) G416R probably damaging Het
Hoxa5 C T 6: 52,181,023 (GRCm39) C103Y probably damaging Het
Kansl3 G T 1: 36,390,848 (GRCm39) D395E possibly damaging Het
Marchf10 A G 11: 105,299,502 (GRCm39) S116P probably benign Het
Med12l C T 3: 59,001,180 (GRCm39) Q748* probably null Het
Mroh7 T A 4: 106,577,791 (GRCm39) N296Y probably damaging Het
Mtbp T G 15: 55,421,961 (GRCm39) D61E probably benign Het
Muc5b A T 7: 141,411,391 (GRCm39) I1446L unknown Het
Myh15 T C 16: 48,901,705 (GRCm39) V266A possibly damaging Het
Napsa A G 7: 44,235,159 (GRCm39) T315A probably benign Het
Nlrc5 A T 8: 95,206,350 (GRCm39) I734F probably damaging Het
Nnt A G 13: 119,531,198 (GRCm39) V183A probably damaging Het
Nploc4 A T 11: 120,276,614 (GRCm39) D477E probably benign Het
Nrip3 A G 7: 109,364,695 (GRCm39) S144P probably damaging Het
Ntng1 A T 3: 109,842,445 (GRCm39) F109L probably benign Het
Or5p61 A G 7: 107,758,883 (GRCm39) Y66H probably damaging Het
Or5v1 T A 17: 37,809,776 (GRCm39) V78D probably damaging Het
Or6aa1 G A 7: 86,044,752 (GRCm39) probably benign Het
Or8b36 A G 9: 37,937,795 (GRCm39) E231G probably benign Het
Pacsin1 G A 17: 27,921,707 (GRCm39) D30N probably damaging Het
Pbld2 A T 10: 62,860,368 (GRCm39) probably benign Het
Pcnx4 C T 12: 72,613,750 (GRCm39) T565I probably damaging Het
Pdzk1 A T 3: 96,763,246 (GRCm39) T225S probably benign Het
Phyhip T G 14: 70,704,639 (GRCm39) I286S probably benign Het
Pkd1 T A 17: 24,813,086 (GRCm39) Y3903N probably damaging Het
Plcb3 A T 19: 6,942,698 (GRCm39) L222Q probably damaging Het
Plcd4 T A 1: 74,593,662 (GRCm39) H262Q probably benign Het
Plekhh1 C T 12: 79,109,390 (GRCm39) A474V probably benign Het
Plppr3 T C 10: 79,701,537 (GRCm39) E435G probably damaging Het
Poln T A 5: 34,276,340 (GRCm39) N305I possibly damaging Het
Pou3f2 T C 4: 22,486,874 (GRCm39) T420A probably benign Het
Ppdpf T C 2: 180,829,523 (GRCm39) Y17H probably damaging Het
Prrx2 C A 2: 30,768,485 (GRCm39) T104K probably damaging Het
Ptprj A T 2: 90,294,822 (GRCm39) L462H probably benign Het
Radil T C 5: 142,471,304 (GRCm39) T991A probably damaging Het
Rbsn T C 6: 92,178,608 (GRCm39) E147G probably damaging Het
Ror2 C T 13: 53,300,742 (GRCm39) V35M probably benign Het
Rps6ka1 T C 4: 133,599,373 (GRCm39) Q18R probably benign Het
Setbp1 T A 18: 78,902,734 (GRCm39) D311V possibly damaging Het
Setd2 C T 9: 110,377,865 (GRCm39) S560L possibly damaging Het
Slc12a5 A T 2: 164,816,878 (GRCm39) I134F probably damaging Het
Speer1h C T 5: 11,647,706 (GRCm39) T148I possibly damaging Het
Svil A G 18: 5,116,080 (GRCm39) D2035G probably damaging Het
Syngap1 T C 17: 27,178,985 (GRCm39) Y665H probably damaging Het
Tbc1d9b T C 11: 50,043,519 (GRCm39) Y547H possibly damaging Het
Tgm2 A G 2: 157,980,812 (GRCm39) V83A probably benign Het
Tmem233 T C 5: 116,189,429 (GRCm39) I117V probably benign Het
Tsen34 A G 7: 3,703,640 (GRCm39) T293A probably damaging Het
Ttn A G 2: 76,709,023 (GRCm39) V8752A unknown Het
Ubac1 A G 2: 25,904,974 (GRCm39) V88A probably benign Het
Uchl4 T C 9: 64,142,621 (GRCm39) V34A probably damaging Het
Ugt2a2 C T 5: 87,608,435 (GRCm39) R468H probably benign Het
Vmn2r102 A T 17: 19,897,749 (GRCm39) T255S probably benign Het
Wdr6 T A 9: 108,450,564 (GRCm39) N988I probably damaging Het
Wnk1 A T 6: 119,903,389 (GRCm39) I2359N unknown Het
Ybey A G 10: 76,304,025 (GRCm39) V59A probably benign Het
Zfp268 T A 4: 145,349,375 (GRCm39) C271S possibly damaging Het
Zfp397 A G 18: 24,090,122 (GRCm39) N142S probably benign Het
Zfy1 A T Y: 725,788 (GRCm39) V659E probably damaging Het
Other mutations in Nap1l1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01154:Nap1l1 APN 10 111,322,536 (GRCm39) missense probably damaging 0.98
IGL01453:Nap1l1 APN 10 111,328,839 (GRCm39) missense probably benign 0.09
IGL01734:Nap1l1 APN 10 111,328,760 (GRCm39) missense probably benign 0.26
IGL01843:Nap1l1 APN 10 111,328,772 (GRCm39) missense possibly damaging 0.93
PIT1430001:Nap1l1 UTSW 10 111,322,597 (GRCm39) missense probably damaging 1.00
PIT4131001:Nap1l1 UTSW 10 111,322,583 (GRCm39) missense probably null
R0020:Nap1l1 UTSW 10 111,326,884 (GRCm39) missense probably benign 0.01
R0020:Nap1l1 UTSW 10 111,326,884 (GRCm39) missense probably benign 0.01
R0131:Nap1l1 UTSW 10 111,321,370 (GRCm39) missense probably benign 0.17
R0131:Nap1l1 UTSW 10 111,321,370 (GRCm39) missense probably benign 0.17
R0132:Nap1l1 UTSW 10 111,321,370 (GRCm39) missense probably benign 0.17
R0601:Nap1l1 UTSW 10 111,326,224 (GRCm39) splice site probably benign
R1576:Nap1l1 UTSW 10 111,330,681 (GRCm39) missense probably damaging 1.00
R1619:Nap1l1 UTSW 10 111,329,240 (GRCm39) missense possibly damaging 0.77
R1969:Nap1l1 UTSW 10 111,326,914 (GRCm39) missense probably benign 0.03
R2071:Nap1l1 UTSW 10 111,328,761 (GRCm39) missense possibly damaging 0.46
R2383:Nap1l1 UTSW 10 111,329,272 (GRCm39) missense probably damaging 1.00
R3836:Nap1l1 UTSW 10 111,331,183 (GRCm39) splice site probably null
R3837:Nap1l1 UTSW 10 111,331,183 (GRCm39) splice site probably null
R3838:Nap1l1 UTSW 10 111,331,183 (GRCm39) splice site probably null
R3839:Nap1l1 UTSW 10 111,331,183 (GRCm39) splice site probably null
R4084:Nap1l1 UTSW 10 111,325,938 (GRCm39) missense possibly damaging 0.92
R4609:Nap1l1 UTSW 10 111,328,741 (GRCm39) nonsense probably null
R4985:Nap1l1 UTSW 10 111,325,944 (GRCm39) missense probably benign 0.01
R5906:Nap1l1 UTSW 10 111,326,891 (GRCm39) nonsense probably null
R5982:Nap1l1 UTSW 10 111,331,229 (GRCm39) missense possibly damaging 0.71
R6522:Nap1l1 UTSW 10 111,330,084 (GRCm39) missense probably damaging 0.99
R6868:Nap1l1 UTSW 10 111,330,669 (GRCm39) missense probably damaging 1.00
R7202:Nap1l1 UTSW 10 111,326,964 (GRCm39) missense probably damaging 1.00
R7789:Nap1l1 UTSW 10 111,326,317 (GRCm39) missense probably benign 0.01
R7950:Nap1l1 UTSW 10 111,328,769 (GRCm39) missense probably damaging 1.00
R8404:Nap1l1 UTSW 10 111,317,162 (GRCm39) start codon destroyed probably null 0.53
R8502:Nap1l1 UTSW 10 111,317,162 (GRCm39) start codon destroyed probably null 0.53
R8933:Nap1l1 UTSW 10 111,328,710 (GRCm39) missense probably benign 0.04
R9680:Nap1l1 UTSW 10 111,330,657 (GRCm39) missense probably damaging 0.99
R9772:Nap1l1 UTSW 10 111,325,911 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- ATACGGGTAATACAGAGTCTGC -3'
(R):5'- AGAGCTGATAACCCTGCAGC -3'

Sequencing Primer
(F):5'- TACAGAGTCTGCAAAGAAAGGGTAG -3'
(R):5'- CCCTGCAGCAGAACAAAATTATTTG -3'
Posted On 2019-05-15