Incidental Mutation 'R7796:Nrsn2'
ID 600211
Institutional Source Beutler Lab
Gene Symbol Nrsn2
Ensembl Gene ENSMUSG00000059361
Gene Name neurensin 2
Synonyms LOC228777, Neurensin-2
MMRRC Submission 045852-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.051) question?
Stock # R7796 (G1)
Quality Score 130.008
Status Validated
Chromosome 2
Chromosomal Location 152210675-152218558 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to A at 152218471 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000078260 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079278]
AlphaFold Q5HZK2
Predicted Effect probably benign
Transcript: ENSMUST00000079278
SMART Domains Protein: ENSMUSP00000078260
Gene: ENSMUSG00000059361

DomainStartEndE-ValueType
Pfam:Neurensin 20 154 1.5e-37 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.4%
Validation Efficiency 100% (54/54)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A630089N07Rik T A 16: 97,867,024 (GRCm39) I313F probably benign Het
Acot2 T A 12: 84,035,257 (GRCm39) probably null Het
Agbl4 G T 4: 110,518,165 (GRCm39) G152V unknown Het
Arap2 A G 5: 62,888,105 (GRCm39) S414P probably damaging Het
Cep85l A C 10: 53,157,497 (GRCm39) N735K probably damaging Het
Col12a1 T C 9: 79,585,833 (GRCm39) S1209G possibly damaging Het
Dennd1b G A 1: 138,990,611 (GRCm39) E192K probably damaging Het
Dpf1 C G 7: 29,011,106 (GRCm39) N168K possibly damaging Het
Dync1li2 T A 8: 105,157,181 (GRCm39) Y184F probably damaging Het
Epb41l2 A G 10: 25,319,727 (GRCm39) T187A probably benign Het
Fam50b G A 13: 34,931,084 (GRCm39) E187K possibly damaging Het
Fndc3b G A 3: 27,515,892 (GRCm39) T638I probably benign Het
Gm11564 A G 11: 99,706,424 (GRCm39) V2A unknown Het
Gm3159 A G 14: 4,400,560 (GRCm38) *206W probably null Het
Gm32742 A G 9: 51,071,123 (GRCm39) probably null Het
Gm4847 G A 1: 166,469,819 (GRCm39) H85Y probably damaging Het
Gprc5c A T 11: 114,755,358 (GRCm39) D345V probably damaging Het
Kalrn A T 16: 34,007,854 (GRCm39) Y1363* probably null Het
Kdm5a T C 6: 120,367,724 (GRCm39) V473A probably damaging Het
Kidins220 T C 12: 25,032,350 (GRCm39) C28R probably damaging Het
Klhl5 T C 5: 65,321,965 (GRCm39) Y664H probably damaging Het
Krt17 A G 11: 100,151,698 (GRCm39) S32P probably benign Het
Krt87 A G 15: 101,383,865 (GRCm39) V424A possibly damaging Het
Lipo3 T C 19: 33,759,634 (GRCm39) T201A possibly damaging Het
Map2 A G 1: 66,455,654 (GRCm39) probably null Het
Megf10 C A 18: 57,410,731 (GRCm39) T680N possibly damaging Het
Metap1d T A 2: 71,342,506 (GRCm39) D178E probably damaging Het
Miip C T 4: 147,947,375 (GRCm39) G236S probably benign Het
Mki67 A G 7: 135,299,923 (GRCm39) S1704P probably damaging Het
Nr2f2 A G 7: 70,007,901 (GRCm39) S194P probably benign Het
Ociad1 C T 5: 73,452,290 (GRCm39) P27L probably damaging Het
Or13p5 T A 4: 118,591,882 (GRCm39) I52N probably damaging Het
Or4a39 T A 2: 89,237,157 (GRCm39) T89S possibly damaging Het
Patj A T 4: 98,435,220 (GRCm39) M1L probably benign Het
Pcdhb2 A G 18: 37,428,446 (GRCm39) I140V possibly damaging Het
Pla2g6 T C 15: 79,202,025 (GRCm39) N49D probably benign Het
Pramel22 T A 4: 143,380,727 (GRCm39) D432V possibly damaging Het
Pxdc1 T A 13: 34,836,354 (GRCm39) N22I probably damaging Het
Rpgrip1l A G 8: 91,996,865 (GRCm39) Y672H probably damaging Het
Rps23rg1 T C 8: 3,634,160 (GRCm39) V111A probably benign Het
Safb2 T C 17: 56,873,327 (GRCm39) R779G possibly damaging Het
Skic2 C T 17: 35,063,394 (GRCm39) G628S probably damaging Het
Smg5 A T 3: 88,256,739 (GRCm39) Q299L probably damaging Het
Sptbn2 C G 19: 4,799,040 (GRCm39) R2037G probably benign Het
Sulf1 T C 1: 12,929,044 (GRCm39) L864S probably benign Het
Tas1r1 A G 4: 152,119,212 (GRCm39) V119A probably benign Het
Tasp1 T C 2: 139,850,705 (GRCm39) N106S probably damaging Het
Tcf4 T A 18: 69,697,140 (GRCm39) N156K probably benign Het
Trav14n-3 T A 14: 53,607,827 (GRCm39) Y52* probably null Het
Ttn T C 2: 76,665,222 (GRCm39) E11598G unknown Het
Unc80 A G 1: 66,542,873 (GRCm39) I376V probably benign Het
Ybx3 T C 6: 131,345,479 (GRCm39) E298G probably damaging Het
Yipf7 T C 5: 69,684,596 (GRCm39) Y73C possibly damaging Het
Zdbf2 G A 1: 63,342,583 (GRCm39) A321T possibly damaging Het
Zfp369 A G 13: 65,444,029 (GRCm39) R391G probably benign Het
Zfp54 A G 17: 21,654,982 (GRCm39) E492G probably damaging Het
Zfp971 A G 2: 177,673,403 (GRCm39) T51A probably benign Het
Other mutations in Nrsn2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03303:Nrsn2 APN 2 152,216,131 (GRCm39) missense possibly damaging 0.65
R0403:Nrsn2 UTSW 2 152,211,710 (GRCm39) missense probably damaging 1.00
R0714:Nrsn2 UTSW 2 152,216,042 (GRCm39) nonsense probably null
R2570:Nrsn2 UTSW 2 152,211,741 (GRCm39) missense possibly damaging 0.55
R4840:Nrsn2 UTSW 2 152,211,552 (GRCm39) missense probably benign 0.42
R4856:Nrsn2 UTSW 2 152,211,531 (GRCm39) missense probably benign 0.09
R4886:Nrsn2 UTSW 2 152,211,531 (GRCm39) missense probably benign 0.09
R6641:Nrsn2 UTSW 2 152,211,830 (GRCm39) missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- CTTGTCTATAAGCCCTGGGGTG -3'
(R):5'- CACAGGACTACAGTCTGCAG -3'

Sequencing Primer
(F):5'- CTATAAGCCCTGGGGTGTCGAG -3'
(R):5'- AGCAAACTCGCTCTGCT -3'
Posted On 2019-11-26