Incidental Mutation 'R5555:Nbeal1'
ID 435319
Institutional Source Beutler Lab
Gene Symbol Nbeal1
Ensembl Gene ENSMUSG00000073664
Gene Name neurobeachin like 1
Synonyms A530083I02Rik, A530050O19Rik, ALS2CR17, 2310076G13Rik
MMRRC Submission 043112-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5555 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 60180599-60338328 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to G at 60237152 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 684 (V684G)
Ref Sequence ENSEMBL: ENSMUSP00000124056 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000160834] [ENSMUST00000160980]
AlphaFold E9PYP2
Predicted Effect possibly damaging
Transcript: ENSMUST00000160834
AA Change: V684G

PolyPhen 2 Score 0.926 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000124056
Gene: ENSMUSG00000073664
AA Change: V684G

DomainStartEndE-ValueType
low complexity region 522 541 N/A INTRINSIC
Pfam:Laminin_G_3 567 801 8.3e-9 PFAM
low complexity region 1383 1401 N/A INTRINSIC
low complexity region 1849 1865 N/A INTRINSIC
Pfam:PH_BEACH 1882 1975 4.9e-32 PFAM
Beach 1998 2278 7.2e-199 SMART
Blast:Beach 2342 2405 6e-30 BLAST
WD40 2425 2463 5.52e-2 SMART
WD40 2475 2514 4.95e-4 SMART
WD40 2604 2649 7.64e1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000160980
SMART Domains Protein: ENSMUSP00000125147
Gene: ENSMUSG00000073664

DomainStartEndE-ValueType
low complexity region 278 297 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188450
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.4%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI

All alleles(16) : Targeted(1) Gene trapped(15)

Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atg7 T C 6: 114,702,053 (GRCm38) V366A probably damaging Het
Cadm2 A T 16: 66,784,815 (GRCm38) V192E probably damaging Het
Chil6 C T 3: 106,389,952 (GRCm38) S291N possibly damaging Het
D7Ertd443e T C 7: 134,349,591 (GRCm38) T118A probably benign Het
Dennd4b G A 3: 90,268,368 (GRCm38) R148Q probably damaging Het
Dnah1 T A 14: 31,290,819 (GRCm38) T1837S probably damaging Het
Elapor2 T A 5: 9,422,296 (GRCm38) probably null Het
Ext1 A G 15: 53,088,143 (GRCm38) V515A probably damaging Het
Fer1l4 T C 2: 156,048,189 (GRCm38) E272G probably damaging Het
Fras1 T A 5: 96,677,377 (GRCm38) H1475Q probably benign Het
Grid1 T C 14: 35,520,705 (GRCm38) S672P possibly damaging Het
Gtpbp4 A G 13: 8,979,427 (GRCm38) probably null Het
Hsp90aa1 A T 12: 110,692,734 (GRCm38) V543E probably damaging Het
Irf5 T C 6: 29,531,146 (GRCm38) S4P probably benign Het
Kif2b G T 11: 91,575,460 (GRCm38) Q666K probably benign Het
Macc1 A T 12: 119,450,375 (GRCm38) H762L probably benign Het
Map1s C T 8: 70,917,107 (GRCm38) T941M probably damaging Het
Mrgprb1 T A 7: 48,447,775 (GRCm38) I130F probably benign Het
Ngly1 C T 14: 16,270,508 (GRCm38) Q173* probably null Het
Plcb3 A T 19: 6,966,219 (GRCm38) M104K probably benign Het
Plcg2 T A 8: 117,612,995 (GRCm38) Y1048* probably null Het
Ptprf T C 4: 118,224,924 (GRCm38) Y1039C probably damaging Het
Rab38 A G 7: 88,430,487 (GRCm38) Y29C probably damaging Het
Rcan2 T A 17: 44,037,030 (GRCm38) V210E probably damaging Het
Rptn A T 3: 93,396,701 (GRCm38) Q447L probably benign Het
Scel G A 14: 103,602,206 (GRCm38) R495K probably benign Het
Scn11a G T 9: 119,755,238 (GRCm38) P1437Q probably damaging Het
Sim2 A G 16: 94,109,456 (GRCm38) D239G probably damaging Het
Skap2 A G 6: 51,860,018 (GRCm38) Y356H probably damaging Het
Skint11 A G 4: 114,194,601 (GRCm38) T49A probably benign Het
Snx33 G A 9: 56,925,397 (GRCm38) H463Y probably benign Het
Steap2 T C 5: 5,677,544 (GRCm38) T264A possibly damaging Het
Stk40 T A 4: 126,135,059 (GRCm38) V238E probably damaging Het
Sun2 T C 15: 79,734,127 (GRCm38) D277G probably benign Het
Ttll9 T C 2: 152,990,100 (GRCm38) probably null Het
Vmn1r54 G A 6: 90,269,365 (GRCm38) C87Y probably benign Het
Other mutations in Nbeal1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Nbeal1 APN 1 60,235,191 (GRCm38) nonsense probably null 0.00
IGL00334:Nbeal1 APN 1 60,281,883 (GRCm38) missense probably damaging 0.98
IGL00334:Nbeal1 APN 1 60,328,103 (GRCm38) missense probably damaging 1.00
IGL00514:Nbeal1 APN 1 60,217,225 (GRCm38) missense probably benign 0.31
IGL00596:Nbeal1 APN 1 60,181,741 (GRCm38) missense probably damaging 0.96
IGL00654:Nbeal1 APN 1 60,195,011 (GRCm38) critical splice acceptor site probably benign 0.00
IGL00757:Nbeal1 APN 1 60,195,143 (GRCm38) missense possibly damaging 0.82
IGL00771:Nbeal1 APN 1 60,235,353 (GRCm38) missense probably benign 0.11
IGL01315:Nbeal1 APN 1 60,281,341 (GRCm38) missense probably damaging 1.00
IGL01445:Nbeal1 APN 1 60,242,625 (GRCm38) critical splice donor site probably null
IGL01456:Nbeal1 APN 1 60,230,628 (GRCm38) missense probably damaging 1.00
IGL01458:Nbeal1 APN 1 60,242,625 (GRCm38) critical splice donor site probably null
IGL01535:Nbeal1 APN 1 60,217,255 (GRCm38) missense probably damaging 1.00
IGL01608:Nbeal1 APN 1 60,242,535 (GRCm38) critical splice acceptor site probably benign 0.00
IGL02006:Nbeal1 APN 1 60,272,259 (GRCm38) critical splice donor site probably null
IGL02105:Nbeal1 APN 1 60,253,501 (GRCm38) missense probably damaging 1.00
IGL02409:Nbeal1 APN 1 60,329,335 (GRCm38) missense probably benign 0.01
IGL02713:Nbeal1 APN 1 60,235,237 (GRCm38) missense possibly damaging 0.94
IGL02720:Nbeal1 APN 1 60,283,987 (GRCm38) missense probably damaging 0.98
IGL02887:Nbeal1 APN 1 60,287,444 (GRCm38) splice site probably benign
IGL02945:Nbeal1 APN 1 60,206,410 (GRCm38) missense probably damaging 1.00
IGL03023:Nbeal1 APN 1 60,253,413 (GRCm38) missense probably damaging 0.98
IGL03114:Nbeal1 APN 1 60,278,727 (GRCm38) missense probably damaging 1.00
IGL03231:Nbeal1 APN 1 60,236,459 (GRCm38) missense probably benign 0.44
IGL03241:Nbeal1 APN 1 60,234,868 (GRCm38) missense possibly damaging 0.46
IGL03241:Nbeal1 APN 1 60,234,869 (GRCm38) missense probably benign 0.44
IGL03382:Nbeal1 APN 1 60,261,586 (GRCm38) critical splice donor site probably null
IGL03412:Nbeal1 APN 1 60,242,567 (GRCm38) nonsense probably null
coach UTSW 1 60,253,481 (GRCm38) nonsense probably null
Committee UTSW 1 60,292,903 (GRCm38) missense probably damaging 1.00
Disgrace UTSW 1 60,281,310 (GRCm38) nonsense probably null
Dravrah UTSW 1 60,284,092 (GRCm38) missense probably damaging 1.00
Harvard UTSW 1 60,235,563 (GRCm38) splice site probably null
horrified UTSW 1 60,244,824 (GRCm38) missense probably damaging 1.00
Lampoon UTSW 1 60,261,586 (GRCm38) critical splice donor site probably null
lawyer UTSW 1 60,310,224 (GRCm38) nonsense probably null
magistrate UTSW 1 60,194,597 (GRCm38) critical splice donor site probably null
Maratimus UTSW 1 60,291,888 (GRCm38) missense probably damaging 1.00
National UTSW 1 60,222,263 (GRCm38) missense possibly damaging 0.95
phainopepla UTSW 1 60,319,687 (GRCm38) missense probably damaging 1.00
R3875_Nbeal1_770 UTSW 1 60,194,599 (GRCm38) splice site probably benign
satirical UTSW 1 60,235,562 (GRCm38) critical splice donor site probably null
silky UTSW 1 60,330,878 (GRCm38) splice site probably benign
stiggs UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
3-1:Nbeal1 UTSW 1 60,264,272 (GRCm38) splice site probably benign
P0007:Nbeal1 UTSW 1 60,319,688 (GRCm38) missense probably damaging 0.98
P0028:Nbeal1 UTSW 1 60,291,937 (GRCm38) missense probably damaging 1.00
R0041:Nbeal1 UTSW 1 60,281,871 (GRCm38) missense probably benign 0.05
R0051:Nbeal1 UTSW 1 60,310,263 (GRCm38) missense probably benign 0.19
R0052:Nbeal1 UTSW 1 60,228,612 (GRCm38) splice site probably benign
R0054:Nbeal1 UTSW 1 60,287,401 (GRCm38) utr 3 prime probably benign
R0062:Nbeal1 UTSW 1 60,247,717 (GRCm38) missense probably benign 0.01
R0062:Nbeal1 UTSW 1 60,247,717 (GRCm38) missense probably benign 0.01
R0094:Nbeal1 UTSW 1 60,305,309 (GRCm38) missense possibly damaging 0.62
R0310:Nbeal1 UTSW 1 60,305,370 (GRCm38) splice site probably benign
R0324:Nbeal1 UTSW 1 60,292,873 (GRCm38) missense probably damaging 1.00
R0329:Nbeal1 UTSW 1 60,268,063 (GRCm38) missense probably damaging 1.00
R0330:Nbeal1 UTSW 1 60,268,063 (GRCm38) missense probably damaging 1.00
R0417:Nbeal1 UTSW 1 60,247,734 (GRCm38) missense probably benign 0.00
R0421:Nbeal1 UTSW 1 60,268,439 (GRCm38) missense probably benign 0.08
R0617:Nbeal1 UTSW 1 60,281,832 (GRCm38) nonsense probably null
R1034:Nbeal1 UTSW 1 60,290,006 (GRCm38) nonsense probably null
R1082:Nbeal1 UTSW 1 60,312,226 (GRCm38) missense probably damaging 0.99
R1123:Nbeal1 UTSW 1 60,260,269 (GRCm38) missense probably benign
R1187:Nbeal1 UTSW 1 60,194,528 (GRCm38) missense probably damaging 1.00
R1484:Nbeal1 UTSW 1 60,200,939 (GRCm38) missense probably damaging 1.00
R1594:Nbeal1 UTSW 1 60,305,291 (GRCm38) missense possibly damaging 0.91
R1651:Nbeal1 UTSW 1 60,200,119 (GRCm38) missense probably damaging 1.00
R1678:Nbeal1 UTSW 1 60,260,334 (GRCm38) missense probably benign 0.00
R1806:Nbeal1 UTSW 1 60,284,092 (GRCm38) missense probably damaging 1.00
R1937:Nbeal1 UTSW 1 60,267,941 (GRCm38) nonsense probably null
R1952:Nbeal1 UTSW 1 60,234,840 (GRCm38) missense probably damaging 1.00
R1953:Nbeal1 UTSW 1 60,234,840 (GRCm38) missense probably damaging 1.00
R2038:Nbeal1 UTSW 1 60,206,344 (GRCm38) missense probably benign 0.00
R2044:Nbeal1 UTSW 1 60,319,687 (GRCm38) missense probably damaging 1.00
R2050:Nbeal1 UTSW 1 60,292,964 (GRCm38) splice site probably null
R2055:Nbeal1 UTSW 1 60,311,057 (GRCm38) missense probably damaging 1.00
R2064:Nbeal1 UTSW 1 60,270,356 (GRCm38) missense possibly damaging 0.89
R2100:Nbeal1 UTSW 1 60,305,271 (GRCm38) splice site probably null
R2181:Nbeal1 UTSW 1 60,278,780 (GRCm38) missense probably damaging 1.00
R2192:Nbeal1 UTSW 1 60,281,895 (GRCm38) missense probably damaging 1.00
R2203:Nbeal1 UTSW 1 60,284,006 (GRCm38) missense probably benign 0.21
R2267:Nbeal1 UTSW 1 60,330,878 (GRCm38) splice site probably benign
R2268:Nbeal1 UTSW 1 60,330,878 (GRCm38) splice site probably benign
R2351:Nbeal1 UTSW 1 60,237,098 (GRCm38) missense possibly damaging 0.90
R2366:Nbeal1 UTSW 1 60,251,352 (GRCm38) missense probably damaging 0.97
R2393:Nbeal1 UTSW 1 60,251,370 (GRCm38) missense probably damaging 0.98
R3545:Nbeal1 UTSW 1 60,278,780 (GRCm38) missense probably damaging 1.00
R3546:Nbeal1 UTSW 1 60,278,780 (GRCm38) missense probably damaging 1.00
R3547:Nbeal1 UTSW 1 60,278,780 (GRCm38) missense probably damaging 1.00
R3701:Nbeal1 UTSW 1 60,251,413 (GRCm38) splice site probably benign
R3747:Nbeal1 UTSW 1 60,195,023 (GRCm38) missense probably damaging 0.98
R3875:Nbeal1 UTSW 1 60,194,599 (GRCm38) splice site probably benign
R4119:Nbeal1 UTSW 1 60,291,870 (GRCm38) missense probably damaging 0.99
R4256:Nbeal1 UTSW 1 60,330,948 (GRCm38) missense probably benign 0.19
R4371:Nbeal1 UTSW 1 60,289,946 (GRCm38) missense possibly damaging 0.95
R4450:Nbeal1 UTSW 1 60,267,774 (GRCm38) missense probably damaging 0.97
R4558:Nbeal1 UTSW 1 60,281,310 (GRCm38) nonsense probably null
R4618:Nbeal1 UTSW 1 60,228,731 (GRCm38) intron probably benign
R4673:Nbeal1 UTSW 1 60,329,390 (GRCm38) missense probably damaging 1.00
R4719:Nbeal1 UTSW 1 60,235,563 (GRCm38) splice site probably null
R4798:Nbeal1 UTSW 1 60,222,193 (GRCm38) splice site probably null
R4826:Nbeal1 UTSW 1 60,251,342 (GRCm38) missense possibly damaging 0.79
R4841:Nbeal1 UTSW 1 60,253,375 (GRCm38) missense probably damaging 1.00
R4842:Nbeal1 UTSW 1 60,253,375 (GRCm38) missense probably damaging 1.00
R4895:Nbeal1 UTSW 1 60,292,903 (GRCm38) missense probably damaging 1.00
R4929:Nbeal1 UTSW 1 60,238,654 (GRCm38) missense probably damaging 1.00
R5026:Nbeal1 UTSW 1 60,237,179 (GRCm38) missense probably damaging 1.00
R5243:Nbeal1 UTSW 1 60,270,328 (GRCm38) missense probably damaging 0.99
R5300:Nbeal1 UTSW 1 60,235,559 (GRCm38) nonsense probably null
R5345:Nbeal1 UTSW 1 60,328,210 (GRCm38) critical splice donor site probably null
R5502:Nbeal1 UTSW 1 60,310,999 (GRCm38) missense probably damaging 1.00
R5542:Nbeal1 UTSW 1 60,277,194 (GRCm38) missense probably benign 0.00
R5580:Nbeal1 UTSW 1 60,242,602 (GRCm38) missense probably benign 0.45
R5765:Nbeal1 UTSW 1 60,291,847 (GRCm38) missense probably damaging 1.00
R5802:Nbeal1 UTSW 1 60,272,221 (GRCm38) missense probably benign 0.01
R5907:Nbeal1 UTSW 1 60,228,791 (GRCm38) intron probably benign
R5918:Nbeal1 UTSW 1 60,267,892 (GRCm38) missense possibly damaging 0.90
R5923:Nbeal1 UTSW 1 60,248,395 (GRCm38) missense probably damaging 1.00
R6066:Nbeal1 UTSW 1 60,248,405 (GRCm38) missense probably benign 0.29
R6091:Nbeal1 UTSW 1 60,181,556 (GRCm38) start gained probably benign
R6113:Nbeal1 UTSW 1 60,222,263 (GRCm38) missense possibly damaging 0.95
R6143:Nbeal1 UTSW 1 60,251,307 (GRCm38) missense possibly damaging 0.81
R6194:Nbeal1 UTSW 1 60,257,484 (GRCm38) missense possibly damaging 0.80
R6197:Nbeal1 UTSW 1 60,222,128 (GRCm38) missense probably damaging 0.99
R6228:Nbeal1 UTSW 1 60,295,924 (GRCm38) missense probably benign 0.00
R6229:Nbeal1 UTSW 1 60,248,365 (GRCm38) missense possibly damaging 0.88
R6309:Nbeal1 UTSW 1 60,238,719 (GRCm38) missense probably benign
R6457:Nbeal1 UTSW 1 60,253,474 (GRCm38) missense probably benign 0.31
R6489:Nbeal1 UTSW 1 60,330,942 (GRCm38) missense possibly damaging 0.89
R6845:Nbeal1 UTSW 1 60,281,310 (GRCm38) nonsense probably null
R7021:Nbeal1 UTSW 1 60,261,586 (GRCm38) critical splice donor site probably null
R7033:Nbeal1 UTSW 1 60,310,947 (GRCm38) missense probably damaging 1.00
R7144:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7145:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7146:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7157:Nbeal1 UTSW 1 60,260,634 (GRCm38) nonsense probably null
R7157:Nbeal1 UTSW 1 60,237,158 (GRCm38) missense probably damaging 1.00
R7209:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7210:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7211:Nbeal1 UTSW 1 60,200,951 (GRCm38) missense probably damaging 1.00
R7212:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7213:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7214:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7283:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7285:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7287:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7296:Nbeal1 UTSW 1 60,310,224 (GRCm38) nonsense probably null
R7312:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7313:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7329:Nbeal1 UTSW 1 60,217,196 (GRCm38) missense probably benign 0.39
R7380:Nbeal1 UTSW 1 60,244,810 (GRCm38) missense probably damaging 1.00
R7414:Nbeal1 UTSW 1 60,194,597 (GRCm38) critical splice donor site probably null
R7477:Nbeal1 UTSW 1 60,261,584 (GRCm38) missense probably benign
R7507:Nbeal1 UTSW 1 60,235,467 (GRCm38) missense probably damaging 1.00
R7642:Nbeal1 UTSW 1 60,277,227 (GRCm38) missense probably benign 0.31
R7678:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7689:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7728:Nbeal1 UTSW 1 60,244,824 (GRCm38) missense probably damaging 1.00
R7757:Nbeal1 UTSW 1 60,257,450 (GRCm38) missense probably damaging 0.97
R7761:Nbeal1 UTSW 1 60,319,341 (GRCm38) missense probably benign 0.00
R7813:Nbeal1 UTSW 1 60,291,889 (GRCm38) missense probably damaging 1.00
R7829:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R7891:Nbeal1 UTSW 1 60,260,432 (GRCm38) missense probably benign
R7902:Nbeal1 UTSW 1 60,291,870 (GRCm38) missense probably damaging 0.99
R8022:Nbeal1 UTSW 1 60,260,272 (GRCm38) nonsense probably null
R8053:Nbeal1 UTSW 1 60,279,795 (GRCm38) missense probably damaging 0.98
R8169:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R8170:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R8178:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R8182:Nbeal1 UTSW 1 60,200,133 (GRCm38) missense probably benign 0.00
R8186:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R8187:Nbeal1 UTSW 1 60,237,151 (GRCm38) missense probably benign 0.11
R8193:Nbeal1 UTSW 1 60,253,481 (GRCm38) nonsense probably null
R8209:Nbeal1 UTSW 1 60,277,177 (GRCm38) missense probably damaging 0.99
R8226:Nbeal1 UTSW 1 60,277,177 (GRCm38) missense probably damaging 0.99
R8549:Nbeal1 UTSW 1 60,235,562 (GRCm38) critical splice donor site probably null
R8560:Nbeal1 UTSW 1 60,235,157 (GRCm38) missense probably benign 0.38
R8753:Nbeal1 UTSW 1 60,268,383 (GRCm38) missense probably damaging 1.00
R8769:Nbeal1 UTSW 1 60,235,211 (GRCm38) missense probably damaging 0.99
R8771:Nbeal1 UTSW 1 60,261,584 (GRCm38) missense probably benign
R8952:Nbeal1 UTSW 1 60,260,300 (GRCm38) missense probably benign 0.01
R9014:Nbeal1 UTSW 1 60,289,959 (GRCm38) missense probably damaging 1.00
R9056:Nbeal1 UTSW 1 60,278,726 (GRCm38) missense probably damaging 1.00
R9091:Nbeal1 UTSW 1 60,268,389 (GRCm38) missense possibly damaging 0.50
R9138:Nbeal1 UTSW 1 60,247,745 (GRCm38) nonsense probably null
R9168:Nbeal1 UTSW 1 60,291,888 (GRCm38) missense probably damaging 1.00
R9200:Nbeal1 UTSW 1 60,281,266 (GRCm38) missense probably damaging 1.00
R9205:Nbeal1 UTSW 1 60,278,680 (GRCm38) missense probably damaging 1.00
R9270:Nbeal1 UTSW 1 60,268,389 (GRCm38) missense possibly damaging 0.50
R9322:Nbeal1 UTSW 1 60,258,659 (GRCm38) missense possibly damaging 0.91
R9405:Nbeal1 UTSW 1 60,310,265 (GRCm38) missense probably damaging 1.00
R9554:Nbeal1 UTSW 1 60,251,128 (GRCm38) nonsense probably null
R9557:Nbeal1 UTSW 1 60,235,350 (GRCm38) missense probably benign
R9560:Nbeal1 UTSW 1 60,329,385 (GRCm38) missense probably damaging 1.00
R9641:Nbeal1 UTSW 1 60,311,088 (GRCm38) missense probably damaging 1.00
R9784:Nbeal1 UTSW 1 60,260,582 (GRCm38) nonsense probably null
X0022:Nbeal1 UTSW 1 60,277,232 (GRCm38) missense probably benign
Predicted Primers PCR Primer
(F):5'- ATCTTTGAAGATTTCCTAGGCTGG -3'
(R):5'- TGCTGAACCTACTTCTCCAAAC -3'

Sequencing Primer
(F):5'- TGTTAAACCAGTTATCTCTGTTGC -3'
(R):5'- ACATCTGAAATTATCTAATGGCAGAC -3'
Posted On 2016-10-24