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 60219758-60377487 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 60276311 bp (GRCm39)
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: 114,679,014 (GRCm39) V366A probably damaging Het
Cadm2 A T 16: 66,581,702 (GRCm39) V192E probably damaging Het
Chil6 C T 3: 106,297,268 (GRCm39) S291N possibly damaging Het
D7Ertd443e T C 7: 133,951,320 (GRCm39) T118A probably benign Het
Dennd4b G A 3: 90,175,675 (GRCm39) R148Q probably damaging Het
Dnah1 T A 14: 31,012,776 (GRCm39) T1837S probably damaging Het
Elapor2 T A 5: 9,472,296 (GRCm39) probably null Het
Ext1 A G 15: 52,951,539 (GRCm39) V515A probably damaging Het
Fer1l4 T C 2: 155,890,109 (GRCm39) E272G probably damaging Het
Fras1 T A 5: 96,825,236 (GRCm39) H1475Q probably benign Het
Grid1 T C 14: 35,242,662 (GRCm39) S672P possibly damaging Het
Gtpbp4 A G 13: 9,029,463 (GRCm39) probably null Het
Hsp90aa1 A T 12: 110,659,168 (GRCm39) V543E probably damaging Het
Irf5 T C 6: 29,531,145 (GRCm39) S4P probably benign Het
Kif2b G T 11: 91,466,286 (GRCm39) Q666K probably benign Het
Macc1 A T 12: 119,414,110 (GRCm39) H762L probably benign Het
Map1s C T 8: 71,369,751 (GRCm39) T941M probably damaging Het
Mrgprb1 T A 7: 48,097,523 (GRCm39) I130F probably benign Het
Ngly1 C T 14: 16,270,508 (GRCm38) Q173* probably null Het
Plcb3 A T 19: 6,943,587 (GRCm39) M104K probably benign Het
Plcg2 T A 8: 118,339,734 (GRCm39) Y1048* probably null Het
Ptprf T C 4: 118,082,121 (GRCm39) Y1039C probably damaging Het
Rab38 A G 7: 88,079,695 (GRCm39) Y29C probably damaging Het
Rcan2 T A 17: 44,347,921 (GRCm39) V210E probably damaging Het
Rptn A T 3: 93,304,008 (GRCm39) Q447L probably benign Het
Scel G A 14: 103,839,642 (GRCm39) R495K probably benign Het
Scn11a G T 9: 119,584,304 (GRCm39) P1437Q probably damaging Het
Sim2 A G 16: 93,910,315 (GRCm39) D239G probably damaging Het
Skap2 A G 6: 51,836,998 (GRCm39) Y356H probably damaging Het
Skint11 A G 4: 114,051,798 (GRCm39) T49A probably benign Het
Snx33 G A 9: 56,832,681 (GRCm39) H463Y probably benign Het
Steap2 T C 5: 5,727,544 (GRCm39) T264A possibly damaging Het
Stk40 T A 4: 126,028,852 (GRCm39) V238E probably damaging Het
Sun2 T C 15: 79,618,328 (GRCm39) D277G probably benign Het
Ttll9 T C 2: 152,832,020 (GRCm39) probably null Het
Vmn1r54 G A 6: 90,246,347 (GRCm39) C87Y probably benign Het
Other mutations in Nbeal1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Nbeal1 APN 1 60,274,350 (GRCm39) nonsense probably null 0.00
IGL00334:Nbeal1 APN 1 60,321,042 (GRCm39) missense probably damaging 0.98
IGL00334:Nbeal1 APN 1 60,367,262 (GRCm39) missense probably damaging 1.00
IGL00514:Nbeal1 APN 1 60,256,384 (GRCm39) missense probably benign 0.31
IGL00596:Nbeal1 APN 1 60,220,900 (GRCm39) missense probably damaging 0.96
IGL00654:Nbeal1 APN 1 60,234,170 (GRCm39) critical splice acceptor site probably benign 0.00
IGL00757:Nbeal1 APN 1 60,234,302 (GRCm39) missense possibly damaging 0.82
IGL00771:Nbeal1 APN 1 60,274,512 (GRCm39) missense probably benign 0.11
IGL01315:Nbeal1 APN 1 60,320,500 (GRCm39) missense probably damaging 1.00
IGL01445:Nbeal1 APN 1 60,281,784 (GRCm39) critical splice donor site probably null
IGL01456:Nbeal1 APN 1 60,269,787 (GRCm39) missense probably damaging 1.00
IGL01458:Nbeal1 APN 1 60,281,784 (GRCm39) critical splice donor site probably null
IGL01535:Nbeal1 APN 1 60,256,414 (GRCm39) missense probably damaging 1.00
IGL01608:Nbeal1 APN 1 60,281,694 (GRCm39) critical splice acceptor site probably benign 0.00
IGL02006:Nbeal1 APN 1 60,311,418 (GRCm39) critical splice donor site probably null
IGL02105:Nbeal1 APN 1 60,292,660 (GRCm39) missense probably damaging 1.00
IGL02409:Nbeal1 APN 1 60,368,494 (GRCm39) missense probably benign 0.01
IGL02713:Nbeal1 APN 1 60,274,396 (GRCm39) missense possibly damaging 0.94
IGL02720:Nbeal1 APN 1 60,323,146 (GRCm39) missense probably damaging 0.98
IGL02887:Nbeal1 APN 1 60,326,603 (GRCm39) splice site probably benign
IGL02945:Nbeal1 APN 1 60,245,569 (GRCm39) missense probably damaging 1.00
IGL03023:Nbeal1 APN 1 60,292,572 (GRCm39) missense probably damaging 0.98
IGL03114:Nbeal1 APN 1 60,317,886 (GRCm39) missense probably damaging 1.00
IGL03231:Nbeal1 APN 1 60,275,618 (GRCm39) missense probably benign 0.44
IGL03241:Nbeal1 APN 1 60,274,027 (GRCm39) missense possibly damaging 0.46
IGL03241:Nbeal1 APN 1 60,274,028 (GRCm39) missense probably benign 0.44
IGL03382:Nbeal1 APN 1 60,300,745 (GRCm39) critical splice donor site probably null
IGL03412:Nbeal1 APN 1 60,281,726 (GRCm39) nonsense probably null
coach UTSW 1 60,292,640 (GRCm39) nonsense probably null
Committee UTSW 1 60,332,062 (GRCm39) missense probably damaging 1.00
Disgrace UTSW 1 60,320,469 (GRCm39) nonsense probably null
Dravrah UTSW 1 60,323,251 (GRCm39) missense probably damaging 1.00
Harvard UTSW 1 60,274,722 (GRCm39) splice site probably null
horrified UTSW 1 60,283,983 (GRCm39) missense probably damaging 1.00
Lampoon UTSW 1 60,300,745 (GRCm39) critical splice donor site probably null
lawyer UTSW 1 60,349,383 (GRCm39) nonsense probably null
magistrate UTSW 1 60,233,756 (GRCm39) critical splice donor site probably null
Maratimus UTSW 1 60,331,047 (GRCm39) missense probably damaging 1.00
National UTSW 1 60,261,422 (GRCm39) missense possibly damaging 0.95
phainopepla UTSW 1 60,358,846 (GRCm39) missense probably damaging 1.00
R3875_Nbeal1_770 UTSW 1 60,233,758 (GRCm39) splice site probably benign
satirical UTSW 1 60,274,721 (GRCm39) critical splice donor site probably null
silky UTSW 1 60,370,037 (GRCm39) splice site probably benign
stiggs UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
3-1:Nbeal1 UTSW 1 60,303,431 (GRCm39) splice site probably benign
P0007:Nbeal1 UTSW 1 60,358,847 (GRCm39) missense probably damaging 0.98
P0028:Nbeal1 UTSW 1 60,331,096 (GRCm39) missense probably damaging 1.00
R0041:Nbeal1 UTSW 1 60,321,030 (GRCm39) missense probably benign 0.05
R0051:Nbeal1 UTSW 1 60,349,422 (GRCm39) missense probably benign 0.19
R0052:Nbeal1 UTSW 1 60,267,771 (GRCm39) splice site probably benign
R0054:Nbeal1 UTSW 1 60,326,560 (GRCm39) utr 3 prime probably benign
R0062:Nbeal1 UTSW 1 60,286,876 (GRCm39) missense probably benign 0.01
R0062:Nbeal1 UTSW 1 60,286,876 (GRCm39) missense probably benign 0.01
R0094:Nbeal1 UTSW 1 60,344,468 (GRCm39) missense possibly damaging 0.62
R0310:Nbeal1 UTSW 1 60,344,529 (GRCm39) splice site probably benign
R0324:Nbeal1 UTSW 1 60,332,032 (GRCm39) missense probably damaging 1.00
R0329:Nbeal1 UTSW 1 60,307,222 (GRCm39) missense probably damaging 1.00
R0330:Nbeal1 UTSW 1 60,307,222 (GRCm39) missense probably damaging 1.00
R0417:Nbeal1 UTSW 1 60,286,893 (GRCm39) missense probably benign 0.00
R0421:Nbeal1 UTSW 1 60,307,598 (GRCm39) missense probably benign 0.08
R0617:Nbeal1 UTSW 1 60,320,991 (GRCm39) nonsense probably null
R1034:Nbeal1 UTSW 1 60,329,165 (GRCm39) nonsense probably null
R1082:Nbeal1 UTSW 1 60,351,385 (GRCm39) missense probably damaging 0.99
R1123:Nbeal1 UTSW 1 60,299,428 (GRCm39) missense probably benign
R1187:Nbeal1 UTSW 1 60,233,687 (GRCm39) missense probably damaging 1.00
R1484:Nbeal1 UTSW 1 60,240,098 (GRCm39) missense probably damaging 1.00
R1594:Nbeal1 UTSW 1 60,344,450 (GRCm39) missense possibly damaging 0.91
R1651:Nbeal1 UTSW 1 60,239,278 (GRCm39) missense probably damaging 1.00
R1678:Nbeal1 UTSW 1 60,299,493 (GRCm39) missense probably benign 0.00
R1806:Nbeal1 UTSW 1 60,323,251 (GRCm39) missense probably damaging 1.00
R1937:Nbeal1 UTSW 1 60,307,100 (GRCm39) nonsense probably null
R1952:Nbeal1 UTSW 1 60,273,999 (GRCm39) missense probably damaging 1.00
R1953:Nbeal1 UTSW 1 60,273,999 (GRCm39) missense probably damaging 1.00
R2038:Nbeal1 UTSW 1 60,245,503 (GRCm39) missense probably benign 0.00
R2044:Nbeal1 UTSW 1 60,358,846 (GRCm39) missense probably damaging 1.00
R2050:Nbeal1 UTSW 1 60,332,123 (GRCm39) splice site probably null
R2055:Nbeal1 UTSW 1 60,350,216 (GRCm39) missense probably damaging 1.00
R2064:Nbeal1 UTSW 1 60,309,515 (GRCm39) missense possibly damaging 0.89
R2100:Nbeal1 UTSW 1 60,344,430 (GRCm39) splice site probably null
R2181:Nbeal1 UTSW 1 60,317,939 (GRCm39) missense probably damaging 1.00
R2192:Nbeal1 UTSW 1 60,321,054 (GRCm39) missense probably damaging 1.00
R2203:Nbeal1 UTSW 1 60,323,165 (GRCm39) missense probably benign 0.21
R2267:Nbeal1 UTSW 1 60,370,037 (GRCm39) splice site probably benign
R2268:Nbeal1 UTSW 1 60,370,037 (GRCm39) splice site probably benign
R2351:Nbeal1 UTSW 1 60,276,257 (GRCm39) missense possibly damaging 0.90
R2366:Nbeal1 UTSW 1 60,290,511 (GRCm39) missense probably damaging 0.97
R2393:Nbeal1 UTSW 1 60,290,529 (GRCm39) missense probably damaging 0.98
R3545:Nbeal1 UTSW 1 60,317,939 (GRCm39) missense probably damaging 1.00
R3546:Nbeal1 UTSW 1 60,317,939 (GRCm39) missense probably damaging 1.00
R3547:Nbeal1 UTSW 1 60,317,939 (GRCm39) missense probably damaging 1.00
R3701:Nbeal1 UTSW 1 60,290,572 (GRCm39) splice site probably benign
R3747:Nbeal1 UTSW 1 60,234,182 (GRCm39) missense probably damaging 0.98
R3875:Nbeal1 UTSW 1 60,233,758 (GRCm39) splice site probably benign
R4119:Nbeal1 UTSW 1 60,331,029 (GRCm39) missense probably damaging 0.99
R4256:Nbeal1 UTSW 1 60,370,107 (GRCm39) missense probably benign 0.19
R4371:Nbeal1 UTSW 1 60,329,105 (GRCm39) missense possibly damaging 0.95
R4450:Nbeal1 UTSW 1 60,306,933 (GRCm39) missense probably damaging 0.97
R4558:Nbeal1 UTSW 1 60,320,469 (GRCm39) nonsense probably null
R4618:Nbeal1 UTSW 1 60,267,890 (GRCm39) intron probably benign
R4673:Nbeal1 UTSW 1 60,368,549 (GRCm39) missense probably damaging 1.00
R4719:Nbeal1 UTSW 1 60,274,722 (GRCm39) splice site probably null
R4798:Nbeal1 UTSW 1 60,261,352 (GRCm39) splice site probably null
R4826:Nbeal1 UTSW 1 60,290,501 (GRCm39) missense possibly damaging 0.79
R4841:Nbeal1 UTSW 1 60,292,534 (GRCm39) missense probably damaging 1.00
R4842:Nbeal1 UTSW 1 60,292,534 (GRCm39) missense probably damaging 1.00
R4895:Nbeal1 UTSW 1 60,332,062 (GRCm39) missense probably damaging 1.00
R4929:Nbeal1 UTSW 1 60,277,813 (GRCm39) missense probably damaging 1.00
R5026:Nbeal1 UTSW 1 60,276,338 (GRCm39) missense probably damaging 1.00
R5243:Nbeal1 UTSW 1 60,309,487 (GRCm39) missense probably damaging 0.99
R5300:Nbeal1 UTSW 1 60,274,718 (GRCm39) nonsense probably null
R5345:Nbeal1 UTSW 1 60,367,369 (GRCm39) critical splice donor site probably null
R5502:Nbeal1 UTSW 1 60,350,158 (GRCm39) missense probably damaging 1.00
R5542:Nbeal1 UTSW 1 60,316,353 (GRCm39) missense probably benign 0.00
R5580:Nbeal1 UTSW 1 60,281,761 (GRCm39) missense probably benign 0.45
R5765:Nbeal1 UTSW 1 60,331,006 (GRCm39) missense probably damaging 1.00
R5802:Nbeal1 UTSW 1 60,311,380 (GRCm39) missense probably benign 0.01
R5907:Nbeal1 UTSW 1 60,267,950 (GRCm39) intron probably benign
R5918:Nbeal1 UTSW 1 60,307,051 (GRCm39) missense possibly damaging 0.90
R5923:Nbeal1 UTSW 1 60,287,554 (GRCm39) missense probably damaging 1.00
R6066:Nbeal1 UTSW 1 60,287,564 (GRCm39) missense probably benign 0.29
R6091:Nbeal1 UTSW 1 60,220,715 (GRCm39) start gained probably benign
R6113:Nbeal1 UTSW 1 60,261,422 (GRCm39) missense possibly damaging 0.95
R6143:Nbeal1 UTSW 1 60,290,466 (GRCm39) missense possibly damaging 0.81
R6194:Nbeal1 UTSW 1 60,296,643 (GRCm39) missense possibly damaging 0.80
R6197:Nbeal1 UTSW 1 60,261,287 (GRCm39) missense probably damaging 0.99
R6228:Nbeal1 UTSW 1 60,335,083 (GRCm39) missense probably benign 0.00
R6229:Nbeal1 UTSW 1 60,287,524 (GRCm39) missense possibly damaging 0.88
R6309:Nbeal1 UTSW 1 60,277,878 (GRCm39) missense probably benign
R6457:Nbeal1 UTSW 1 60,292,633 (GRCm39) missense probably benign 0.31
R6489:Nbeal1 UTSW 1 60,370,101 (GRCm39) missense possibly damaging 0.89
R6845:Nbeal1 UTSW 1 60,320,469 (GRCm39) nonsense probably null
R7021:Nbeal1 UTSW 1 60,300,745 (GRCm39) critical splice donor site probably null
R7033:Nbeal1 UTSW 1 60,350,106 (GRCm39) missense probably damaging 1.00
R7144:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7145:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7146:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7157:Nbeal1 UTSW 1 60,299,793 (GRCm39) nonsense probably null
R7157:Nbeal1 UTSW 1 60,276,317 (GRCm39) missense probably damaging 1.00
R7209:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7210:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7211:Nbeal1 UTSW 1 60,240,110 (GRCm39) missense probably damaging 1.00
R7212:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7213:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7214:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7283:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7285:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7287:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7296:Nbeal1 UTSW 1 60,349,383 (GRCm39) nonsense probably null
R7312:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7313:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7329:Nbeal1 UTSW 1 60,256,355 (GRCm39) missense probably benign 0.39
R7380:Nbeal1 UTSW 1 60,283,969 (GRCm39) missense probably damaging 1.00
R7414:Nbeal1 UTSW 1 60,233,756 (GRCm39) critical splice donor site probably null
R7477:Nbeal1 UTSW 1 60,300,743 (GRCm39) missense probably benign
R7507:Nbeal1 UTSW 1 60,274,626 (GRCm39) missense probably damaging 1.00
R7642:Nbeal1 UTSW 1 60,316,386 (GRCm39) missense probably benign 0.31
R7678:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7689:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7728:Nbeal1 UTSW 1 60,283,983 (GRCm39) missense probably damaging 1.00
R7757:Nbeal1 UTSW 1 60,296,609 (GRCm39) missense probably damaging 0.97
R7761:Nbeal1 UTSW 1 60,358,500 (GRCm39) missense probably benign 0.00
R7813:Nbeal1 UTSW 1 60,331,048 (GRCm39) missense probably damaging 1.00
R7829:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R7891:Nbeal1 UTSW 1 60,299,591 (GRCm39) missense probably benign
R7902:Nbeal1 UTSW 1 60,331,029 (GRCm39) missense probably damaging 0.99
R8022:Nbeal1 UTSW 1 60,299,431 (GRCm39) nonsense probably null
R8053:Nbeal1 UTSW 1 60,318,954 (GRCm39) missense probably damaging 0.98
R8169:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R8170:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R8178:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R8182:Nbeal1 UTSW 1 60,239,292 (GRCm39) missense probably benign 0.00
R8186:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R8187:Nbeal1 UTSW 1 60,276,310 (GRCm39) missense probably benign 0.11
R8193:Nbeal1 UTSW 1 60,292,640 (GRCm39) nonsense probably null
R8209:Nbeal1 UTSW 1 60,316,336 (GRCm39) missense probably damaging 0.99
R8226:Nbeal1 UTSW 1 60,316,336 (GRCm39) missense probably damaging 0.99
R8549:Nbeal1 UTSW 1 60,274,721 (GRCm39) critical splice donor site probably null
R8560:Nbeal1 UTSW 1 60,274,316 (GRCm39) missense probably benign 0.38
R8753:Nbeal1 UTSW 1 60,307,542 (GRCm39) missense probably damaging 1.00
R8769:Nbeal1 UTSW 1 60,274,370 (GRCm39) missense probably damaging 0.99
R8771:Nbeal1 UTSW 1 60,300,743 (GRCm39) missense probably benign
R8952:Nbeal1 UTSW 1 60,299,459 (GRCm39) missense probably benign 0.01
R9014:Nbeal1 UTSW 1 60,329,118 (GRCm39) missense probably damaging 1.00
R9056:Nbeal1 UTSW 1 60,317,885 (GRCm39) missense probably damaging 1.00
R9091:Nbeal1 UTSW 1 60,307,548 (GRCm39) missense possibly damaging 0.50
R9138:Nbeal1 UTSW 1 60,286,904 (GRCm39) nonsense probably null
R9168:Nbeal1 UTSW 1 60,331,047 (GRCm39) missense probably damaging 1.00
R9200:Nbeal1 UTSW 1 60,320,425 (GRCm39) missense probably damaging 1.00
R9205:Nbeal1 UTSW 1 60,317,839 (GRCm39) missense probably damaging 1.00
R9270:Nbeal1 UTSW 1 60,307,548 (GRCm39) missense possibly damaging 0.50
R9322:Nbeal1 UTSW 1 60,297,818 (GRCm39) missense possibly damaging 0.91
R9405:Nbeal1 UTSW 1 60,349,424 (GRCm39) missense probably damaging 1.00
R9554:Nbeal1 UTSW 1 60,290,287 (GRCm39) nonsense probably null
R9557:Nbeal1 UTSW 1 60,274,509 (GRCm39) missense probably benign
R9560:Nbeal1 UTSW 1 60,368,544 (GRCm39) missense probably damaging 1.00
R9641:Nbeal1 UTSW 1 60,350,247 (GRCm39) missense probably damaging 1.00
R9784:Nbeal1 UTSW 1 60,299,741 (GRCm39) nonsense probably null
X0022:Nbeal1 UTSW 1 60,316,391 (GRCm39) 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