Incidental Mutation 'R5202:Nbeal2'
ID 400915
Institutional Source Beutler Lab
Gene Symbol Nbeal2
Ensembl Gene ENSMUSG00000056724
Gene Name neurobeachin-like 2
Synonyms 1110014F23Rik
MMRRC Submission 042777-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.228) question?
Stock # R5202 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 110624789-110654161 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 110644666 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 28 (E28G)
Ref Sequence ENSEMBL: ENSMUSP00000119254 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000133191] [ENSMUST00000149089] [ENSMUST00000167320] [ENSMUST00000196488]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000133191
AA Change: E35G

PolyPhen 2 Score 0.903 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000121373
Gene: ENSMUSG00000056724
AA Change: E35G

DomainStartEndE-ValueType
low complexity region 56 84 N/A INTRINSIC
low complexity region 192 201 N/A INTRINSIC
low complexity region 227 238 N/A INTRINSIC
low complexity region 514 522 N/A INTRINSIC
low complexity region 527 542 N/A INTRINSIC
Pfam:Laminin_G_3 578 818 5.9e-8 PFAM
low complexity region 1014 1028 N/A INTRINSIC
low complexity region 1128 1136 N/A INTRINSIC
low complexity region 1149 1163 N/A INTRINSIC
low complexity region 1359 1375 N/A INTRINSIC
low complexity region 1515 1530 N/A INTRINSIC
low complexity region 1621 1647 N/A INTRINSIC
low complexity region 1875 1904 N/A INTRINSIC
Pfam:PH_BEACH 1908 2002 6.2e-28 PFAM
Beach 2054 2334 5.2e-205 SMART
WD40 2432 2477 1.03e1 SMART
WD40 2480 2519 6.19e-5 SMART
WD40 2531 2570 1.02e-5 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000149089
AA Change: E28G

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000119254
Gene: ENSMUSG00000056724
AA Change: E28G

DomainStartEndE-ValueType
low complexity region 49 77 N/A INTRINSIC
low complexity region 185 194 N/A INTRINSIC
low complexity region 220 231 N/A INTRINSIC
low complexity region 480 488 N/A INTRINSIC
low complexity region 493 508 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000167320
AA Change: E35G

PolyPhen 2 Score 0.916 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000128586
Gene: ENSMUSG00000056724
AA Change: E35G

DomainStartEndE-ValueType
low complexity region 56 84 N/A INTRINSIC
low complexity region 192 201 N/A INTRINSIC
low complexity region 227 238 N/A INTRINSIC
low complexity region 514 522 N/A INTRINSIC
low complexity region 527 542 N/A INTRINSIC
low complexity region 763 775 N/A INTRINSIC
Pfam:DUF4704 872 1148 9.2e-32 PFAM
low complexity region 1149 1163 N/A INTRINSIC
low complexity region 1366 1382 N/A INTRINSIC
low complexity region 1522 1537 N/A INTRINSIC
Pfam:DUF4800 1590 1856 1.5e-112 PFAM
low complexity region 1882 1911 N/A INTRINSIC
Pfam:PH_BEACH 1922 2009 3.1e-21 PFAM
Beach 2061 2341 5.2e-205 SMART
WD40 2439 2484 1.03e1 SMART
WD40 2487 2526 6.19e-5 SMART
WD40 2538 2577 1.02e-5 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000196488
AA Change: E35G

PolyPhen 2 Score 0.932 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000143265
Gene: ENSMUSG00000056724
AA Change: E35G

DomainStartEndE-ValueType
low complexity region 56 84 N/A INTRINSIC
low complexity region 192 201 N/A INTRINSIC
low complexity region 227 238 N/A INTRINSIC
low complexity region 487 495 N/A INTRINSIC
low complexity region 500 515 N/A INTRINSIC
Pfam:Laminin_G_3 551 791 5.3e-6 PFAM
low complexity region 987 1001 N/A INTRINSIC
low complexity region 1101 1109 N/A INTRINSIC
low complexity region 1122 1136 N/A INTRINSIC
low complexity region 1332 1348 N/A INTRINSIC
low complexity region 1488 1503 N/A INTRINSIC
low complexity region 1594 1620 N/A INTRINSIC
low complexity region 1848 1877 N/A INTRINSIC
Pfam:PH_BEACH 1881 1975 3.1e-25 PFAM
Beach 2027 2307 3.8e-209 SMART
WD40 2405 2450 6.3e-2 SMART
WD40 2453 2492 3.8e-7 SMART
WD40 2504 2543 6.5e-8 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a beige and Chediak-Higashi (BEACH) domain and multiple WD40 domains, and may play a role in megakaryocyte alpha-granule biogenesis. Mutations in this gene are a cause of gray platelet syndrome. [provided by RefSeq, Dec 2011]
PHENOTYPE: Homozygous null mice exhibit megakaryocyte and platelet abnormalities resulting in impaired arterial thrombus formation and protection from infarction following cerebral ischemia. Wound repair is impaired. These abnormalities result in a bleeding disorder similiar to Gray Platelet Syndrome. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932414N04Rik A T 2: 68,731,964 (GRCm38) M312L probably benign Het
Adam7 C A 14: 68,507,856 (GRCm38) D640Y possibly damaging Het
Alcam T C 16: 52,274,236 (GRCm38) Y384C probably damaging Het
Apob A G 12: 8,013,737 (GRCm38) E289G probably damaging Het
Arhgap15 A T 2: 44,063,857 (GRCm38) R198S probably benign Het
Bbs2 G T 8: 94,092,414 (GRCm38) S109* probably null Het
Bfsp1 T C 2: 143,826,971 (GRCm38) S569G probably benign Het
Chst9 A T 18: 15,453,239 (GRCm38) I89N probably benign Het
Cntln A C 4: 84,971,229 (GRCm38) E316D probably benign Het
Csde1 T G 3: 103,039,934 (GRCm38) D67E probably damaging Het
Csf2rb T G 15: 78,349,057 (GRCm38) S855A possibly damaging Het
Cyp4a10 T A 4: 115,532,615 (GRCm38) D472E probably damaging Het
Cyp4f18 C A 8: 72,009,096 (GRCm38) R49L probably benign Het
Daam1 G T 12: 71,944,274 (GRCm38) V221L unknown Het
Dbr1 T G 9: 99,583,891 (GRCm38) D507E probably benign Het
Dhrs7c A G 11: 67,815,801 (GRCm38) M188V probably benign Het
Dicer1 A T 12: 104,694,731 (GRCm38) L1688* probably null Het
Dmpk C G 7: 19,088,019 (GRCm38) L301V probably benign Het
E2f3 G A 13: 29,918,636 (GRCm38) T91I probably damaging Het
Etaa1 A T 11: 17,947,853 (GRCm38) V157E probably damaging Het
Foxp2 A T 6: 15,394,771 (GRCm38) T157S probably benign Het
Frem2 A G 3: 53,551,346 (GRCm38) V2034A probably benign Het
Fzd10 T C 5: 128,602,116 (GRCm38) V300A possibly damaging Het
Gbf1 A T 19: 46,268,454 (GRCm38) M778L probably benign Het
Gm17472 T A 6: 42,981,134 (GRCm38) N112K probably benign Het
Gria4 T C 9: 4,424,330 (GRCm38) K845R probably benign Het
Hspa4l T A 3: 40,781,569 (GRCm38) S541T probably benign Het
Igkv4-68 G A 6: 69,304,942 (GRCm38) R82C probably damaging Het
Itgb1 A T 8: 128,720,010 (GRCm38) I383F probably damaging Het
Kcnk12 T A 17: 87,746,605 (GRCm38) K210* probably null Het
Limch1 C G 5: 66,993,173 (GRCm38) D163E probably damaging Het
Mbd4 A T 6: 115,849,402 (GRCm38) D188E probably damaging Het
Myh9 C T 15: 77,781,110 (GRCm38) probably null Het
Nfatc4 A G 14: 55,826,659 (GRCm38) E201G probably damaging Het
Nrap G A 19: 56,335,151 (GRCm38) H1330Y probably damaging Het
Nudt14 A G 12: 112,935,028 (GRCm38) S151P probably damaging Het
Olfr297 C A 7: 86,527,116 (GRCm38) R120S probably damaging Het
Olfr58 T A 9: 19,783,218 (GRCm38) F28L possibly damaging Het
Olfr706 T A 7: 106,886,596 (GRCm38) T74S possibly damaging Het
Otx1 C A 11: 21,997,037 (GRCm38) A91S probably damaging Het
Paqr9 A G 9: 95,560,110 (GRCm38) D51G probably damaging Het
Pcgf5 T A 19: 36,437,183 (GRCm38) F80I probably damaging Het
Pkhd1 T G 1: 20,547,341 (GRCm38) S1007R probably benign Het
Rab30 T C 7: 92,835,913 (GRCm38) Y196H probably benign Het
Setd2 A T 9: 110,551,230 (GRCm38) D1371V probably damaging Het
Slc48a1 A T 15: 97,790,700 (GRCm38) I140F possibly damaging Het
Sorl1 A G 9: 42,033,583 (GRCm38) V882A probably benign Het
Sptbn2 G T 19: 4,724,184 (GRCm38) G88W probably damaging Het
Tdrd12 A G 7: 35,490,030 (GRCm38) V427A possibly damaging Het
Tekt2 T C 4: 126,324,670 (GRCm38) D69G probably benign Het
Tie1 C T 4: 118,480,510 (GRCm38) V463I probably benign Het
Tmem150c G T 5: 100,079,954 (GRCm38) H217N probably damaging Het
Tnks2 G A 19: 36,888,852 (GRCm38) G1080R probably damaging Het
Ttll4 G A 1: 74,687,852 (GRCm38) probably null Het
Other mutations in Nbeal2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00229:Nbeal2 APN 9 110,635,869 (GRCm38) missense probably damaging 1.00
IGL00784:Nbeal2 APN 9 110,629,763 (GRCm38) splice site probably benign
IGL00826:Nbeal2 APN 9 110,626,903 (GRCm38) missense probably benign
IGL00885:Nbeal2 APN 9 110,638,661 (GRCm38) missense probably damaging 1.00
IGL01348:Nbeal2 APN 9 110,629,146 (GRCm38) missense probably damaging 0.99
IGL01511:Nbeal2 APN 9 110,629,234 (GRCm38) missense probably damaging 1.00
IGL01571:Nbeal2 APN 9 110,632,758 (GRCm38) missense possibly damaging 0.63
IGL01612:Nbeal2 APN 9 110,644,678 (GRCm38) missense probably damaging 1.00
IGL01924:Nbeal2 APN 9 110,631,414 (GRCm38) missense probably benign 0.23
IGL02056:Nbeal2 APN 9 110,627,324 (GRCm38) missense probably benign 0.17
IGL02481:Nbeal2 APN 9 110,625,995 (GRCm38) nonsense probably null
IGL02483:Nbeal2 APN 9 110,625,995 (GRCm38) nonsense probably null
IGL02502:Nbeal2 APN 9 110,633,768 (GRCm38) missense probably damaging 1.00
IGL02631:Nbeal2 APN 9 110,630,208 (GRCm38) missense probably damaging 0.99
IGL02637:Nbeal2 APN 9 110,625,977 (GRCm38) missense possibly damaging 0.62
IGL02727:Nbeal2 APN 9 110,639,285 (GRCm38) splice site probably benign
IGL02887:Nbeal2 APN 9 110,628,276 (GRCm38) missense probably damaging 1.00
IGL02896:Nbeal2 APN 9 110,639,292 (GRCm38) critical splice donor site probably null
IGL03110:Nbeal2 APN 9 110,631,433 (GRCm38) missense probably damaging 1.00
Antonym UTSW 9 110,630,252 (GRCm38) missense probably damaging 1.00
Beowulf UTSW 9 110,637,937 (GRCm38) missense possibly damaging 0.65
Blackmail UTSW 9 110,629,639 (GRCm38) missense probably damaging 1.00
dog UTSW 9 110,635,341 (GRCm38) missense possibly damaging 0.89
extortion UTSW 9 110,630,243 (GRCm38) missense probably damaging 1.00
legion UTSW 9 110,629,179 (GRCm38) missense probably damaging 1.00
litigious UTSW 9 110,628,195 (GRCm38) missense probably damaging 1.00
mall UTSW 9 110,632,886 (GRCm38) missense probably damaging 1.00
Mollusca UTSW 9 110,645,438 (GRCm38) splice site probably null
Schleuter UTSW 9 110,628,744 (GRCm38) missense possibly damaging 0.69
shellfish UTSW 9 110,628,720 (GRCm38) missense probably damaging 1.00
Sophomoric UTSW 9 110,633,047 (GRCm38) missense probably damaging 1.00
F5770:Nbeal2 UTSW 9 110,637,937 (GRCm38) missense possibly damaging 0.65
R0032:Nbeal2 UTSW 9 110,637,868 (GRCm38) splice site probably benign
R0084:Nbeal2 UTSW 9 110,643,710 (GRCm38) critical splice donor site probably null
R0147:Nbeal2 UTSW 9 110,642,143 (GRCm38) nonsense probably null
R0294:Nbeal2 UTSW 9 110,632,859 (GRCm38) missense probably damaging 1.00
R0310:Nbeal2 UTSW 9 110,638,163 (GRCm38) missense probably damaging 1.00
R0494:Nbeal2 UTSW 9 110,627,187 (GRCm38) missense probably damaging 1.00
R0550:Nbeal2 UTSW 9 110,642,158 (GRCm38) missense probably benign 0.01
R0630:Nbeal2 UTSW 9 110,636,034 (GRCm38) splice site probably benign
R0762:Nbeal2 UTSW 9 110,643,808 (GRCm38) splice site probably benign
R0862:Nbeal2 UTSW 9 110,628,195 (GRCm38) missense probably damaging 1.00
R0864:Nbeal2 UTSW 9 110,628,195 (GRCm38) missense probably damaging 1.00
R1225:Nbeal2 UTSW 9 110,632,886 (GRCm38) missense probably damaging 1.00
R1240:Nbeal2 UTSW 9 110,627,108 (GRCm38) missense probably damaging 0.98
R1450:Nbeal2 UTSW 9 110,633,672 (GRCm38) splice site probably benign
R1519:Nbeal2 UTSW 9 110,636,305 (GRCm38) missense probably damaging 1.00
R1655:Nbeal2 UTSW 9 110,632,872 (GRCm38) missense probably damaging 1.00
R1668:Nbeal2 UTSW 9 110,638,893 (GRCm38) missense probably damaging 1.00
R1705:Nbeal2 UTSW 9 110,625,196 (GRCm38) missense probably damaging 1.00
R1784:Nbeal2 UTSW 9 110,630,857 (GRCm38) nonsense probably null
R1834:Nbeal2 UTSW 9 110,627,129 (GRCm38) missense probably damaging 1.00
R1997:Nbeal2 UTSW 9 110,632,198 (GRCm38) missense probably damaging 1.00
R2013:Nbeal2 UTSW 9 110,634,071 (GRCm38) missense probably benign 0.09
R2014:Nbeal2 UTSW 9 110,634,071 (GRCm38) missense probably benign 0.09
R2055:Nbeal2 UTSW 9 110,635,307 (GRCm38) missense possibly damaging 0.92
R2086:Nbeal2 UTSW 9 110,634,071 (GRCm38) missense probably benign 0.09
R2113:Nbeal2 UTSW 9 110,625,406 (GRCm38) missense probably damaging 1.00
R2167:Nbeal2 UTSW 9 110,638,308 (GRCm38) missense probably damaging 1.00
R2201:Nbeal2 UTSW 9 110,630,250 (GRCm38) missense probably benign 0.16
R2309:Nbeal2 UTSW 9 110,626,570 (GRCm38) missense probably damaging 1.00
R2378:Nbeal2 UTSW 9 110,630,808 (GRCm38) missense probably damaging 0.99
R2945:Nbeal2 UTSW 9 110,628,068 (GRCm38) missense possibly damaging 0.82
R3052:Nbeal2 UTSW 9 110,633,085 (GRCm38) missense possibly damaging 0.93
R3076:Nbeal2 UTSW 9 110,631,700 (GRCm38) missense probably damaging 1.00
R3176:Nbeal2 UTSW 9 110,636,887 (GRCm38) splice site probably benign
R3974:Nbeal2 UTSW 9 110,633,846 (GRCm38) missense probably damaging 1.00
R4183:Nbeal2 UTSW 9 110,636,675 (GRCm38) missense probably benign
R4342:Nbeal2 UTSW 9 110,631,793 (GRCm38) intron probably benign
R4654:Nbeal2 UTSW 9 110,632,004 (GRCm38) missense probably damaging 1.00
R4707:Nbeal2 UTSW 9 110,632,055 (GRCm38) missense probably benign 0.10
R4822:Nbeal2 UTSW 9 110,636,315 (GRCm38) missense possibly damaging 0.82
R4854:Nbeal2 UTSW 9 110,631,396 (GRCm38) missense probably damaging 1.00
R4860:Nbeal2 UTSW 9 110,635,194 (GRCm38) missense probably benign 0.00
R4860:Nbeal2 UTSW 9 110,635,194 (GRCm38) missense probably benign 0.00
R4990:Nbeal2 UTSW 9 110,634,803 (GRCm38) missense probably benign 0.10
R4991:Nbeal2 UTSW 9 110,638,767 (GRCm38) missense probably damaging 1.00
R5021:Nbeal2 UTSW 9 110,637,463 (GRCm38) missense probably damaging 0.99
R5057:Nbeal2 UTSW 9 110,631,005 (GRCm38) missense probably damaging 1.00
R5092:Nbeal2 UTSW 9 110,626,728 (GRCm38) splice site probably null
R5161:Nbeal2 UTSW 9 110,629,868 (GRCm38) missense probably benign
R5217:Nbeal2 UTSW 9 110,632,090 (GRCm38) missense possibly damaging 0.56
R5408:Nbeal2 UTSW 9 110,637,520 (GRCm38) missense possibly damaging 0.91
R5540:Nbeal2 UTSW 9 110,631,733 (GRCm38) missense probably damaging 1.00
R5866:Nbeal2 UTSW 9 110,631,492 (GRCm38) missense probably damaging 1.00
R5925:Nbeal2 UTSW 9 110,629,880 (GRCm38) missense probably benign 0.00
R6057:Nbeal2 UTSW 9 110,641,877 (GRCm38) missense possibly damaging 0.81
R6180:Nbeal2 UTSW 9 110,625,147 (GRCm38) missense probably damaging 1.00
R6191:Nbeal2 UTSW 9 110,627,990 (GRCm38) critical splice donor site probably null
R6232:Nbeal2 UTSW 9 110,638,734 (GRCm38) missense probably damaging 1.00
R6372:Nbeal2 UTSW 9 110,628,744 (GRCm38) missense possibly damaging 0.69
R6423:Nbeal2 UTSW 9 110,625,994 (GRCm38) missense probably damaging 1.00
R6543:Nbeal2 UTSW 9 110,644,458 (GRCm38) missense probably benign
R6648:Nbeal2 UTSW 9 110,637,642 (GRCm38) missense probably damaging 1.00
R6722:Nbeal2 UTSW 9 110,632,992 (GRCm38) missense probably damaging 1.00
R6738:Nbeal2 UTSW 9 110,636,905 (GRCm38) missense possibly damaging 0.93
R6916:Nbeal2 UTSW 9 110,626,108 (GRCm38) missense probably damaging 1.00
R6935:Nbeal2 UTSW 9 110,639,391 (GRCm38) missense probably damaging 1.00
R7022:Nbeal2 UTSW 9 110,638,618 (GRCm38) missense probably damaging 1.00
R7023:Nbeal2 UTSW 9 110,638,618 (GRCm38) missense probably damaging 1.00
R7050:Nbeal2 UTSW 9 110,628,720 (GRCm38) missense probably damaging 1.00
R7072:Nbeal2 UTSW 9 110,626,051 (GRCm38) missense probably benign 0.01
R7073:Nbeal2 UTSW 9 110,626,109 (GRCm38) missense probably damaging 0.99
R7099:Nbeal2 UTSW 9 110,645,438 (GRCm38) splice site probably null
R7354:Nbeal2 UTSW 9 110,629,179 (GRCm38) missense probably damaging 1.00
R7394:Nbeal2 UTSW 9 110,630,189 (GRCm38) critical splice donor site probably null
R7397:Nbeal2 UTSW 9 110,628,032 (GRCm38) missense possibly damaging 0.78
R7552:Nbeal2 UTSW 9 110,653,917 (GRCm38) missense probably benign 0.16
R7619:Nbeal2 UTSW 9 110,625,818 (GRCm38) missense probably benign 0.19
R7821:Nbeal2 UTSW 9 110,630,252 (GRCm38) missense probably damaging 1.00
R7902:Nbeal2 UTSW 9 110,637,547 (GRCm38) missense probably benign
R7923:Nbeal2 UTSW 9 110,631,446 (GRCm38) nonsense probably null
R8018:Nbeal2 UTSW 9 110,629,157 (GRCm38) unclassified probably benign
R8190:Nbeal2 UTSW 9 110,626,090 (GRCm38) missense probably benign 0.04
R8297:Nbeal2 UTSW 9 110,635,341 (GRCm38) missense possibly damaging 0.89
R8404:Nbeal2 UTSW 9 110,634,389 (GRCm38) missense possibly damaging 0.48
R8502:Nbeal2 UTSW 9 110,634,389 (GRCm38) missense possibly damaging 0.48
R8737:Nbeal2 UTSW 9 110,627,881 (GRCm38) missense probably damaging 1.00
R8782:Nbeal2 UTSW 9 110,630,805 (GRCm38) missense probably benign 0.04
R8807:Nbeal2 UTSW 9 110,629,639 (GRCm38) missense probably damaging 1.00
R8877:Nbeal2 UTSW 9 110,630,243 (GRCm38) missense probably damaging 1.00
R9057:Nbeal2 UTSW 9 110,627,150 (GRCm38) missense probably benign
R9267:Nbeal2 UTSW 9 110,633,047 (GRCm38) missense probably damaging 1.00
R9313:Nbeal2 UTSW 9 110,634,368 (GRCm38) missense probably damaging 1.00
R9352:Nbeal2 UTSW 9 110,627,848 (GRCm38) missense probably benign 0.03
R9482:Nbeal2 UTSW 9 110,633,998 (GRCm38) missense probably benign 0.25
R9533:Nbeal2 UTSW 9 110,644,661 (GRCm38) missense probably benign 0.01
R9566:Nbeal2 UTSW 9 110,628,921 (GRCm38) missense probably benign 0.00
R9769:Nbeal2 UTSW 9 110,626,279 (GRCm38) missense probably benign 0.01
V7583:Nbeal2 UTSW 9 110,637,937 (GRCm38) missense possibly damaging 0.65
X0017:Nbeal2 UTSW 9 110,644,278 (GRCm38) missense probably benign 0.02
X0065:Nbeal2 UTSW 9 110,644,413 (GRCm38) splice site probably benign
Z1088:Nbeal2 UTSW 9 110,632,372 (GRCm38) missense possibly damaging 0.51
Z1176:Nbeal2 UTSW 9 110,638,835 (GRCm38) missense probably benign
Z1176:Nbeal2 UTSW 9 110,625,816 (GRCm38) missense probably benign 0.01
Z1177:Nbeal2 UTSW 9 110,629,854 (GRCm38) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- ATGTAGAGCATCTAGGGGTAGC -3'
(R):5'- ACCACAGTCCTCTGGTTCTG -3'

Sequencing Primer
(F):5'- CTAGGGGTAGCAGAGGCACTTC -3'
(R):5'- TGACCTTCCACGTCCCGG -3'
Posted On 2016-07-06