Incidental Mutation 'R7260:Fbn2'
ID 564582
Institutional Source Beutler Lab
Gene Symbol Fbn2
Ensembl Gene ENSMUSG00000024598
Gene Name fibrillin 2
Synonyms sy, Sne, Fib-2
MMRRC Submission 045352-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.923) question?
Stock # R7260 (G1)
Quality Score 225.009
Status Validated
Chromosome 18
Chromosomal Location 58141689-58343200 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 58199188 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 1360 (D1360G)
Ref Sequence ENSEMBL: ENSMUSP00000025497 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025497]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000025497
AA Change: D1360G

PolyPhen 2 Score 0.140 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000025497
Gene: ENSMUSG00000024598
AA Change: D1360G

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
low complexity region 29 52 N/A INTRINSIC
low complexity region 68 77 N/A INTRINSIC
EGF 148 176 1.15e1 SMART
EGF 179 208 1.26e-2 SMART
Pfam:TB 224 262 3.7e-10 PFAM
EGF_CA 276 317 8.3e-12 SMART
EGF_CA 318 359 9.25e-10 SMART
Pfam:TB 374 416 4.3e-13 PFAM
low complexity region 435 450 N/A INTRINSIC
low complexity region 463 475 N/A INTRINSIC
EGF 490 527 1.13e-4 SMART
EGF_CA 528 567 2.26e-13 SMART
EGF_CA 568 609 9.03e-13 SMART
EGF_CA 610 650 6.2e-11 SMART
EGF_CA 651 691 7.75e-12 SMART
Pfam:TB 707 748 5.2e-15 PFAM
EGF_CA 761 802 6.29e-12 SMART
EGF_CA 803 844 1.97e-13 SMART
EGF_CA 845 884 1.61e-9 SMART
Pfam:TB 899 935 1.8e-9 PFAM
EGF_CA 948 989 4.7e-11 SMART
Pfam:TB 1004 1044 1.3e-16 PFAM
EGF_CA 1066 1107 3.05e-10 SMART
EGF_CA 1108 1150 2.19e-11 SMART
EGF_CA 1151 1192 2.04e-11 SMART
EGF_CA 1193 1234 3.15e-12 SMART
EGF_CA 1235 1275 1.82e-8 SMART
EGF_CA 1276 1317 9.91e-10 SMART
EGF_CA 1318 1359 1.48e-8 SMART
EGF_CA 1360 1400 6.54e-10 SMART
EGF_CA 1401 1441 4.63e-10 SMART
EGF_CA 1442 1483 7.75e-12 SMART
EGF_CA 1484 1524 5.23e-9 SMART
EGF_CA 1525 1565 2.13e-9 SMART
Pfam:TB 1585 1625 3.4e-15 PFAM
EGF_CA 1643 1684 6.74e-12 SMART
EGF_CA 1685 1726 1.06e-9 SMART
Pfam:TB 1741 1783 1.2e-17 PFAM
EGF_CA 1801 1842 7.34e-13 SMART
EGF_CA 1843 1884 4.15e-12 SMART
EGF_CA 1885 1926 5.23e-9 SMART
EGF_CA 1927 1965 5.87e-12 SMART
EGF_CA 1966 2008 1.11e-12 SMART
EGF_CA 2009 2048 1.26e-11 SMART
EGF_CA 2049 2090 7.12e-11 SMART
Pfam:TB 2105 2147 1.2e-15 PFAM
EGF_CA 2164 2205 2.89e-11 SMART
EGF_CA 2206 2245 1.1e-11 SMART
EGF_CA 2246 2286 3.76e-10 SMART
EGF_CA 2287 2330 1.44e-6 SMART
EGF_CA 2331 2372 1.16e-10 SMART
Pfam:TB 2387 2429 1.9e-16 PFAM
EGF_CA 2442 2483 8.43e-13 SMART
EGF_CA 2484 2524 4.96e-10 SMART
EGF_CA 2525 2563 7.63e-11 SMART
EGF_CA 2564 2606 6.44e-9 SMART
EGF_CA 2607 2646 2.28e-9 SMART
EGF_CA 2647 2687 1.79e-7 SMART
EGF_CA 2688 2727 3.45e-9 SMART
low complexity region 2774 2786 N/A INTRINSIC
Meta Mutation Damage Score 0.9415 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 98% (78/80)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for spontaneous, chemically-induced, and targeted null mutations show bilateral syndactyly with fusion of both soft and hard tissues. Deafness found in an X-ray induced allelic mutant is apparently due to the joint disruption of a linked gene. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 81 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310057J18Rik A G 10: 28,849,882 (GRCm39) S293P probably benign Het
Actn2 T C 13: 12,291,376 (GRCm39) N676S probably benign Het
Amfr C T 8: 94,702,776 (GRCm39) M463I possibly damaging Het
Ankdd1a G T 9: 65,411,834 (GRCm39) A325D probably damaging Het
Apba2 A G 7: 64,389,493 (GRCm39) D463G probably damaging Het
Arid5b A G 10: 67,933,637 (GRCm39) V755A probably damaging Het
Boc A T 16: 44,310,533 (GRCm39) F796I Het
Ccnt1 G A 15: 98,463,005 (GRCm39) Q56* probably null Het
Cd248 T A 19: 5,119,383 (GRCm39) Y410* probably null Het
Chd9 T A 8: 91,721,171 (GRCm39) N986K unknown Het
Col6a6 T C 9: 105,661,168 (GRCm39) T314A probably benign Het
Cpped1 A G 16: 11,646,327 (GRCm39) F142L possibly damaging Het
Csmd1 C T 8: 16,050,574 (GRCm39) A2221T probably damaging Het
Cyp2c69 C A 19: 39,831,344 (GRCm39) V490L probably benign Het
Cyrib A T 15: 63,829,438 (GRCm39) F23L possibly damaging Het
Dcst2 T C 3: 89,273,593 (GRCm39) F157S probably damaging Het
Ddx54 G T 5: 120,764,985 (GRCm39) R788L probably benign Het
Dnah1 T C 14: 30,991,343 (GRCm39) Y3145C probably damaging Het
Dnah14 A T 1: 181,534,309 (GRCm39) R2320W probably damaging Het
Dnai3 T A 3: 145,752,295 (GRCm39) M794L probably benign Het
Emilin2 T C 17: 71,581,785 (GRCm39) T314A probably benign Het
Eml2 A G 7: 18,934,515 (GRCm39) S405G probably benign Het
Ephb2 A G 4: 136,498,885 (GRCm39) F65L probably damaging Het
Fbxo22 A G 9: 55,125,754 (GRCm39) T206A probably benign Het
Filip1l A G 16: 57,391,287 (GRCm39) E625G probably damaging Het
Gen1 A C 12: 11,306,849 (GRCm39) M172R probably damaging Het
Gk5 A G 9: 96,001,663 (GRCm39) K54E probably benign Het
Glis3 T C 19: 28,508,802 (GRCm39) E394G probably benign Het
Helq T A 5: 100,939,793 (GRCm39) E373D probably damaging Het
Ighv1-74 A G 12: 115,766,372 (GRCm39) F83L probably benign Het
Ints15 A G 5: 143,297,594 (GRCm39) V151A probably benign Het
Iqcn T C 8: 71,161,397 (GRCm39) Y197H probably benign Het
Kdm4d T C 9: 14,374,454 (GRCm39) D468G probably benign Het
Kif20b A G 19: 34,927,610 (GRCm39) I957M probably damaging Het
Ldhal6b A G 17: 5,468,535 (GRCm39) F133S possibly damaging Het
Loxhd1 T C 18: 77,420,338 (GRCm39) Y321H possibly damaging Het
Ltbp1 A T 17: 75,373,139 (GRCm39) M261L probably benign Het
Mical2 A T 7: 111,919,001 (GRCm39) Q430L probably benign Het
Mroh4 A T 15: 74,479,978 (GRCm39) N885K possibly damaging Het
Ms4a7 A G 19: 11,299,710 (GRCm39) Y231H probably damaging Het
Msh2 G T 17: 88,025,047 (GRCm39) V642F probably damaging Het
Muc5b G T 7: 141,396,385 (GRCm39) A166S unknown Het
Myo18b T C 5: 112,923,154 (GRCm39) I1868V probably benign Het
Nfatc3 T C 8: 106,835,578 (GRCm39) S975P probably benign Het
Oacyl T C 18: 65,831,438 (GRCm39) L25P probably damaging Het
Or12e10 A G 2: 87,640,731 (GRCm39) N189S probably damaging Het
Or5b109 T C 19: 13,212,388 (GRCm39) F258S probably damaging Het
Or5w15 T C 2: 87,568,852 (GRCm39) probably null Het
Or6c69 T A 10: 129,748,156 (GRCm39) probably benign Het
Or8a1 T A 9: 37,642,049 (GRCm39) I77F probably damaging Het
Patj A G 4: 98,304,970 (GRCm39) I275V possibly damaging Het
Pdcd11 G A 19: 47,117,673 (GRCm39) R1674Q possibly damaging Het
Peg10 CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG CCACATCAGGATCCACATCAGGATGCACATCAG 6: 4,756,398 (GRCm39) probably benign Het
Phkb T A 8: 86,604,759 (GRCm39) Y55N probably benign Het
Pias4 A G 10: 80,993,302 (GRCm39) V207A possibly damaging Het
Plxna4 C A 6: 32,216,455 (GRCm39) R540L possibly damaging Het
Psapl1 G A 5: 36,362,556 (GRCm39) V383M probably benign Het
Rars1 C A 11: 35,725,281 (GRCm39) A10S probably benign Het
Rhobtb1 A T 10: 69,106,610 (GRCm39) K454* probably null Het
Rmnd1 A T 10: 4,364,803 (GRCm39) probably null Het
Rnf213 A G 11: 119,343,401 (GRCm39) I3589V Het
Rngtt T C 4: 33,356,176 (GRCm39) S338P possibly damaging Het
Sh3bgr A G 16: 96,025,681 (GRCm39) E189G unknown Het
Slc30a3 G A 5: 31,245,690 (GRCm39) T281I probably damaging Het
Smok3c T A 5: 138,063,885 (GRCm39) D457E possibly damaging Het
Stard9 C A 2: 120,537,419 (GRCm39) Q4274K possibly damaging Het
Syne2 G T 12: 75,991,853 (GRCm39) L1938F probably damaging Het
Tmem70 C A 1: 16,735,590 (GRCm39) T20K possibly damaging Het
Tnrc6a A G 7: 122,785,813 (GRCm39) E1502G probably benign Het
Tpp1 A T 7: 105,396,704 (GRCm39) S438T probably benign Het
Tubb2a T A 13: 34,259,397 (GRCm39) Q131L probably damaging Het
Ube2v1 A G 2: 167,471,114 (GRCm39) S26P probably benign Het
Unc13a G T 8: 72,113,229 (GRCm39) S207R possibly damaging Het
Usp35 T G 7: 96,969,286 (GRCm39) D362A probably damaging Het
Utp20 A G 10: 88,587,334 (GRCm39) I2487T probably benign Het
Vmn2r111 T C 17: 22,778,032 (GRCm39) N549S possibly damaging Het
Vmn2r117 T A 17: 23,694,359 (GRCm39) H496L probably benign Het
Vmn2r92 C T 17: 18,387,138 (GRCm39) A159V probably damaging Het
Wiz T C 17: 32,578,085 (GRCm39) K467E probably damaging Het
Zfp534 T C 4: 147,759,461 (GRCm39) T403A probably benign Het
Zswim5 T C 4: 116,819,843 (GRCm39) L416P probably damaging Het
Other mutations in Fbn2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00694:Fbn2 APN 18 58,170,881 (GRCm39) missense possibly damaging 0.81
IGL00780:Fbn2 APN 18 58,229,060 (GRCm39) missense probably damaging 1.00
IGL00923:Fbn2 APN 18 58,145,397 (GRCm39) missense probably benign 0.00
IGL01011:Fbn2 APN 18 58,228,312 (GRCm39) splice site probably benign
IGL01123:Fbn2 APN 18 58,237,153 (GRCm39) missense possibly damaging 0.62
IGL01304:Fbn2 APN 18 58,194,817 (GRCm39) missense probably damaging 0.97
IGL01339:Fbn2 APN 18 58,246,442 (GRCm39) missense possibly damaging 0.75
IGL01465:Fbn2 APN 18 58,336,905 (GRCm39) missense probably null 0.67
IGL01608:Fbn2 APN 18 58,186,776 (GRCm39) nonsense probably null
IGL01682:Fbn2 APN 18 58,205,743 (GRCm39) missense probably damaging 1.00
IGL01752:Fbn2 APN 18 58,209,049 (GRCm39) splice site probably null
IGL01764:Fbn2 APN 18 58,178,423 (GRCm39) missense probably damaging 1.00
IGL02002:Fbn2 APN 18 58,247,625 (GRCm39) missense probably benign 0.01
IGL02010:Fbn2 APN 18 58,170,794 (GRCm39) missense probably damaging 0.99
IGL02029:Fbn2 APN 18 58,342,675 (GRCm39) missense probably benign 0.04
IGL02037:Fbn2 APN 18 58,229,087 (GRCm39) missense probably damaging 1.00
IGL02350:Fbn2 APN 18 58,237,067 (GRCm39) missense possibly damaging 0.71
IGL02357:Fbn2 APN 18 58,237,067 (GRCm39) missense possibly damaging 0.71
IGL02653:Fbn2 APN 18 58,209,777 (GRCm39) missense probably benign
IGL03233:Fbn2 APN 18 58,235,449 (GRCm39) missense probably benign 0.39
IGL03347:Fbn2 APN 18 58,146,737 (GRCm39) missense probably damaging 1.00
IGL03410:Fbn2 APN 18 58,183,315 (GRCm39) missense possibly damaging 0.95
pinch UTSW 18 58,202,256 (GRCm39) missense probably damaging 1.00
stick UTSW 18 58,204,891 (GRCm39) missense possibly damaging 0.94
tweak UTSW 18 58,191,461 (GRCm39) missense probably damaging 1.00
BB009:Fbn2 UTSW 18 58,153,555 (GRCm39) missense possibly damaging 0.61
BB019:Fbn2 UTSW 18 58,153,555 (GRCm39) missense possibly damaging 0.61
PIT4434001:Fbn2 UTSW 18 58,229,134 (GRCm39) missense probably damaging 0.99
R0020:Fbn2 UTSW 18 58,238,236 (GRCm39) missense probably damaging 1.00
R0069:Fbn2 UTSW 18 58,202,256 (GRCm39) missense probably damaging 1.00
R0107:Fbn2 UTSW 18 58,189,275 (GRCm39) missense probably benign 0.00
R0116:Fbn2 UTSW 18 58,235,445 (GRCm39) nonsense probably null
R0277:Fbn2 UTSW 18 58,178,389 (GRCm39) missense probably damaging 1.00
R0284:Fbn2 UTSW 18 58,183,362 (GRCm39) splice site probably benign
R0316:Fbn2 UTSW 18 58,246,397 (GRCm39) missense probably damaging 1.00
R0323:Fbn2 UTSW 18 58,178,389 (GRCm39) missense probably damaging 1.00
R0421:Fbn2 UTSW 18 58,160,876 (GRCm39) splice site probably benign
R0455:Fbn2 UTSW 18 58,168,408 (GRCm39) missense probably damaging 1.00
R0504:Fbn2 UTSW 18 58,172,532 (GRCm39) missense possibly damaging 0.94
R0520:Fbn2 UTSW 18 58,146,821 (GRCm39) missense probably damaging 1.00
R0632:Fbn2 UTSW 18 58,170,819 (GRCm39) missense probably damaging 1.00
R0638:Fbn2 UTSW 18 58,178,446 (GRCm39) missense probably damaging 0.98
R0645:Fbn2 UTSW 18 58,191,461 (GRCm39) missense probably damaging 1.00
R1051:Fbn2 UTSW 18 58,145,425 (GRCm39) missense probably damaging 0.99
R1209:Fbn2 UTSW 18 58,203,088 (GRCm39) missense probably benign 0.00
R1319:Fbn2 UTSW 18 58,333,682 (GRCm39) missense possibly damaging 0.88
R1400:Fbn2 UTSW 18 58,213,265 (GRCm39) missense possibly damaging 0.90
R1437:Fbn2 UTSW 18 58,186,731 (GRCm39) missense possibly damaging 0.68
R1463:Fbn2 UTSW 18 58,143,452 (GRCm39) missense probably benign
R1612:Fbn2 UTSW 18 58,194,824 (GRCm39) missense probably damaging 1.00
R1623:Fbn2 UTSW 18 58,181,620 (GRCm39) missense possibly damaging 0.61
R1629:Fbn2 UTSW 18 58,159,610 (GRCm39) missense probably damaging 1.00
R1639:Fbn2 UTSW 18 58,191,534 (GRCm39) missense probably benign 0.41
R1722:Fbn2 UTSW 18 58,181,124 (GRCm39) critical splice acceptor site probably null
R1749:Fbn2 UTSW 18 58,183,348 (GRCm39) missense probably benign 0.35
R1802:Fbn2 UTSW 18 58,186,048 (GRCm39) nonsense probably null
R1850:Fbn2 UTSW 18 58,172,377 (GRCm39) splice site probably benign
R1913:Fbn2 UTSW 18 58,194,814 (GRCm39) missense probably damaging 1.00
R2045:Fbn2 UTSW 18 58,223,730 (GRCm39) missense probably damaging 1.00
R2064:Fbn2 UTSW 18 58,181,921 (GRCm39) missense probably damaging 0.99
R2143:Fbn2 UTSW 18 58,186,065 (GRCm39) missense possibly damaging 0.65
R2144:Fbn2 UTSW 18 58,186,065 (GRCm39) missense possibly damaging 0.65
R2149:Fbn2 UTSW 18 58,235,397 (GRCm39) splice site probably null
R2207:Fbn2 UTSW 18 58,214,471 (GRCm39) nonsense probably null
R2219:Fbn2 UTSW 18 58,186,035 (GRCm39) missense possibly damaging 0.79
R2263:Fbn2 UTSW 18 58,228,248 (GRCm39) splice site probably benign
R2375:Fbn2 UTSW 18 58,169,038 (GRCm39) missense probably damaging 1.00
R2424:Fbn2 UTSW 18 58,336,859 (GRCm39) missense probably damaging 0.99
R2504:Fbn2 UTSW 18 58,226,431 (GRCm39) missense probably damaging 0.99
R2879:Fbn2 UTSW 18 58,202,314 (GRCm39) missense probably damaging 0.97
R3040:Fbn2 UTSW 18 58,226,459 (GRCm39) missense probably damaging 1.00
R3080:Fbn2 UTSW 18 58,282,122 (GRCm39) missense probably damaging 0.97
R3625:Fbn2 UTSW 18 58,194,814 (GRCm39) missense probably damaging 1.00
R3901:Fbn2 UTSW 18 58,199,083 (GRCm39) missense probably damaging 0.97
R4089:Fbn2 UTSW 18 58,186,841 (GRCm39) missense probably benign 0.01
R4133:Fbn2 UTSW 18 58,229,034 (GRCm39) missense possibly damaging 0.82
R4155:Fbn2 UTSW 18 58,156,359 (GRCm39) nonsense probably null
R4288:Fbn2 UTSW 18 58,168,411 (GRCm39) missense probably damaging 0.98
R4289:Fbn2 UTSW 18 58,168,411 (GRCm39) missense probably damaging 0.98
R4363:Fbn2 UTSW 18 58,282,122 (GRCm39) missense probably damaging 0.97
R4559:Fbn2 UTSW 18 58,209,146 (GRCm39) missense probably benign 0.00
R4601:Fbn2 UTSW 18 58,186,805 (GRCm39) missense probably damaging 1.00
R4609:Fbn2 UTSW 18 58,323,341 (GRCm39) nonsense probably null
R4626:Fbn2 UTSW 18 58,146,819 (GRCm39) nonsense probably null
R4638:Fbn2 UTSW 18 58,143,376 (GRCm39) missense probably benign 0.01
R4675:Fbn2 UTSW 18 58,173,265 (GRCm39) missense possibly damaging 0.95
R4707:Fbn2 UTSW 18 58,189,344 (GRCm39) missense probably damaging 1.00
R4758:Fbn2 UTSW 18 58,159,458 (GRCm39) missense probably benign 0.00
R4945:Fbn2 UTSW 18 58,183,325 (GRCm39) missense possibly damaging 0.53
R4955:Fbn2 UTSW 18 58,191,455 (GRCm39) missense possibly damaging 0.61
R4980:Fbn2 UTSW 18 58,143,703 (GRCm39) missense probably benign 0.05
R4998:Fbn2 UTSW 18 58,205,703 (GRCm39) missense probably damaging 1.00
R5133:Fbn2 UTSW 18 58,172,412 (GRCm39) missense probably damaging 0.99
R5322:Fbn2 UTSW 18 58,172,387 (GRCm39) missense probably benign 0.00
R5414:Fbn2 UTSW 18 58,226,477 (GRCm39) missense probably damaging 0.96
R5538:Fbn2 UTSW 18 58,204,973 (GRCm39) missense probably benign 0.22
R5557:Fbn2 UTSW 18 58,248,731 (GRCm39) missense probably benign 0.00
R5754:Fbn2 UTSW 18 58,257,383 (GRCm39) missense probably benign 0.04
R5769:Fbn2 UTSW 18 58,238,271 (GRCm39) missense probably damaging 1.00
R5790:Fbn2 UTSW 18 58,209,768 (GRCm39) missense probably benign 0.34
R5830:Fbn2 UTSW 18 58,247,541 (GRCm39) missense probably benign 0.01
R5845:Fbn2 UTSW 18 58,186,840 (GRCm39) missense possibly damaging 0.89
R5880:Fbn2 UTSW 18 58,156,354 (GRCm39) nonsense probably null
R5907:Fbn2 UTSW 18 58,178,409 (GRCm39) missense probably damaging 1.00
R5948:Fbn2 UTSW 18 58,170,121 (GRCm39) missense probably damaging 1.00
R5955:Fbn2 UTSW 18 58,177,328 (GRCm39) missense probably damaging 1.00
R5974:Fbn2 UTSW 18 58,181,992 (GRCm39) missense probably damaging 1.00
R6010:Fbn2 UTSW 18 58,202,596 (GRCm39) missense probably benign 0.31
R6024:Fbn2 UTSW 18 58,209,908 (GRCm39) missense probably benign 0.03
R6037:Fbn2 UTSW 18 58,177,295 (GRCm39) missense probably benign 0.05
R6037:Fbn2 UTSW 18 58,177,295 (GRCm39) missense probably benign 0.05
R6315:Fbn2 UTSW 18 58,188,025 (GRCm39) critical splice acceptor site probably null
R6437:Fbn2 UTSW 18 58,246,435 (GRCm39) missense probably damaging 1.00
R6519:Fbn2 UTSW 18 58,196,647 (GRCm39) missense possibly damaging 0.61
R6520:Fbn2 UTSW 18 58,235,462 (GRCm39) missense probably damaging 1.00
R6734:Fbn2 UTSW 18 58,169,032 (GRCm39) missense probably damaging 1.00
R6755:Fbn2 UTSW 18 58,246,405 (GRCm39) missense possibly damaging 0.89
R6789:Fbn2 UTSW 18 58,143,686 (GRCm39) missense probably benign 0.00
R6801:Fbn2 UTSW 18 58,246,420 (GRCm39) missense probably benign 0.04
R6862:Fbn2 UTSW 18 58,257,393 (GRCm39) missense probably benign 0.04
R6900:Fbn2 UTSW 18 58,209,903 (GRCm39) missense probably benign
R6906:Fbn2 UTSW 18 58,204,891 (GRCm39) missense possibly damaging 0.94
R6919:Fbn2 UTSW 18 58,257,259 (GRCm39) splice site probably null
R6950:Fbn2 UTSW 18 58,168,993 (GRCm39) missense probably null 0.21
R6985:Fbn2 UTSW 18 58,201,460 (GRCm39) missense probably damaging 1.00
R7056:Fbn2 UTSW 18 58,209,798 (GRCm39) missense probably benign
R7199:Fbn2 UTSW 18 58,186,833 (GRCm39) nonsense probably null
R7219:Fbn2 UTSW 18 58,186,099 (GRCm39) missense probably benign 0.04
R7226:Fbn2 UTSW 18 58,170,142 (GRCm39) missense probably damaging 1.00
R7414:Fbn2 UTSW 18 58,229,122 (GRCm39) missense probably damaging 1.00
R7485:Fbn2 UTSW 18 58,204,912 (GRCm39) missense possibly damaging 0.50
R7523:Fbn2 UTSW 18 58,199,152 (GRCm39) missense probably benign 0.01
R7549:Fbn2 UTSW 18 58,153,536 (GRCm39) nonsense probably null
R7619:Fbn2 UTSW 18 58,213,299 (GRCm39) missense possibly damaging 0.46
R7638:Fbn2 UTSW 18 58,238,208 (GRCm39) missense probably damaging 1.00
R7789:Fbn2 UTSW 18 58,172,385 (GRCm39) missense probably benign 0.22
R7932:Fbn2 UTSW 18 58,153,555 (GRCm39) missense possibly damaging 0.61
R8013:Fbn2 UTSW 18 58,237,153 (GRCm39) missense possibly damaging 0.62
R8076:Fbn2 UTSW 18 58,159,496 (GRCm39) nonsense probably null
R8300:Fbn2 UTSW 18 58,342,687 (GRCm39) missense probably benign
R8345:Fbn2 UTSW 18 58,191,503 (GRCm39) missense probably damaging 1.00
R8487:Fbn2 UTSW 18 58,153,462 (GRCm39) missense possibly damaging 0.53
R8520:Fbn2 UTSW 18 58,171,270 (GRCm39) critical splice donor site probably null
R8781:Fbn2 UTSW 18 58,194,719 (GRCm39) missense possibly damaging 0.88
R8801:Fbn2 UTSW 18 58,287,021 (GRCm39) missense probably damaging 1.00
R8857:Fbn2 UTSW 18 58,286,933 (GRCm39) missense probably damaging 1.00
R8878:Fbn2 UTSW 18 58,257,318 (GRCm39) missense probably benign 0.30
R8909:Fbn2 UTSW 18 58,192,508 (GRCm39) missense possibly damaging 0.88
R8973:Fbn2 UTSW 18 58,286,928 (GRCm39) missense probably damaging 1.00
R8975:Fbn2 UTSW 18 58,286,928 (GRCm39) missense probably damaging 1.00
R8979:Fbn2 UTSW 18 58,286,928 (GRCm39) missense probably damaging 1.00
R8991:Fbn2 UTSW 18 58,239,395 (GRCm39) missense probably damaging 1.00
R9003:Fbn2 UTSW 18 58,176,591 (GRCm39) missense probably damaging 1.00
R9205:Fbn2 UTSW 18 58,192,428 (GRCm39) missense probably damaging 1.00
R9215:Fbn2 UTSW 18 58,209,747 (GRCm39) missense probably damaging 1.00
R9263:Fbn2 UTSW 18 58,257,344 (GRCm39) missense probably damaging 1.00
R9307:Fbn2 UTSW 18 58,342,856 (GRCm39) missense probably benign
R9337:Fbn2 UTSW 18 58,342,723 (GRCm39) missense probably benign
R9403:Fbn2 UTSW 18 58,199,179 (GRCm39) missense probably damaging 1.00
R9501:Fbn2 UTSW 18 58,209,130 (GRCm39) missense probably damaging 1.00
R9503:Fbn2 UTSW 18 58,171,313 (GRCm39) missense probably damaging 1.00
R9509:Fbn2 UTSW 18 58,247,550 (GRCm39) missense probably benign 0.22
R9561:Fbn2 UTSW 18 58,181,611 (GRCm39) nonsense probably null
R9565:Fbn2 UTSW 18 58,228,298 (GRCm39) missense probably benign 0.20
R9652:Fbn2 UTSW 18 58,146,722 (GRCm39) critical splice donor site probably null
R9659:Fbn2 UTSW 18 58,342,654 (GRCm39) missense probably damaging 0.98
R9679:Fbn2 UTSW 18 58,201,433 (GRCm39) missense probably damaging 1.00
R9683:Fbn2 UTSW 18 58,186,099 (GRCm39) missense probably benign 0.04
R9773:Fbn2 UTSW 18 58,143,481 (GRCm39) missense probably benign
X0062:Fbn2 UTSW 18 58,189,285 (GRCm39) missense probably damaging 1.00
Z1177:Fbn2 UTSW 18 58,202,262 (GRCm39) missense probably damaging 1.00
Z1177:Fbn2 UTSW 18 58,188,554 (GRCm39) missense probably benign 0.00
Z1177:Fbn2 UTSW 18 58,143,451 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AACGGTCAGTAACGACACTG -3'
(R):5'- TTCCTGTGACGAAGGGCTTG -3'

Sequencing Primer
(F):5'- TCAGTAACGACACTGGGCCTTC -3'
(R):5'- GGTCACGATCATGAAGTTATAGATC -3'
Posted On 2019-06-26