Mutagenetix > Incidental Mutation

Incidental Mutation 'R6862:Fbn2'

535725

Institutional Source

Beutler Lab

Gene Symbol

Fbn2

Ensembl Gene

ENSMUSG00000024598

Gene Name

fibrillin 2

Synonyms

Fib-2, sy, Sne

MMRRC Submission

045026-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.926) question?

Stock #

R6862 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

58008623-58209926 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 58124321 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 325 (I325F)

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: I325F

PolyPhen 2 Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000025497
Gene: ENSMUSG00000024598
AA Change: I325F

Domain	Start	End	E-Value	Type
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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.0%

Validation Efficiency

98% (57/58)

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: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579F01Rik	C	T	3: 138,186,188 (GRCm38)		probably benign	Het
Adgra2	C	A	8: 27,113,436 (GRCm38)	H416Q	probably benign	Het
Adgra2	T	A	8: 27,113,437 (GRCm38)	C417S	probably damaging	Het
Aff3	C	A	1: 38,406,497 (GRCm38)	R307L	possibly damaging	Het
Arhgap17	T	C	7: 123,321,901 (GRCm38)	D121G	probably damaging	Het
Ascc3	G	T	10: 50,849,646 (GRCm38)	R2155I	probably null	Het
Ccdc115	C	T	1: 34,439,283 (GRCm38)	S19N	possibly damaging	Het
Ccser2	T	C	14: 36,940,081 (GRCm38)	N382S	probably benign	Het
Cct6b	A	T	11: 82,719,959 (GRCm38)	V500E	probably damaging	Het
Cenpo	A	T	12: 4,216,539 (GRCm38)	Y190N	probably damaging	Het
Cfh	T	A	1: 140,102,362 (GRCm38)	K924N	probably damaging	Het
Col4a1	A	G	8: 11,202,926 (GRCm38)		probably benign	Het
Coro1b	T	C	19: 4,150,771 (GRCm38)	V234A	probably benign	Het
Crot	T	C	5: 8,989,641 (GRCm38)	K69E	probably damaging	Het
Cyp2d11	A	T	15: 82,390,138 (GRCm38)	H347Q	probably benign	Het
Fam71b	G	A	11: 46,407,591 (GRCm38)	G574D	possibly damaging	Het
Fbxw4	T	A	19: 45,582,748 (GRCm38)	R41S	probably benign	Het
Fn1	T	A	1: 71,613,907 (GRCm38)	I1308F	probably benign	Het
Frem1	C	A	4: 83,012,014 (GRCm38)	E232*	probably null	Het
Gabrg3	T	C	7: 56,773,311 (GRCm38)	Q213R	possibly damaging	Het
Gm11639	A	T	11: 104,721,458 (GRCm38)	K636*	probably null	Het
Gm428	A	G	4: 73,687,384 (GRCm38)	N344S	probably benign	Het
Gsdme	A	T	6: 50,227,398 (GRCm38)	V193E	probably damaging	Het
Hadha	C	A	5: 30,147,979 (GRCm38)		probably null	Het
Hdgfl2	C	A	17: 56,099,211 (GRCm38)	A533E	probably damaging	Het
Hivep2	T	C	10: 14,130,583 (GRCm38)	F975S	probably damaging	Het
Htatip2	T	A	7: 49,770,918 (GRCm38)	S171T	probably benign	Het
Ift57	A	T	16: 49,763,804 (GRCm38)	I307F	possibly damaging	Het
Il22	A	T	10: 118,205,810 (GRCm38)	R110W	probably benign	Het
Kcnk13	G	T	12: 100,061,689 (GRCm38)	R341L	probably damaging	Het
Kif2b	G	A	11: 91,575,915 (GRCm38)	T514M	probably damaging	Het
Kmt2c	A	C	5: 25,310,517 (GRCm38)	I2776S	probably damaging	Het
Ly9	T	C	1: 171,601,155 (GRCm38)	D189G	probably benign	Het
Mal2	T	C	15: 54,588,357 (GRCm38)	V58A	probably damaging	Het
Mettl21e	T	A	1: 44,206,366 (GRCm38)	N240I	probably benign	Het
Muc5ac	C	T	7: 141,809,744 (GRCm38)		probably benign	Het
Nacc1	G	A	8: 84,673,215 (GRCm38)	R458C	probably damaging	Het
Ncapd3	T	C	9: 27,030,809 (GRCm38)	C14R	probably damaging	Het
Obscn	G	T	11: 58,995,453 (GRCm38)		probably benign	Het
Olfr273	A	G	4: 52,855,695 (GRCm38)	F273L	probably benign	Het
Olfr350	A	T	2: 36,850,222 (GRCm38)	M59L	possibly damaging	Het
Olfr930	T	A	9: 38,930,476 (GRCm38)	F102I	possibly damaging	Het
Parp12	T	C	6: 39,111,736 (GRCm38)	I189V	probably benign	Het
Pde4dip	C	A	3: 97,767,024 (GRCm38)	R192L	possibly damaging	Het
Pdlim4	C	A	11: 54,055,848 (GRCm38)	E204D	probably damaging	Het
Phf3	T	C	1: 30,813,982 (GRCm38)	Q1049R	probably damaging	Het
Prr14l	A	G	5: 32,827,759 (GRCm38)	L1464P	probably damaging	Het
Psg25	C	T	7: 18,521,398 (GRCm38)	V398I	probably benign	Het
Ptprq	T	A	10: 107,686,225 (GRCm38)	N622Y	probably damaging	Het
Rsf1	CG	CGACGGCGGTG	7: 97,579,908 (GRCm38)		probably benign	Het
Tex36	A	G	7: 133,587,273 (GRCm38)	L190P	probably benign	Het
Tk1	A	G	11: 117,816,494 (GRCm38)	C156R	probably damaging	Het
Tmem144	T	A	3: 79,832,099 (GRCm38)	M126L	probably benign	Het
Tmem208	G	A	8: 105,328,230 (GRCm38)		probably null	Het
Trappc13	T	C	13: 104,150,152 (GRCm38)	Q199R	probably damaging	Het
Trim30b	T	A	7: 104,363,753 (GRCm38)	K156N	probably damaging	Het
Trps1	A	G	15: 50,831,605 (GRCm38)		probably null	Het
Washc4	T	A	10: 83,558,893 (GRCm38)	F329Y	possibly damaging	Het
Zbed5	T	G	5: 129,903,185 (GRCm38)	D658E	probably benign	Het
Zfyve28	T	G	5: 34,288,105 (GRCm38)	K11N	probably benign	Het
Zp1	C	T	19: 10,916,513 (GRCm38)	V443I	possibly damaging	Het

Other mutations in Fbn2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00694:Fbn2	APN	18	58,037,809 (GRCm38)	missense	possibly damaging	0.81
IGL00780:Fbn2	APN	18	58,095,988 (GRCm38)	missense	probably damaging	1.00
IGL00923:Fbn2	APN	18	58,012,325 (GRCm38)	missense	probably benign	0.00
IGL01011:Fbn2	APN	18	58,095,240 (GRCm38)	splice site	probably benign
IGL01123:Fbn2	APN	18	58,104,081 (GRCm38)	missense	possibly damaging	0.62
IGL01304:Fbn2	APN	18	58,061,745 (GRCm38)	missense	probably damaging	0.97
IGL01339:Fbn2	APN	18	58,113,370 (GRCm38)	missense	possibly damaging	0.75
IGL01465:Fbn2	APN	18	58,203,833 (GRCm38)	missense	probably null	0.67
IGL01608:Fbn2	APN	18	58,053,704 (GRCm38)	nonsense	probably null
IGL01682:Fbn2	APN	18	58,072,671 (GRCm38)	missense	probably damaging	1.00
IGL01752:Fbn2	APN	18	58,075,977 (GRCm38)	splice site	probably null
IGL01764:Fbn2	APN	18	58,045,351 (GRCm38)	missense	probably damaging	1.00
IGL02002:Fbn2	APN	18	58,114,553 (GRCm38)	missense	probably benign	0.01
IGL02010:Fbn2	APN	18	58,037,722 (GRCm38)	missense	probably damaging	0.99
IGL02029:Fbn2	APN	18	58,209,603 (GRCm38)	missense	probably benign	0.04
IGL02037:Fbn2	APN	18	58,096,015 (GRCm38)	missense	probably damaging	1.00
IGL02350:Fbn2	APN	18	58,103,995 (GRCm38)	missense	possibly damaging	0.71
IGL02357:Fbn2	APN	18	58,103,995 (GRCm38)	missense	possibly damaging	0.71
IGL02653:Fbn2	APN	18	58,076,705 (GRCm38)	missense	probably benign
IGL03233:Fbn2	APN	18	58,102,377 (GRCm38)	missense	probably benign	0.39
IGL03347:Fbn2	APN	18	58,013,665 (GRCm38)	missense	probably damaging	1.00
IGL03410:Fbn2	APN	18	58,050,243 (GRCm38)	missense	possibly damaging	0.95
pinch	UTSW	18	58,069,184 (GRCm38)	missense	probably damaging	1.00
stick	UTSW	18	58,071,819 (GRCm38)	missense	possibly damaging	0.94
tweak	UTSW	18	58,058,389 (GRCm38)	missense	probably damaging	1.00
BB009:Fbn2	UTSW	18	58,020,483 (GRCm38)	missense	possibly damaging	0.61
BB019:Fbn2	UTSW	18	58,020,483 (GRCm38)	missense	possibly damaging	0.61
PIT4434001:Fbn2	UTSW	18	58,096,062 (GRCm38)	missense	probably damaging	0.99
R0020:Fbn2	UTSW	18	58,105,164 (GRCm38)	missense	probably damaging	1.00
R0069:Fbn2	UTSW	18	58,069,184 (GRCm38)	missense	probably damaging	1.00
R0107:Fbn2	UTSW	18	58,056,203 (GRCm38)	missense	probably benign	0.00
R0116:Fbn2	UTSW	18	58,102,373 (GRCm38)	nonsense	probably null
R0277:Fbn2	UTSW	18	58,045,317 (GRCm38)	missense	probably damaging	1.00
R0284:Fbn2	UTSW	18	58,050,290 (GRCm38)	splice site	probably benign
R0316:Fbn2	UTSW	18	58,113,325 (GRCm38)	missense	probably damaging	1.00
R0323:Fbn2	UTSW	18	58,045,317 (GRCm38)	missense	probably damaging	1.00
R0421:Fbn2	UTSW	18	58,027,804 (GRCm38)	splice site	probably benign
R0455:Fbn2	UTSW	18	58,035,336 (GRCm38)	missense	probably damaging	1.00
R0504:Fbn2	UTSW	18	58,039,460 (GRCm38)	missense	possibly damaging	0.94
R0520:Fbn2	UTSW	18	58,013,749 (GRCm38)	missense	probably damaging	1.00
R0632:Fbn2	UTSW	18	58,037,747 (GRCm38)	missense	probably damaging	1.00
R0638:Fbn2	UTSW	18	58,045,374 (GRCm38)	missense	probably damaging	0.98
R0645:Fbn2	UTSW	18	58,058,389 (GRCm38)	missense	probably damaging	1.00
R1051:Fbn2	UTSW	18	58,012,353 (GRCm38)	missense	probably damaging	0.99
R1209:Fbn2	UTSW	18	58,070,016 (GRCm38)	missense	probably benign	0.00
R1319:Fbn2	UTSW	18	58,200,610 (GRCm38)	missense	possibly damaging	0.88
R1400:Fbn2	UTSW	18	58,080,193 (GRCm38)	missense	possibly damaging	0.90
R1437:Fbn2	UTSW	18	58,053,659 (GRCm38)	missense	possibly damaging	0.68
R1463:Fbn2	UTSW	18	58,010,380 (GRCm38)	missense	probably benign
R1612:Fbn2	UTSW	18	58,061,752 (GRCm38)	missense	probably damaging	1.00
R1623:Fbn2	UTSW	18	58,048,548 (GRCm38)	missense	possibly damaging	0.61
R1629:Fbn2	UTSW	18	58,026,538 (GRCm38)	missense	probably damaging	1.00
R1639:Fbn2	UTSW	18	58,058,462 (GRCm38)	missense	probably benign	0.41
R1722:Fbn2	UTSW	18	58,048,052 (GRCm38)	critical splice acceptor site	probably null
R1749:Fbn2	UTSW	18	58,050,276 (GRCm38)	missense	probably benign	0.35
R1802:Fbn2	UTSW	18	58,052,976 (GRCm38)	nonsense	probably null
R1850:Fbn2	UTSW	18	58,039,305 (GRCm38)	splice site	probably benign
R1913:Fbn2	UTSW	18	58,061,742 (GRCm38)	missense	probably damaging	1.00
R2045:Fbn2	UTSW	18	58,090,658 (GRCm38)	missense	probably damaging	1.00
R2064:Fbn2	UTSW	18	58,048,849 (GRCm38)	missense	probably damaging	0.99
R2143:Fbn2	UTSW	18	58,052,993 (GRCm38)	missense	possibly damaging	0.65
R2144:Fbn2	UTSW	18	58,052,993 (GRCm38)	missense	possibly damaging	0.65
R2149:Fbn2	UTSW	18	58,102,325 (GRCm38)	splice site	probably null
R2207:Fbn2	UTSW	18	58,081,399 (GRCm38)	nonsense	probably null
R2219:Fbn2	UTSW	18	58,052,963 (GRCm38)	missense	possibly damaging	0.79
R2263:Fbn2	UTSW	18	58,095,176 (GRCm38)	splice site	probably benign
R2375:Fbn2	UTSW	18	58,035,966 (GRCm38)	missense	probably damaging	1.00
R2424:Fbn2	UTSW	18	58,203,787 (GRCm38)	missense	probably damaging	0.99
R2504:Fbn2	UTSW	18	58,093,359 (GRCm38)	missense	probably damaging	0.99
R2879:Fbn2	UTSW	18	58,069,242 (GRCm38)	missense	probably damaging	0.97
R3040:Fbn2	UTSW	18	58,093,387 (GRCm38)	missense	probably damaging	1.00
R3080:Fbn2	UTSW	18	58,149,050 (GRCm38)	missense	probably damaging	0.97
R3625:Fbn2	UTSW	18	58,061,742 (GRCm38)	missense	probably damaging	1.00
R3901:Fbn2	UTSW	18	58,066,011 (GRCm38)	missense	probably damaging	0.97
R4089:Fbn2	UTSW	18	58,053,769 (GRCm38)	missense	probably benign	0.01
R4133:Fbn2	UTSW	18	58,095,962 (GRCm38)	missense	possibly damaging	0.82
R4155:Fbn2	UTSW	18	58,023,287 (GRCm38)	nonsense	probably null
R4288:Fbn2	UTSW	18	58,035,339 (GRCm38)	missense	probably damaging	0.98
R4289:Fbn2	UTSW	18	58,035,339 (GRCm38)	missense	probably damaging	0.98
R4363:Fbn2	UTSW	18	58,149,050 (GRCm38)	missense	probably damaging	0.97
R4559:Fbn2	UTSW	18	58,076,074 (GRCm38)	missense	probably benign	0.00
R4601:Fbn2	UTSW	18	58,053,733 (GRCm38)	missense	probably damaging	1.00
R4609:Fbn2	UTSW	18	58,190,269 (GRCm38)	nonsense	probably null
R4626:Fbn2	UTSW	18	58,013,747 (GRCm38)	nonsense	probably null
R4638:Fbn2	UTSW	18	58,010,304 (GRCm38)	missense	probably benign	0.01
R4675:Fbn2	UTSW	18	58,040,193 (GRCm38)	missense	possibly damaging	0.95
R4707:Fbn2	UTSW	18	58,056,272 (GRCm38)	missense	probably damaging	1.00
R4758:Fbn2	UTSW	18	58,026,386 (GRCm38)	missense	probably benign	0.00
R4945:Fbn2	UTSW	18	58,050,253 (GRCm38)	missense	possibly damaging	0.53
R4955:Fbn2	UTSW	18	58,058,383 (GRCm38)	missense	possibly damaging	0.61
R4980:Fbn2	UTSW	18	58,010,631 (GRCm38)	missense	probably benign	0.05
R4998:Fbn2	UTSW	18	58,072,631 (GRCm38)	missense	probably damaging	1.00
R5133:Fbn2	UTSW	18	58,039,340 (GRCm38)	missense	probably damaging	0.99
R5322:Fbn2	UTSW	18	58,039,315 (GRCm38)	missense	probably benign	0.00
R5414:Fbn2	UTSW	18	58,093,405 (GRCm38)	missense	probably damaging	0.96
R5538:Fbn2	UTSW	18	58,071,901 (GRCm38)	missense	probably benign	0.22
R5557:Fbn2	UTSW	18	58,115,659 (GRCm38)	missense	probably benign	0.00
R5754:Fbn2	UTSW	18	58,124,311 (GRCm38)	missense	probably benign	0.04
R5769:Fbn2	UTSW	18	58,105,199 (GRCm38)	missense	probably damaging	1.00
R5790:Fbn2	UTSW	18	58,076,696 (GRCm38)	missense	probably benign	0.34
R5830:Fbn2	UTSW	18	58,114,469 (GRCm38)	missense	probably benign	0.01
R5845:Fbn2	UTSW	18	58,053,768 (GRCm38)	missense	possibly damaging	0.89
R5880:Fbn2	UTSW	18	58,023,282 (GRCm38)	nonsense	probably null
R5907:Fbn2	UTSW	18	58,045,337 (GRCm38)	missense	probably damaging	1.00
R5948:Fbn2	UTSW	18	58,037,049 (GRCm38)	missense	probably damaging	1.00
R5955:Fbn2	UTSW	18	58,044,256 (GRCm38)	missense	probably damaging	1.00
R5974:Fbn2	UTSW	18	58,048,920 (GRCm38)	missense	probably damaging	1.00
R6010:Fbn2	UTSW	18	58,069,524 (GRCm38)	missense	probably benign	0.31
R6024:Fbn2	UTSW	18	58,076,836 (GRCm38)	missense	probably benign	0.03
R6037:Fbn2	UTSW	18	58,044,223 (GRCm38)	missense	probably benign	0.05
R6037:Fbn2	UTSW	18	58,044,223 (GRCm38)	missense	probably benign	0.05
R6315:Fbn2	UTSW	18	58,054,953 (GRCm38)	critical splice acceptor site	probably null
R6437:Fbn2	UTSW	18	58,113,363 (GRCm38)	missense	probably damaging	1.00
R6519:Fbn2	UTSW	18	58,063,575 (GRCm38)	missense	possibly damaging	0.61
R6520:Fbn2	UTSW	18	58,102,390 (GRCm38)	missense	probably damaging	1.00
R6734:Fbn2	UTSW	18	58,035,960 (GRCm38)	missense	probably damaging	1.00
R6755:Fbn2	UTSW	18	58,113,333 (GRCm38)	missense	possibly damaging	0.89
R6789:Fbn2	UTSW	18	58,010,614 (GRCm38)	missense	probably benign	0.00
R6801:Fbn2	UTSW	18	58,113,348 (GRCm38)	missense	probably benign	0.04
R6900:Fbn2	UTSW	18	58,076,831 (GRCm38)	missense	probably benign
R6906:Fbn2	UTSW	18	58,071,819 (GRCm38)	missense	possibly damaging	0.94
R6919:Fbn2	UTSW	18	58,124,187 (GRCm38)	splice site	probably null
R6950:Fbn2	UTSW	18	58,035,921 (GRCm38)	missense	probably null	0.21
R6985:Fbn2	UTSW	18	58,068,388 (GRCm38)	missense	probably damaging	1.00
R7056:Fbn2	UTSW	18	58,076,726 (GRCm38)	missense	probably benign
R7199:Fbn2	UTSW	18	58,053,761 (GRCm38)	nonsense	probably null
R7219:Fbn2	UTSW	18	58,053,027 (GRCm38)	missense	probably benign	0.04
R7226:Fbn2	UTSW	18	58,037,070 (GRCm38)	missense	probably damaging	1.00
R7260:Fbn2	UTSW	18	58,066,116 (GRCm38)	missense	probably benign	0.14
R7414:Fbn2	UTSW	18	58,096,050 (GRCm38)	missense	probably damaging	1.00
R7485:Fbn2	UTSW	18	58,071,840 (GRCm38)	missense	possibly damaging	0.50
R7523:Fbn2	UTSW	18	58,066,080 (GRCm38)	missense	probably benign	0.01
R7549:Fbn2	UTSW	18	58,020,464 (GRCm38)	nonsense	probably null
R7619:Fbn2	UTSW	18	58,080,227 (GRCm38)	missense	possibly damaging	0.46
R7638:Fbn2	UTSW	18	58,105,136 (GRCm38)	missense	probably damaging	1.00
R7789:Fbn2	UTSW	18	58,039,313 (GRCm38)	missense	probably benign	0.22
R7932:Fbn2	UTSW	18	58,020,483 (GRCm38)	missense	possibly damaging	0.61
R8013:Fbn2	UTSW	18	58,104,081 (GRCm38)	missense	possibly damaging	0.62
R8076:Fbn2	UTSW	18	58,026,424 (GRCm38)	nonsense	probably null
R8300:Fbn2	UTSW	18	58,209,615 (GRCm38)	missense	probably benign
R8345:Fbn2	UTSW	18	58,058,431 (GRCm38)	missense	probably damaging	1.00
R8487:Fbn2	UTSW	18	58,020,390 (GRCm38)	missense	possibly damaging	0.53
R8520:Fbn2	UTSW	18	58,038,198 (GRCm38)	critical splice donor site	probably null
R8781:Fbn2	UTSW	18	58,061,647 (GRCm38)	missense	possibly damaging	0.88
R8801:Fbn2	UTSW	18	58,153,949 (GRCm38)	missense	probably damaging	1.00
R8857:Fbn2	UTSW	18	58,153,861 (GRCm38)	missense	probably damaging	1.00
R8878:Fbn2	UTSW	18	58,124,246 (GRCm38)	missense	probably benign	0.30
R8909:Fbn2	UTSW	18	58,059,436 (GRCm38)	missense	possibly damaging	0.88
R8973:Fbn2	UTSW	18	58,153,856 (GRCm38)	missense	probably damaging	1.00
R8975:Fbn2	UTSW	18	58,153,856 (GRCm38)	missense	probably damaging	1.00
R8979:Fbn2	UTSW	18	58,153,856 (GRCm38)	missense	probably damaging	1.00
R8991:Fbn2	UTSW	18	58,106,323 (GRCm38)	missense	probably damaging	1.00
R9003:Fbn2	UTSW	18	58,043,519 (GRCm38)	missense	probably damaging	1.00
R9205:Fbn2	UTSW	18	58,059,356 (GRCm38)	missense	probably damaging	1.00
R9215:Fbn2	UTSW	18	58,076,675 (GRCm38)	missense	probably damaging	1.00
R9263:Fbn2	UTSW	18	58,124,272 (GRCm38)	missense	probably damaging	1.00
R9307:Fbn2	UTSW	18	58,209,784 (GRCm38)	missense	probably benign
R9337:Fbn2	UTSW	18	58,209,651 (GRCm38)	missense	probably benign
R9403:Fbn2	UTSW	18	58,066,107 (GRCm38)	missense	probably damaging	1.00
R9501:Fbn2	UTSW	18	58,076,058 (GRCm38)	missense	probably damaging	1.00
R9503:Fbn2	UTSW	18	58,038,241 (GRCm38)	missense	probably damaging	1.00
R9509:Fbn2	UTSW	18	58,114,478 (GRCm38)	missense	probably benign	0.22
R9561:Fbn2	UTSW	18	58,048,539 (GRCm38)	nonsense	probably null
R9565:Fbn2	UTSW	18	58,095,226 (GRCm38)	missense	probably benign	0.20
R9652:Fbn2	UTSW	18	58,013,650 (GRCm38)	critical splice donor site	probably null
R9659:Fbn2	UTSW	18	58,209,582 (GRCm38)	missense	probably damaging	0.98
R9679:Fbn2	UTSW	18	58,068,361 (GRCm38)	missense	probably damaging	1.00
R9683:Fbn2	UTSW	18	58,053,027 (GRCm38)	missense	probably benign	0.04
R9773:Fbn2	UTSW	18	58,010,409 (GRCm38)	missense	probably benign
X0062:Fbn2	UTSW	18	58,056,213 (GRCm38)	missense	probably damaging	1.00
Z1177:Fbn2	UTSW	18	58,069,190 (GRCm38)	missense	probably damaging	1.00
Z1177:Fbn2	UTSW	18	58,055,482 (GRCm38)	missense	probably benign	0.00
Z1177:Fbn2	UTSW	18	58,010,379 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AGAGCAATCCTTTCATCCGTTC -3'
(R):5'- AGTTCCCAGAGATACGTGCG -3'

Sequencing Primer
(F):5'- ATCCGTTCGCCCAATGG -3'
(R):5'- TACGTGCGAGAAATTCCTCAG -3'

Posted On

2018-10-18