Mutagenetix > Incidental Mutation

Incidental Mutation 'R7570:Fbn1'

585688

Institutional Source

Beutler Lab

Gene Symbol

Fbn1

Ensembl Gene

ENSMUSG00000027204

Gene Name

fibrillin 1

Synonyms

Fib-1

MMRRC Submission

045631-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.916) question?

Stock #

R7570 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

125300594-125507993 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 125397852 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Lysine at position 305 (T305K)

Ref Sequence

ENSEMBL: ENSMUSP00000028633 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028633] [ENSMUST00000103234]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000028633
AA Change: T305K

PolyPhen 2 Score 0.294 (Sensitivity: 0.91; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000028633
Gene: ENSMUSG00000027204
AA Change: T305K

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
low complexity region	38	49	N/A	INTRINSIC
EGF	118	146	8.52e0	SMART
EGF	149	178	5.4e-2	SMART
Pfam:TB	193	235	6.9e-17	PFAM
EGF_CA	246	287	3.56e-11	SMART
EGF_CA	288	329	9.39e-11	SMART
Pfam:TB	343	388	2.3e-17	PFAM
low complexity region	394	445	N/A	INTRINSIC
EGF	454	491	8.57e-5	SMART
EGF_CA	492	531	9.39e-11	SMART
EGF_CA	532	573	2.38e-12	SMART
EGF_CA	574	614	5.48e-12	SMART
EGF_CA	615	655	5.39e-11	SMART
Pfam:TB	670	712	1.4e-17	PFAM
EGF_CA	725	766	1.53e-10	SMART
EGF_CA	767	808	2.42e-13	SMART
EGF_CA	809	848	2.44e-9	SMART
Pfam:TB	862	902	2.1e-14	PFAM
EGF_CA	912	953	3.32e-11	SMART
Pfam:TB	967	1009	3.9e-17	PFAM
EGF_CA	1030	1071	5.11e-12	SMART
EGF_CA	1072	1114	5.39e-11	SMART
EGF_CA	1115	1156	1.55e-11	SMART
EGF_CA	1157	1198	5.48e-12	SMART
EGF_CA	1199	1239	5.61e-9	SMART
EGF_CA	1240	1281	1.22e-9	SMART
EGF_CA	1282	1323	2.62e-9	SMART
EGF_CA	1324	1364	3.27e-10	SMART
EGF_CA	1365	1405	4.7e-11	SMART
EGF_CA	1406	1447	1.91e-11	SMART
EGF_CA	1448	1488	1.98e-9	SMART
EGF_CA	1489	1529	2.13e-9	SMART
Pfam:TB	1549	1590	3.5e-18	PFAM
EGF_CA	1608	1649	2.19e-11	SMART
EGF_CA	1650	1690	3.97e-9	SMART
Pfam:TB	1706	1749	9.7e-18	PFAM
EGF_CA	1768	1809	5.11e-12	SMART
EGF_CA	1810	1850	1.1e-11	SMART
EGF_CA	1851	1892	5.69e-10	SMART
EGF_CA	1893	1931	6.1e-10	SMART
EGF_CA	1932	1974	2.11e-13	SMART
EGF_CA	1975	2014	7.23e-12	SMART
EGF_CA	2015	2056	3.15e-12	SMART
Pfam:TB	2070	2112	3.7e-17	PFAM
EGF_CA	2129	2167	1.24e-10	SMART
EGF_CA	2168	2207	3.81e-11	SMART
EGF_CA	2208	2248	3.81e-11	SMART
EGF	2252	2292	5.24e0	SMART
EGF_CA	2293	2334	9.91e-10	SMART
Pfam:TB	2348	2391	8.5e-18	PFAM
EGF_CA	2404	2445	1.26e-11	SMART
EGF_CA	2446	2486	1.06e-9	SMART
EGF_CA	2487	2525	3.1e-11	SMART
EGF_CA	2526	2568	1.48e-8	SMART
EGF_CA	2569	2608	1.14e-9	SMART
EGF_CA	2609	2649	3.97e-9	SMART
EGF_CA	2650	2689	1.98e-9	SMART
low complexity region	2691	2698	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000103234
AA Change: T305K

PolyPhen 2 Score 0.294 (Sensitivity: 0.91; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000099524
Gene: ENSMUSG00000027204
AA Change: T305K

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
low complexity region	38	49	N/A	INTRINSIC
EGF	118	146	8.52e0	SMART
EGF	149	178	5.4e-2	SMART
Pfam:TB	194	232	3.5e-10	PFAM
EGF_CA	246	287	3.56e-11	SMART
EGF_CA	288	329	9.39e-11	SMART
Pfam:TB	344	388	6.8e-15	PFAM
low complexity region	394	445	N/A	INTRINSIC
EGF	454	491	8.57e-5	SMART
EGF_CA	492	531	9.39e-11	SMART
EGF_CA	532	573	2.38e-12	SMART
EGF_CA	574	614	5.48e-12	SMART
EGF_CA	615	655	5.39e-11	SMART
Pfam:TB	671	712	8.3e-16	PFAM
EGF_CA	725	766	1.53e-10	SMART
EGF_CA	767	808	2.42e-13	SMART
EGF_CA	809	848	2.44e-9	SMART
Pfam:TB	863	898	3.1e-8	PFAM
EGF_CA	912	953	3.32e-11	SMART
Pfam:TB	968	1009	1.5e-15	PFAM
EGF_CA	1030	1071	5.11e-12	SMART
EGF_CA	1072	1114	5.39e-11	SMART
EGF_CA	1115	1156	1.55e-11	SMART
EGF_CA	1157	1198	5.48e-12	SMART
EGF_CA	1199	1239	5.61e-9	SMART
EGF_CA	1240	1281	1.22e-9	SMART
EGF_CA	1282	1323	2.62e-9	SMART
EGF_CA	1324	1364	3.27e-10	SMART
EGF_CA	1365	1405	4.7e-11	SMART
EGF_CA	1406	1447	1.91e-11	SMART
EGF_CA	1448	1488	1.98e-9	SMART
EGF_CA	1489	1529	2.13e-9	SMART
Pfam:TB	1550	1590	5.3e-17	PFAM
EGF_CA	1608	1649	2.19e-11	SMART
EGF_CA	1650	1690	3.97e-9	SMART
Pfam:TB	1707	1749	1.6e-16	PFAM
EGF_CA	1768	1809	5.11e-12	SMART
EGF_CA	1810	1850	1.1e-11	SMART
EGF_CA	1851	1892	5.69e-10	SMART
EGF_CA	1893	1931	6.1e-10	SMART
EGF_CA	1932	1974	2.11e-13	SMART
EGF_CA	1975	2014	7.23e-12	SMART
EGF_CA	2015	2056	3.15e-12	SMART
Pfam:TB	2071	2112	1.9e-15	PFAM
EGF_CA	2129	2167	1.24e-10	SMART
EGF_CA	2168	2207	3.81e-11	SMART
EGF_CA	2208	2248	3.81e-11	SMART
EGF	2252	2292	5.24e0	SMART
EGF_CA	2293	2334	9.91e-10	SMART
Pfam:TB	2349	2391	5.8e-15	PFAM
EGF_CA	2404	2445	1.26e-11	SMART
EGF_CA	2446	2486	1.06e-9	SMART
EGF_CA	2487	2525	3.1e-11	SMART
EGF_CA	2526	2568	1.48e-8	SMART
EGF_CA	2569	2608	1.14e-9	SMART
EGF_CA	2609	2649	3.97e-9	SMART
EGF_CA	2650	2689	1.98e-9	SMART
low complexity region	2691	2698	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

98% (104/106)

MGI Phenotype

Strain: 1934905; 4880665
Lethality: D7-D10
FUNCTION: This gene encodes a member of the fibrillin family of proteins. The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin. Fibrillin-1 is an extracellular matrix glycoprotein that serves as a structural component of calcium-binding microfibrils. Asprosin, secreted by white adipose tissue, has been shown to regulate glucose homeostasis. Homozygous knockout mice for this gene exhibit impaired aortic development and early postnatal death, which was attributed to a deficiency in the fibrillin-1 protein. Mice with a hypomorphic allele of this gene exhibit impaired glucose homeostasis, likely due to a reduction in serum asprosin levels. [provided by RefSeq, Apr 2016]
PHENOTYPE: Lethality among homozygotes for spontaneous and targeted mutations ranges from embryonic death to death around 4 months. Abnormalities include vascular defects, excess bone growth, connective tissue hyperplasia, and lung emphysema. Mice heterozygous for a knock-in allele exhibit scleroderma. [provided by MGI curators]

Allele List at MGI

All alleles(10) : Targeted(9) Spontaneous(1)

Other mutations in this stock

Total: 106 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930590J08Rik	C	T	6: 91,934,610 (GRCm38)	T613I	probably benign	Het
9130019O22Rik	T	A	7: 127,385,283 (GRCm38)	S216C	probably benign	Het
Ajuba	T	C	14: 54,576,402 (GRCm38)	E288G	probably damaging	Het
Ankrd12	C	T	17: 65,985,360 (GRCm38)	R1026K	probably benign	Het
Apol7b	T	C	15: 77,423,474 (GRCm38)	T274A	probably benign	Het
Arid4a	A	T	12: 71,063,142 (GRCm38)	R86*	probably null	Het
Asnsd1	C	T	1: 53,348,258 (GRCm38)	G70D	probably damaging	Het
Atg4c	T	A	4: 99,228,560 (GRCm38)	V313D	possibly damaging	Het
Atp13a5	A	C	16: 29,266,963 (GRCm38)	C885G	probably damaging	Het
Bpifb9a	A	T	2: 154,262,263 (GRCm38)	I209F	possibly damaging	Het
Bsn	T	C	9: 108,113,543 (GRCm38)	D1670G	probably damaging	Het
Cct8	T	A	16: 87,491,322 (GRCm38)	I121F	probably benign	Het
Cd209a	T	G	8: 3,744,151 (GRCm38)	D217A	probably damaging	Het
Cdk19	C	T	10: 40,477,958 (GRCm38)	S456L	possibly damaging	Het
Chd9	C	T	8: 90,994,580 (GRCm38)	H999Y	unknown	Het
Col5a1	G	A	2: 27,951,383 (GRCm38)	V339M	unknown	Het
Cr2	G	A	1: 195,169,340 (GRCm38)	R115*	probably null	Het
Cyb561	A	T	11: 105,937,644 (GRCm38)	F62I	probably damaging	Het
Cyp2c38	A	T	19: 39,404,743 (GRCm38)	N293K	possibly damaging	Het
Cyp2c69	A	T	19: 39,859,898 (GRCm38)	D293E	probably damaging	Het
Dcbld2	T	A	16: 58,424,569 (GRCm38)	C69S	possibly damaging	Het
Dcdc2a	T	C	13: 25,119,373 (GRCm38)	S296P	probably benign	Het
Dmxl1	T	A	18: 49,893,957 (GRCm38)	I2044K	possibly damaging	Het
Dnah5	A	G	15: 28,346,952 (GRCm38)	D2527G	probably damaging	Het
Dnah6	T	C	6: 73,149,430 (GRCm38)	T1305A	probably benign	Het
Dnajc9	A	G	14: 20,388,644 (GRCm38)	V47A	probably benign	Het
Dnmt3b	A	G	2: 153,676,699 (GRCm38)	Y594C	probably damaging	Het
Dph7	A	G	2: 24,965,630 (GRCm38)	D147G	probably damaging	Het
Drap1	T	C	19: 5,423,352 (GRCm38)	H164R	possibly damaging	Het
Dsg3	T	A	18: 20,527,780 (GRCm38)	V392E	possibly damaging	Het
Dxo	A	G	17: 34,837,640 (GRCm38)	D81G	probably benign	Het
E230025N22Rik	G	T	18: 36,695,592 (GRCm38)	T11K	probably benign	Het
Esyt1	A	G	10: 128,518,932 (GRCm38)	V533A	possibly damaging	Het
Etv3	T	A	3: 87,536,031 (GRCm38)	C307*	probably null	Het
Fam114a1	T	A	5: 65,030,059 (GRCm38)		probably null	Het
Fam208b	A	G	13: 3,573,621 (GRCm38)	Y2110H	probably damaging	Het
Fam3c	T	A	6: 22,326,405 (GRCm38)		probably benign	Het
Ggt1	A	T	10: 75,585,594 (GRCm38)	I484F	probably damaging	Het
Gm10639	A	T	9: 78,304,469 (GRCm38)	D171V	possibly damaging	Het
Gpatch1	T	C	7: 35,293,812 (GRCm38)	D536G	probably damaging	Het
Gpx4	T	C	10: 80,055,041 (GRCm38)	I189T	probably damaging	Het
Gsr	T	A	8: 33,669,165 (GRCm38)	C85S	probably damaging	Het
Havcr1	T	A	11: 46,770,542 (GRCm38)		probably null	Het
Heatr4	T	C	12: 83,979,644 (GRCm38)	T280A	probably benign	Het
Hmcn2	A	T	2: 31,423,911 (GRCm38)	E3532D	probably benign	Het
Hnrnpc	T	C	14: 52,075,099 (GRCm38)	N308S	possibly damaging	Het
Ighv8-9	A	G	12: 115,468,738 (GRCm38)	V13A	probably benign	Het
Itgb2l	A	T	16: 96,426,239 (GRCm38)	F535I	probably benign	Het
Kdm5a	T	G	6: 120,427,842 (GRCm38)	D1348E	probably damaging	Het
Kndc1	CT	C	7: 139,923,775 (GRCm38)		probably null	Het
Ky	A	G	9: 102,542,329 (GRCm38)	I512V	probably benign	Het
Lamc1	A	T	1: 153,243,275 (GRCm38)	F866Y	possibly damaging	Het
Lbx1	C	A	19: 45,235,248 (GRCm38)		probably benign	Het
Magel2	A	G	7: 62,378,910 (GRCm38)	T521A	possibly damaging	Het
Mgam	A	T	6: 40,746,433 (GRCm38)	I491L	probably benign	Het
Mitd1	T	C	1: 37,890,192 (GRCm38)	E40G	probably damaging	Het
Mpzl3	A	G	9: 45,070,687 (GRCm38)	T218A	probably benign	Het
Mrpl42	A	G	10: 95,480,965 (GRCm38)	S77P	probably benign	Het
Mup5	C	T	4: 61,834,674 (GRCm38)	W37*	probably null	Het
Myh14	T	C	7: 44,632,426 (GRCm38)	I803V	probably benign	Het
Ncor2	T	A	5: 125,030,089 (GRCm38)	T744S		Het
Ndufv3	A	G	17: 31,527,622 (GRCm38)	D162G	probably damaging	Het
Nostrin	A	G	2: 69,175,806 (GRCm38)	E278G	probably damaging	Het
Nrxn1	T	G	17: 90,162,379 (GRCm38)	E1288A	probably benign	Het
Olfr1205	A	G	2: 88,831,128 (GRCm38)	N4D	possibly damaging	Het
Olfr623	C	A	7: 103,660,881 (GRCm38)	R123L	probably damaging	Het
Olfr648	T	A	7: 104,179,748 (GRCm38)	Y220F	probably damaging	Het
Olfr972	A	T	9: 39,873,455 (GRCm38)	Y60F	possibly damaging	Het
Patj	T	A	4: 98,424,500 (GRCm38)		probably null	Het
Pcm1	T	G	8: 41,267,344 (GRCm38)	I314R	possibly damaging	Het
Pcsk6	A	G	7: 66,033,898 (GRCm38)	T754A	probably benign	Het
Pde2a	A	T	7: 101,502,834 (GRCm38)	N326I	probably benign	Het
Plekhg4	T	C	8: 105,378,684 (GRCm38)	S594P	possibly damaging	Het
Plekhm3	T	C	1: 64,937,906 (GRCm38)	D135G	probably damaging	Het
Plin4	A	T	17: 56,106,776 (GRCm38)	M283K	probably benign	Het
Ppfia3	T	C	7: 45,340,748 (GRCm38)		probably null	Het
Prdm9	T	C	17: 15,555,652 (GRCm38)	N179S	probably benign	Het
Prrt3	T	C	6: 113,494,488 (GRCm38)	S908G	probably damaging	Het
Psg22	C	A	7: 18,722,735 (GRCm38)	S181Y	possibly damaging	Het
Rcor3	C	A	1: 192,137,876 (GRCm38)	G8V	probably damaging	Het
Rp1l1	T	A	14: 64,031,574 (GRCm38)	C1536*	probably null	Het
Rpp25l	T	C	4: 41,712,529 (GRCm38)	H82R	probably damaging	Het
Rps3a1	T	A	3: 86,139,089 (GRCm38)	M172L	probably benign	Het
Rtbdn	T	C	8: 84,952,927 (GRCm38)	L110P	probably damaging	Het
Ryr1	T	A	7: 29,078,585 (GRCm38)	Q2169L	probably damaging	Het
Scn4a	A	T	11: 106,320,473 (GRCm38)	C1573S	possibly damaging	Het
Sec16b	A	T	1: 157,531,395 (GRCm38)		probably null	Het
Serpina1a	A	T	12: 103,853,837 (GRCm38)	D383E	possibly damaging	Het
Sh3gl3	T	C	7: 82,285,077 (GRCm38)	M262T	probably benign	Het
Sos2	G	A	12: 69,590,880 (GRCm38)	T1052M	probably damaging	Het
Spag16	G	A	1: 69,996,841 (GRCm38)	V343I	probably benign	Het
Spocd1	T	G	4: 129,930,164 (GRCm38)	D251E		Het
Stc2	G	T	11: 31,367,798 (GRCm38)	N74K	probably damaging	Het
Thbs3	C	T	3: 89,219,052 (GRCm38)	Q227*	probably null	Het
Tmem92	A	C	11: 94,778,990 (GRCm38)	I105R	probably benign	Het
Tmod1	T	A	4: 46,083,632 (GRCm38)	N20K	probably benign	Het
Tns1	T	C	1: 73,953,479 (GRCm38)	D53G	probably damaging	Het
Tspan33	T	A	6: 29,717,338 (GRCm38)	L246Q	probably damaging	Het
Ttc16	A	G	2: 32,768,968 (GRCm38)	L392P	probably damaging	Het
Uggt1	T	A	1: 36,185,838 (GRCm38)	T572S	probably benign	Het
Usp17la	A	T	7: 104,860,397 (GRCm38)	T70S	probably damaging	Het
Usp31	C	T	7: 121,674,963 (GRCm38)	R370H	probably damaging	Het
Wdr83	C	T	8: 85,079,834 (GRCm38)	V112M	probably damaging	Het
Zbtb25	T	A	12: 76,369,592 (GRCm38)		probably benign	Het
Zfp110	T	A	7: 12,849,340 (GRCm38)	N638K	possibly damaging	Het
Zfp820	T	C	17: 21,819,013 (GRCm38)	T445A	probably benign	Het

Other mutations in Fbn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Fbn1	APN	2	125,324,947 (GRCm38)	missense	probably damaging	1.00
IGL00159:Fbn1	APN	2	125,397,873 (GRCm38)	missense	probably benign	0.14
IGL00500:Fbn1	APN	2	125,317,516 (GRCm38)	missense	probably damaging	0.99
IGL00558:Fbn1	APN	2	125,329,128 (GRCm38)	splice site	probably benign
IGL00645:Fbn1	APN	2	125,317,103 (GRCm38)	splice site	probably benign
IGL00863:Fbn1	APN	2	125,403,219 (GRCm38)	missense	possibly damaging	0.84
IGL00926:Fbn1	APN	2	125,319,042 (GRCm38)	missense	possibly damaging	0.84
IGL00935:Fbn1	APN	2	125,377,910 (GRCm38)	nonsense	probably null
IGL00950:Fbn1	APN	2	125,358,823 (GRCm38)	missense	probably damaging	1.00
IGL01090:Fbn1	APN	2	125,394,776 (GRCm38)	splice site	probably benign
IGL01106:Fbn1	APN	2	125,351,706 (GRCm38)	missense	possibly damaging	0.55
IGL01486:Fbn1	APN	2	125,389,978 (GRCm38)	missense	probably benign	0.03
IGL01519:Fbn1	APN	2	125,317,019 (GRCm38)	missense	probably benign	0.07
IGL01585:Fbn1	APN	2	125,360,110 (GRCm38)	missense	probably damaging	0.98
IGL01730:Fbn1	APN	2	125,312,974 (GRCm38)	splice site	probably benign
IGL01793:Fbn1	APN	2	125,387,293 (GRCm38)	missense	possibly damaging	0.67
IGL01803:Fbn1	APN	2	125,350,287 (GRCm38)	missense	probably damaging	1.00
IGL01803:Fbn1	APN	2	125,301,725 (GRCm38)	missense	probably benign
IGL01916:Fbn1	APN	2	125,315,446 (GRCm38)	missense	possibly damaging	0.55
IGL02035:Fbn1	APN	2	125,335,362 (GRCm38)	splice site	probably null
IGL02097:Fbn1	APN	2	125,363,969 (GRCm38)	missense	probably damaging	1.00
IGL02233:Fbn1	APN	2	125,321,610 (GRCm38)	splice site	probably benign
IGL02512:Fbn1	APN	2	125,338,460 (GRCm38)	missense	probably damaging	1.00
IGL02552:Fbn1	APN	2	125,412,713 (GRCm38)	missense	possibly damaging	0.86
IGL02657:Fbn1	APN	2	125,352,025 (GRCm38)	missense	possibly damaging	0.86
IGL02718:Fbn1	APN	2	125,369,886 (GRCm38)	missense	probably damaging	1.00
IGL02863:Fbn1	APN	2	125,303,256 (GRCm38)	missense	possibly damaging	0.80
IGL02974:Fbn1	APN	2	125,346,330 (GRCm38)	missense	probably null	0.99
IGL03058:Fbn1	APN	2	125,403,200 (GRCm38)	missense	probably benign	0.03
IGL03172:Fbn1	APN	2	125,320,968 (GRCm38)	missense	possibly damaging	0.92
IGL03288:Fbn1	APN	2	125,303,183 (GRCm38)	missense	probably benign	0.13
Carinatum	UTSW	2	125,342,830 (GRCm38)	missense	possibly damaging	0.70
Elasticity	UTSW	2	125,403,132 (GRCm38)	missense	possibly damaging	0.63
Excavatum	UTSW	2	125,335,487 (GRCm38)	missense	probably damaging	1.00
Exceedingly	UTSW	2	125,344,095 (GRCm38)	critical splice acceptor site	probably benign
Extensor	UTSW	2	125,328,158 (GRCm38)	missense	probably damaging	1.00
lincoln	UTSW	2	125,403,170 (GRCm38)	missense	possibly damaging	0.50
Long	UTSW	2	125,317,038 (GRCm38)	missense	probably damaging	1.00
Pectus	UTSW	2	125,321,691 (GRCm38)	missense	possibly damaging	0.82
Reach	UTSW	2	125,382,034 (GRCm38)	nonsense	probably null
reaper	UTSW	2	125,315,404 (GRCm38)	missense	probably damaging	0.98
Scythe	UTSW	2	125,403,228 (GRCm38)	missense	possibly damaging	0.84
String_bean	UTSW	2	125,379,134 (GRCm38)	splice site	probably null
wirey	UTSW	2	125,309,495 (GRCm38)	missense	probably benign
3-1:Fbn1	UTSW	2	125,394,605 (GRCm38)	splice site	probably benign
BB004:Fbn1	UTSW	2	125,383,736 (GRCm38)	missense	possibly damaging	0.82
BB014:Fbn1	UTSW	2	125,383,736 (GRCm38)	missense	possibly damaging	0.82
P0012:Fbn1	UTSW	2	125,369,321 (GRCm38)	splice site	probably benign
PIT4403001:Fbn1	UTSW	2	125,342,911 (GRCm38)	missense	probably damaging	1.00
PIT4466001:Fbn1	UTSW	2	125,306,501 (GRCm38)	missense	possibly damaging	0.90
PIT4472001:Fbn1	UTSW	2	125,306,501 (GRCm38)	missense	possibly damaging	0.90
PIT4651001:Fbn1	UTSW	2	125,363,989 (GRCm38)	critical splice acceptor site	probably null
R0226:Fbn1	UTSW	2	125,320,910 (GRCm38)	missense	possibly damaging	0.86
R0310:Fbn1	UTSW	2	125,363,644 (GRCm38)	missense	probably damaging	1.00
R0362:Fbn1	UTSW	2	125,309,777 (GRCm38)	missense	probably damaging	0.99
R0374:Fbn1	UTSW	2	125,321,676 (GRCm38)	missense	possibly damaging	0.86
R0433:Fbn1	UTSW	2	125,348,215 (GRCm38)	missense	possibly damaging	0.95
R0441:Fbn1	UTSW	2	125,309,755 (GRCm38)	critical splice donor site	probably null
R0501:Fbn1	UTSW	2	125,301,749 (GRCm38)	missense	probably benign	0.23
R0510:Fbn1	UTSW	2	125,342,925 (GRCm38)	splice site	probably benign
R0573:Fbn1	UTSW	2	125,389,249 (GRCm38)	missense	probably damaging	0.99
R0622:Fbn1	UTSW	2	125,379,024 (GRCm38)	missense	possibly damaging	0.88
R0630:Fbn1	UTSW	2	125,394,770 (GRCm38)	missense	possibly damaging	0.48
R0724:Fbn1	UTSW	2	125,352,064 (GRCm38)	missense	probably benign	0.14
R0739:Fbn1	UTSW	2	125,367,630 (GRCm38)	missense	probably benign	0.18
R0744:Fbn1	UTSW	2	125,314,814 (GRCm38)	splice site	probably benign
R0811:Fbn1	UTSW	2	125,403,170 (GRCm38)	missense	possibly damaging	0.50
R0812:Fbn1	UTSW	2	125,403,170 (GRCm38)	missense	possibly damaging	0.50
R0862:Fbn1	UTSW	2	125,342,891 (GRCm38)	nonsense	probably null
R0864:Fbn1	UTSW	2	125,342,891 (GRCm38)	nonsense	probably null
R1061:Fbn1	UTSW	2	125,345,963 (GRCm38)	missense	probably benign	0.01
R1126:Fbn1	UTSW	2	125,321,192 (GRCm38)	splice site	probably null
R1172:Fbn1	UTSW	2	125,394,687 (GRCm38)	missense	probably benign	0.13
R1175:Fbn1	UTSW	2	125,394,687 (GRCm38)	missense	probably benign	0.13
R1183:Fbn1	UTSW	2	125,321,617 (GRCm38)	missense	probably benign	0.07
R1218:Fbn1	UTSW	2	125,412,749 (GRCm38)	missense	possibly damaging	0.71
R1241:Fbn1	UTSW	2	125,372,527 (GRCm38)	splice site	probably benign
R1248:Fbn1	UTSW	2	125,301,609 (GRCm38)	missense	probably benign	0.01
R1345:Fbn1	UTSW	2	125,314,671 (GRCm38)	missense	probably damaging	1.00
R1374:Fbn1	UTSW	2	125,346,434 (GRCm38)	missense	probably damaging	0.99
R1458:Fbn1	UTSW	2	125,301,929 (GRCm38)	missense	probably benign	0.01
R1474:Fbn1	UTSW	2	125,361,265 (GRCm38)	missense	possibly damaging	0.72
R1496:Fbn1	UTSW	2	125,309,495 (GRCm38)	missense	probably benign
R1502:Fbn1	UTSW	2	125,363,706 (GRCm38)	nonsense	probably null
R1511:Fbn1	UTSW	2	125,306,285 (GRCm38)	missense	probably benign	0.00
R1588:Fbn1	UTSW	2	125,319,114 (GRCm38)	missense	probably benign	0.19
R1626:Fbn1	UTSW	2	125,341,279 (GRCm38)	missense	probably damaging	1.00
R1676:Fbn1	UTSW	2	125,309,781 (GRCm38)	missense	probably damaging	1.00
R1712:Fbn1	UTSW	2	125,346,434 (GRCm38)	missense	probably damaging	0.99
R1772:Fbn1	UTSW	2	125,403,228 (GRCm38)	missense	possibly damaging	0.84
R1776:Fbn1	UTSW	2	125,321,734 (GRCm38)	missense	possibly damaging	0.71
R1869:Fbn1	UTSW	2	125,352,027 (GRCm38)	missense	probably benign	0.00
R1894:Fbn1	UTSW	2	125,394,621 (GRCm38)	missense	probably damaging	0.96
R1925:Fbn1	UTSW	2	125,363,629 (GRCm38)	missense	probably damaging	1.00
R1957:Fbn1	UTSW	2	125,367,654 (GRCm38)	missense	possibly damaging	0.93
R1995:Fbn1	UTSW	2	125,350,373 (GRCm38)	critical splice acceptor site	probably null
R2140:Fbn1	UTSW	2	125,343,810 (GRCm38)	missense	probably damaging	1.00
R2142:Fbn1	UTSW	2	125,412,708 (GRCm38)	missense	possibly damaging	0.93
R2268:Fbn1	UTSW	2	125,321,741 (GRCm38)	missense	possibly damaging	0.49
R3409:Fbn1	UTSW	2	125,412,665 (GRCm38)	missense	possibly damaging	0.92
R3418:Fbn1	UTSW	2	125,320,926 (GRCm38)	missense	possibly damaging	0.55
R3508:Fbn1	UTSW	2	125,306,327 (GRCm38)	missense	probably benign	0.19
R3778:Fbn1	UTSW	2	125,317,086 (GRCm38)	missense	probably damaging	1.00
R3800:Fbn1	UTSW	2	125,345,974 (GRCm38)	missense	possibly damaging	0.63
R4001:Fbn1	UTSW	2	125,477,495 (GRCm38)	critical splice donor site	probably null
R4169:Fbn1	UTSW	2	125,363,952 (GRCm38)	missense	possibly damaging	0.86
R4398:Fbn1	UTSW	2	125,397,781 (GRCm38)	missense	probably benign	0.32
R4482:Fbn1	UTSW	2	125,363,610 (GRCm38)	critical splice donor site	probably null
R4559:Fbn1	UTSW	2	125,351,714 (GRCm38)	missense	possibly damaging	0.65
R4608:Fbn1	UTSW	2	125,306,500 (GRCm38)	missense	probably benign	0.05
R4634:Fbn1	UTSW	2	125,344,061 (GRCm38)	missense	probably damaging	1.00
R4706:Fbn1	UTSW	2	125,370,149 (GRCm38)	missense	probably benign	0.21
R4712:Fbn1	UTSW	2	125,341,316 (GRCm38)	missense	probably benign	0.12
R4783:Fbn1	UTSW	2	125,324,919 (GRCm38)	missense	probably damaging	1.00
R4784:Fbn1	UTSW	2	125,324,919 (GRCm38)	missense	probably damaging	1.00
R4785:Fbn1	UTSW	2	125,324,919 (GRCm38)	missense	probably damaging	1.00
R4793:Fbn1	UTSW	2	125,321,235 (GRCm38)	nonsense	probably null
R4838:Fbn1	UTSW	2	125,372,399 (GRCm38)	missense	probably benign	0.01
R4864:Fbn1	UTSW	2	125,372,397 (GRCm38)	missense	possibly damaging	0.92
R4887:Fbn1	UTSW	2	125,309,774 (GRCm38)	missense	probably damaging	1.00
R4942:Fbn1	UTSW	2	125,383,616 (GRCm38)	missense	possibly damaging	0.88
R4952:Fbn1	UTSW	2	125,317,534 (GRCm38)	missense	probably damaging	1.00
R5030:Fbn1	UTSW	2	125,412,704 (GRCm38)	missense	possibly damaging	0.51
R5044:Fbn1	UTSW	2	125,329,102 (GRCm38)	missense	probably damaging	0.97
R5057:Fbn1	UTSW	2	125,466,695 (GRCm38)	missense	probably benign	0.33
R5115:Fbn1	UTSW	2	125,332,383 (GRCm38)	missense	probably damaging	1.00
R5399:Fbn1	UTSW	2	125,332,333 (GRCm38)	missense	possibly damaging	0.69
R5498:Fbn1	UTSW	2	125,360,176 (GRCm38)	missense	probably damaging	1.00
R5526:Fbn1	UTSW	2	125,365,639 (GRCm38)	missense	possibly damaging	0.83
R5529:Fbn1	UTSW	2	125,373,950 (GRCm38)	missense	probably benign	0.01
R5602:Fbn1	UTSW	2	125,321,741 (GRCm38)	missense	possibly damaging	0.49
R5760:Fbn1	UTSW	2	125,361,247 (GRCm38)	missense	probably damaging	1.00
R5837:Fbn1	UTSW	2	125,379,134 (GRCm38)	splice site	probably null
R5955:Fbn1	UTSW	2	125,358,882 (GRCm38)	missense	probably damaging	1.00
R5980:Fbn1	UTSW	2	125,315,404 (GRCm38)	missense	probably damaging	0.98
R6039:Fbn1	UTSW	2	125,363,880 (GRCm38)	missense	probably damaging	1.00
R6039:Fbn1	UTSW	2	125,363,880 (GRCm38)	missense	probably damaging	1.00
R6058:Fbn1	UTSW	2	125,466,612 (GRCm38)	missense	possibly damaging	0.73
R6089:Fbn1	UTSW	2	125,321,225 (GRCm38)	missense	possibly damaging	0.55
R6136:Fbn1	UTSW	2	125,403,132 (GRCm38)	missense	possibly damaging	0.63
R6161:Fbn1	UTSW	2	125,369,801 (GRCm38)	nonsense	probably null
R6162:Fbn1	UTSW	2	125,360,227 (GRCm38)	missense	probably damaging	1.00
R6165:Fbn1	UTSW	2	125,332,363 (GRCm38)	missense	probably damaging	0.99
R6169:Fbn1	UTSW	2	125,335,489 (GRCm38)	critical splice acceptor site	probably null
R6221:Fbn1	UTSW	2	125,320,921 (GRCm38)	missense	probably benign	0.07
R6223:Fbn1	UTSW	2	125,412,671 (GRCm38)	missense	possibly damaging	0.86
R6225:Fbn1	UTSW	2	125,330,543 (GRCm38)	missense	probably damaging	1.00
R6238:Fbn1	UTSW	2	125,324,945 (GRCm38)	missense	probably damaging	0.98
R6329:Fbn1	UTSW	2	125,308,473 (GRCm38)	missense	possibly damaging	0.70
R6401:Fbn1	UTSW	2	125,346,450 (GRCm38)	missense	probably damaging	0.98
R6480:Fbn1	UTSW	2	125,335,418 (GRCm38)	missense	probably benign	0.05
R6513:Fbn1	UTSW	2	125,383,671 (GRCm38)	missense	probably damaging	1.00
R6530:Fbn1	UTSW	2	125,389,270 (GRCm38)	missense	probably damaging	0.99
R6595:Fbn1	UTSW	2	125,342,830 (GRCm38)	missense	possibly damaging	0.70
R6781:Fbn1	UTSW	2	125,317,038 (GRCm38)	missense	probably damaging	1.00
R6849:Fbn1	UTSW	2	125,321,691 (GRCm38)	missense	possibly damaging	0.82
R6860:Fbn1	UTSW	2	125,328,158 (GRCm38)	missense	probably damaging	1.00
R6960:Fbn1	UTSW	2	125,382,060 (GRCm38)	missense	probably benign	0.16
R7134:Fbn1	UTSW	2	125,382,049 (GRCm38)	missense	probably benign	0.03
R7241:Fbn1	UTSW	2	125,306,495 (GRCm38)	missense	possibly damaging	0.86
R7295:Fbn1	UTSW	2	125,335,487 (GRCm38)	missense	probably damaging	1.00
R7312:Fbn1	UTSW	2	125,466,674 (GRCm38)	missense	possibly damaging	0.53
R7322:Fbn1	UTSW	2	125,479,195 (GRCm38)	missense	possibly damaging	0.92
R7349:Fbn1	UTSW	2	125,315,401 (GRCm38)	missense	possibly damaging	0.84
R7365:Fbn1	UTSW	2	125,352,049 (GRCm38)	missense	probably damaging	0.97
R7392:Fbn1	UTSW	2	125,343,924 (GRCm38)	missense	probably damaging	1.00
R7442:Fbn1	UTSW	2	125,403,212 (GRCm38)	missense	possibly damaging	0.45
R7452:Fbn1	UTSW	2	125,505,455 (GRCm38)	missense	possibly damaging	0.53
R7453:Fbn1	UTSW	2	125,320,959 (GRCm38)	missense	possibly damaging	0.93
R7457:Fbn1	UTSW	2	125,351,747 (GRCm38)	missense	possibly damaging	0.90
R7458:Fbn1	UTSW	2	125,319,116 (GRCm38)	missense	probably benign	0.14
R7549:Fbn1	UTSW	2	125,344,027 (GRCm38)	missense	probably damaging	0.99
R7666:Fbn1	UTSW	2	125,306,471 (GRCm38)	missense	probably damaging	1.00
R7723:Fbn1	UTSW	2	125,382,034 (GRCm38)	nonsense	probably null
R7745:Fbn1	UTSW	2	125,303,195 (GRCm38)	missense	probably benign	0.06
R7754:Fbn1	UTSW	2	125,479,280 (GRCm38)	splice site	probably null
R7780:Fbn1	UTSW	2	125,301,758 (GRCm38)	missense	probably benign	0.15
R7849:Fbn1	UTSW	2	125,309,485 (GRCm38)	missense	probably damaging	0.98
R7927:Fbn1	UTSW	2	125,383,736 (GRCm38)	missense	possibly damaging	0.82
R7942:Fbn1	UTSW	2	125,412,786 (GRCm38)	missense	possibly damaging	0.53
R7948:Fbn1	UTSW	2	125,341,299 (GRCm38)	missense	probably damaging	1.00
R7985:Fbn1	UTSW	2	125,301,878 (GRCm38)	missense	probably benign	0.01
R8051:Fbn1	UTSW	2	125,306,463 (GRCm38)	missense	possibly damaging	0.86
R8054:Fbn1	UTSW	2	125,346,018 (GRCm38)	missense	possibly damaging	0.93
R8058:Fbn1	UTSW	2	125,351,969 (GRCm38)	missense	possibly damaging	0.46
R8113:Fbn1	UTSW	2	125,477,569 (GRCm38)	missense	probably damaging	1.00
R8307:Fbn1	UTSW	2	125,505,482 (GRCm38)	missense	possibly damaging	0.53
R8472:Fbn1	UTSW	2	125,309,802 (GRCm38)	missense	probably damaging	1.00
R8690:Fbn1	UTSW	2	125,344,095 (GRCm38)	critical splice acceptor site	probably benign
R8724:Fbn1	UTSW	2	125,360,146 (GRCm38)	missense	probably damaging	0.98
R8856:Fbn1	UTSW	2	125,314,717 (GRCm38)	missense	probably damaging	1.00
R8916:Fbn1	UTSW	2	125,403,229 (GRCm38)	missense	possibly damaging	0.63
R8931:Fbn1	UTSW	2	125,360,175 (GRCm38)	missense	probably damaging	1.00
R8988:Fbn1	UTSW	2	125,370,806 (GRCm38)	missense	possibly damaging	0.88
R9127:Fbn1	UTSW	2	125,382,065 (GRCm38)	missense	possibly damaging	0.86
R9161:Fbn1	UTSW	2	125,350,350 (GRCm38)	missense	probably damaging	1.00
R9495:Fbn1	UTSW	2	125,319,064 (GRCm38)	missense	probably damaging	0.96
R9515:Fbn1	UTSW	2	125,365,631 (GRCm38)	missense	probably benign	0.03
R9557:Fbn1	UTSW	2	125,338,538 (GRCm38)	missense	probably damaging	0.99
R9597:Fbn1	UTSW	2	125,345,986 (GRCm38)	missense	probably benign
R9680:Fbn1	UTSW	2	125,468,564 (GRCm38)	missense	probably benign	0.29
R9723:Fbn1	UTSW	2	125,360,199 (GRCm38)	nonsense	probably null
R9734:Fbn1	UTSW	2	125,389,978 (GRCm38)	missense	probably benign	0.03
R9796:Fbn1	UTSW	2	125,317,021 (GRCm38)	missense	probably benign	0.19
X0019:Fbn1	UTSW	2	125,383,643 (GRCm38)	missense	possibly damaging	0.82
X0020:Fbn1	UTSW	2	125,369,340 (GRCm38)	missense	probably damaging	1.00
X0028:Fbn1	UTSW	2	125,342,798 (GRCm38)	critical splice donor site	probably null
X0067:Fbn1	UTSW	2	125,369,914 (GRCm38)	missense	possibly damaging	0.95
Z1088:Fbn1	UTSW	2	125,350,288 (GRCm38)	missense	probably damaging	0.99
Z1176:Fbn1	UTSW	2	125,387,350 (GRCm38)	missense	possibly damaging	0.51
Z1177:Fbn1	UTSW	2	125,389,231 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACAGGCTCTCTACTCTTGAATGC -3'
(R):5'- GGGAATGTCTGTCTACATCGG -3'

Sequencing Primer
(F):5'- AGGCTCTCTACTCTTGAATGCATTTC -3'
(R):5'- ACATCGGCTCTTCTCTGGTCAG -3'

Posted On

2019-10-17