Mutagenetix > Incidental Mutation

Incidental Mutation 'R4887:Fbn1'

376947

Institutional Source

Beutler Lab

Gene Symbol

Fbn1

Ensembl Gene

ENSMUSG00000027204

Gene Name

fibrillin 1

Synonyms

Fib-1

MMRRC Submission

041979-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.916) question?

Stock #

R4887 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

125300594-125507993 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 125309774 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 2520 (H2520L)

Ref Sequence

ENSEMBL: ENSMUSP00000099524 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000028633
AA Change: H2520L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000028633
Gene: ENSMUSG00000027204
AA Change: H2520L

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 damaging
Transcript: ENSMUST00000103234
AA Change: H2520L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000099524
Gene: ENSMUSG00000027204
AA Change: H2520L

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: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.2%

Validation Efficiency

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: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310009B15Rik	A	C	1: 138,852,165 (GRCm38)	Y116*	probably null	Het
Abtb3	C	T	10: 85,387,378 (GRCm38)	T17M	unknown	Het
Acer3	T	C	7: 98,257,701 (GRCm38)	T91A	possibly damaging	Het
Acsbg3	A	T	17: 56,876,324 (GRCm38)	I22F	possibly damaging	Het
Adam12	T	C	7: 134,172,821 (GRCm38)	K20E	possibly damaging	Het
Adamtsl3	T	C	7: 82,574,614 (GRCm38)	V275A	possibly damaging	Het
Afg1l	C	T	10: 42,454,378 (GRCm38)	V98I	probably benign	Het
Ajm1	G	A	2: 25,579,747 (GRCm38)	R51C	possibly damaging	Het
Alpk1	C	T	3: 127,673,475 (GRCm38)	G1052R	probably damaging	Het
Anln	A	T	9: 22,380,188 (GRCm38)	S115T	possibly damaging	Het
Apob	T	A	12: 8,013,099 (GRCm38)	N3827K	probably damaging	Het
Aqr	G	A	2: 114,150,509 (GRCm38)	L264F	probably damaging	Het
Arhgap33	T	C	7: 30,532,192 (GRCm38)	S123G	probably damaging	Het
Arvcf	C	T	16: 18,398,113 (GRCm38)	R333*	probably null	Het
Brca2	T	A	5: 150,556,937 (GRCm38)	L2724Q	probably damaging	Het
C2cd6	T	A	1: 59,094,734 (GRCm38)	T43S	probably benign	Het
Cacna1h	A	G	17: 25,377,287 (GRCm38)	V1920A	possibly damaging	Het
Capsl	A	T	15: 9,457,772 (GRCm38)	I26F	possibly damaging	Het
Card10	A	T	15: 78,781,524 (GRCm38)	V673E	possibly damaging	Het
Ccar1	A	G	10: 62,753,218 (GRCm38)	S829P	unknown	Het
Ccdc121	A	G	5: 31,486,252 (GRCm38)	I109V	probably benign	Het
Cdc42bpa	T	C	1: 180,144,635 (GRCm38)	M1334T	possibly damaging	Het
Ceacam2	C	T	7: 25,520,832 (GRCm38)	C267Y	probably benign	Het
Cep68	G	A	11: 20,239,239 (GRCm38)	T591M	probably benign	Het
Chil4	T	C	3: 106,204,144 (GRCm38)	K218R	probably benign	Het
Cldn14	G	T	16: 93,919,859 (GRCm38)	T33K	possibly damaging	Het
Copa	T	A	1: 172,092,276 (GRCm38)	C140S	probably benign	Het
Coq6	T	C	12: 84,372,296 (GRCm38)	L358P	probably damaging	Het
Cyfip1	C	T	7: 55,872,068 (GRCm38)	P40L	probably damaging	Het
Dennd2a	A	C	6: 39,497,159 (GRCm38)	S414A	probably benign	Het
Dpm1	T	C	2: 168,217,759 (GRCm38)	N139S	probably benign	Het
Dpp7	T	A	2: 25,352,758 (GRCm38)		probably null	Het
Ednrb	T	C	14: 103,820,011 (GRCm38)	I372V	possibly damaging	Het
Edrf1	G	T	7: 133,658,610 (GRCm38)	M83I	probably damaging	Het
Fam135a	G	A	1: 24,024,253 (GRCm38)	Q1087*	probably null	Het
Fancg	T	C	4: 43,006,866 (GRCm38)	T275A	probably benign	Het
Fmn2	T	C	1: 174,581,961 (GRCm38)	S587P	unknown	Het
Foxr2	A	G	X: 153,130,316 (GRCm38)	Q61R	probably damaging	Het
Frrs1	A	G	3: 116,902,416 (GRCm38)	*124W	probably null	Het
Gm16432	A	G	1: 178,103,949 (GRCm38)	Y478C	unknown	Het
Gm7535	T	A	17: 17,911,071 (GRCm38)		probably benign	Het
H4c1	T	C	13: 23,760,952 (GRCm38)	D69G	probably damaging	Het
Herc3	T	C	6: 58,887,499 (GRCm38)	V706A	probably damaging	Het
Hivep3	A	G	4: 120,122,934 (GRCm38)	E1723G	probably damaging	Het
Igsf9b	A	G	9: 27,322,650 (GRCm38)	I382V	probably benign	Het
Ints1	G	T	5: 139,771,156 (GRCm38)	T467N	possibly damaging	Het
Iqca1	G	A	1: 90,045,701 (GRCm38)	T783M	probably damaging	Het
Kng1	A	G	16: 23,067,698 (GRCm38)	K131R	possibly damaging	Het
Krt35	T	C	11: 100,093,130 (GRCm38)	Y348C	probably damaging	Het
Ldlrad3	A	G	2: 102,113,536 (GRCm38)	C64R	probably damaging	Het
Lilrb4b	C	T	10: 51,484,520 (GRCm38)	A272V	possibly damaging	Het
Lrrc37	T	C	11: 103,614,872 (GRCm38)	H2090R	probably benign	Het
Ltn1	A	T	16: 87,398,809 (GRCm38)	C1276*	probably null	Het
Matn1	G	A	4: 130,952,114 (GRCm38)	A360T	probably benign	Het
Minpp1	G	A	19: 32,498,384 (GRCm38)	V306I	probably benign	Het
Mkx	G	A	18: 6,992,904 (GRCm38)	R127W	probably damaging	Het
Mrpl48	G	T	7: 100,546,409 (GRCm38)		probably benign	Het
Ms4a2	A	G	19: 11,618,429 (GRCm38)	L166S	possibly damaging	Het
Mtus2	T	A	5: 148,077,103 (GRCm38)	Y235*	probably null	Het
Myh4	G	T	11: 67,241,054 (GRCm38)	W113C	probably damaging	Het
Nav2	T	A	7: 49,548,434 (GRCm38)	C1270*	probably null	Het
Ncoa5	A	G	2: 165,002,150 (GRCm38)	L111P	probably damaging	Het
Nup107	T	C	10: 117,770,478 (GRCm38)	Y453C	probably damaging	Het
Oca2	C	T	7: 56,330,358 (GRCm38)	Q604*	probably null	Het
Or13a19	T	C	7: 140,323,101 (GRCm38)	M134T	probably benign	Het
Or13p5	A	C	4: 118,734,688 (GRCm38)	H53P	probably benign	Het
Or14j10	A	T	17: 37,623,891 (GRCm38)	V248D	probably damaging	Het
Or5p58	T	A	7: 108,095,096 (GRCm38)	N158I	probably benign	Het
Or8g33	T	C	9: 39,426,235 (GRCm38)	T279A	possibly damaging	Het
Pde3a	G	T	6: 141,470,942 (GRCm38)	G514V	possibly damaging	Het
Pik3cb	A	T	9: 99,101,328 (GRCm38)	C76S	probably damaging	Het
Plk1	T	C	7: 122,168,605 (GRCm38)	V411A	probably damaging	Het
Pole	C	T	5: 110,324,753 (GRCm38)	P1600L	probably damaging	Het
Prr36	T	C	8: 4,210,881 (GRCm38)	T979A	probably benign	Het
Rdh7	T	A	10: 127,885,721 (GRCm38)	T229S	probably benign	Het
Rnpepl1	A	T	1: 92,915,113 (GRCm38)	T140S	probably damaging	Het
Rps6kc1	A	T	1: 190,798,694 (GRCm38)	S947T	probably benign	Het
Rtl1	A	G	12: 109,591,704 (GRCm38)	F1234L	probably damaging	Het
Sdc1	G	A	12: 8,791,708 (GRCm38)	M279I	probably damaging	Het
Siae	T	C	9: 37,627,800 (GRCm38)	L169P	possibly damaging	Het
Slc22a22	C	T	15: 57,249,752 (GRCm38)	V364I	probably benign	Het
Sltm	G	T	9: 70,588,978 (GRCm38)	V932F	probably damaging	Het
Smad1	A	G	8: 79,349,752 (GRCm38)	L279P	probably damaging	Het
Spag17	G	T	3: 100,050,831 (GRCm38)	G935V	probably damaging	Het
Srgap3	A	G	6: 112,746,934 (GRCm38)	S546P	probably damaging	Het
Stxbp5	T	C	10: 9,809,100 (GRCm38)	I519V	probably benign	Het
Syt16	A	T	12: 74,129,386 (GRCm38)	I10F	probably damaging	Het
Trim43b	C	G	9: 89,091,312 (GRCm38)	G123R	probably damaging	Het
Ubr3	T	C	2: 70,013,131 (GRCm38)	Y1572H	probably damaging	Het
Umodl1	G	A	17: 31,008,665 (GRCm38)	R1324H	probably benign	Het
Vmn2r44	A	T	7: 8,377,986 (GRCm38)	W303R	probably benign	Het
Wdr93	T	C	7: 79,785,774 (GRCm38)	Y684H	probably damaging	Het
Wnk2	G	A	13: 49,071,002 (GRCm38)	R268C	probably damaging	Het
Zfp438	C	T	18: 5,213,776 (GRCm38)	C394Y	possibly damaging	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
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
R7570:Fbn1	UTSW	2	125,397,852 (GRCm38)	missense	probably benign	0.29
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'- AGGTTGACCCAGAGAAGTCC -3'
(R):5'- AGAGGAACTGCTAGGCCTTG -3'

Sequencing Primer
(F):5'- GTCCAAAATAGGGTCAATAACTTCC -3'
(R):5'- AACTGCTAGGCCTTGGGTCC -3'

Posted On

2016-03-17