Mutagenetix > Incidental Mutations

Incidental Mutation 'R2145:Fn1'

233683

Institutional Source

Beutler Lab

Gene Symbol

Fn1

Ensembl Gene

ENSMUSG00000026193

Gene Name

fibronectin 1

Synonyms

Fn-1, Fn

MMRRC Submission

040148-MU

Accession Numbers

Is this an essential gene?

Essential (E-score: 1.000) question?

Stock #

R2145 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

71585520-71653200 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 71606004 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Aspartic acid at position 1552 (V1552D)

Ref Sequence

ENSEMBL: ENSMUSP00000140816 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055226] [ENSMUST00000186129] [ENSMUST00000187938] [ENSMUST00000188674] [ENSMUST00000188894] [ENSMUST00000189821] [ENSMUST00000190780]

Predicted Effect

probably damaging
Transcript: ENSMUST00000055226
AA Change: V1643D

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

SMART Domains

Protein: ENSMUSP00000054499
Gene: ENSMUSG00000026193
AA Change: V1643D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1264	1346	4.22e-9	SMART
FN3	1357	1437	9.6e-13	SMART
FN3	1448	1527	1.82e-13	SMART
FN3	1538	1617	6.69e-12	SMART
FN3	1632	1711	2.72e-12	SMART
FN3	1722	1801	8.9e-8	SMART
FN3	1812	1891	1.66e-7	SMART
FN3	1904	1983	4.92e-10	SMART
FN3	1993	2074	3.64e-13	SMART
low complexity region	2148	2165	N/A	INTRINSIC
FN3	2193	2272	2.9e0	SMART
FN1	2296	2340	3.72e-19	SMART
FN1	2341	2383	2.49e-20	SMART
FN1	2385	2425	2.69e-16	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185408

Predicted Effect

probably damaging
Transcript: ENSMUST00000186129
AA Change: V1552D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000141123
Gene: ENSMUSG00000026193
AA Change: V1552D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1266	1346	9.6e-13	SMART
FN3	1357	1436	1.82e-13	SMART
FN3	1447	1526	6.69e-12	SMART
FN3	1541	1620	2.72e-12	SMART
FN3	1631	1710	1.66e-7	SMART
FN3	1723	1802	4.92e-10	SMART
FN3	1812	1893	3.64e-13	SMART
low complexity region	1967	1984	N/A	INTRINSIC
FN3	2012	2091	2.9e0	SMART
FN1	2115	2159	3.72e-19	SMART
FN1	2160	2202	2.49e-20	SMART
FN1	2204	2244	2.69e-16	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000186985

Predicted Effect

probably damaging
Transcript: ENSMUST00000187938
AA Change: V1552D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000140975
Gene: ENSMUSG00000026193
AA Change: V1552D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1266	1346	9.6e-13	SMART
FN3	1357	1436	1.82e-13	SMART
FN3	1447	1526	6.69e-12	SMART
FN3	1541	1620	2.72e-12	SMART
FN3	1631	1710	8.9e-8	SMART
FN3	1721	1800	1.66e-7	SMART
FN3	1813	1892	4.92e-10	SMART
FN3	1902	1983	3.64e-13	SMART
low complexity region	2032	2049	N/A	INTRINSIC
FN3	2077	2156	2.9e0	SMART
FN1	2180	2224	3.72e-19	SMART
FN1	2225	2267	2.49e-20	SMART
FN1	2269	2309	2.69e-16	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000188092

Predicted Effect

probably damaging
Transcript: ENSMUST00000188674
AA Change: V1552D

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

SMART Domains

Protein: ENSMUSP00000140907
Gene: ENSMUSG00000026193
AA Change: V1552D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1266	1346	9.6e-13	SMART
FN3	1357	1436	1.82e-13	SMART
FN3	1447	1526	6.69e-12	SMART
FN3	1541	1620	2.72e-12	SMART
FN3	1631	1710	8.9e-8	SMART
FN3	1721	1800	1.66e-7	SMART
FN3	1813	1892	4.92e-10	SMART
FN3	1902	1981	6.79e-13	SMART
FN3	1983	2061	1.01e1	SMART
FN1	2085	2129	3.72e-19	SMART
FN1	2130	2172	2.49e-20	SMART
FN1	2174	2214	2.69e-16	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000188894
AA Change: V1552D

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

SMART Domains

Protein: ENSMUSP00000140471
Gene: ENSMUSG00000026193
AA Change: V1552D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1266	1346	9.6e-13	SMART
FN3	1357	1436	1.82e-13	SMART
FN3	1447	1526	6.69e-12	SMART
FN3	1541	1620	2.72e-12	SMART
FN3	1631	1710	8.9e-8	SMART
FN3	1721	1800	1.66e-7	SMART
FN3	1813	1892	4.92e-10	SMART
FN3	1902	1983	3.64e-13	SMART
low complexity region	2057	2074	N/A	INTRINSIC
FN3	2102	2181	2.9e0	SMART
FN1	2205	2249	3.72e-19	SMART
FN1	2250	2292	2.49e-20	SMART
FN1	2294	2334	2.69e-16	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000189160

Predicted Effect

probably damaging
Transcript: ENSMUST00000189821
AA Change: V1552D

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

SMART Domains

Protein: ENSMUSP00000139702
Gene: ENSMUSG00000026193
AA Change: V1552D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1266	1346	9.6e-13	SMART
FN3	1357	1436	1.82e-13	SMART
FN3	1447	1526	6.69e-12	SMART
FN3	1541	1620	2.72e-12	SMART
FN3	1631	1710	1.66e-7	SMART
FN3	1723	1802	4.92e-10	SMART
FN3	1812	1891	6.79e-13	SMART
FN3	1893	1971	1.01e1	SMART
FN1	1995	2039	3.72e-19	SMART
FN1	2040	2082	2.49e-20	SMART
FN1	2084	2124	2.69e-16	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000190780
AA Change: V1552D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000140816
Gene: ENSMUSG00000026193
AA Change: V1552D

Domain	Start	End	E-Value	Type
low complexity region	2	19	N/A	INTRINSIC
FN1	53	93	6.38e-18	SMART
FN1	98	141	6.04e-19	SMART
FN1	142	185	6.94e-19	SMART
FN1	187	231	3.47e-19	SMART
FN1	232	276	6.04e-19	SMART
FN1	308	347	5.91e-13	SMART
FN2	353	401	6.66e-30	SMART
FN2	413	461	5.05e-30	SMART
FN1	470	513	2.59e-18	SMART
FN1	518	560	1.68e-17	SMART
FN1	561	604	5.69e-15	SMART
FN3	609	688	3.79e-2	SMART
FN3	719	798	1.27e-3	SMART
FN3	810	888	7.92e-14	SMART
FN3	906	985	4.28e-10	SMART
FN3	996	1074	2.53e-12	SMART
FN3	1086	1160	1.31e-5	SMART
FN3	1173	1255	1.13e-9	SMART
FN3	1266	1346	9.6e-13	SMART
FN3	1357	1436	1.82e-13	SMART
FN3	1447	1526	6.69e-12	SMART
FN3	1541	1620	2.72e-12	SMART
FN3	1631	1710	1.66e-7	SMART
FN3	1723	1802	4.92e-10	SMART
FN3	1812	1893	3.64e-13	SMART
low complexity region	1942	1959	N/A	INTRINSIC
FN3	1987	2066	2.9e0	SMART
FN1	2090	2134	3.72e-19	SMART
FN1	2135	2177	2.49e-20	SMART
FN1	2179	2219	2.69e-16	SMART

Meta Mutation Damage Score

0.8552

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.6%

Validation Efficiency

97% (101/104)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes fibronectin, a glycoprotein present in a soluble dimeric form in plasma, and in a dimeric or multimeric form at the cell surface and in extracellular matrix. The encoded preproprotein is proteolytically processed to generate the mature protein. Fibronectin is involved in cell adhesion and migration processes including embryogenesis, wound healing, blood coagulation, host defense, and metastasis. The gene has three regions subject to alternative splicing, with the potential to produce 20 different transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing. The full-length nature of some variants has not been determined. [provided by RefSeq, Jan 2016]
PHENOTYPE: Mutants are defective in mesodermal function. Null mutants are embryonic lethal with major patterning and organizational defects. Conditional mutants live and show increased neuronal apoptosis and susceptibility to induced cerebral ischemia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 104 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110032A03Rik	T	C	9: 50,764,874	Y32C	probably damaging	Het
Abca15	A	G	7: 120,354,478	N535S	probably benign	Het
Abcc6	A	T	7: 45,998,741	L717Q	probably benign	Het
Abraxas2	C	A	7: 132,883,061	Q278K	probably benign	Het
Acap2	A	T	16: 31,105,524	D637E	probably benign	Het
AI661453	A	G	17: 47,466,098		probably benign	Het
Aoah	A	T	13: 20,840,096	E74V	probably damaging	Het
Appl1	A	G	14: 26,949,619	L292S	possibly damaging	Het
Astl	T	A	2: 127,347,189	V166E	probably damaging	Het
Atp5s	A	G	12: 69,741,054	Q88R	probably damaging	Het
Bbs1	T	G	19: 4,903,707	K143Q	possibly damaging	Het
Bbx	T	C	16: 50,274,544		probably benign	Het
Birc6	A	T	17: 74,660,413	Q4103L	possibly damaging	Het
C1qtnf2	T	G	11: 43,490,984	F178V	probably damaging	Het
Camta2	A	G	11: 70,671,575	F999L	probably benign	Het
Clcn7	A	G	17: 25,144,451	I34V	probably benign	Het
Cntn5	G	T	9: 9,748,415	P487Q	probably damaging	Het
Ctu2	T	A	8: 122,479,152	I213K	probably benign	Het
Des	C	A	1: 75,363,464		probably benign	Het
Dgcr8	A	T	16: 18,280,230	D432E	probably benign	Het
Dlgap5	G	A	14: 47,395,923	R549*	probably null	Het
Dmxl2	T	C	9: 54,415,910	T1397A	probably damaging	Het
Dnmt1	T	A	9: 20,937,155		probably benign	Het
Doxl2	A	T	6: 48,976,695	D518V	probably damaging	Het
Dstyk	T	A	1: 132,463,375	M838K	probably damaging	Het
Dtwd1	C	A	2: 126,159,984	T208N	probably damaging	Het
Dvl1	G	A	4: 155,847,816	V28I	possibly damaging	Het
Dync1i2	T	A	2: 71,214,563		probably benign	Het
Fer1l6	T	A	15: 58,627,534	M1251K	probably benign	Het
Fmod	T	C	1: 134,040,518	Y99H	probably benign	Het
Fnip2	A	T	3: 79,500,432	S281T	probably damaging	Het
Glb1	A	G	9: 114,464,165	H536R	probably benign	Het
Glis2	T	A	16: 4,613,642	S344R	possibly damaging	Het
Gm1966	T	A	7: 106,603,008	H343L	possibly damaging	Het
Gm4847	A	T	1: 166,634,903	S339R	probably benign	Het
Gpr155	A	G	2: 73,356,658	S44P	probably benign	Het
Gprin1	G	A	13: 54,738,632	P610S	probably damaging	Het
H2-Ob	A	T	17: 34,242,580	M98L	probably benign	Het
Hist1h3e	T	C	13: 23,562,356	T4A	probably benign	Het
Hmcn2	T	C	2: 31,333,931		probably benign	Het
Ikbke	C	A	1: 131,273,474	V176L	probably damaging	Het
Il13	T	C	11: 53,632,524	T85A	possibly damaging	Het
Inpp5k	A	T	11: 75,647,191		probably null	Het
Irgm2	T	C	11: 58,220,529	S361P	possibly damaging	Het
Itga11	C	T	9: 62,732,204		probably benign	Het
Kalrn	G	T	16: 34,009,262		probably benign	Het
Kcng1	C	A	2: 168,269,032	G71C	probably damaging	Het
Kcnq5	T	A	1: 21,505,349	D291V	probably damaging	Het
Klhl7	A	T	5: 24,100,863	M37L	probably benign	Het
Letm1	A	AG	5: 33,769,515		probably null	Het
Lhx6	C	T	2: 36,087,466	V325I	probably benign	Het
Lipc	A	G	9: 70,934,535	I9T	possibly damaging	Het
Lsmem1	GTACATACATACATACATACATACATACA	GTACATACATACATACATACATACATACATACA	12: 40,185,261		probably null	Het
Mast1	C	A	8: 84,921,478	G458V	probably damaging	Het
Mga	T	C	2: 119,964,157	V2565A	possibly damaging	Het
Mkl2	T	C	16: 13,412,586	I1045T	probably damaging	Het
Mpzl2	C	G	9: 45,044,173	D127E	probably benign	Het
Myh3	T	A	11: 67,091,056	C793S	probably benign	Het
Nomo1	T	C	7: 46,066,504	L765P	probably damaging	Het
Nup210	A	G	6: 91,028,876	I1335T	possibly damaging	Het
Olfr549	T	C	7: 102,555,060		probably null	Het
Oxr1	T	A	15: 41,819,944	S254R	probably damaging	Het
Pan3	A	G	5: 147,530,098	I592V	possibly damaging	Het
Pask	C	T	1: 93,321,297	A794T	probably benign	Het
Pex2	T	C	3: 5,561,590	E53G	probably damaging	Het
Pfkfb2	T	C	1: 130,698,723	T438A	probably benign	Het
Phactr4	T	C	4: 132,370,784	E391G	probably damaging	Het
Pira2	A	T	7: 3,844,345	L115Q	probably damaging	Het
Pkhd1l1	A	T	15: 44,512,877		probably null	Het
Pnlip	A	G	19: 58,676,444	S235G	probably benign	Het
Prkd1	A	G	12: 50,489,911	V130A	possibly damaging	Het
Ptpn13	A	G	5: 103,556,133	T1344A	probably benign	Het
Ptprc	T	C	1: 138,073,681	Y780C	probably damaging	Het
Pxn	T	A	5: 115,552,756		probably benign	Het
Rap1gap2	G	A	11: 74,425,976	T245M	probably damaging	Het
Rc3h1	G	T	1: 160,930,257	K48N	probably damaging	Het
Rfwd3	T	C	8: 111,282,613	I444V	probably benign	Het
Rictor	C	T	15: 6,765,107	R293C	probably damaging	Het
Rif1	T	A	2: 52,111,400	I1622N	possibly damaging	Het
Rnf213	T	C	11: 119,415,193	V609A	probably benign	Het
Scgb1b2	G	T	7: 31,291,763		probably benign	Het
Serac1	A	T	17: 6,050,785	I448N	probably damaging	Het
Sh3kbp1	C	A	X: 159,824,496	T200K	probably benign	Het
Sned1	T	A	1: 93,271,684	F495L	probably damaging	Het
Socs7	T	C	11: 97,373,124	F281L	probably benign	Het
Spta1	C	T	1: 174,212,614	L1214F	probably benign	Het
Ssu72	A	G	4: 155,705,443	E21G	probably damaging	Het
Syngr4	A	G	7: 45,887,040	V186A	probably benign	Het
Tarsl2	G	A	7: 65,655,791	M254I	possibly damaging	Het
Tmem130	C	A	5: 144,743,785	V270L	probably benign	Het
Trim66	A	T	7: 109,475,113	I647N	probably damaging	Het
Tspyl2	A	T	X: 152,338,894	D572E	probably benign	Het
Unc45b	G	A	11: 82,917,754	R222H	probably benign	Het
Uxs1	T	C	1: 43,827,623	Y29C	probably damaging	Het
Virma	T	A	4: 11,548,726		probably benign	Het
Vmn1r202	C	T	13: 22,501,783	G155S	possibly damaging	Het
Vmn2r24	T	A	6: 123,779,013	F15I	probably benign	Het
Wdr64	A	G	1: 175,767,095	T471A	probably benign	Het
Zfa-ps	T	A	10: 52,543,277		noncoding transcript	Het
Zfp260	A	G	7: 30,105,340	K222E	probably damaging	Het
Zfp300	A	G	X: 21,081,951	S525P	possibly damaging	Het
Zfp821	A	G	8: 109,724,347	D324G	probably damaging	Het
Zfp934	T	C	13: 62,517,834	D331G	probably damaging	Het
Zscan29	T	C	2: 121,170,106	R7G	probably damaging	Het

Other mutations in Fn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00236:Fn1	APN	1	71652873	missense	probably benign	0.28
IGL00402:Fn1	APN	1	71641163	missense	probably damaging	1.00
IGL00946:Fn1	APN	1	71645540	splice site	probably benign
IGL01311:Fn1	APN	1	71628140	missense	probably damaging	1.00
IGL01338:Fn1	APN	1	71626210	missense	probably damaging	0.98
IGL01353:Fn1	APN	1	71586939	missense	probably damaging	1.00
IGL01674:Fn1	APN	1	71606741	missense	probably damaging	1.00
IGL01701:Fn1	APN	1	71629853	splice site	probably benign
IGL01734:Fn1	APN	1	71619485	missense	probably damaging	1.00
IGL01788:Fn1	APN	1	71613837	missense	probably damaging	1.00
IGL02186:Fn1	APN	1	71638534	missense	probably damaging	1.00
IGL02398:Fn1	APN	1	71618670	splice site	probably null
IGL02425:Fn1	APN	1	71641143	splice site	probably benign
IGL02516:Fn1	APN	1	71637323	missense	possibly damaging	0.78
IGL02593:Fn1	APN	1	71602432	missense	probably benign
IGL02651:Fn1	APN	1	71597676	missense	possibly damaging	0.65
IGL02681:Fn1	APN	1	71619482	missense	probably damaging	1.00
IGL02890:Fn1	APN	1	71598372	critical splice donor site	probably null
IGL02929:Fn1	APN	1	71595662	critical splice donor site	probably null
IGL03036:Fn1	APN	1	71629773	missense	probably damaging	1.00
IGL03088:Fn1	APN	1	71614038	splice site	probably null
IGL03142:Fn1	APN	1	71637296	missense	probably damaging	1.00
IGL03172:Fn1	APN	1	71641262	missense	probably damaging	0.99
IGL03184:Fn1	APN	1	71609497	missense	probably benign	0.02
IGL03212:Fn1	APN	1	71641325	nonsense	probably null
IGL03246:Fn1	APN	1	71624296	missense	possibly damaging	0.89
IGL03367:Fn1	APN	1	71597553	missense	probably benign	0.27
PIT4514001:Fn1	UTSW	1	71628456	missense	probably benign	0.01
R0008:Fn1	UTSW	1	71595720	missense	probably damaging	0.98
R0112:Fn1	UTSW	1	71609653	missense	probably damaging	1.00
R0138:Fn1	UTSW	1	71624110	missense	possibly damaging	0.82
R0383:Fn1	UTSW	1	71597685	missense	probably damaging	0.99
R0386:Fn1	UTSW	1	71595786	missense	probably damaging	1.00
R0648:Fn1	UTSW	1	71597585	missense	possibly damaging	0.79
R0684:Fn1	UTSW	1	71595809	splice site	probably null
R1054:Fn1	UTSW	1	71586214	makesense	probably null
R1183:Fn1	UTSW	1	71586245	missense	probably damaging	0.98
R1405:Fn1	UTSW	1	71642078	missense	probably damaging	1.00
R1405:Fn1	UTSW	1	71642078	missense	probably damaging	1.00
R1414:Fn1	UTSW	1	71601303	splice site	probably benign
R1677:Fn1	UTSW	1	71597655	missense	probably benign	0.00
R1773:Fn1	UTSW	1	71637383	missense	probably damaging	1.00
R1830:Fn1	UTSW	1	71624259	missense	probably damaging	1.00
R1987:Fn1	UTSW	1	71651625	missense	probably damaging	1.00
R1989:Fn1	UTSW	1	71651625	missense	probably damaging	1.00
R2068:Fn1	UTSW	1	71600439	missense	probably damaging	1.00
R2113:Fn1	UTSW	1	71626164	missense	probably damaging	1.00
R2246:Fn1	UTSW	1	71628535	missense	probably benign	0.10
R2273:Fn1	UTSW	1	71613943	missense	probably null	1.00
R2274:Fn1	UTSW	1	71613943	missense	probably null	1.00
R2275:Fn1	UTSW	1	71613943	missense	probably null	1.00
R2303:Fn1	UTSW	1	71614036	critical splice acceptor site	probably null
R2379:Fn1	UTSW	1	71649284	nonsense	probably null
R2382:Fn1	UTSW	1	71648119	missense	probably damaging	1.00
R2567:Fn1	UTSW	1	71597736	nonsense	probably null
R2864:Fn1	UTSW	1	71602419	missense	probably damaging	0.99
R3154:Fn1	UTSW	1	71593083	missense	probably damaging	1.00
R3837:Fn1	UTSW	1	71653155	splice site	probably null
R3844:Fn1	UTSW	1	71609574	missense	possibly damaging	0.61
R3886:Fn1	UTSW	1	71640306	missense	probably damaging	1.00
R3887:Fn1	UTSW	1	71640306	missense	probably damaging	1.00
R3888:Fn1	UTSW	1	71640306	missense	probably damaging	1.00
R3889:Fn1	UTSW	1	71640306	missense	probably damaging	1.00
R3905:Fn1	UTSW	1	71607913	missense	probably damaging	1.00
R3906:Fn1	UTSW	1	71607913	missense	probably damaging	1.00
R3907:Fn1	UTSW	1	71607913	missense	probably damaging	1.00
R3909:Fn1	UTSW	1	71607913	missense	probably damaging	1.00
R4611:Fn1	UTSW	1	71624178	nonsense	probably null
R4724:Fn1	UTSW	1	71648148	critical splice acceptor site	probably null
R4732:Fn1	UTSW	1	71602512	splice site	probably null
R4733:Fn1	UTSW	1	71602512	splice site	probably null
R4756:Fn1	UTSW	1	71590808	missense	probably damaging	1.00
R4809:Fn1	UTSW	1	71652800	intron	probably benign
R4839:Fn1	UTSW	1	71642083	missense	probably damaging	1.00
R4915:Fn1	UTSW	1	71595809	splice site	probably null
R4917:Fn1	UTSW	1	71595809	splice site	probably null
R4918:Fn1	UTSW	1	71595809	splice site	probably null
R5002:Fn1	UTSW	1	71629728	missense	possibly damaging	0.48
R5015:Fn1	UTSW	1	71626177	missense	probably damaging	0.98
R5022:Fn1	UTSW	1	71624179	missense	probably damaging	1.00
R5109:Fn1	UTSW	1	71649235	missense	probably damaging	1.00
R5267:Fn1	UTSW	1	71629704	missense	probably damaging	1.00
R5323:Fn1	UTSW	1	71597432	missense	probably benign	0.09
R5333:Fn1	UTSW	1	71624180	missense	probably damaging	1.00
R5631:Fn1	UTSW	1	71590196	missense	probably damaging	1.00
R5644:Fn1	UTSW	1	71627250	missense	probably damaging	1.00
R5754:Fn1	UTSW	1	71600322	missense	probably damaging	1.00
R5807:Fn1	UTSW	1	71648059	missense	probably damaging	1.00
R6053:Fn1	UTSW	1	71599290	missense	probably damaging	1.00
R6133:Fn1	UTSW	1	71597727	missense	probably damaging	1.00
R6186:Fn1	UTSW	1	71637290	missense	probably damaging	1.00
R6270:Fn1	UTSW	1	71637275	missense	probably damaging	1.00
R6332:Fn1	UTSW	1	71628071	missense	probably benign	0.01
R6431:Fn1	UTSW	1	71647844	splice site	probably null
R6571:Fn1	UTSW	1	71626190	missense	probably damaging	1.00
R6596:Fn1	UTSW	1	71609482	missense	probably damaging	1.00
R6862:Fn1	UTSW	1	71613907	missense	probably benign	0.43
R6898:Fn1	UTSW	1	71600413	missense	probably damaging	1.00
R6984:Fn1	UTSW	1	71626079	missense	probably damaging	1.00
R7107:Fn1	UTSW	1	71627249	missense	probably damaging	1.00
R7121:Fn1	UTSW	1	71600538	intron	probably benign
R7127:Fn1	UTSW	1	71597544	missense	probably benign	0.16
R7194:Fn1	UTSW	1	71602323	missense	probably damaging	1.00
R7274:Fn1	UTSW	1	71628113	missense	probably benign
R7285:Fn1	UTSW	1	71637339	missense	probably damaging	1.00
R7426:Fn1	UTSW	1	71649225	missense	probably damaging	1.00
R7453:Fn1	UTSW	1	71590880	missense	probably damaging	1.00
R7508:Fn1	UTSW	1	71597516	missense	probably benign	0.01
R7724:Fn1	UTSW	1	71603735	missense	probably benign	0.02
R7848:Fn1	UTSW	1	71650601	missense	probably damaging	1.00
R7992:Fn1	UTSW	1	71599666	missense	probably benign	0.34
R8036:Fn1	UTSW	1	71590151	nonsense	probably null
R8077:Fn1	UTSW	1	71612602	missense	probably damaging	1.00
R8175:Fn1	UTSW	1	71599665	missense	probably damaging	1.00
R8177:Fn1	UTSW	1	71609587	missense	probably benign
R8212:Fn1	UTSW	1	71642905	missense	probably benign	0.01
R8322:Fn1	UTSW	1	71628459	missense	probably benign	0.04
X0023:Fn1	UTSW	1	71598373	critical splice donor site	probably null
Z1088:Fn1	UTSW	1	71649292	missense	probably damaging	1.00
Z1176:Fn1	UTSW	1	71597411	missense	probably benign	0.10

Predicted Primers

PCR Primer
(F):5'- GCAACTTCTGAGCTCCTACAG -3'
(R):5'- TAATAGTGACTGGATGCATGGC -3'

Sequencing Primer
(F):5'- AACTTCTGAGCTCCTACAGTGTTTC -3'
(R):5'- ACTGGATGCATGGCTTTCC -3'

Posted On

2014-10-01