Mutagenetix > Incidental Mutation

Incidental Mutation 'R4849:Fat3'

373403

Institutional Source

Beutler Lab

Gene Symbol

Fat3

Ensembl Gene

ENSMUSG00000074505

Gene Name

FAT atypical cadherin 3

Synonyms

D430038H04Rik, LOC382129, LOC234973, 9430076A06Rik

MMRRC Submission

042461-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.631) question?

Stock #

R4849 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

15821485-16412581 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 16289244 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Serine at position 93 (I93S)

Ref Sequence

ENSEMBL: ENSMUSP00000148968 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000082170] [ENSMUST00000217308]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000082170
AA Change: I93S

PolyPhen 2 Score 0.034 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000080808
Gene: ENSMUSG00000074505
AA Change: I93S

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
CA	65	151	3e-7	SMART
CA	175	259	8.9e-22	SMART
CA	280	368	8.9e-4	SMART
CA	389	465	2.6e-11	SMART
CA	489	571	2e-29	SMART
low complexity region	684	697	N/A	INTRINSIC
CA	743	824	1e-24	SMART
low complexity region	830	840	N/A	INTRINSIC
CA	848	929	7.6e-26	SMART
CA	953	1034	1.5e-25	SMART
CA	1060	1141	6.6e-32	SMART
CA	1165	1247	1.5e-30	SMART
CA	1273	1349	1.8e-8	SMART
CA	1375	1453	2.9e-12	SMART
CA	1477	1559	3e-22	SMART
CA	1583	1664	3.1e-16	SMART
CA	1688	1762	4.2e-22	SMART
CA	1793	1876	2.5e-26	SMART
CA	1900	1975	1.5e-8	SMART
low complexity region	1983	1994	N/A	INTRINSIC
CA	1999	2077	1.4e-18	SMART
CA	2101	2179	6.6e-10	SMART
CA	2203	2280	4.9e-19	SMART
CA	2304	2387	4.3e-29	SMART
CA	2411	2489	4.2e-11	SMART
CA	2513	2593	2.8e-22	SMART
CA	2617	2701	4.3e-10	SMART
CA	2719	2807	2.5e-7	SMART
CA	2831	2917	3.3e-27	SMART
CA	2941	3022	9.4e-23	SMART
CA	3046	3124	2.4e-26	SMART
CA	3148	3229	1.3e-32	SMART
CA	3253	3334	1.3e-29	SMART
CA	3358	3439	4.9e-28	SMART
CA	3463	3544	6.4e-12	SMART
EGF	3793	3828	1.3e-1	SMART
LamG	3852	3989	4.3e-25	SMART
EGF	4019	4053	2.7e-6	SMART
EGF	4058	4091	4.5e-6	SMART
EGF_CA	4093	4129	3.9e-11	SMART
transmembrane domain	4151	4170	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000217308
AA Change: I93S

PolyPhen 2 Score 0.034 (Sensitivity: 0.95; Specificity: 0.82)

Meta Mutation Damage Score

0.0625

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.2%

Validation Efficiency

98% (90/92)

MGI Phenotype

PHENOTYPE: Mice homozgyous for a knock-out allele exhibit abnormal amacrine cell differentiation and migration that result in the formation of two additional plexiform layers and thickened retinal ganglion layer. [provided by MGI curators]

Allele List at MGI

All alleles(3) : Gene trapped(3)

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acp7	G	T	7: 28,314,877 (GRCm39)	R239S	possibly damaging	Het
Angptl1	C	A	1: 156,684,735 (GRCm39)	N301K	probably benign	Het
Ankrd26	T	A	6: 118,509,257 (GRCm39)	T603S	probably benign	Het
App	T	C	16: 84,853,322 (GRCm39)	D252G	unknown	Het
Atxn3	A	G	12: 101,900,627 (GRCm39)	S219P	probably benign	Het
Birc6	T	C	17: 74,954,383 (GRCm39)	S3397P	probably damaging	Het
Bivm	A	G	1: 44,182,033 (GRCm39)	I414V	possibly damaging	Het
Cemip	A	G	7: 83,584,945 (GRCm39)	F1324L	possibly damaging	Het
Ckap5	T	A	2: 91,445,616 (GRCm39)	N1724K	probably damaging	Het
Corin	T	A	5: 72,460,178 (GRCm39)	M1035L	probably damaging	Het
Ctnna3	T	C	10: 64,709,094 (GRCm39)	I711T	probably damaging	Het
Cts6	A	T	13: 61,349,415 (GRCm39)	W98R	probably null	Het
Dip2a	A	G	10: 76,130,367 (GRCm39)	S580P	probably damaging	Het
Dock6	A	G	9: 21,723,068 (GRCm39)		probably null	Het
Dusp15	T	A	2: 152,791,002 (GRCm39)	T32S	probably damaging	Het
Eogt	T	A	6: 97,093,016 (GRCm39)	N387I	probably damaging	Het
Evx2	T	C	2: 74,489,675 (GRCm39)	D29G	probably benign	Het
Fat1	A	G	8: 45,466,007 (GRCm39)	N1422S	probably benign	Het
Fat2	T	C	11: 55,201,463 (GRCm39)	D537G	probably damaging	Het
Fem1b	T	C	9: 62,704,576 (GRCm39)	E228G	probably damaging	Het
Fh1	A	G	1: 175,448,072 (GRCm39)	T25A	probably benign	Het
Fndc3b	A	G	3: 27,514,097 (GRCm39)	W695R	probably damaging	Het
Gaa	G	A	11: 119,163,813 (GRCm39)	V222I	possibly damaging	Het
Ggnbp1	T	C	17: 27,251,947 (GRCm39)		probably null	Het
Gipc1	A	G	8: 84,388,756 (GRCm39)	Y154C	probably benign	Het
Gm5356	G	T	8: 89,913,670 (GRCm39)		noncoding transcript	Het
Gnl1	T	A	17: 36,298,603 (GRCm39)		probably null	Het
Gpcpd1	C	T	2: 132,376,019 (GRCm39)	G605R	probably damaging	Het
Guca1a	T	C	17: 47,705,662 (GRCm39)	T177A	possibly damaging	Het
Ifit1bl1	T	C	19: 34,572,076 (GRCm39)	E127G	probably damaging	Het
Ift81	A	T	5: 122,729,282 (GRCm39)	I350N	probably damaging	Het
Ikbke	GCC	G	1: 131,203,004 (GRCm39)		probably null	Het
Ing4	A	G	6: 125,020,946 (GRCm39)	R23G	probably damaging	Het
Ins1	A	G	19: 52,253,384 (GRCm39)	N108S	probably damaging	Het
Iqce	A	T	5: 140,679,214 (GRCm39)	M72K	possibly damaging	Het
Itga3	C	A	11: 94,967,097 (GRCm39)	M22I	probably benign	Het
Kctd18	T	C	1: 58,001,152 (GRCm39)	E201G	probably damaging	Het
Klc1	A	G	12: 111,748,129 (GRCm39)	N344S	probably damaging	Het
Klrb1f	A	T	6: 129,033,347 (GRCm39)	I192F	probably damaging	Het
Klrg2	A	T	6: 38,607,214 (GRCm39)		probably null	Het
Kntc1	A	C	5: 123,897,128 (GRCm39)	I164L	probably benign	Het
Ltf	T	A	9: 110,855,058 (GRCm39)	I357K	probably benign	Het
Mr1	T	C	1: 155,006,436 (GRCm39)	T304A	probably benign	Het
Msh6	C	T	17: 88,290,947 (GRCm39)	R178C	possibly damaging	Het
Mtch1	T	C	17: 29,566,565 (GRCm39)	D66G	probably benign	Het
Mtmr7	A	G	8: 41,062,040 (GRCm39)	V15A	probably benign	Het
Mtss2	A	T	8: 111,452,875 (GRCm39)	H40L	possibly damaging	Het
Mxra8	A	G	4: 155,925,331 (GRCm39)		probably benign	Het
Myo3b	T	C	2: 70,075,253 (GRCm39)	L535P	probably damaging	Het
Neurl2	T	A	2: 164,674,739 (GRCm39)		probably null	Het
Nfia	A	C	4: 97,970,048 (GRCm39)	T503P	probably damaging	Het
Noa1	T	C	5: 77,454,179 (GRCm39)	E487G	possibly damaging	Het
Nuak1	A	T	10: 84,211,143 (GRCm39)	V315D	probably damaging	Het
Nup205	A	G	6: 35,207,505 (GRCm39)	N1519S	possibly damaging	Het
Or10x1	T	A	1: 174,196,966 (GRCm39)	I161K	probably damaging	Het
Or1l4b	T	C	2: 37,036,266 (GRCm39)	L14P	probably damaging	Het
Or1o1	T	C	17: 37,716,589 (GRCm39)	V50A	probably benign	Het
Or51f1e	A	G	7: 102,747,526 (GRCm39)	I193V	possibly damaging	Het
Or6b13	G	T	7: 139,782,340 (GRCm39)	C114*	probably null	Het
Or9s18	G	A	13: 65,300,493 (GRCm39)	V152M	possibly damaging	Het
Peli1	T	A	11: 21,098,528 (GRCm39)		probably benign	Het
Ppp6r1	A	G	7: 4,646,206 (GRCm39)	L175P	probably damaging	Het
Prkcd	A	G	14: 30,321,700 (GRCm39)	L498P	probably damaging	Het
Prss30	T	A	17: 24,191,769 (GRCm39)	I251F	probably benign	Het
Psme3	A	T	11: 101,207,907 (GRCm39)	N21Y	probably benign	Het
Ptpra	T	C	2: 130,374,081 (GRCm39)	Y271H	probably damaging	Het
Ralgapa1	T	A	12: 55,745,588 (GRCm39)	N1303Y	probably damaging	Het
Rims4	T	C	2: 163,707,463 (GRCm39)	I121V	probably benign	Het
Rnf123	A	T	9: 107,933,290 (GRCm39)	L1149Q	probably damaging	Het
Ryr3	T	A	2: 112,738,807 (GRCm39)	L593F	probably damaging	Het
Sec23b	T	C	2: 144,427,519 (GRCm39)	F582S	probably damaging	Het
Sgpl1	T	C	10: 60,940,297 (GRCm39)	K335R	probably benign	Het
Sirpa	C	T	2: 129,451,163 (GRCm39)	T141I	probably damaging	Het
Slit1	G	T	19: 41,637,983 (GRCm39)	A270E	probably benign	Het
Snap91	T	C	9: 86,674,613 (GRCm39)	T533A	possibly damaging	Het
Sphkap	T	G	1: 83,255,105 (GRCm39)	E881D	probably benign	Het
Sptan1	C	A	2: 29,901,054 (GRCm39)	R1407S	probably damaging	Het
Tfdp1	A	G	8: 13,423,895 (GRCm39)	T353A	probably benign	Het
Ttyh1	A	G	7: 4,125,533 (GRCm39)	I62V	possibly damaging	Het
Vwde	A	T	6: 13,196,047 (GRCm39)	V326D	possibly damaging	Het
Zfp398	T	C	6: 47,836,446 (GRCm39)	I82T	possibly damaging	Het
Zp1	A	G	19: 10,896,198 (GRCm39)	Y176H	possibly damaging	Het

Other mutations in Fat3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00662:Fat3	APN	9	15,907,723 (GRCm39)	missense	possibly damaging	0.77
IGL00962:Fat3	APN	9	15,826,815 (GRCm39)	missense	probably benign	0.14
IGL00966:Fat3	APN	9	15,910,390 (GRCm39)	missense	possibly damaging	0.69
IGL01100:Fat3	APN	9	16,286,524 (GRCm39)	missense	probably damaging	1.00
IGL01104:Fat3	APN	9	16,287,024 (GRCm39)	missense	possibly damaging	0.92
IGL01104:Fat3	APN	9	15,909,756 (GRCm39)	missense	probably damaging	1.00
IGL01121:Fat3	APN	9	15,909,697 (GRCm39)	missense	probably benign	0.00
IGL01407:Fat3	APN	9	16,289,319 (GRCm39)	missense	probably benign	0.01
IGL01444:Fat3	APN	9	15,910,144 (GRCm39)	missense	probably damaging	1.00
IGL01634:Fat3	APN	9	15,909,654 (GRCm39)	missense	probably damaging	1.00
IGL01649:Fat3	APN	9	16,288,015 (GRCm39)	missense	possibly damaging	0.95
IGL01839:Fat3	APN	9	15,909,168 (GRCm39)	missense	probably damaging	1.00
IGL01867:Fat3	APN	9	16,289,197 (GRCm39)	missense	probably benign	0.03
IGL01894:Fat3	APN	9	16,287,145 (GRCm39)	missense	probably benign
IGL01913:Fat3	APN	9	15,910,086 (GRCm39)	missense	probably damaging	0.99
IGL02033:Fat3	APN	9	15,826,648 (GRCm39)	missense	possibly damaging	0.50
IGL02035:Fat3	APN	9	16,289,266 (GRCm39)	missense	probably benign	0.06
IGL02146:Fat3	APN	9	15,910,878 (GRCm39)	missense	probably benign
IGL02147:Fat3	APN	9	15,907,281 (GRCm39)	missense	probably damaging	1.00
IGL02161:Fat3	APN	9	15,908,346 (GRCm39)	missense	probably benign	0.10
IGL02161:Fat3	APN	9	15,908,347 (GRCm39)	nonsense	probably null
IGL02164:Fat3	APN	9	15,942,720 (GRCm39)	splice site	probably benign
IGL02269:Fat3	APN	9	15,826,873 (GRCm39)	missense	possibly damaging	0.84
IGL02314:Fat3	APN	9	15,881,134 (GRCm39)	missense	possibly damaging	0.61
IGL02393:Fat3	APN	9	15,899,708 (GRCm39)	nonsense	probably null
IGL02410:Fat3	APN	9	15,909,141 (GRCm39)	missense	probably damaging	1.00
IGL02504:Fat3	APN	9	15,871,094 (GRCm39)	missense	probably damaging	1.00
IGL02572:Fat3	APN	9	15,871,802 (GRCm39)	missense	probably benign
IGL02623:Fat3	APN	9	15,908,433 (GRCm39)	missense	probably damaging	1.00
IGL02654:Fat3	APN	9	15,908,271 (GRCm39)	missense	possibly damaging	0.84
IGL02749:Fat3	APN	9	15,918,007 (GRCm39)	missense	possibly damaging	0.93
IGL02810:Fat3	APN	9	16,288,146 (GRCm39)	missense	probably damaging	1.00
IGL02839:Fat3	APN	9	15,830,466 (GRCm39)	missense	probably damaging	1.00
IGL02890:Fat3	APN	9	15,826,636 (GRCm39)	missense	probably benign	0.03
IGL02892:Fat3	APN	9	16,288,858 (GRCm39)	missense	probably damaging	1.00
IGL03090:Fat3	APN	9	16,288,535 (GRCm39)	nonsense	probably null
IGL03144:Fat3	APN	9	16,286,541 (GRCm39)	missense	probably damaging	1.00
IGL03199:Fat3	APN	9	16,288,344 (GRCm39)	missense	possibly damaging	0.83
IGL03365:Fat3	APN	9	15,907,765 (GRCm39)	missense	probably damaging	1.00
IGL03392:Fat3	APN	9	15,915,158 (GRCm39)	missense	probably benign
IGL03408:Fat3	APN	9	15,909,253 (GRCm39)	nonsense	probably null
gagged	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
hushed	UTSW	9	15,871,165 (GRCm39)	missense	possibly damaging	0.72
Muffled	UTSW	9	15,849,287 (GRCm39)	critical splice donor site	probably null
muted	UTSW	9	15,908,773 (GRCm39)	missense	possibly damaging	0.93
Softened	UTSW	9	16,289,481 (GRCm39)	missense	probably benign
BB001:Fat3	UTSW	9	15,910,593 (GRCm39)	missense	probably damaging	1.00
BB002:Fat3	UTSW	9	15,942,656 (GRCm39)	missense	possibly damaging	0.77
BB011:Fat3	UTSW	9	15,910,593 (GRCm39)	missense	probably damaging	1.00
BB012:Fat3	UTSW	9	15,942,656 (GRCm39)	missense	possibly damaging	0.77
F6893:Fat3	UTSW	9	15,918,085 (GRCm39)	missense	probably damaging	0.99
IGL03050:Fat3	UTSW	9	15,907,896 (GRCm39)	missense	probably benign	0.04
PIT4142001:Fat3	UTSW	9	15,903,414 (GRCm39)	critical splice donor site	probably null
PIT4283001:Fat3	UTSW	9	15,917,897 (GRCm39)	missense	possibly damaging	0.77
PIT4378001:Fat3	UTSW	9	16,288,104 (GRCm39)	missense	probably benign	0.05
PIT4434001:Fat3	UTSW	9	15,907,612 (GRCm39)	missense	probably benign	0.00
PIT4468001:Fat3	UTSW	9	15,907,647 (GRCm39)	missense	probably benign	0.06
R0001:Fat3	UTSW	9	16,289,169 (GRCm39)	missense	probably damaging	0.99
R0005:Fat3	UTSW	9	15,874,162 (GRCm39)	missense	probably damaging	1.00
R0005:Fat3	UTSW	9	15,874,162 (GRCm39)	missense	probably damaging	1.00
R0038:Fat3	UTSW	9	15,826,306 (GRCm39)	missense	probably damaging	1.00
R0046:Fat3	UTSW	9	15,877,275 (GRCm39)	missense	possibly damaging	0.65
R0089:Fat3	UTSW	9	15,849,501 (GRCm39)	missense	probably benign
R0135:Fat3	UTSW	9	15,918,073 (GRCm39)	missense	probably damaging	1.00
R0255:Fat3	UTSW	9	15,881,002 (GRCm39)	splice site	probably benign
R0349:Fat3	UTSW	9	15,942,476 (GRCm39)	missense	probably damaging	1.00
R0361:Fat3	UTSW	9	15,909,699 (GRCm39)	missense	possibly damaging	0.77
R0382:Fat3	UTSW	9	15,871,052 (GRCm39)	missense	probably damaging	1.00
R0418:Fat3	UTSW	9	16,158,192 (GRCm39)	missense	probably damaging	1.00
R0419:Fat3	UTSW	9	15,903,552 (GRCm39)	missense	probably damaging	1.00
R0437:Fat3	UTSW	9	15,908,228 (GRCm39)	missense	probably damaging	1.00
R0441:Fat3	UTSW	9	15,856,304 (GRCm39)	splice site	probably benign
R0480:Fat3	UTSW	9	15,909,025 (GRCm39)	missense	probably benign	0.00
R0510:Fat3	UTSW	9	15,910,981 (GRCm39)	nonsense	probably null
R0665:Fat3	UTSW	9	15,908,698 (GRCm39)	missense	probably benign
R0715:Fat3	UTSW	9	16,286,419 (GRCm39)	missense	probably benign
R0727:Fat3	UTSW	9	15,907,995 (GRCm39)	missense	probably damaging	1.00
R0882:Fat3	UTSW	9	15,942,664 (GRCm39)	missense	possibly damaging	0.84
R0946:Fat3	UTSW	9	15,909,100 (GRCm39)	missense	possibly damaging	0.95
R1068:Fat3	UTSW	9	15,881,330 (GRCm39)	missense	probably benign
R1081:Fat3	UTSW	9	16,286,580 (GRCm39)	missense	possibly damaging	0.62
R1082:Fat3	UTSW	9	15,917,911 (GRCm39)	missense	probably damaging	1.00
R1148:Fat3	UTSW	9	15,908,070 (GRCm39)	missense	probably damaging	1.00
R1148:Fat3	UTSW	9	15,908,070 (GRCm39)	missense	probably damaging	1.00
R1233:Fat3	UTSW	9	15,834,041 (GRCm39)	missense	probably benign
R1306:Fat3	UTSW	9	16,287,975 (GRCm39)	missense	probably damaging	1.00
R1311:Fat3	UTSW	9	15,932,706 (GRCm39)	missense	probably damaging	1.00
R1338:Fat3	UTSW	9	15,836,387 (GRCm39)	missense	probably benign	0.00
R1395:Fat3	UTSW	9	16,158,212 (GRCm39)	missense	probably benign	0.00
R1466:Fat3	UTSW	9	16,286,778 (GRCm39)	missense	probably damaging	0.96
R1466:Fat3	UTSW	9	16,286,778 (GRCm39)	missense	probably damaging	0.96
R1510:Fat3	UTSW	9	15,871,351 (GRCm39)	missense	probably damaging	1.00
R1528:Fat3	UTSW	9	15,836,387 (GRCm39)	missense	probably benign	0.00
R1531:Fat3	UTSW	9	15,908,761 (GRCm39)	missense	probably damaging	1.00
R1659:Fat3	UTSW	9	15,908,479 (GRCm39)	missense	possibly damaging	0.91
R1697:Fat3	UTSW	9	15,856,176 (GRCm39)	missense	probably benign	0.05
R1699:Fat3	UTSW	9	15,849,694 (GRCm39)	missense	probably damaging	1.00
R1728:Fat3	UTSW	9	15,907,611 (GRCm39)	missense	possibly damaging	0.65
R1729:Fat3	UTSW	9	15,907,611 (GRCm39)	missense	possibly damaging	0.65
R1731:Fat3	UTSW	9	15,907,233 (GRCm39)	missense	probably benign
R1784:Fat3	UTSW	9	15,907,611 (GRCm39)	missense	possibly damaging	0.65
R1789:Fat3	UTSW	9	16,288,281 (GRCm39)	missense	probably benign	0.00
R1794:Fat3	UTSW	9	15,908,434 (GRCm39)	missense	probably benign	0.15
R1794:Fat3	UTSW	9	15,908,432 (GRCm39)	nonsense	probably null
R1830:Fat3	UTSW	9	15,826,636 (GRCm39)	missense	probably benign	0.03
R1835:Fat3	UTSW	9	15,909,384 (GRCm39)	missense	probably damaging	1.00
R1887:Fat3	UTSW	9	15,878,357 (GRCm39)	missense	probably damaging	1.00
R1898:Fat3	UTSW	9	15,871,426 (GRCm39)	missense	probably damaging	1.00
R1909:Fat3	UTSW	9	15,909,411 (GRCm39)	missense	probably benign
R1912:Fat3	UTSW	9	15,881,284 (GRCm39)	missense	probably damaging	1.00
R1917:Fat3	UTSW	9	15,908,353 (GRCm39)	missense	possibly damaging	0.55
R1967:Fat3	UTSW	9	15,879,591 (GRCm39)	missense	probably benign	0.00
R2070:Fat3	UTSW	9	15,910,666 (GRCm39)	missense	probably benign	0.21
R2100:Fat3	UTSW	9	16,288,726 (GRCm39)	missense	possibly damaging	0.73
R2104:Fat3	UTSW	9	15,909,813 (GRCm39)	missense	possibly damaging	0.77
R2113:Fat3	UTSW	9	15,911,082 (GRCm39)	missense	probably damaging	1.00
R2132:Fat3	UTSW	9	16,158,015 (GRCm39)	critical splice donor site	probably null
R2136:Fat3	UTSW	9	16,288,347 (GRCm39)	missense	probably benign	0.01
R2146:Fat3	UTSW	9	15,901,808 (GRCm39)	missense	probably benign	0.01
R2233:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R2234:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R2273:Fat3	UTSW	9	15,826,558 (GRCm39)	missense	probably benign
R2285:Fat3	UTSW	9	16,287,469 (GRCm39)	missense	probably damaging	1.00
R2363:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R2365:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R2367:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R2403:Fat3	UTSW	9	15,881,167 (GRCm39)	missense	probably damaging	1.00
R2447:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R2496:Fat3	UTSW	9	15,877,399 (GRCm39)	missense	probably benign	0.01
R2509:Fat3	UTSW	9	15,836,310 (GRCm39)	missense	possibly damaging	0.82
R2932:Fat3	UTSW	9	16,287,240 (GRCm39)	missense	probably damaging	1.00
R2986:Fat3	UTSW	9	15,903,424 (GRCm39)	missense	probably damaging	1.00
R3054:Fat3	UTSW	9	15,871,792 (GRCm39)	missense	probably benign
R3056:Fat3	UTSW	9	15,871,792 (GRCm39)	missense	probably benign
R3729:Fat3	UTSW	9	16,158,337 (GRCm39)	splice site	probably benign
R3745:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R3806:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R3859:Fat3	UTSW	9	15,908,524 (GRCm39)	nonsense	probably null
R3862:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R3890:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R3892:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R3950:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R3972:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4004:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4005:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4086:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4111:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4113:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4227:Fat3	UTSW	9	16,288,989 (GRCm39)	missense	probably damaging	1.00
R4352:Fat3	UTSW	9	16,158,074 (GRCm39)	missense	possibly damaging	0.55
R4394:Fat3	UTSW	9	15,834,088 (GRCm39)	missense	probably benign	0.11
R4403:Fat3	UTSW	9	15,856,169 (GRCm39)	missense	probably damaging	1.00
R4433:Fat3	UTSW	9	15,942,448 (GRCm39)	missense	probably damaging	0.99
R4453:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4479:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4480:Fat3	UTSW	9	15,909,567 (GRCm39)	missense	probably damaging	1.00
R4521:Fat3	UTSW	9	15,834,238 (GRCm39)	missense	probably null	0.71
R4620:Fat3	UTSW	9	15,908,190 (GRCm39)	missense	probably damaging	1.00
R4700:Fat3	UTSW	9	15,942,469 (GRCm39)	missense	probably damaging	1.00
R4721:Fat3	UTSW	9	15,941,262 (GRCm39)	missense	probably damaging	1.00
R4790:Fat3	UTSW	9	15,909,780 (GRCm39)	missense	probably damaging	1.00
R4796:Fat3	UTSW	9	15,911,028 (GRCm39)	missense	probably benign	0.17
R4823:Fat3	UTSW	9	15,907,803 (GRCm39)	missense	probably benign
R4836:Fat3	UTSW	9	16,289,019 (GRCm39)	missense	probably damaging	1.00
R4842:Fat3	UTSW	9	15,908,883 (GRCm39)	missense	probably damaging	1.00
R4856:Fat3	UTSW	9	15,932,626 (GRCm39)	missense	probably benign
R4869:Fat3	UTSW	9	16,288,773 (GRCm39)	missense	probably damaging	0.98
R4886:Fat3	UTSW	9	15,932,626 (GRCm39)	missense	probably benign
R4899:Fat3	UTSW	9	15,881,095 (GRCm39)	missense	probably damaging	1.00
R4941:Fat3	UTSW	9	16,286,448 (GRCm39)	missense	probably damaging	1.00
R4986:Fat3	UTSW	9	15,909,636 (GRCm39)	missense	probably damaging	1.00
R5058:Fat3	UTSW	9	15,908,154 (GRCm39)	missense	probably damaging	1.00
R5079:Fat3	UTSW	9	15,910,423 (GRCm39)	missense	probably benign	0.01
R5080:Fat3	UTSW	9	15,910,634 (GRCm39)	missense	probably benign	0.35
R5174:Fat3	UTSW	9	15,910,866 (GRCm39)	missense	probably damaging	1.00
R5183:Fat3	UTSW	9	15,871,609 (GRCm39)	missense	probably damaging	0.99
R5203:Fat3	UTSW	9	16,289,438 (GRCm39)	missense	possibly damaging	0.79
R5216:Fat3	UTSW	9	16,288,833 (GRCm39)	missense	probably damaging	1.00
R5230:Fat3	UTSW	9	15,901,856 (GRCm39)	missense	possibly damaging	0.51
R5318:Fat3	UTSW	9	16,287,925 (GRCm39)	missense	probably damaging	1.00
R5377:Fat3	UTSW	9	16,287,739 (GRCm39)	missense	probably benign	0.05
R5385:Fat3	UTSW	9	15,833,971 (GRCm39)	missense	possibly damaging	0.82
R5436:Fat3	UTSW	9	15,871,810 (GRCm39)	missense	probably benign	0.02
R5437:Fat3	UTSW	9	15,996,604 (GRCm39)	missense	probably damaging	1.00
R5453:Fat3	UTSW	9	15,908,160 (GRCm39)	missense	probably damaging	1.00
R5460:Fat3	UTSW	9	15,830,463 (GRCm39)	missense	probably damaging	1.00
R5516:Fat3	UTSW	9	15,910,005 (GRCm39)	missense	probably damaging	1.00
R5568:Fat3	UTSW	9	16,288,219 (GRCm39)	nonsense	probably null
R5628:Fat3	UTSW	9	15,877,392 (GRCm39)	missense	probably damaging	1.00
R5835:Fat3	UTSW	9	16,287,129 (GRCm39)	missense	probably damaging	1.00
R5845:Fat3	UTSW	9	16,288,506 (GRCm39)	missense	probably damaging	1.00
R5898:Fat3	UTSW	9	15,849,757 (GRCm39)	missense	probably benign	0.15
R5941:Fat3	UTSW	9	15,910,797 (GRCm39)	missense	probably benign	0.07
R5974:Fat3	UTSW	9	15,917,824 (GRCm39)	critical splice donor site	probably null
R5986:Fat3	UTSW	9	15,909,613 (GRCm39)	missense	probably benign	0.22
R6015:Fat3	UTSW	9	16,287,346 (GRCm39)	missense	possibly damaging	0.55
R6031:Fat3	UTSW	9	15,899,788 (GRCm39)	missense	probably benign	0.02
R6031:Fat3	UTSW	9	15,899,788 (GRCm39)	missense	probably benign	0.02
R6042:Fat3	UTSW	9	16,289,113 (GRCm39)	missense	probably benign	0.12
R6051:Fat3	UTSW	9	16,286,751 (GRCm39)	missense	possibly damaging	0.83
R6052:Fat3	UTSW	9	15,833,975 (GRCm39)	missense	probably null
R6119:Fat3	UTSW	9	16,287,864 (GRCm39)	missense	possibly damaging	0.82
R6161:Fat3	UTSW	9	16,288,818 (GRCm39)	missense	probably damaging	1.00
R6254:Fat3	UTSW	9	15,907,441 (GRCm39)	missense	probably benign	0.19
R6318:Fat3	UTSW	9	15,828,280 (GRCm39)	intron	probably benign
R6347:Fat3	UTSW	9	15,909,668 (GRCm39)	missense	probably damaging	1.00
R6348:Fat3	UTSW	9	15,849,287 (GRCm39)	critical splice donor site	probably null
R6351:Fat3	UTSW	9	15,849,694 (GRCm39)	missense	probably damaging	1.00
R6450:Fat3	UTSW	9	15,910,466 (GRCm39)	missense	possibly damaging	0.51
R6460:Fat3	UTSW	9	15,878,296 (GRCm39)	missense	probably damaging	1.00
R6524:Fat3	UTSW	9	15,903,552 (GRCm39)	missense	probably damaging	1.00
R6533:Fat3	UTSW	9	15,910,195 (GRCm39)	missense	probably benign	0.02
R6565:Fat3	UTSW	9	15,826,623 (GRCm39)	missense	probably benign
R6576:Fat3	UTSW	9	16,288,506 (GRCm39)	missense	probably damaging	1.00
R6649:Fat3	UTSW	9	16,288,038 (GRCm39)	missense	probably damaging	1.00
R6716:Fat3	UTSW	9	15,830,565 (GRCm39)	missense	probably benign
R6719:Fat3	UTSW	9	15,907,440 (GRCm39)	missense	probably benign
R6753:Fat3	UTSW	9	15,826,357 (GRCm39)	missense	possibly damaging	0.82
R6754:Fat3	UTSW	9	15,826,357 (GRCm39)	missense	possibly damaging	0.82
R6755:Fat3	UTSW	9	15,826,357 (GRCm39)	missense	possibly damaging	0.82
R6792:Fat3	UTSW	9	16,286,940 (GRCm39)	missense	probably damaging	1.00
R6802:Fat3	UTSW	9	15,826,357 (GRCm39)	missense	possibly damaging	0.82
R6803:Fat3	UTSW	9	15,908,083 (GRCm39)	missense	probably damaging	0.99
R6831:Fat3	UTSW	9	16,287,847 (GRCm39)	missense	probably damaging	0.98
R6831:Fat3	UTSW	9	15,826,357 (GRCm39)	missense	possibly damaging	0.82
R6833:Fat3	UTSW	9	15,826,357 (GRCm39)	missense	possibly damaging	0.82
R6877:Fat3	UTSW	9	15,910,564 (GRCm39)	missense	probably benign
R6894:Fat3	UTSW	9	15,909,072 (GRCm39)	missense	probably damaging	1.00
R6915:Fat3	UTSW	9	16,289,044 (GRCm39)	missense	probably benign	0.37
R6931:Fat3	UTSW	9	15,871,238 (GRCm39)	missense	possibly damaging	0.89
R6934:Fat3	UTSW	9	16,288,252 (GRCm39)	missense	probably damaging	0.98
R6940:Fat3	UTSW	9	15,828,096 (GRCm39)	splice site	probably null
R6959:Fat3	UTSW	9	15,908,181 (GRCm39)	missense	possibly damaging	0.91
R6969:Fat3	UTSW	9	15,941,212 (GRCm39)	missense	probably benign	0.29
R6986:Fat3	UTSW	9	15,932,631 (GRCm39)	missense	probably damaging	1.00
R6993:Fat3	UTSW	9	15,830,517 (GRCm39)	missense	probably damaging	1.00
R7039:Fat3	UTSW	9	16,287,561 (GRCm39)	missense	probably damaging	1.00
R7051:Fat3	UTSW	9	16,289,123 (GRCm39)	missense	probably damaging	1.00
R7089:Fat3	UTSW	9	15,908,214 (GRCm39)	missense	probably benign	0.01
R7136:Fat3	UTSW	9	16,289,481 (GRCm39)	missense	probably benign
R7137:Fat3	UTSW	9	15,908,444 (GRCm39)	missense	probably damaging	1.00
R7154:Fat3	UTSW	9	15,908,160 (GRCm39)	missense	probably damaging	1.00
R7170:Fat3	UTSW	9	15,917,870 (GRCm39)	missense	probably damaging	0.99
R7183:Fat3	UTSW	9	15,834,133 (GRCm39)	missense	possibly damaging	0.81
R7237:Fat3	UTSW	9	16,288,510 (GRCm39)	missense	probably damaging	1.00
R7288:Fat3	UTSW	9	15,909,888 (GRCm39)	missense	probably damaging	1.00
R7293:Fat3	UTSW	9	15,826,592 (GRCm39)	missense
R7293:Fat3	UTSW	9	15,826,336 (GRCm39)	missense
R7381:Fat3	UTSW	9	16,158,283 (GRCm39)	missense	probably damaging	1.00
R7438:Fat3	UTSW	9	15,899,778 (GRCm39)	missense	probably benign
R7537:Fat3	UTSW	9	15,849,615 (GRCm39)	missense	probably damaging	1.00
R7560:Fat3	UTSW	9	15,908,138 (GRCm39)	missense	probably damaging	1.00
R7585:Fat3	UTSW	9	15,909,558 (GRCm39)	missense	probably benign	0.03
R7623:Fat3	UTSW	9	15,899,620 (GRCm39)	missense	probably damaging	1.00
R7624:Fat3	UTSW	9	15,871,165 (GRCm39)	missense	possibly damaging	0.72
R7684:Fat3	UTSW	9	15,899,564 (GRCm39)	critical splice donor site	probably null
R7690:Fat3	UTSW	9	15,909,477 (GRCm39)	missense	probably damaging	1.00
R7804:Fat3	UTSW	9	15,901,888 (GRCm39)	missense	probably benign	0.01
R7809:Fat3	UTSW	9	15,917,924 (GRCm39)	missense	probably damaging	1.00
R7924:Fat3	UTSW	9	15,910,593 (GRCm39)	missense	probably damaging	1.00
R7925:Fat3	UTSW	9	15,942,656 (GRCm39)	missense	possibly damaging	0.77
R7954:Fat3	UTSW	9	15,909,708 (GRCm39)	missense	probably damaging	1.00
R8021:Fat3	UTSW	9	15,910,405 (GRCm39)	missense	probably damaging	0.99
R8118:Fat3	UTSW	9	15,871,400 (GRCm39)	missense	probably benign
R8141:Fat3	UTSW	9	15,908,362 (GRCm39)	missense	possibly damaging	0.79
R8163:Fat3	UTSW	9	15,871,055 (GRCm39)	missense	probably damaging	1.00
R8170:Fat3	UTSW	9	15,858,792 (GRCm39)	missense	probably damaging	0.97
R8201:Fat3	UTSW	9	15,908,773 (GRCm39)	missense	possibly damaging	0.93
R8258:Fat3	UTSW	9	15,901,887 (GRCm39)	missense	possibly damaging	0.79
R8259:Fat3	UTSW	9	15,901,887 (GRCm39)	missense	possibly damaging	0.79
R8274:Fat3	UTSW	9	16,288,786 (GRCm39)	nonsense	probably null
R8275:Fat3	UTSW	9	16,158,046 (GRCm39)	missense	probably damaging	1.00
R8345:Fat3	UTSW	9	15,910,570 (GRCm39)	missense	probably benign	0.08
R8350:Fat3	UTSW	9	15,826,435 (GRCm39)	missense
R8405:Fat3	UTSW	9	15,907,167 (GRCm39)	missense	probably damaging	1.00
R8421:Fat3	UTSW	9	15,909,480 (GRCm39)	missense	probably damaging	1.00
R8450:Fat3	UTSW	9	15,826,435 (GRCm39)	missense
R8472:Fat3	UTSW	9	16,286,563 (GRCm39)	missense	possibly damaging	0.90
R8482:Fat3	UTSW	9	16,158,263 (GRCm39)	missense	probably benign	0.02
R8680:Fat3	UTSW	9	15,908,703 (GRCm39)	missense	probably damaging	0.99
R8690:Fat3	UTSW	9	15,878,397 (GRCm39)	missense	probably benign	0.45
R8748:Fat3	UTSW	9	15,834,161 (GRCm39)	missense	possibly damaging	0.70
R8756:Fat3	UTSW	9	16,287,885 (GRCm39)	missense	probably damaging	1.00
R8834:Fat3	UTSW	9	15,942,493 (GRCm39)	missense	probably damaging	1.00
R8848:Fat3	UTSW	9	15,878,398 (GRCm39)	missense	probably damaging	1.00
R8884:Fat3	UTSW	9	15,941,280 (GRCm39)	missense	probably damaging	1.00
R8898:Fat3	UTSW	9	15,858,822 (GRCm39)	missense	probably benign	0.04
R8930:Fat3	UTSW	9	15,910,819 (GRCm39)	missense	probably benign	0.06
R8932:Fat3	UTSW	9	15,910,819 (GRCm39)	missense	probably benign	0.06
R8954:Fat3	UTSW	9	16,287,864 (GRCm39)	missense	probably benign	0.00
R8995:Fat3	UTSW	9	16,286,898 (GRCm39)	missense	probably damaging	1.00
R9000:Fat3	UTSW	9	15,918,095 (GRCm39)	missense	probably benign	0.12
R9000:Fat3	UTSW	9	15,871,816 (GRCm39)	missense	possibly damaging	0.82
R9060:Fat3	UTSW	9	15,910,782 (GRCm39)	missense	possibly damaging	0.80
R9116:Fat3	UTSW	9	15,909,421 (GRCm39)	missense	probably benign	0.34
R9136:Fat3	UTSW	9	15,833,738 (GRCm39)	missense
R9193:Fat3	UTSW	9	15,910,248 (GRCm39)	missense	probably benign
R9235:Fat3	UTSW	9	15,833,674 (GRCm39)	missense	probably null
R9257:Fat3	UTSW	9	15,907,863 (GRCm39)	missense	probably benign
R9297:Fat3	UTSW	9	15,908,996 (GRCm39)	missense	probably damaging	1.00
R9307:Fat3	UTSW	9	15,932,719 (GRCm39)	missense	probably damaging	1.00
R9412:Fat3	UTSW	9	15,908,703 (GRCm39)	missense	probably damaging	0.99
R9427:Fat3	UTSW	9	16,288,691 (GRCm39)	nonsense	probably null
R9430:Fat3	UTSW	9	16,287,381 (GRCm39)	missense	probably damaging	1.00
R9480:Fat3	UTSW	9	15,942,703 (GRCm39)	missense	probably damaging	1.00
R9497:Fat3	UTSW	9	15,903,504 (GRCm39)	missense	probably damaging	0.99
R9547:Fat3	UTSW	9	15,911,142 (GRCm39)	missense	possibly damaging	0.86
R9569:Fat3	UTSW	9	15,830,495 (GRCm39)	missense
R9591:Fat3	UTSW	9	16,288,336 (GRCm39)	missense	probably benign	0.01
R9615:Fat3	UTSW	9	16,289,343 (GRCm39)	missense	probably benign	0.00
R9649:Fat3	UTSW	9	15,908,054 (GRCm39)	missense	possibly damaging	0.57
R9671:Fat3	UTSW	9	16,286,871 (GRCm39)	missense	possibly damaging	0.93
R9750:Fat3	UTSW	9	15,915,157 (GRCm39)	missense	probably benign	0.00
R9777:Fat3	UTSW	9	15,826,537 (GRCm39)	missense	probably benign
RF006:Fat3	UTSW	9	15,909,913 (GRCm39)	missense	probably benign	0.36
X0021:Fat3	UTSW	9	15,941,227 (GRCm39)	missense	probably null	0.66
X0026:Fat3	UTSW	9	15,907,629 (GRCm39)	missense	probably benign
X0064:Fat3	UTSW	9	15,830,573 (GRCm39)	missense	probably benign
Z1176:Fat3	UTSW	9	16,286,913 (GRCm39)	missense	probably benign
Z1176:Fat3	UTSW	9	16,286,725 (GRCm39)	missense	probably damaging	1.00
Z1176:Fat3	UTSW	9	15,858,822 (GRCm39)	missense	probably damaging	0.98
Z1177:Fat3	UTSW	9	15,877,287 (GRCm39)	missense	possibly damaging	0.68
Z1177:Fat3	UTSW	9	15,858,834 (GRCm39)	missense	probably damaging	1.00
Z1177:Fat3	UTSW	9	15,834,322 (GRCm39)	missense	possibly damaging	0.81
Z1177:Fat3	UTSW	9	15,881,131 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AGGCCTCAAGTCATTCATGTC -3'
(R):5'- GAAGCTGTTTGCCACTGTCTC -3'

Sequencing Primer
(F):5'- CTAAAACCTGGATGTTCACTTTGGTC -3'
(R):5'- ACTGTCTCCCAGGGGTTG -3'

Posted On

2016-03-01