Mutagenetix > Incidental Mutation

Incidental Mutation 'R5898:Fat3'

512272

Institutional Source

Beutler Lab

Gene Symbol

Fat3

Ensembl Gene

ENSMUSG00000074505

Gene Name

FAT atypical cadherin 3

Synonyms

9430076A06Rik, D430038H04Rik, LOC382129, LOC234973

MMRRC Submission

044097-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.417) question?

Stock #

R5898 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

15910189-16501285 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 15938461 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 3882 (I3882V)

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: I3882V

PolyPhen 2 Score 0.149 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000080808
Gene: ENSMUSG00000074505
AA Change: I3882V

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

noncoding transcript
Transcript: ENSMUST00000215388

Predicted Effect

probably benign
Transcript: ENSMUST00000217308
AA Change: I3882V

PolyPhen 2 Score 0.149 (Sensitivity: 0.92; Specificity: 0.87)

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.9%
20x: 93.8%

Validation Efficiency

96% (86/90)

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: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017N19Rik	G	A	10: 100,615,208 (GRCm38)	M179I	probably benign	Het
1700017N19Rik	G	T	10: 100,612,900 (GRCm38)	R158L	possibly damaging	Het
Abhd12	T	C	2: 150,839,778 (GRCm38)	I231V	possibly damaging	Het
Adsl	A	G	15: 80,961,353 (GRCm38)		probably null	Het
Ahnak	T	C	19: 9,018,211 (GRCm38)	S5620P	probably damaging	Het
Ahnak	C	A	19: 9,013,767 (GRCm38)	N4138K	possibly damaging	Het
Akap13	C	T	7: 75,729,146 (GRCm38)	T2145I	probably damaging	Het
Alpk2	T	A	18: 65,307,623 (GRCm38)	Q700L	probably damaging	Het
Apobec1	T	C	6: 122,580,773 (GRCm38)	Y159C	probably damaging	Het
Atg9a	T	C	1: 75,186,272 (GRCm38)	T395A	probably damaging	Het
Atp6v1f	A	G	6: 29,467,958 (GRCm38)	I48V	probably benign	Het
BC051665	A	C	13: 60,782,704 (GRCm38)	V278G	probably damaging	Het
Bicd1	A	T	6: 149,513,703 (GRCm38)	H638L	probably damaging	Het
Cacna2d4	A	G	6: 119,274,231 (GRCm38)	Y460C	probably damaging	Het
Ccdc157	C	A	11: 4,144,538 (GRCm38)	R496L	probably benign	Het
Cdcp3	T	G	7: 131,241,967 (GRCm38)		probably null	Het
Cep44	C	G	8: 56,541,021 (GRCm38)	V174L	probably damaging	Het
Clca1	G	T	3: 145,016,761 (GRCm38)	F283L	possibly damaging	Het
Csk	T	C	9: 57,630,302 (GRCm38)	T110A	probably benign	Het
Cspg4	T	A	9: 56,885,222 (GRCm38)		probably null	Het
Cutc	A	G	19: 43,760,029 (GRCm38)	I124V	probably benign	Het
Cyp2d9	A	G	15: 82,455,524 (GRCm38)	T104A	probably benign	Het
Cyp2j9	G	T	4: 96,577,714 (GRCm38)	T294K	probably benign	Het
D630003M21Rik	T	A	2: 158,204,657 (GRCm38)		probably null	Het
Dcaf15	G	T	8: 84,098,452 (GRCm38)	F450L	probably damaging	Het
Ddhd1	A	T	14: 45,602,668 (GRCm38)	I723K	probably damaging	Het
Dnah17	C	T	11: 118,114,213 (GRCm38)	A782T	probably benign	Het
Dnah3	T	C	7: 120,078,501 (GRCm38)	D399G	probably benign	Het
Dync2h1	T	C	9: 7,148,717 (GRCm38)	N909S	probably benign	Het
Erbin	A	G	13: 103,839,305 (GRCm38)		probably null	Het
Fanci	G	A	7: 79,433,321 (GRCm38)	V682I	probably benign	Het
Fap	A	T	2: 62,573,503 (GRCm38)	F9L	probably benign	Het
Fkbp15	A	T	4: 62,326,057 (GRCm38)		probably null	Het
Fsd2	T	C	7: 81,537,227 (GRCm38)	Y601C	probably damaging	Het
Gm5900	T	C	7: 104,950,261 (GRCm38)		noncoding transcript	Het
Gramd4	G	T	15: 86,100,784 (GRCm38)	G82V	probably damaging	Het
Hc	C	T	2: 34,997,437 (GRCm38)	V1352I	probably benign	Het
Hsph1	A	T	5: 149,625,158 (GRCm38)	N466K	probably damaging	Het
Ice2	T	A	9: 69,408,262 (GRCm38)	D133E	probably benign	Het
Ifi213	T	C	1: 173,568,979 (GRCm38)	M510V	probably benign	Het
Itpkb	T	G	1: 180,421,315 (GRCm38)	L861R	probably damaging	Het
Kbtbd3	T	A	9: 4,330,476 (GRCm38)	D283E	probably damaging	Het
Man2a1	A	G	17: 64,625,380 (GRCm38)	K154R	probably benign	Het
Masp1	T	A	16: 23,491,927 (GRCm38)	I252F	probably damaging	Het
Megf11	G	T	9: 64,685,964 (GRCm38)	C586F	probably damaging	Het
Myh2	C	A	11: 67,192,719 (GRCm38)	A1476E	possibly damaging	Het
Myo18b	A	T	5: 112,802,330 (GRCm38)		probably null	Het
Naip6	A	T	13: 100,299,321 (GRCm38)	V898E	possibly damaging	Het
Nav1	T	C	1: 135,585,146 (GRCm38)	M59V	probably benign	Het
Nlrp3	A	T	11: 59,546,852 (GRCm38)	Y119F	probably benign	Het
Oxa1l	T	A	14: 54,363,301 (GRCm38)	I77N	possibly damaging	Het
Pcdhb8	T	A	18: 37,357,484 (GRCm38)	D738E	possibly damaging	Het
Pdia5	A	T	16: 35,422,965 (GRCm38)	W269R	probably damaging	Het
Peak1	T	A	9: 56,207,338 (GRCm38)	T1440S	probably benign	Het
Piezo1	A	G	8: 122,487,943 (GRCm38)	V1547A	probably benign	Het
Pkp1	T	C	1: 135,882,521 (GRCm38)	Y437C	probably damaging	Het
Pla2r1	T	C	2: 60,422,760 (GRCm38)	D1329G	probably damaging	Het
Ppip5k2	T	C	1: 97,744,162 (GRCm38)		probably benign	Het
Prrg4	C	T	2: 104,845,033 (GRCm38)	S75N	probably benign	Het
Psmb9	T	A	17: 34,182,292 (GRCm38)	I198F	probably damaging	Het
Rcbtb2	T	A	14: 73,161,965 (GRCm38)	L23*	probably null	Het
Sbno1	A	T	5: 124,386,791 (GRCm38)		probably benign	Het
Scn3a	T	C	2: 65,514,695 (GRCm38)	E483G	probably damaging	Het
Sdccag8	T	A	1: 176,824,822 (GRCm38)	D46E	probably benign	Het
Selenov	A	G	7: 28,288,154 (GRCm38)	F293L	probably damaging	Het
Septin2	A	C	1: 93,479,301 (GRCm38)	D20A	probably benign	Het
Shc1	T	A	3: 89,426,967 (GRCm38)	Y313*	probably null	Het
Siglec1	T	A	2: 131,073,633 (GRCm38)	Y1346F	probably damaging	Het
Slc22a5	T	A	11: 53,873,733 (GRCm38)	I296F	probably damaging	Het
Slc9c1	A	G	16: 45,544,760 (GRCm38)	N152S	probably damaging	Het
Smoc1	C	T	12: 81,104,757 (GRCm38)	R83*	probably null	Het
Ssx2ip	A	G	3: 146,427,831 (GRCm38)	D227G	possibly damaging	Het
Tbrg4	T	C	11: 6,617,372 (GRCm38)	D576G	probably damaging	Het
Tbx20	T	A	9: 24,758,859 (GRCm38)	Y226F	probably damaging	Het
Trav10d	G	T	14: 52,811,472 (GRCm38)	A107S	probably damaging	Het
Trim60	A	T	8: 65,000,364 (GRCm38)	L411*	probably null	Het
Ttbk2	A	T	2: 120,745,040 (GRCm38)	V1083D	probably benign	Het
Unc93a	T	A	17: 13,125,577 (GRCm38)	Q26L	probably damaging	Het
Usp14	T	A	18: 10,022,819 (GRCm38)	N65I	possibly damaging	Het
Vip	A	T	10: 5,643,988 (GRCm38)	S114C	probably damaging	Het
Vmn1r237	A	T	17: 21,314,551 (GRCm38)	I179F	probably damaging	Het
Wdr47	T	A	3: 108,637,885 (GRCm38)		probably null	Het
Zfp975	A	T	7: 42,662,539 (GRCm38)	C217S	probably damaging	Het

Other mutations in Fat3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00662:Fat3	APN	9	15,996,427 (GRCm38)	missense	possibly damaging	0.77
IGL00962:Fat3	APN	9	15,915,519 (GRCm38)	missense	probably benign	0.14
IGL00966:Fat3	APN	9	15,999,094 (GRCm38)	missense	possibly damaging	0.69
IGL01100:Fat3	APN	9	16,375,228 (GRCm38)	missense	probably damaging	1.00
IGL01104:Fat3	APN	9	16,375,728 (GRCm38)	missense	possibly damaging	0.92
IGL01104:Fat3	APN	9	15,998,460 (GRCm38)	missense	probably damaging	1.00
IGL01121:Fat3	APN	9	15,998,401 (GRCm38)	missense	probably benign	0.00
IGL01407:Fat3	APN	9	16,378,023 (GRCm38)	missense	probably benign	0.01
IGL01444:Fat3	APN	9	15,998,848 (GRCm38)	missense	probably damaging	1.00
IGL01634:Fat3	APN	9	15,998,358 (GRCm38)	missense	probably damaging	1.00
IGL01649:Fat3	APN	9	16,376,719 (GRCm38)	missense	possibly damaging	0.95
IGL01839:Fat3	APN	9	15,997,872 (GRCm38)	missense	probably damaging	1.00
IGL01867:Fat3	APN	9	16,377,901 (GRCm38)	missense	probably benign	0.03
IGL01894:Fat3	APN	9	16,375,849 (GRCm38)	missense	probably benign
IGL01913:Fat3	APN	9	15,998,790 (GRCm38)	missense	probably damaging	0.99
IGL02033:Fat3	APN	9	15,915,352 (GRCm38)	missense	possibly damaging	0.50
IGL02035:Fat3	APN	9	16,377,970 (GRCm38)	missense	probably benign	0.06
IGL02146:Fat3	APN	9	15,999,582 (GRCm38)	missense	probably benign
IGL02147:Fat3	APN	9	15,995,985 (GRCm38)	missense	probably damaging	1.00
IGL02161:Fat3	APN	9	15,997,050 (GRCm38)	missense	probably benign	0.10
IGL02161:Fat3	APN	9	15,997,051 (GRCm38)	nonsense	probably null
IGL02164:Fat3	APN	9	16,031,424 (GRCm38)	splice site	probably benign
IGL02269:Fat3	APN	9	15,915,577 (GRCm38)	missense	possibly damaging	0.84
IGL02314:Fat3	APN	9	15,969,838 (GRCm38)	missense	possibly damaging	0.61
IGL02393:Fat3	APN	9	15,988,412 (GRCm38)	nonsense	probably null
IGL02410:Fat3	APN	9	15,997,845 (GRCm38)	missense	probably damaging	1.00
IGL02504:Fat3	APN	9	15,959,798 (GRCm38)	missense	probably damaging	1.00
IGL02572:Fat3	APN	9	15,960,506 (GRCm38)	missense	probably benign
IGL02623:Fat3	APN	9	15,997,137 (GRCm38)	missense	probably damaging	1.00
IGL02654:Fat3	APN	9	15,996,975 (GRCm38)	missense	possibly damaging	0.84
IGL02749:Fat3	APN	9	16,006,711 (GRCm38)	missense	possibly damaging	0.93
IGL02810:Fat3	APN	9	16,376,850 (GRCm38)	missense	probably damaging	1.00
IGL02839:Fat3	APN	9	15,919,170 (GRCm38)	missense	probably damaging	1.00
IGL02890:Fat3	APN	9	15,915,340 (GRCm38)	missense	probably benign	0.03
IGL02892:Fat3	APN	9	16,377,562 (GRCm38)	missense	probably damaging	1.00
IGL03090:Fat3	APN	9	16,377,239 (GRCm38)	nonsense	probably null
IGL03144:Fat3	APN	9	16,375,245 (GRCm38)	missense	probably damaging	1.00
IGL03199:Fat3	APN	9	16,377,048 (GRCm38)	missense	possibly damaging	0.83
IGL03365:Fat3	APN	9	15,996,469 (GRCm38)	missense	probably damaging	1.00
IGL03392:Fat3	APN	9	16,003,862 (GRCm38)	missense	probably benign
IGL03408:Fat3	APN	9	15,997,957 (GRCm38)	nonsense	probably null
gagged	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
hushed	UTSW	9	15,959,869 (GRCm38)	missense	possibly damaging	0.72
Muffled	UTSW	9	15,937,991 (GRCm38)	critical splice donor site	probably null
muted	UTSW	9	15,997,477 (GRCm38)	missense	possibly damaging	0.93
Softened	UTSW	9	16,378,185 (GRCm38)	missense	probably benign
BB001:Fat3	UTSW	9	15,999,297 (GRCm38)	missense	probably damaging	1.00
BB002:Fat3	UTSW	9	16,031,360 (GRCm38)	missense	possibly damaging	0.77
BB011:Fat3	UTSW	9	15,999,297 (GRCm38)	missense	probably damaging	1.00
BB012:Fat3	UTSW	9	16,031,360 (GRCm38)	missense	possibly damaging	0.77
F6893:Fat3	UTSW	9	16,006,789 (GRCm38)	missense	probably damaging	0.99
IGL03050:Fat3	UTSW	9	15,996,600 (GRCm38)	missense	probably benign	0.04
PIT4142001:Fat3	UTSW	9	15,992,118 (GRCm38)	critical splice donor site	probably null
PIT4283001:Fat3	UTSW	9	16,006,601 (GRCm38)	missense	possibly damaging	0.77
PIT4378001:Fat3	UTSW	9	16,376,808 (GRCm38)	missense	probably benign	0.05
PIT4434001:Fat3	UTSW	9	15,996,316 (GRCm38)	missense	probably benign	0.00
PIT4468001:Fat3	UTSW	9	15,996,351 (GRCm38)	missense	probably benign	0.06
R0001:Fat3	UTSW	9	16,377,873 (GRCm38)	missense	probably damaging	0.99
R0005:Fat3	UTSW	9	15,962,866 (GRCm38)	missense	probably damaging	1.00
R0005:Fat3	UTSW	9	15,962,866 (GRCm38)	missense	probably damaging	1.00
R0038:Fat3	UTSW	9	15,915,010 (GRCm38)	missense	probably damaging	1.00
R0046:Fat3	UTSW	9	15,965,979 (GRCm38)	missense	possibly damaging	0.65
R0089:Fat3	UTSW	9	15,938,205 (GRCm38)	missense	probably benign
R0135:Fat3	UTSW	9	16,006,777 (GRCm38)	missense	probably damaging	1.00
R0255:Fat3	UTSW	9	15,969,706 (GRCm38)	splice site	probably benign
R0349:Fat3	UTSW	9	16,031,180 (GRCm38)	missense	probably damaging	1.00
R0361:Fat3	UTSW	9	15,998,403 (GRCm38)	missense	possibly damaging	0.77
R0382:Fat3	UTSW	9	15,959,756 (GRCm38)	missense	probably damaging	1.00
R0418:Fat3	UTSW	9	16,246,896 (GRCm38)	missense	probably damaging	1.00
R0419:Fat3	UTSW	9	15,992,256 (GRCm38)	missense	probably damaging	1.00
R0437:Fat3	UTSW	9	15,996,932 (GRCm38)	missense	probably damaging	1.00
R0441:Fat3	UTSW	9	15,945,008 (GRCm38)	splice site	probably benign
R0480:Fat3	UTSW	9	15,997,729 (GRCm38)	missense	probably benign	0.00
R0510:Fat3	UTSW	9	15,999,685 (GRCm38)	nonsense	probably null
R0665:Fat3	UTSW	9	15,997,402 (GRCm38)	missense	probably benign
R0715:Fat3	UTSW	9	16,375,123 (GRCm38)	missense	probably benign
R0727:Fat3	UTSW	9	15,996,699 (GRCm38)	missense	probably damaging	1.00
R0882:Fat3	UTSW	9	16,031,368 (GRCm38)	missense	possibly damaging	0.84
R0946:Fat3	UTSW	9	15,997,804 (GRCm38)	missense	possibly damaging	0.95
R1068:Fat3	UTSW	9	15,970,034 (GRCm38)	missense	probably benign
R1081:Fat3	UTSW	9	16,375,284 (GRCm38)	missense	possibly damaging	0.62
R1082:Fat3	UTSW	9	16,006,615 (GRCm38)	missense	probably damaging	1.00
R1148:Fat3	UTSW	9	15,996,774 (GRCm38)	missense	probably damaging	1.00
R1148:Fat3	UTSW	9	15,996,774 (GRCm38)	missense	probably damaging	1.00
R1233:Fat3	UTSW	9	15,922,745 (GRCm38)	missense	probably benign
R1306:Fat3	UTSW	9	16,376,679 (GRCm38)	missense	probably damaging	1.00
R1311:Fat3	UTSW	9	16,021,410 (GRCm38)	missense	probably damaging	1.00
R1338:Fat3	UTSW	9	15,925,091 (GRCm38)	missense	probably benign	0.00
R1395:Fat3	UTSW	9	16,246,916 (GRCm38)	missense	probably benign	0.00
R1466:Fat3	UTSW	9	16,375,482 (GRCm38)	missense	probably damaging	0.96
R1466:Fat3	UTSW	9	16,375,482 (GRCm38)	missense	probably damaging	0.96
R1510:Fat3	UTSW	9	15,960,055 (GRCm38)	missense	probably damaging	1.00
R1528:Fat3	UTSW	9	15,925,091 (GRCm38)	missense	probably benign	0.00
R1531:Fat3	UTSW	9	15,997,465 (GRCm38)	missense	probably damaging	1.00
R1659:Fat3	UTSW	9	15,997,183 (GRCm38)	missense	possibly damaging	0.91
R1697:Fat3	UTSW	9	15,944,880 (GRCm38)	missense	probably benign	0.05
R1699:Fat3	UTSW	9	15,938,398 (GRCm38)	missense	probably damaging	1.00
R1728:Fat3	UTSW	9	15,996,315 (GRCm38)	missense	possibly damaging	0.65
R1729:Fat3	UTSW	9	15,996,315 (GRCm38)	missense	possibly damaging	0.65
R1731:Fat3	UTSW	9	15,995,937 (GRCm38)	missense	probably benign
R1784:Fat3	UTSW	9	15,996,315 (GRCm38)	missense	possibly damaging	0.65
R1789:Fat3	UTSW	9	16,376,985 (GRCm38)	missense	probably benign	0.00
R1794:Fat3	UTSW	9	15,997,138 (GRCm38)	missense	probably benign	0.15
R1794:Fat3	UTSW	9	15,997,136 (GRCm38)	nonsense	probably null
R1830:Fat3	UTSW	9	15,915,340 (GRCm38)	missense	probably benign	0.03
R1835:Fat3	UTSW	9	15,998,088 (GRCm38)	missense	probably damaging	1.00
R1887:Fat3	UTSW	9	15,967,061 (GRCm38)	missense	probably damaging	1.00
R1898:Fat3	UTSW	9	15,960,130 (GRCm38)	missense	probably damaging	1.00
R1909:Fat3	UTSW	9	15,998,115 (GRCm38)	missense	probably benign
R1912:Fat3	UTSW	9	15,969,988 (GRCm38)	missense	probably damaging	1.00
R1917:Fat3	UTSW	9	15,997,057 (GRCm38)	missense	possibly damaging	0.55
R1967:Fat3	UTSW	9	15,968,295 (GRCm38)	missense	probably benign	0.00
R2070:Fat3	UTSW	9	15,999,370 (GRCm38)	missense	probably benign	0.21
R2100:Fat3	UTSW	9	16,377,430 (GRCm38)	missense	possibly damaging	0.73
R2104:Fat3	UTSW	9	15,998,517 (GRCm38)	missense	possibly damaging	0.77
R2113:Fat3	UTSW	9	15,999,786 (GRCm38)	missense	probably damaging	1.00
R2132:Fat3	UTSW	9	16,246,719 (GRCm38)	critical splice donor site	probably null
R2136:Fat3	UTSW	9	16,377,051 (GRCm38)	missense	probably benign	0.01
R2146:Fat3	UTSW	9	15,990,512 (GRCm38)	missense	probably benign	0.01
R2233:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R2234:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R2273:Fat3	UTSW	9	15,915,262 (GRCm38)	missense	probably benign
R2285:Fat3	UTSW	9	16,376,173 (GRCm38)	missense	probably damaging	1.00
R2363:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R2365:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R2367:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R2403:Fat3	UTSW	9	15,969,871 (GRCm38)	missense	probably damaging	1.00
R2447:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R2496:Fat3	UTSW	9	15,966,103 (GRCm38)	missense	probably benign	0.01
R2509:Fat3	UTSW	9	15,925,014 (GRCm38)	missense	possibly damaging	0.82
R2932:Fat3	UTSW	9	16,375,944 (GRCm38)	missense	probably damaging	1.00
R2986:Fat3	UTSW	9	15,992,128 (GRCm38)	missense	probably damaging	1.00
R3054:Fat3	UTSW	9	15,960,496 (GRCm38)	missense	probably benign
R3056:Fat3	UTSW	9	15,960,496 (GRCm38)	missense	probably benign
R3729:Fat3	UTSW	9	16,247,041 (GRCm38)	splice site	probably benign
R3745:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R3806:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R3859:Fat3	UTSW	9	15,997,228 (GRCm38)	nonsense	probably null
R3862:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R3890:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R3892:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R3950:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R3972:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4004:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4005:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4086:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4111:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4113:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4227:Fat3	UTSW	9	16,377,693 (GRCm38)	missense	probably damaging	1.00
R4352:Fat3	UTSW	9	16,246,778 (GRCm38)	missense	possibly damaging	0.55
R4394:Fat3	UTSW	9	15,922,792 (GRCm38)	missense	probably benign	0.11
R4403:Fat3	UTSW	9	15,944,873 (GRCm38)	missense	probably damaging	1.00
R4433:Fat3	UTSW	9	16,031,152 (GRCm38)	missense	probably damaging	0.99
R4453:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4479:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4480:Fat3	UTSW	9	15,998,271 (GRCm38)	missense	probably damaging	1.00
R4521:Fat3	UTSW	9	15,922,942 (GRCm38)	missense	probably null	0.71
R4620:Fat3	UTSW	9	15,996,894 (GRCm38)	missense	probably damaging	1.00
R4700:Fat3	UTSW	9	16,031,173 (GRCm38)	missense	probably damaging	1.00
R4721:Fat3	UTSW	9	16,029,966 (GRCm38)	missense	probably damaging	1.00
R4790:Fat3	UTSW	9	15,998,484 (GRCm38)	missense	probably damaging	1.00
R4796:Fat3	UTSW	9	15,999,732 (GRCm38)	missense	probably benign	0.17
R4823:Fat3	UTSW	9	15,996,507 (GRCm38)	missense	probably benign
R4836:Fat3	UTSW	9	16,377,723 (GRCm38)	missense	probably damaging	1.00
R4842:Fat3	UTSW	9	15,997,587 (GRCm38)	missense	probably damaging	1.00
R4849:Fat3	UTSW	9	16,377,948 (GRCm38)	missense	probably benign	0.03
R4856:Fat3	UTSW	9	16,021,330 (GRCm38)	missense	probably benign
R4869:Fat3	UTSW	9	16,377,477 (GRCm38)	missense	probably damaging	0.98
R4886:Fat3	UTSW	9	16,021,330 (GRCm38)	missense	probably benign
R4899:Fat3	UTSW	9	15,969,799 (GRCm38)	missense	probably damaging	1.00
R4941:Fat3	UTSW	9	16,375,152 (GRCm38)	missense	probably damaging	1.00
R4986:Fat3	UTSW	9	15,998,340 (GRCm38)	missense	probably damaging	1.00
R5058:Fat3	UTSW	9	15,996,858 (GRCm38)	missense	probably damaging	1.00
R5079:Fat3	UTSW	9	15,999,127 (GRCm38)	missense	probably benign	0.01
R5080:Fat3	UTSW	9	15,999,338 (GRCm38)	missense	probably benign	0.35
R5174:Fat3	UTSW	9	15,999,570 (GRCm38)	missense	probably damaging	1.00
R5183:Fat3	UTSW	9	15,960,313 (GRCm38)	missense	probably damaging	0.99
R5203:Fat3	UTSW	9	16,378,142 (GRCm38)	missense	possibly damaging	0.79
R5216:Fat3	UTSW	9	16,377,537 (GRCm38)	missense	probably damaging	1.00
R5230:Fat3	UTSW	9	15,990,560 (GRCm38)	missense	possibly damaging	0.51
R5318:Fat3	UTSW	9	16,376,629 (GRCm38)	missense	probably damaging	1.00
R5377:Fat3	UTSW	9	16,376,443 (GRCm38)	missense	probably benign	0.05
R5385:Fat3	UTSW	9	15,922,675 (GRCm38)	missense	possibly damaging	0.82
R5436:Fat3	UTSW	9	15,960,514 (GRCm38)	missense	probably benign	0.02
R5437:Fat3	UTSW	9	16,085,308 (GRCm38)	missense	probably damaging	1.00
R5453:Fat3	UTSW	9	15,996,864 (GRCm38)	missense	probably damaging	1.00
R5460:Fat3	UTSW	9	15,919,167 (GRCm38)	missense	probably damaging	1.00
R5516:Fat3	UTSW	9	15,998,709 (GRCm38)	missense	probably damaging	1.00
R5568:Fat3	UTSW	9	16,376,923 (GRCm38)	nonsense	probably null
R5628:Fat3	UTSW	9	15,966,096 (GRCm38)	missense	probably damaging	1.00
R5835:Fat3	UTSW	9	16,375,833 (GRCm38)	missense	probably damaging	1.00
R5845:Fat3	UTSW	9	16,377,210 (GRCm38)	missense	probably damaging	1.00
R5941:Fat3	UTSW	9	15,999,501 (GRCm38)	missense	probably benign	0.07
R5974:Fat3	UTSW	9	16,006,528 (GRCm38)	critical splice donor site	probably null
R5986:Fat3	UTSW	9	15,998,317 (GRCm38)	missense	probably benign	0.22
R6015:Fat3	UTSW	9	16,376,050 (GRCm38)	missense	possibly damaging	0.55
R6031:Fat3	UTSW	9	15,988,492 (GRCm38)	missense	probably benign	0.02
R6031:Fat3	UTSW	9	15,988,492 (GRCm38)	missense	probably benign	0.02
R6042:Fat3	UTSW	9	16,377,817 (GRCm38)	missense	probably benign	0.12
R6051:Fat3	UTSW	9	16,375,455 (GRCm38)	missense	possibly damaging	0.83
R6052:Fat3	UTSW	9	15,922,679 (GRCm38)	missense	probably null
R6119:Fat3	UTSW	9	16,376,568 (GRCm38)	missense	possibly damaging	0.82
R6161:Fat3	UTSW	9	16,377,522 (GRCm38)	missense	probably damaging	1.00
R6254:Fat3	UTSW	9	15,996,145 (GRCm38)	missense	probably benign	0.19
R6318:Fat3	UTSW	9	15,916,984 (GRCm38)	intron	probably benign
R6347:Fat3	UTSW	9	15,998,372 (GRCm38)	missense	probably damaging	1.00
R6348:Fat3	UTSW	9	15,937,991 (GRCm38)	critical splice donor site	probably null
R6351:Fat3	UTSW	9	15,938,398 (GRCm38)	missense	probably damaging	1.00
R6450:Fat3	UTSW	9	15,999,170 (GRCm38)	missense	possibly damaging	0.51
R6460:Fat3	UTSW	9	15,967,000 (GRCm38)	missense	probably damaging	1.00
R6524:Fat3	UTSW	9	15,992,256 (GRCm38)	missense	probably damaging	1.00
R6533:Fat3	UTSW	9	15,998,899 (GRCm38)	missense	probably benign	0.02
R6565:Fat3	UTSW	9	15,915,327 (GRCm38)	missense	probably benign
R6576:Fat3	UTSW	9	16,377,210 (GRCm38)	missense	probably damaging	1.00
R6649:Fat3	UTSW	9	16,376,742 (GRCm38)	missense	probably damaging	1.00
R6716:Fat3	UTSW	9	15,919,269 (GRCm38)	missense	probably benign
R6719:Fat3	UTSW	9	15,996,144 (GRCm38)	missense	probably benign
R6753:Fat3	UTSW	9	15,915,061 (GRCm38)	missense	possibly damaging	0.82
R6754:Fat3	UTSW	9	15,915,061 (GRCm38)	missense	possibly damaging	0.82
R6755:Fat3	UTSW	9	15,915,061 (GRCm38)	missense	possibly damaging	0.82
R6792:Fat3	UTSW	9	16,375,644 (GRCm38)	missense	probably damaging	1.00
R6802:Fat3	UTSW	9	15,915,061 (GRCm38)	missense	possibly damaging	0.82
R6803:Fat3	UTSW	9	15,996,787 (GRCm38)	missense	probably damaging	0.99
R6831:Fat3	UTSW	9	16,376,551 (GRCm38)	missense	probably damaging	0.98
R6831:Fat3	UTSW	9	15,915,061 (GRCm38)	missense	possibly damaging	0.82
R6833:Fat3	UTSW	9	15,915,061 (GRCm38)	missense	possibly damaging	0.82
R6877:Fat3	UTSW	9	15,999,268 (GRCm38)	missense	probably benign
R6894:Fat3	UTSW	9	15,997,776 (GRCm38)	missense	probably damaging	1.00
R6915:Fat3	UTSW	9	16,377,748 (GRCm38)	missense	probably benign	0.37
R6931:Fat3	UTSW	9	15,959,942 (GRCm38)	missense	possibly damaging	0.89
R6934:Fat3	UTSW	9	16,376,956 (GRCm38)	missense	probably damaging	0.98
R6940:Fat3	UTSW	9	15,916,800 (GRCm38)	splice site	probably null
R6959:Fat3	UTSW	9	15,996,885 (GRCm38)	missense	possibly damaging	0.91
R6969:Fat3	UTSW	9	16,029,916 (GRCm38)	missense	probably benign	0.29
R6986:Fat3	UTSW	9	16,021,335 (GRCm38)	missense	probably damaging	1.00
R6993:Fat3	UTSW	9	15,919,221 (GRCm38)	missense	probably damaging	1.00
R7039:Fat3	UTSW	9	16,376,265 (GRCm38)	missense	probably damaging	1.00
R7051:Fat3	UTSW	9	16,377,827 (GRCm38)	missense	probably damaging	1.00
R7089:Fat3	UTSW	9	15,996,918 (GRCm38)	missense	probably benign	0.01
R7136:Fat3	UTSW	9	16,378,185 (GRCm38)	missense	probably benign
R7137:Fat3	UTSW	9	15,997,148 (GRCm38)	missense	probably damaging	1.00
R7154:Fat3	UTSW	9	15,996,864 (GRCm38)	missense	probably damaging	1.00
R7170:Fat3	UTSW	9	16,006,574 (GRCm38)	missense	probably damaging	0.99
R7183:Fat3	UTSW	9	15,922,837 (GRCm38)	missense	possibly damaging	0.81
R7237:Fat3	UTSW	9	16,377,214 (GRCm38)	missense	probably damaging	1.00
R7288:Fat3	UTSW	9	15,998,592 (GRCm38)	missense	probably damaging	1.00
R7293:Fat3	UTSW	9	15,915,296 (GRCm38)	missense
R7293:Fat3	UTSW	9	15,915,040 (GRCm38)	missense
R7381:Fat3	UTSW	9	16,246,987 (GRCm38)	missense	probably damaging	1.00
R7438:Fat3	UTSW	9	15,988,482 (GRCm38)	missense	probably benign
R7537:Fat3	UTSW	9	15,938,319 (GRCm38)	missense	probably damaging	1.00
R7560:Fat3	UTSW	9	15,996,842 (GRCm38)	missense	probably damaging	1.00
R7585:Fat3	UTSW	9	15,998,262 (GRCm38)	missense	probably benign	0.03
R7623:Fat3	UTSW	9	15,988,324 (GRCm38)	missense	probably damaging	1.00
R7624:Fat3	UTSW	9	15,959,869 (GRCm38)	missense	possibly damaging	0.72
R7684:Fat3	UTSW	9	15,988,268 (GRCm38)	critical splice donor site	probably null
R7690:Fat3	UTSW	9	15,998,181 (GRCm38)	missense	probably damaging	1.00
R7804:Fat3	UTSW	9	15,990,592 (GRCm38)	missense	probably benign	0.01
R7809:Fat3	UTSW	9	16,006,628 (GRCm38)	missense	probably damaging	1.00
R7924:Fat3	UTSW	9	15,999,297 (GRCm38)	missense	probably damaging	1.00
R7925:Fat3	UTSW	9	16,031,360 (GRCm38)	missense	possibly damaging	0.77
R7954:Fat3	UTSW	9	15,998,412 (GRCm38)	missense	probably damaging	1.00
R8021:Fat3	UTSW	9	15,999,109 (GRCm38)	missense	probably damaging	0.99
R8118:Fat3	UTSW	9	15,960,104 (GRCm38)	missense	probably benign
R8141:Fat3	UTSW	9	15,997,066 (GRCm38)	missense	possibly damaging	0.79
R8163:Fat3	UTSW	9	15,959,759 (GRCm38)	missense	probably damaging	1.00
R8170:Fat3	UTSW	9	15,947,496 (GRCm38)	missense	probably damaging	0.97
R8201:Fat3	UTSW	9	15,997,477 (GRCm38)	missense	possibly damaging	0.93
R8258:Fat3	UTSW	9	15,990,591 (GRCm38)	missense	possibly damaging	0.79
R8259:Fat3	UTSW	9	15,990,591 (GRCm38)	missense	possibly damaging	0.79
R8274:Fat3	UTSW	9	16,377,490 (GRCm38)	nonsense	probably null
R8275:Fat3	UTSW	9	16,246,750 (GRCm38)	missense	probably damaging	1.00
R8345:Fat3	UTSW	9	15,999,274 (GRCm38)	missense	probably benign	0.08
R8350:Fat3	UTSW	9	15,915,139 (GRCm38)	missense
R8405:Fat3	UTSW	9	15,995,871 (GRCm38)	missense	probably damaging	1.00
R8421:Fat3	UTSW	9	15,998,184 (GRCm38)	missense	probably damaging	1.00
R8450:Fat3	UTSW	9	15,915,139 (GRCm38)	missense
R8472:Fat3	UTSW	9	16,375,267 (GRCm38)	missense	possibly damaging	0.90
R8482:Fat3	UTSW	9	16,246,967 (GRCm38)	missense	probably benign	0.02
R8680:Fat3	UTSW	9	15,997,407 (GRCm38)	missense	probably damaging	0.99
R8690:Fat3	UTSW	9	15,967,101 (GRCm38)	missense	probably benign	0.45
R8748:Fat3	UTSW	9	15,922,865 (GRCm38)	missense	possibly damaging	0.70
R8756:Fat3	UTSW	9	16,376,589 (GRCm38)	missense	probably damaging	1.00
R8834:Fat3	UTSW	9	16,031,197 (GRCm38)	missense	probably damaging	1.00
R8848:Fat3	UTSW	9	15,967,102 (GRCm38)	missense	probably damaging	1.00
R8884:Fat3	UTSW	9	16,029,984 (GRCm38)	missense	probably damaging	1.00
R8898:Fat3	UTSW	9	15,947,526 (GRCm38)	missense	probably benign	0.04
R8930:Fat3	UTSW	9	15,999,523 (GRCm38)	missense	probably benign	0.06
R8932:Fat3	UTSW	9	15,999,523 (GRCm38)	missense	probably benign	0.06
R8954:Fat3	UTSW	9	16,376,568 (GRCm38)	missense	probably benign	0.00
R8995:Fat3	UTSW	9	16,375,602 (GRCm38)	missense	probably damaging	1.00
R9000:Fat3	UTSW	9	16,006,799 (GRCm38)	missense	probably benign	0.12
R9000:Fat3	UTSW	9	15,960,520 (GRCm38)	missense	possibly damaging	0.82
R9060:Fat3	UTSW	9	15,999,486 (GRCm38)	missense	possibly damaging	0.80
R9116:Fat3	UTSW	9	15,998,125 (GRCm38)	missense	probably benign	0.34
R9136:Fat3	UTSW	9	15,922,442 (GRCm38)	missense
R9193:Fat3	UTSW	9	15,998,952 (GRCm38)	missense	probably benign
R9235:Fat3	UTSW	9	15,922,378 (GRCm38)	missense	probably null
R9257:Fat3	UTSW	9	15,996,567 (GRCm38)	missense	probably benign
R9297:Fat3	UTSW	9	15,997,700 (GRCm38)	missense	probably damaging	1.00
R9307:Fat3	UTSW	9	16,021,423 (GRCm38)	missense	probably damaging	1.00
R9412:Fat3	UTSW	9	15,997,407 (GRCm38)	missense	probably damaging	0.99
R9427:Fat3	UTSW	9	16,377,395 (GRCm38)	nonsense	probably null
R9430:Fat3	UTSW	9	16,376,085 (GRCm38)	missense	probably damaging	1.00
R9480:Fat3	UTSW	9	16,031,407 (GRCm38)	missense	probably damaging	1.00
R9497:Fat3	UTSW	9	15,992,208 (GRCm38)	missense	probably damaging	0.99
R9547:Fat3	UTSW	9	15,999,846 (GRCm38)	missense	possibly damaging	0.86
R9569:Fat3	UTSW	9	15,919,199 (GRCm38)	missense
R9591:Fat3	UTSW	9	16,377,040 (GRCm38)	missense	probably benign	0.01
R9615:Fat3	UTSW	9	16,378,047 (GRCm38)	missense	probably benign	0.00
R9649:Fat3	UTSW	9	15,996,758 (GRCm38)	missense	possibly damaging	0.57
R9671:Fat3	UTSW	9	16,375,575 (GRCm38)	missense	possibly damaging	0.93
R9750:Fat3	UTSW	9	16,003,861 (GRCm38)	missense	probably benign	0.00
R9777:Fat3	UTSW	9	15,915,241 (GRCm38)	missense	probably benign
RF006:Fat3	UTSW	9	15,998,617 (GRCm38)	missense	probably benign	0.36
X0021:Fat3	UTSW	9	16,029,931 (GRCm38)	missense	probably null	0.66
X0026:Fat3	UTSW	9	15,996,333 (GRCm38)	missense	probably benign
X0064:Fat3	UTSW	9	15,919,277 (GRCm38)	missense	probably benign
Z1176:Fat3	UTSW	9	16,375,617 (GRCm38)	missense	probably benign
Z1176:Fat3	UTSW	9	16,375,429 (GRCm38)	missense	probably damaging	1.00
Z1176:Fat3	UTSW	9	15,947,526 (GRCm38)	missense	probably damaging	0.98
Z1177:Fat3	UTSW	9	15,965,991 (GRCm38)	missense	possibly damaging	0.68
Z1177:Fat3	UTSW	9	15,947,538 (GRCm38)	missense	probably damaging	1.00
Z1177:Fat3	UTSW	9	15,923,026 (GRCm38)	missense	possibly damaging	0.81
Z1177:Fat3	UTSW	9	15,969,835 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- ACCAAAGAAGATGGCACTGTC -3'
(R):5'- ATACCACCATGTGCTTCCTGG -3'

Sequencing Primer
(F):5'- CAGTGCTTAGCGTCTGGAAGTAC -3'
(R):5'- GACGTCCCTATGATTGGTAGCAG -3'

Posted On

2018-04-19