Mutagenetix > Incidental Mutation

Incidental Mutation 'R1729:Fat3'

198916

Institutional Source

Beutler Lab

Gene Symbol

Fat3

Ensembl Gene

ENSMUSG00000074505

Gene Name

FAT atypical cadherin 3

Synonyms

9430076A06Rik, D430038H04Rik, LOC382129, LOC234973

MMRRC Submission

039761-MU

Accession Numbers

Genbank: NM_001080814; MGI: 2444314

Essential gene?

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

Stock #

R1729 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

15910189-16501285 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 15996315 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 2797 (V2797G)

Ref Sequence

ENSEMBL: ENSMUSP00000148968 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000082170
AA Change: V2797G

PolyPhen 2 Score 0.652 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000080808
Gene: ENSMUSG00000074505
AA Change: V2797G

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

possibly damaging
Transcript: ENSMUST00000217308
AA Change: V2797G

PolyPhen 2 Score 0.652 (Sensitivity: 0.87; Specificity: 0.91)

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.0%
20x: 91.6%

Validation Efficiency

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: 225 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447A16Rik	G	A	15: 37,439,600 (GRCm38)		probably benign	Het
4930453N24Rik	T	C	16: 64,769,022 (GRCm38)	I90V	probably damaging	Het
Aadat	A	G	8: 60,526,712 (GRCm38)	T203A	probably damaging	Het
Adamts17	C	T	7: 67,149,956 (GRCm38)	R1060*	probably null	Het
Adamts5	T	A	16: 85,877,915 (GRCm38)	K454*	probably null	Het
Adgrg6	T	C	10: 14,439,782 (GRCm38)	T593A	probably damaging	Het
Aldh1l2	T	A	10: 83,508,082 (GRCm38)	K377*	probably null	Het
Aldh4a1	A	G	4: 139,644,161 (GRCm38)	Y462C	probably damaging	Het
Ankrd12	G	T	17: 65,984,076 (GRCm38)	P1454Q	probably benign	Het
Ap2m1	T	A	16: 20,539,338 (GRCm38)	N35K	probably damaging	Het
Aspm	A	G	1: 139,473,574 (GRCm38)	I1111V	probably benign	Het
Atr	G	A	9: 95,897,581 (GRCm38)	V1331I	probably benign	Het
Boc	T	C	16: 44,496,419 (GRCm38)	T454A	probably benign	Het
C4bp	C	G	1: 130,642,988 (GRCm38)	V284L	probably benign	Het
Cacna1s	T	C	1: 136,118,716 (GRCm38)	F1761S	probably benign	Het
Camsap2	C	T	1: 136,281,315 (GRCm38)	R802Q	probably benign	Het
Capn9	G	A	8: 124,605,711 (GRCm38)	G430R	possibly damaging	Het
Car14	G	A	3: 95,901,248 (GRCm38)	P18L	possibly damaging	Het
Cbs	G	T	17: 31,620,949 (GRCm38)	A337E	probably benign	Het
Ccdc129	T	C	6: 55,968,541 (GRCm38)	F749S	probably benign	Het
Ccdc186	A	C	19: 56,809,220 (GRCm38)	H306Q	probably benign	Het
Ccdc93	C	T	1: 121,456,126 (GRCm38)	P192L	probably benign	Het
Ccdc93	T	C	1: 121,461,939 (GRCm38)	V237A	probably benign	Het
Cd55	C	T	1: 130,449,423 (GRCm38)	V333I	probably benign	Het
Cd55	C	A	1: 130,459,633 (GRCm38)	A143S	probably benign	Het
Cdh19	C	A	1: 110,893,384 (GRCm38)	E541D	probably damaging	Het
Cdh7	C	G	1: 110,065,735 (GRCm38)	L307V	possibly damaging	Het
Cdk12	T	C	11: 98,249,970 (GRCm38)		probably benign	Het
Cep350	A	T	1: 155,911,981 (GRCm38)	H1370Q	probably benign	Het
Cfh	C	T	1: 140,147,697 (GRCm38)	V268I	possibly damaging	Het
Cfh	T	C	1: 140,136,788 (GRCm38)	K374R	probably benign	Het
Cfhr2	A	C	1: 139,813,459 (GRCm38)	N259K	probably benign	Het
Cfhr2	A	G	1: 139,813,442 (GRCm38)	M265T	probably benign	Het
Chat	A	T	14: 32,446,795 (GRCm38)	L261H	probably damaging	Het
Chil1	C	T	1: 134,188,529 (GRCm38)	A250V	probably damaging	Het
Clcn1	T	A	6: 42,299,514 (GRCm38)	F360Y	possibly damaging	Het
Clgn	A	G	8: 83,423,030 (GRCm38)	S387G	probably damaging	Het
Clk1	C	T	1: 58,421,261 (GRCm38)	R70Q	probably damaging	Het
Cntnap5a	T	C	1: 116,455,101 (GRCm38)	L1033S	probably benign	Het
Cntnap5a	C	T	1: 116,455,143 (GRCm38)	T1047I	probably benign	Het
Cntnap5a	C	A	1: 116,455,004 (GRCm38)	L1001I	probably benign	Het
Crb1	A	T	1: 139,237,622 (GRCm38)	H921Q	probably benign	Het
Crb1	G	A	1: 139,241,138 (GRCm38)	P881S	probably damaging	Het
Crb1	C	T	1: 139,242,995 (GRCm38)	G825R	probably damaging	Het
Crb1	T	C	1: 139,234,779 (GRCm38)	M1214V	probably benign	Het
Crb1	C	T	1: 139,243,417 (GRCm38)	R684H	probably benign	Het
Cspg4	G	T	9: 56,898,537 (GRCm38)	V2211L	probably benign	Het
Cwh43	T	C	5: 73,408,218 (GRCm38)	L42P	probably damaging	Het
Cxcr4	C	T	1: 128,589,277 (GRCm38)	V216I	probably benign	Het
Cyb5r1	C	T	1: 134,407,667 (GRCm38)	R147W	probably damaging	Het
D830039M14Rik	C	T	10: 61,475,727 (GRCm38)		probably benign	Het
Ddx59	T	C	1: 136,417,053 (GRCm38)	V154A	probably benign	Het
Dhx30	T	C	9: 110,098,751 (GRCm38)	H101R	probably damaging	Het
Dnah11	T	A	12: 117,916,931 (GRCm38)	D3818V	probably damaging	Het
Dnah9	G	A	11: 66,085,020 (GRCm38)	T1401I	possibly damaging	Het
Dsel	G	C	1: 111,859,994 (GRCm38)	T937S	probably benign	Het
Dsel	T	C	1: 111,859,457 (GRCm38)	N1116S	probably benign	Het
Dstyk	C	T	1: 132,456,984 (GRCm38)	L739F	probably damaging	Het
Ehf	T	G	2: 103,273,906 (GRCm38)	T186P	possibly damaging	Het
Elf2	A	T	3: 51,257,572 (GRCm38)	V277D	probably damaging	Het
Etnk2	G	T	1: 133,365,765 (GRCm38)	G149W	probably damaging	Het
Etnk2	T	A	1: 133,376,915 (GRCm38)	V292E	probably benign	Het
Etnk2	A	G	1: 133,363,923 (GRCm38)	S54G	probably benign	Het
Etnk2	C	T	1: 133,365,816 (GRCm38)	R166*	probably null	Het
Etnk2	C	A	1: 133,365,587 (GRCm38)	D89E	probably benign	Het
Etnk2	G	A	1: 133,365,817 (GRCm38)	R166Q	probably benign	Het
Eya2	G	T	2: 165,687,663 (GRCm38)	G109W	probably damaging	Het
Fam208a	A	T	14: 27,479,633 (GRCm38)	N1367Y	probably damaging	Het
Fam72a	C	T	1: 131,538,895 (GRCm38)	T139M	probably benign	Het
Fam72a	T	C	1: 131,530,668 (GRCm38)	I56T	probably benign	Het
Fam78b	A	G	1: 167,001,630 (GRCm38)	D22G	possibly damaging	Het
Fastkd2	T	A	1: 63,751,300 (GRCm38)	C628*	probably null	Het
Fcamr	A	C	1: 130,804,627 (GRCm38)	N117T	probably benign	Het
Fcamr	A	G	1: 130,812,809 (GRCm38)	M322V	probably benign	Het
Fcamr	C	T	1: 130,812,816 (GRCm38)	P324L	probably benign	Het
Fcamr	A	G	1: 130,812,692 (GRCm38)	I283V	probably benign	Het
Fcamr	A	G	1: 130,814,597 (GRCm38)	N574D	probably benign	Het
Fcamr	A	G	1: 130,811,580 (GRCm38)	I206V	probably benign	Het
Fcamr	G	A	1: 130,812,629 (GRCm38)	G262S	probably benign	Het
Fcamr	T	C	1: 130,812,738 (GRCm38)	V298A	probably benign	Het
Fcmr	T	C	1: 130,878,269 (GRCm38)	S321P	probably benign	Het
Fcmr	A	G	1: 130,875,974 (GRCm38)	T172A	probably benign	Het
Fut10	T	A	8: 31,201,390 (GRCm38)	S88T	probably benign	Het
Gabarap	C	T	11: 69,991,689 (GRCm38)		probably benign	Het
Gli2	G	T	1: 119,002,044 (GRCm38)	H44Q	probably benign	Het
Gli2	C	T	1: 118,868,087 (GRCm38)	A113T	possibly damaging	Het
Gm5346	T	C	8: 43,625,583 (GRCm38)	N535D	probably damaging	Het
Gon4l	T	A	3: 88,903,098 (GRCm38)	D1844E	probably damaging	Het
Gpr25	G	A	1: 136,260,710 (GRCm38)	P55L	probably benign	Het
Guk1	A	T	11: 59,185,312 (GRCm38)	V100E	probably damaging	Het
Ifi44l	T	C	3: 151,762,819 (GRCm38)	I25V	unknown	Het
Igfn1	C	T	1: 135,972,127 (GRCm38)	R482Q	probably benign	Het
Igfn1	G	A	1: 135,982,475 (GRCm38)	R124W	probably benign	Het
Igfn1	G	A	1: 135,959,928 (GRCm38)	P2466L	probably damaging	Het
Igfn1	G	A	1: 135,968,199 (GRCm38)	A1543V	probably benign	Het
Igfn1	T	C	1: 135,998,625 (GRCm38)	E29G	probably benign	Het
Igfn1	T	C	1: 135,998,683 (GRCm38)	I10V	unknown	Het
Igfn1	C	T	1: 135,979,915 (GRCm38)	A231T	probably benign	Het
Igfn1	T	C	1: 135,970,411 (GRCm38)	S806G	probably benign	Het
Ikbke	T	C	1: 131,269,823 (GRCm38)	S447G	probably benign	Het
Ikbke	C	A	1: 131,265,937 (GRCm38)	A459S	probably benign	Het
Ipo9	A	G	1: 135,402,250 (GRCm38)	V484A	probably benign	Het
Ipo9	ATCCTCCTCCTCCTCCTC	ATCCTCCTCCTCCTCCTCCTC	1: 135,386,268 (GRCm38)		probably benign	Het
Jarid2	T	A	13: 44,906,276 (GRCm38)	N661K	probably damaging	Het
Kcnt2	G	A	1: 140,354,547 (GRCm38)	S90N	probably benign	Het
Kif14	C	T	1: 136,503,431 (GRCm38)	L1189F	probably benign	Het
Kif14	T	C	1: 136,525,783 (GRCm38)	V1433A	probably benign	Het
Kif14	G	A	1: 136,478,365 (GRCm38)	A556T	probably benign	Het
Kif14	A	G	1: 136,468,279 (GRCm38)	N108D	probably benign	Het
Kif14	A	G	1: 136,468,975 (GRCm38)	K340E	probably damaging	Het
Kif14	A	G	1: 136,490,332 (GRCm38)	S868G	probably benign	Het
Kif14	T	C	1: 136,515,961 (GRCm38)	F1291L	probably benign	Het
Kif18b	A	G	11: 102,915,541 (GRCm38)		probably null	Het
Kif26a	T	C	12: 112,176,785 (GRCm38)	S1158P	possibly damaging	Het
Kmt2d	A	G	15: 98,865,132 (GRCm38)	C279R	probably damaging	Het
Kremen1	CGGG	CGGGGGG	11: 5,201,791 (GRCm38)		probably benign	Het
Krt23	A	T	11: 99,492,964 (GRCm38)	V34D	probably damaging	Het
Lad1	C	T	1: 135,828,023 (GRCm38)	R346C	probably damaging	Het
Lad1	C	T	1: 135,827,381 (GRCm38)	P132S	possibly damaging	Het
Lax1	T	C	1: 133,680,569 (GRCm38)	N145D	probably benign	Het
Lax1	T	C	1: 133,679,978 (GRCm38)	R342G	probably benign	Het
Lax1	G	A	1: 133,683,634 (GRCm38)	P67S	probably damaging	Het
Lgr6	G	T	1: 134,990,635 (GRCm38)	H263N	probably benign	Het
Lgr6	C	T	1: 135,003,476 (GRCm38)	S3N	probably benign	Het
Lgr6	A	T	1: 134,988,009 (GRCm38)	S334T	probably benign	Het
Lgr6	C	T	1: 134,987,088 (GRCm38)	V641I	probably benign	Het
Lmod1	C	T	1: 135,364,073 (GRCm38)	T222I	probably benign	Het
Mb21d2	A	G	16: 28,828,421 (GRCm38)	V267A	probably benign	Het
Megf10	T	C	18: 57,240,792 (GRCm38)		probably null	Het
Mfrp	A	G	9: 44,104,587 (GRCm38)	T334A	possibly damaging	Het
Miga2	A	G	2: 30,368,968 (GRCm38)	H63R	probably damaging	Het
Mrgbp	T	A	2: 180,585,449 (GRCm38)	N192K	probably damaging	Het
Mrgpra2b	A	G	7: 47,464,879 (GRCm38)	I35T	probably benign	Het
Mroh3	G	C	1: 136,192,144 (GRCm38)	Q440E	possibly damaging	Het
Mybph	C	T	1: 134,197,480 (GRCm38)	R249C	probably benign	Het
Nav1	A	T	1: 135,584,727 (GRCm38)	D198E	possibly damaging	Het
Ndufaf7	A	T	17: 78,937,629 (GRCm38)	K59M	probably damaging	Het
Necab3	T	C	2: 154,546,875 (GRCm38)	S208G	probably benign	Het
Nfrkb	C	T	9: 31,414,636 (GRCm38)	T1125M	probably benign	Het
Npnt	G	A	3: 132,914,397 (GRCm38)	Q112*	probably null	Het
Nr5a2	C	A	1: 136,952,125 (GRCm38)	R35L	probably benign	Het
Nrcam	A	G	12: 44,573,850 (GRCm38)	K893E	probably benign	Het
Obsl1	G	A	1: 75,486,756 (GRCm38)	T1764M	probably benign	Het
Olfr1240	C	T	2: 89,439,583 (GRCm38)	R232H	probably benign	Het
Olfr453	C	A	6: 42,744,135 (GRCm38)	L33M	possibly damaging	Het
Olfr870	A	T	9: 20,170,913 (GRCm38)	Y219*	probably null	Het
Optc	C	G	1: 133,905,170 (GRCm38)	S64T	probably benign	Het
Optc	A	T	1: 133,903,796 (GRCm38)		probably null	Het
Otoa	T	C	7: 121,125,439 (GRCm38)	V447A	probably benign	Het
Patj	G	A	4: 98,431,780 (GRCm38)	G428D	possibly damaging	Het
Pigr	C	T	1: 130,844,522 (GRCm38)	A159V	possibly damaging	Het
Pik3c2b	C	T	1: 133,066,627 (GRCm38)	P110S	probably benign	Het
Pkn2	G	A	3: 142,810,701 (GRCm38)	P555S	probably benign	Het
Pla2g12a	A	G	3: 129,894,940 (GRCm38)	E149G	probably benign	Het
Plec	C	A	15: 76,177,692 (GRCm38)	E2547*	probably null	Het
Plekha6	C	G	1: 133,287,846 (GRCm38)	T792S	probably benign	Het
Ppfia4	G	A	1: 134,299,321 (GRCm38)	P1159S	probably benign	Het
Prelp	C	T	1: 133,915,131 (GRCm38)	R92K	probably benign	Het
Ptpn7	A	G	1: 135,134,475 (GRCm38)	Q53R	probably benign	Het
Ptprc	T	G	1: 138,099,676 (GRCm38)	N478T	probably benign	Het
Ptprc	A	G	1: 138,107,823 (GRCm38)	S405P	probably benign	Het
Ptprc	T	C	1: 138,112,254 (GRCm38)	K212E	possibly damaging	Het
Ptprc	C	A	1: 138,107,824 (GRCm38)	E402D	probably benign	Het
Ptprc	A	G	1: 138,107,837 (GRCm38)	V400A	probably benign	Het
Rab29	A	G	1: 131,872,110 (GRCm38)	Q141R	probably benign	Het
Rab3gap1	T	G	1: 127,942,486 (GRCm38)	L948R	probably damaging	Het
Rbsn	A	T	6: 92,190,019 (GRCm38)	L548Q	possibly damaging	Het
Ren1	C	G	1: 133,360,007 (GRCm38)	L360V	probably benign	Het
Ren1	C	T	1: 133,354,237 (GRCm38)	T32I	probably benign	Het
Ren1	T	A	1: 133,354,206 (GRCm38)	W22R	probably damaging	Het
Ren1	A	T	1: 133,359,079 (GRCm38)	E315D	probably benign	Het
Rint1	T	A	5: 23,809,843 (GRCm38)	D352E	probably benign	Het
Rnpep	G	C	1: 135,283,977 (GRCm38)	A11G	probably benign	Het
Rnpep	C	T	1: 135,263,096 (GRCm38)	A571T	possibly damaging	Het
Sctr	G	A	1: 120,063,257 (GRCm38)	S440N	possibly damaging	Het
Sctr	T	C	1: 120,031,656 (GRCm38)	F110L	probably benign	Het
Sctr	G	T	1: 120,063,246 (GRCm38)	E453D	probably benign	Het
Sept4	A	T	11: 87,583,436 (GRCm38)	Q60L	probably benign	Het
Serpinb10	C	T	1: 107,538,473 (GRCm38)	S63F	probably damaging	Het
Serpinb2	C	T	1: 107,523,890 (GRCm38)	H258Y	probably benign	Het
Serpinb2	C	T	1: 107,523,894 (GRCm38)	T259I	probably benign	Het
Serpinb2	A	C	1: 107,524,543 (GRCm38)	S284R	probably benign	Het
Serpinb2	G	A	1: 107,515,635 (GRCm38)	A55T	probably damaging	Het
Serpinb2	C	A	1: 107,523,834 (GRCm38)	A239E	probably benign	Het
Serpinb8	A	G	1: 107,597,527 (GRCm38)	S20G	probably benign	Het
Serpinb8	A	C	1: 107,607,004 (GRCm38)	L268F	probably benign	Het
Serpinb8	G	A	1: 107,598,954 (GRCm38)	A75T	probably benign	Het
Slain2	A	G	5: 72,957,614 (GRCm38)	H396R	probably damaging	Het
Slc22a5	G	A	11: 53,866,351 (GRCm38)	P491L	probably damaging	Het
Slc26a4	A	G	12: 31,544,494 (GRCm38)	V285A	possibly damaging	Het
Slc26a9	C	A	1: 131,766,012 (GRCm38)	R747S	probably benign	Het
Slc26a9	C	T	1: 131,763,870 (GRCm38)	A617V	probably benign	Het
Slc9a8	T	C	2: 167,424,145 (GRCm38)	F14S	probably benign	Het
Spock3	T	C	8: 63,348,977 (GRCm38)	L330P	probably damaging	Het
Steap3	G	A	1: 120,234,378 (GRCm38)	A350V	probably benign	Het
Steap3	T	C	1: 120,227,750 (GRCm38)	N493S	probably benign	Het
Synpo2l	G	A	14: 20,665,819 (GRCm38)	P233S	probably damaging	Het
Tbc1d19	T	G	5: 53,829,372 (GRCm38)	I41S	probably damaging	Het
Tecta	G	A	9: 42,391,922 (GRCm38)	T138I	probably benign	Het
Thsd7b	T	A	1: 129,667,937 (GRCm38)	F498Y	probably benign	Het
Thsd7b	G	C	1: 129,678,183 (GRCm38)	A554P	probably benign	Het
Thsd7b	C	T	1: 129,628,891 (GRCm38)	T328I	probably damaging	Het
Thsd7b	A	C	1: 130,116,631 (GRCm38)	Q1116P	probably benign	Het
Tmem241	T	A	18: 12,068,312 (GRCm38)	H157L	probably damaging	Het
Tnfrsf25	T	A	4: 152,118,304 (GRCm38)		probably null	Het
Tnnt2	C	T	1: 135,845,506 (GRCm38)		probably benign	Het
Traf3ip3	T	A	1: 193,181,893 (GRCm38)	Q394L	probably benign	Het
Traf7	A	G	17: 24,512,379 (GRCm38)	F228L	probably damaging	Het
Trhr	A	G	15: 44,197,153 (GRCm38)	E23G	probably damaging	Het
Trim59	T	C	3: 69,036,853 (GRCm38)	T385A	probably benign	Het
Trove2	T	C	1: 143,760,034 (GRCm38)	D458G	probably benign	Het
Trove2	C	T	1: 143,760,014 (GRCm38)	V465I	probably benign	Het
Ttn	C	T	2: 76,813,339 (GRCm38)	G11436R	probably damaging	Het
Tubgcp2	T	C	7: 139,998,055 (GRCm38)	T779A	probably benign	Het
Tusc2	A	T	9: 107,564,631 (GRCm38)	I68F	probably damaging	Het
Ube2t	C	T	1: 134,972,167 (GRCm38)	A149V	probably benign	Het
Usp24	A	G	4: 106,360,421 (GRCm38)	N447S	possibly damaging	Het
Usp42	T	C	5: 143,714,626 (GRCm38)	D1214G	probably damaging	Het
Vmn2r73	T	C	7: 85,857,878 (GRCm38)	Y742C	probably damaging	Het
Wdfy4	A	T	14: 33,096,005 (GRCm38)	S1473T	possibly damaging	Het
Zan	C	A	5: 137,415,018 (GRCm38)		probably benign	Het
Zc3h11a	G	A	1: 133,622,154 (GRCm38)	P695S	probably benign	Het
Zfyve9	A	C	4: 108,718,501 (GRCm38)	V461G	possibly damaging	Het
Zp3r	C	A	1: 130,619,414 (GRCm38)	E8D	possibly damaging	Het
Zp3r	A	G	1: 130,596,814 (GRCm38)	L164P	probably benign	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
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
R5898:Fat3	UTSW	9	15,938,461 (GRCm38)	missense	probably benign	0.15
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'- TGTCTCATGGTCCAGGTCCTTCAG -3'
(R):5'- GCCCAATCAAAGTGTCCGGTTCAG -3'

Sequencing Primer
(F):5'- TACCTTTTCAAGATGGGAATCTGAG -3'
(R):5'- AAGTGTCCGGTTCAGCATGG -3'

Posted On

2014-05-23