Mutagenetix > Incidental Mutations

Incidental Mutation 'R7063:Fat1'

548396

Institutional Source

Beutler Lab

Gene Symbol

Fat1

Ensembl Gene

ENSMUSG00000070047

Gene Name

FAT atypical cadherin 1

Synonyms

mFat1, Fath, 2310038E12Rik

MMRRC Submission

Accession Numbers

Genbank: NM_001081286

Is this an essential gene?

Essential (E-score: 1.000) question?

Stock #

R7063 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

44935447-45052257 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 45040775 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 3986 (T3986I)

Ref Sequence

ENSEMBL: ENSMUSP00000149194 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098796] [ENSMUST00000189017] [ENSMUST00000191428] [ENSMUST00000215588]

Predicted Effect

probably benign
Transcript: ENSMUST00000098796
AA Change: T3963I

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000096394
Gene: ENSMUSG00000070047
AA Change: T3963I

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
CA	62	148	3.05e-6	SMART
CA	172	256	3.29e-20	SMART
Blast:CA	277	382	5e-47	BLAST
CA	387	462	2.13e-5	SMART
CA	486	568	8.35e-22	SMART
CA	592	670	2.11e-2	SMART
CA	740	821	5.09e-26	SMART
CA	845	926	6.27e-26	SMART
CA	950	1031	4.07e-25	SMART
CA	1057	1138	5.13e-31	SMART
CA	1162	1244	8.79e-30	SMART
CA	1276	1351	2.06e-3	SMART
CA	1379	1456	1.63e-15	SMART
CA	1480	1562	3.29e-20	SMART
CA	1586	1667	2.34e-16	SMART
CA	1691	1765	1.16e-20	SMART
CA	1796	1879	6.27e-26	SMART
CA	1903	1979	1.47e-8	SMART
CA	2003	2081	2.65e-15	SMART
CA	2105	2181	2.14e-10	SMART
CA	2203	2283	9.82e-19	SMART
CA	2307	2390	7.54e-29	SMART
CA	2414	2492	3.29e-11	SMART
CA	2516	2596	6.48e-19	SMART
CA	2620	2703	3.48e-10	SMART
CA	2719	2809	2.26e-9	SMART
CA	2833	2918	8.08e-29	SMART
CA	2942	3023	5.99e-23	SMART
CA	3047	3125	2.63e-28	SMART
CA	3149	3230	2.79e-32	SMART
CA	3254	3335	5.25e-28	SMART
CA	3359	3440	4.46e-31	SMART
CA	3464	3545	1.25e-11	SMART
CA	3569	3641	5.67e-2	SMART
LamG	3853	3987	6.51e-36	SMART
EGF	4018	4052	8.57e-5	SMART
EGF	4057	4090	3.94e-4	SMART
EGF	4094	4127	4.29e-5	SMART
EGF_CA	4129	4165	1.81e-12	SMART
transmembrane domain	4182	4204	N/A	INTRINSIC
low complexity region	4308	4324	N/A	INTRINSIC
low complexity region	4436	4457	N/A	INTRINSIC
low complexity region	4472	4483	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000186342

Predicted Effect

unknown
Transcript: ENSMUST00000189017
AA Change: T3963I

Predicted Effect

probably benign
Transcript: ENSMUST00000191428
AA Change: T3963I

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000140596
Gene: ENSMUSG00000070047
AA Change: T3963I

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
CA	62	148	3.05e-6	SMART
CA	172	256	3.29e-20	SMART
Blast:CA	277	382	5e-47	BLAST
CA	387	462	2.13e-5	SMART
CA	486	568	8.35e-22	SMART
CA	592	670	2.11e-2	SMART
CA	740	821	5.09e-26	SMART
CA	845	926	6.27e-26	SMART
CA	950	1031	4.07e-25	SMART
CA	1057	1138	5.13e-31	SMART
CA	1162	1244	8.79e-30	SMART
CA	1276	1351	2.06e-3	SMART
CA	1379	1456	1.63e-15	SMART
CA	1480	1562	3.29e-20	SMART
CA	1586	1667	2.34e-16	SMART
CA	1691	1765	1.16e-20	SMART
CA	1796	1879	6.27e-26	SMART
CA	1903	1979	1.47e-8	SMART
CA	2003	2081	2.65e-15	SMART
CA	2105	2181	2.14e-10	SMART
CA	2203	2283	9.82e-19	SMART
CA	2307	2390	7.54e-29	SMART
CA	2414	2492	3.29e-11	SMART
CA	2516	2596	6.48e-19	SMART
CA	2620	2703	3.48e-10	SMART
CA	2719	2809	2.26e-9	SMART
CA	2833	2918	8.08e-29	SMART
CA	2942	3023	5.99e-23	SMART
CA	3047	3125	2.63e-28	SMART
CA	3149	3230	2.79e-32	SMART
CA	3254	3335	5.25e-28	SMART
CA	3359	3440	4.46e-31	SMART
CA	3464	3545	1.25e-11	SMART
CA	3569	3641	5.67e-2	SMART
LamG	3853	3987	6.51e-36	SMART
EGF	4018	4052	8.57e-5	SMART
EGF	4057	4090	3.94e-4	SMART
EGF	4094	4127	4.29e-5	SMART
EGF_CA	4129	4165	1.81e-12	SMART
transmembrane domain	4182	4204	N/A	INTRINSIC
low complexity region	4308	4324	N/A	INTRINSIC
low complexity region	4436	4457	N/A	INTRINSIC
low complexity region	4472	4483	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000215588
AA Change: T3986I

PolyPhen 2 Score 0.088 (Sensitivity: 0.93; Specificity: 0.85)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (43/43)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is an ortholog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has five epidermal growth factor (EGF)-like repeats and one laminin A-G domain. This gene is expressed at high levels in a number of fetal epithelia. Its product probably functions as an adhesion molecule and/or signaling receptor, and is likely to be important in developmental processes and cell communication. Transcript variants derived from alternative splicing and/or alternative promoter usage exist, but they have not been fully described. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit holoprosencephaly, anophthalmia, kidney defects and perinatal lethality. Mice homozygous for a hypomorphic allele exhibit altered shoulder girdle and facial musculature, retinal defects, abnormal inner earpatterning and kidney defects. [provided by MGI curators]

Allele List at MGI

All alleles(56) : Targeted, other(1) Gene trapped(55)

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap35	A	G	7: 16,565,113	V9A	probably benign	Het
Btbd6	A	G	12: 112,977,512	Y148C	probably damaging	Het
C130060K24Rik	A	G	6: 65,441,403		probably benign	Het
Casr	T	C	16: 36,494,574	I968V	probably benign	Het
Celf1	T	C	2: 91,012,844		probably null	Het
Chst2	G	T	9: 95,405,568	R242S	probably benign	Het
Clca3a1	T	A	3: 144,755,206	D228V	probably damaging	Het
Cwf19l2	A	G	9: 3,430,532	Y288C	probably benign	Het
Cyp2r1	A	G	7: 114,552,949	S49P	probably damaging	Het
Dnah5	A	G	15: 28,233,248	E251G	probably benign	Het
Eepd1	A	G	9: 25,483,036	R199G	possibly damaging	Het
Gbp4	G	A	5: 105,118,448	R576C	probably damaging	Het
Glp1r	A	G	17: 30,925,558	Y235C	probably damaging	Het
Gm31371	G	A	8: 19,903,412	C7Y		Het
Gm6408	T	C	5: 146,483,784	I158T	probably benign	Het
Gpr89	C	G	3: 96,875,698	R312P	probably damaging	Het
Idh2	A	G	7: 80,095,684	V403A	probably damaging	Het
Lclat1	A	G	17: 73,239,991	E301G	possibly damaging	Het
Lgmn	A	G	12: 102,402,678	Y181H	probably damaging	Het
Lgr5	T	C	10: 115,456,734	Y417C	probably damaging	Het
Man1a	G	T	10: 54,030,744	N311K	probably damaging	Het
Nat10	G	A	2: 103,748,077	L228F	probably benign	Het
Olfr1417	A	G	19: 11,828,184	F281L	probably damaging	Het
Olfr1445	A	G	19: 12,884,085	D68G	probably damaging	Het
Olfr476	C	A	7: 107,968,204	A269E	probably benign	Het
Olfr958	T	G	9: 39,550,115	Y252S	possibly damaging	Het
Pcmtd2	T	A	2: 181,854,983	Y130*	probably null	Het
Rapgef5	A	G	12: 117,689,129	D62G	possibly damaging	Het
Serpina3m	A	T	12: 104,391,467	I217L	probably benign	Het
Supt16	T	C	14: 52,172,048	R802G	possibly damaging	Het
Sypl2	A	T	3: 108,217,655	M130K	probably benign	Het
Tmtc2	A	T	10: 105,348,525	L503Q	probably damaging	Het
Ubald2	A	G	11: 116,434,617	Q60R	probably benign	Het
Vav1	C	T	17: 57,311,860	Q673*	probably null	Het
Vgll2	T	C	10: 52,027,976	S312P	probably benign	Het
Vmn1r191	C	T	13: 22,178,694	A297T	probably benign	Het
Vmn1r7	T	A	6: 57,024,433	I281F	possibly damaging	Het
Vmn2r108	T	C	17: 20,481,148	Y30C	probably damaging	Het
Vmn2r16	A	G	5: 109,363,784	N619S	probably damaging	Het
Vstm5	A	G	9: 15,239,253		probably benign	Het
Zfp7	A	G	15: 76,891,719	I654V	possibly damaging	Het
Zmat2	A	G	18: 36,796,574	N129S	probably null	Het

Other mutations in Fat1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00088:Fat1	APN	8	45024602	missense	possibly damaging	0.93
IGL00157:Fat1	APN	8	44951670	missense	possibly damaging	0.96
IGL00481:Fat1	APN	8	45050940	missense	probably benign	0.18
IGL00983:Fat1	APN	8	45033390	missense	probably damaging	1.00
IGL01089:Fat1	APN	8	45017857	missense	probably damaging	1.00
IGL01135:Fat1	APN	8	45024840	missense	probably damaging	1.00
IGL01143:Fat1	APN	8	45035532	missense	possibly damaging	0.72
IGL01155:Fat1	APN	8	45023949	missense	probably damaging	1.00
IGL01376:Fat1	APN	8	45026841	missense	probably benign	0.00
IGL01411:Fat1	APN	8	45026800	missense	probably damaging	1.00
IGL01443:Fat1	APN	8	45040576	missense	probably damaging	1.00
IGL01453:Fat1	APN	8	45051270	missense	probably damaging	1.00
IGL01606:Fat1	APN	8	45023049	missense	probably benign	0.26
IGL01622:Fat1	APN	8	45029555	missense	possibly damaging	0.64
IGL01623:Fat1	APN	8	45029555	missense	possibly damaging	0.64
IGL01672:Fat1	APN	8	45040700	missense	probably benign	0.05
IGL01735:Fat1	APN	8	45036239	missense	probably benign	0.07
IGL01793:Fat1	APN	8	44989112	missense	probably benign
IGL01820:Fat1	APN	8	45010502	missense	probably damaging	1.00
IGL01969:Fat1	APN	8	44952599	missense	probably damaging	0.98
IGL02012:Fat1	APN	8	45027540	missense	possibly damaging	0.95
IGL02227:Fat1	APN	8	45023659	missense	probably damaging	1.00
IGL02256:Fat1	APN	8	44950332	missense	probably damaging	1.00
IGL02273:Fat1	APN	8	44950331	missense	probably damaging	1.00
IGL02317:Fat1	APN	8	45025818	missense	probably benign	0.33
IGL02324:Fat1	APN	8	45040556	missense	probably damaging	1.00
IGL02336:Fat1	APN	8	44951583	missense	probably benign	0.16
IGL02442:Fat1	APN	8	44950323	missense	probably benign	0.02
IGL02486:Fat1	APN	8	45025072	missense	probably benign	0.16
IGL02551:Fat1	APN	8	45051398	missense	probably damaging	1.00
IGL02617:Fat1	APN	8	45035591	missense	probably benign	0.31
IGL02698:Fat1	APN	8	45023164	missense	probably benign
IGL02885:Fat1	APN	8	44989167	missense	probably benign	0.01
IGL02904:Fat1	APN	8	45040682	missense	probably damaging	1.00
IGL02953:Fat1	APN	8	45024314	missense	probably damaging	1.00
IGL03108:Fat1	APN	8	45023614	missense	probably damaging	1.00
IGL03153:Fat1	APN	8	45030123	missense	possibly damaging	0.83
IGL03183:Fat1	APN	8	44950586	missense	probably damaging	0.99
IGL03327:Fat1	APN	8	44950468	missense	probably damaging	1.00
IGL03405:Fat1	APN	8	45025241	missense	probably damaging	1.00
Laggardly	UTSW	8	45044464	missense	probably damaging	1.00
only_a_test	UTSW	8	45024495	missense	probably benign	0.41
Shrinkage	UTSW	8	45018037	missense	probably damaging	1.00
F5493:Fat1	UTSW	8	45025480	missense	probably damaging	0.99
G1citation:Fat1	UTSW	8	45026404	missense	probably damaging	1.00
I2289:Fat1	UTSW	8	45024996	missense	probably benign	0.01
IGL02837:Fat1	UTSW	8	45017434	missense	probably benign	0.00
PIT4283001:Fat1	UTSW	8	45029540	missense	probably damaging	1.00
PIT4283001:Fat1	UTSW	8	45037207	missense	probably damaging	1.00
PIT4576001:Fat1	UTSW	8	45024645	missense	probably damaging	1.00
R0040:Fat1	UTSW	8	45026404	missense	probably damaging	1.00
R0040:Fat1	UTSW	8	45026404	missense	probably damaging	1.00
R0078:Fat1	UTSW	8	44953299	missense	probably damaging	1.00
R0197:Fat1	UTSW	8	45026553	missense	probably benign	0.00
R0328:Fat1	UTSW	8	45023790	missense	probably benign	0.35
R0367:Fat1	UTSW	8	45024313	missense	probably damaging	1.00
R0371:Fat1	UTSW	8	44951892	missense	probably damaging	1.00
R0380:Fat1	UTSW	8	45010123	missense	probably damaging	0.97
R0389:Fat1	UTSW	8	44950348	missense	probably benign	0.00
R0433:Fat1	UTSW	8	45024649	missense	possibly damaging	0.51
R0456:Fat1	UTSW	8	45029534	missense	probably damaging	1.00
R0494:Fat1	UTSW	8	44950542	missense	probably damaging	1.00
R0506:Fat1	UTSW	8	45022951	missense	probably damaging	0.99
R0512:Fat1	UTSW	8	44951332	nonsense	probably null
R0624:Fat1	UTSW	8	45051168	missense	possibly damaging	0.46
R0701:Fat1	UTSW	8	45026553	missense	probably benign	0.00
R0723:Fat1	UTSW	8	45026749	missense	probably damaging	1.00
R0787:Fat1	UTSW	8	45040555	missense	probably damaging	1.00
R0788:Fat1	UTSW	8	45023983	missense	probably benign	0.27
R0862:Fat1	UTSW	8	45018037	missense	probably damaging	1.00
R0864:Fat1	UTSW	8	45018037	missense	probably damaging	1.00
R0907:Fat1	UTSW	8	45026598	missense	probably benign	0.08
R0962:Fat1	UTSW	8	45033326	splice site	probably benign
R1051:Fat1	UTSW	8	45044506	missense	probably damaging	1.00
R1156:Fat1	UTSW	8	45039890	missense	possibly damaging	0.94
R1237:Fat1	UTSW	8	45044279	missense	probably damaging	1.00
R1468:Fat1	UTSW	8	45010545	missense	probably damaging	1.00
R1468:Fat1	UTSW	8	45010545	missense	probably damaging	1.00
R1478:Fat1	UTSW	8	45025622	missense	probably damaging	0.99
R1482:Fat1	UTSW	8	44953244	missense	probably benign	0.04
R1496:Fat1	UTSW	8	45033390	missense	probably damaging	1.00
R1498:Fat1	UTSW	8	45025484	nonsense	probably null
R1508:Fat1	UTSW	8	45026862	missense	probably benign	0.01
R1577:Fat1	UTSW	8	45023383	missense	probably benign	0.30
R1646:Fat1	UTSW	8	45018042	missense	probably damaging	1.00
R1652:Fat1	UTSW	8	45025178	nonsense	probably null
R1656:Fat1	UTSW	8	45025530	nonsense	probably null
R1662:Fat1	UTSW	8	44953164	missense	probably benign	0.20
R1672:Fat1	UTSW	8	45036835	missense	probably damaging	1.00
R1704:Fat1	UTSW	8	45025576	missense	probably damaging	1.00
R1708:Fat1	UTSW	8	45024792	missense	probably damaging	1.00
R1710:Fat1	UTSW	8	45010482	missense	probably benign	0.00
R1812:Fat1	UTSW	8	45036803	missense	probably damaging	1.00
R1872:Fat1	UTSW	8	44953304	missense	probably benign	0.01
R1872:Fat1	UTSW	8	45038349	missense	probably damaging	1.00
R1883:Fat1	UTSW	8	45051147	missense	probably benign	0.17
R1893:Fat1	UTSW	8	45023856	missense	probably damaging	1.00
R1930:Fat1	UTSW	8	45044228	missense	possibly damaging	0.91
R1931:Fat1	UTSW	8	45044228	missense	possibly damaging	0.91
R1952:Fat1	UTSW	8	45033926	missense	probably benign	0.00
R1957:Fat1	UTSW	8	45040682	missense	probably damaging	1.00
R1999:Fat1	UTSW	8	44952393	missense	probably damaging	0.96
R2019:Fat1	UTSW	8	45023746	missense	probably damaging	1.00
R2062:Fat1	UTSW	8	45024332	missense	probably damaging	1.00
R2062:Fat1	UTSW	8	45026704	missense	probably damaging	1.00
R2117:Fat1	UTSW	8	45037463	missense	probably benign	0.33
R2196:Fat1	UTSW	8	45024646	missense	probably damaging	1.00
R2204:Fat1	UTSW	8	45023700	missense	probably damaging	1.00
R2256:Fat1	UTSW	8	44950371	missense	probably damaging	1.00
R2257:Fat1	UTSW	8	44950371	missense	probably damaging	1.00
R2409:Fat1	UTSW	8	45040530	splice site	probably benign
R2416:Fat1	UTSW	8	45026383	missense	probably damaging	1.00
R3021:Fat1	UTSW	8	45044011	missense	probably damaging	1.00
R3108:Fat1	UTSW	8	45045173	splice site	probably null
R3109:Fat1	UTSW	8	45045173	splice site	probably null
R3196:Fat1	UTSW	8	44951868	missense	probably benign	0.00
R3683:Fat1	UTSW	8	45017938	missense	probably benign
R3732:Fat1	UTSW	8	44953269	missense	possibly damaging	0.85
R3732:Fat1	UTSW	8	44953269	missense	possibly damaging	0.85
R3733:Fat1	UTSW	8	44953269	missense	possibly damaging	0.85
R3753:Fat1	UTSW	8	45025479	missense	probably damaging	0.97
R3905:Fat1	UTSW	8	45023035	missense	probably benign	0.00
R3907:Fat1	UTSW	8	45023035	missense	probably benign	0.00
R3908:Fat1	UTSW	8	45023035	missense	probably benign	0.00
R4060:Fat1	UTSW	8	45025481	missense	probably benign	0.09
R4061:Fat1	UTSW	8	45025481	missense	probably benign	0.09
R4062:Fat1	UTSW	8	45025481	missense	probably benign	0.09
R4063:Fat1	UTSW	8	45025481	missense	probably benign	0.09
R4078:Fat1	UTSW	8	44989122	missense	probably damaging	0.99
R4105:Fat1	UTSW	8	45036851	missense	probably damaging	1.00
R4118:Fat1	UTSW	8	45010437	missense	probably damaging	1.00
R4118:Fat1	UTSW	8	45050944	missense	probably damaging	1.00
R4161:Fat1	UTSW	8	45036787	missense	probably benign	0.00
R4364:Fat1	UTSW	8	44952962	missense	probably benign	0.01
R4394:Fat1	UTSW	8	44952346	missense	probably damaging	0.98
R4395:Fat1	UTSW	8	44952346	missense	probably damaging	0.98
R4396:Fat1	UTSW	8	44952346	missense	probably damaging	0.98
R4412:Fat1	UTSW	8	45023599	missense	probably damaging	0.99
R4542:Fat1	UTSW	8	45041894	missense	probably damaging	1.00
R4591:Fat1	UTSW	8	45026242	missense	probably benign
R4606:Fat1	UTSW	8	44950683	missense	possibly damaging	0.47
R4612:Fat1	UTSW	8	45025147	missense	probably damaging	1.00
R4730:Fat1	UTSW	8	45033477	missense	probably damaging	1.00
R4778:Fat1	UTSW	8	45038326	missense	probably benign	0.04
R4824:Fat1	UTSW	8	44989114	missense	probably damaging	1.00
R4829:Fat1	UTSW	8	45036162	missense	probably damaging	1.00
R4832:Fat1	UTSW	8	45013065	missense	possibly damaging	0.95
R4849:Fat1	UTSW	8	45012970	missense	probably benign	0.15
R4896:Fat1	UTSW	8	44951280	missense	possibly damaging	0.68
R4927:Fat1	UTSW	8	45022963	missense	probably damaging	0.96
R4941:Fat1	UTSW	8	45036275	missense	probably benign	0.00
R5011:Fat1	UTSW	8	45031263	critical splice acceptor site	probably null
R5040:Fat1	UTSW	8	45023380	missense	probably damaging	1.00
R5112:Fat1	UTSW	8	45024282	missense	probably damaging	1.00
R5151:Fat1	UTSW	8	44951814	missense	possibly damaging	0.74
R5161:Fat1	UTSW	8	44952512	missense	probably benign	0.00
R5162:Fat1	UTSW	8	45025809	missense	probably benign	0.02
R5353:Fat1	UTSW	8	45036131	missense	probably benign	0.13
R5425:Fat1	UTSW	8	45025885	missense	possibly damaging	0.64
R5458:Fat1	UTSW	8	45013053	missense	probably damaging	1.00
R5479:Fat1	UTSW	8	45036875	missense	possibly damaging	0.88
R5543:Fat1	UTSW	8	45023479	missense	probably damaging	0.99
R5569:Fat1	UTSW	8	45039836	missense	probably damaging	0.98
R5610:Fat1	UTSW	8	44953072	nonsense	probably null
R5734:Fat1	UTSW	8	45051209	missense	probably damaging	0.99
R5832:Fat1	UTSW	8	45017423	missense	possibly damaging	0.65
R5860:Fat1	UTSW	8	45051129	missense	probably benign
R5886:Fat1	UTSW	8	45027681	critical splice donor site	probably null
R5886:Fat1	UTSW	8	45033395	missense	probably damaging	1.00
R5919:Fat1	UTSW	8	45026873	critical splice donor site	probably null
R5930:Fat1	UTSW	8	45044036	missense	probably benign	0.10
R5960:Fat1	UTSW	8	45033368	missense	probably damaging	1.00
R5988:Fat1	UTSW	8	45029456	missense	probably benign	0.00
R6166:Fat1	UTSW	8	44952485	missense	probably damaging	1.00
R6184:Fat1	UTSW	8	44953392	missense	probably benign	0.00
R6208:Fat1	UTSW	8	45027613	missense	probably damaging	0.99
R6351:Fat1	UTSW	8	45033495	missense	probably damaging	1.00
R6391:Fat1	UTSW	8	44952342	missense	possibly damaging	0.69
R6701:Fat1	UTSW	8	44950681	missense	probably damaging	1.00
R6702:Fat1	UTSW	8	44953046	missense	probably benign	0.28
R6703:Fat1	UTSW	8	44953046	missense	probably benign	0.28
R6704:Fat1	UTSW	8	45024373	missense	probably damaging	1.00
R6822:Fat1	UTSW	8	45026404	missense	probably damaging	1.00
R6852:Fat1	UTSW	8	45035598	missense	possibly damaging	0.46
R6863:Fat1	UTSW	8	45044464	missense	probably damaging	1.00
R6885:Fat1	UTSW	8	44952452	missense	possibly damaging	0.94
R6912:Fat1	UTSW	8	45051023	missense	probably benign	0.00
R6927:Fat1	UTSW	8	45024495	missense	probably benign	0.41
R6964:Fat1	UTSW	8	45043945	missense	probably damaging	1.00
R7010:Fat1	UTSW	8	44953349	nonsense	probably null
R7062:Fat1	UTSW	8	44950216	start codon destroyed	probably null	0.99
R7071:Fat1	UTSW	8	44989108	missense	possibly damaging	0.67
R7117:Fat1	UTSW	8	45031468	missense	probably damaging	0.98
R7146:Fat1	UTSW	8	44950925	missense	probably benign
R7210:Fat1	UTSW	8	45023503	missense	probably damaging	1.00
R7227:Fat1	UTSW	8	45010609	missense	probably benign	0.08
R7270:Fat1	UTSW	8	45037438	missense	probably damaging	1.00
R7373:Fat1	UTSW	8	45026665	missense	probably damaging	1.00
R7390:Fat1	UTSW	8	44952474	missense	possibly damaging	0.81
R7465:Fat1	UTSW	8	45044152	missense	probably benign	0.35
R7476:Fat1	UTSW	8	45031274	missense	probably benign	0.01
R7483:Fat1	UTSW	8	45023160	missense	probably benign	0.13
R7484:Fat1	UTSW	8	45036184	missense	probably damaging	1.00
R7526:Fat1	UTSW	8	45023427	missense	probably damaging	1.00
R7549:Fat1	UTSW	8	44988994	missense	probably benign	0.01
R7554:Fat1	UTSW	8	45037165	missense	possibly damaging	0.88
R7620:Fat1	UTSW	8	45009850	missense	possibly damaging	0.95
R7652:Fat1	UTSW	8	44953299	missense	probably damaging	1.00
R7694:Fat1	UTSW	8	44988930	critical splice acceptor site	probably null
R7746:Fat1	UTSW	8	44951633	missense	probably damaging	0.96
R7762:Fat1	UTSW	8	45023322	missense	probably damaging	1.00
R7762:Fat1	UTSW	8	45037337	missense	probably damaging	0.99
R7782:Fat1	UTSW	8	44950911	missense	probably damaging	1.00
R7801:Fat1	UTSW	8	45042223	missense	probably damaging	1.00
R7807:Fat1	UTSW	8	45041973	missense	probably damaging	1.00
R7821:Fat1	UTSW	8	44950224	missense	probably benign
R7869:Fat1	UTSW	8	45051222	missense	probably benign	0.02
R8034:Fat1	UTSW	8	44951691	missense	probably benign	0.28
R8094:Fat1	UTSW	8	44952702	missense	probably damaging	0.98
R8111:Fat1	UTSW	8	45026058	missense	possibly damaging	0.94
R8220:Fat1	UTSW	8	45039956	missense	probably null
R8221:Fat1	UTSW	8	44953353	missense
R8233:Fat1	UTSW	8	44952018	missense
R8250:Fat1	UTSW	8	44953299	missense	probably damaging	1.00
R8279:Fat1	UTSW	8	45030347	critical splice donor site	probably null
R8726:Fat1	UTSW	8	45024169	missense	probably benign	0.23
RF001:Fat1	UTSW	8	44988966	missense	probably benign	0.00
X0064:Fat1	UTSW	8	45025734	missense	possibly damaging	0.58
Z1088:Fat1	UTSW	8	45023807	missense	possibly damaging	0.88
Z1176:Fat1	UTSW	8	44950598	missense	probably benign
Z1176:Fat1	UTSW	8	45023596	missense	possibly damaging	0.65
Z1176:Fat1	UTSW	8	45036838	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGCATTCAGGTCAACGACG -3'
(R):5'- TCACGAAGCCTACCTCCAGTAG -3'

Sequencing Primer
(F):5'- TTCAGGTCAACGACGGGCAG -3'
(R):5'- GGGATTGCAAACGCCTCCATTC -3'

Posted On

2019-05-13