Mutagenetix > Incidental Mutation

Incidental Mutation 'R5196:Fbxw19'

400258

Institutional Source

Beutler Lab

Gene Symbol

Fbxw19

Ensembl Gene

ENSMUSG00000074061

Gene Name

F-box and WD-40 domain protein 19

Synonyms

MMRRC Submission

042772-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.066) question?

Stock #

R5196 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

109476654-109495875 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 109484428 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 234 (Y234C)

Ref Sequence

ENSEMBL: ENSMUSP00000075918 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076617]

AlphaFold

Q8C2W8

Predicted Effect

probably benign
Transcript: ENSMUST00000076617
AA Change: Y234C

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000075918
Gene: ENSMUSG00000074061
AA Change: Y234C

Domain	Start	End	E-Value	Type
FBOX	5	45	1.8e-6	SMART
SCOP:d1gxra_	87	284	3e-5	SMART
Blast:WD40	137	176	8e-8	BLAST

Meta Mutation Damage Score

0.0798

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.3%

Validation Efficiency

100% (62/62)

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001O22Rik	T	C	2: 30,796,438	T281A	possibly damaging	Het
4930503B20Rik	A	G	3: 146,646,263		probably benign	Het
6330409D20Rik	T	A	2: 32,740,540		probably benign	Het
Afg3l2	G	T	18: 67,421,259	L458M	probably damaging	Het
Amigo2	A	G	15: 97,246,061	F160S	probably damaging	Het
Arcn1	A	T	9: 44,760,027	L68M	probably damaging	Het
Arhgef25	A	G	10: 127,185,109	S303P	probably damaging	Het
Asph	A	T	4: 9,607,830	S163T	probably damaging	Het
BC003331	T	A	1: 150,382,389	D165V	probably damaging	Het
Birc6	T	C	17: 74,606,141		probably benign	Het
Ccm2	G	A	11: 6,561,181		probably benign	Het
Cdc42bpa	T	C	1: 180,072,413	V431A	probably benign	Het
Cdh7	T	A	1: 110,138,000	M668K	probably damaging	Het
Cfap43	A	T	19: 47,825,925	W157R	probably damaging	Het
Chrm5	T	C	2: 112,480,384	Y129C	probably damaging	Het
Chrna5	A	G	9: 55,006,519	I421V	possibly damaging	Het
Clk1	T	A	1: 58,414,613	T301S	probably benign	Het
Col6a3	G	T	1: 90,816,538		probably null	Het
Eml2	G	A	7: 19,201,163	V432I	probably damaging	Het
Fam198a	T	G	9: 121,965,661	S294A	probably benign	Het
Fgd4	T	A	16: 16,484,142	N183I	probably benign	Het
Fnip2	T	C	3: 79,572,538		probably benign	Het
Gm9847	T	A	12: 14,495,015		noncoding transcript	Het
H2-T23	A	G	17: 36,032,607		probably null	Het
Hdlbp	T	C	1: 93,420,193	E613G	probably damaging	Het
Kat6a	G	A	8: 22,911,713	R366H	probably damaging	Het
Kctd4	A	G	14: 75,962,687	T33A	probably benign	Het
Klrb1c	T	A	6: 128,780,299	S268C	probably benign	Het
Lgr6	C	T	1: 134,994,010	A199T	probably damaging	Het
Lrrfip1	A	G	1: 91,114,608	E245G	probably damaging	Het
Mast3	A	T	8: 70,788,245	I220N	probably damaging	Het
Mfap3	A	G	11: 57,529,813	T207A	probably damaging	Het
Mtdh	G	T	15: 34,118,004	K75N	probably damaging	Het
Mybpc1	A	G	10: 88,536,351	Y806H	probably damaging	Het
Ntng1	T	C	3: 109,934,983	D158G	probably damaging	Het
Olfr1176	A	G	2: 88,339,748	Y61C	possibly damaging	Het
Olfr812	T	A	10: 129,842,781	D87V	possibly damaging	Het
Pask	A	G	1: 93,310,083		probably benign	Het
Pif1	G	T	9: 65,588,092	A95S	probably benign	Het
Plppr2	T	C	9: 21,941,132	F104S	probably damaging	Het
Prmt9	G	A	8: 77,564,997	V333M	probably benign	Het
Pten	A	T	19: 32,815,497	M239L	probably benign	Het
Rb1cc1	A	G	1: 6,234,230	D67G	probably damaging	Het
Reg2	T	A	6: 78,405,547	L12*	probably null	Het
Rufy4	T	C	1: 74,147,663	C537R	probably damaging	Het
Slc5a7	C	A	17: 54,281,722		probably null	Het
Tcaf3	G	T	6: 42,593,715	R368S	probably benign	Het
Tfcp2	A	G	15: 100,520,714	V189A	probably damaging	Het
Uhrf1bp1	A	G	17: 27,856,763	I5V	probably benign	Het
Wdr12	T	C	1: 60,087,084	S191G	probably damaging	Het
Zfp536	G	A	7: 37,480,760	R807W	probably damaging	Het
Zfp647	G	A	15: 76,912,085	P125L	probably damaging	Het

Other mutations in Fbxw19

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01094:Fbxw19	APN	9	109493546	missense	probably benign	0.03
IGL01878:Fbxw19	APN	9	109483279	splice site	probably benign
IGL02622:Fbxw19	APN	9	109493534	missense	probably benign	0.22
IGL02752:Fbxw19	APN	9	109494641	missense	probably benign	0.07
IGL02795:Fbxw19	APN	9	109495818	missense	possibly damaging	0.52
IGL03401:Fbxw19	APN	9	109494970	critical splice donor site	probably null
R0402:Fbxw19	UTSW	9	109484425	missense	probably benign	0.00
R0423:Fbxw19	UTSW	9	109486066	missense	probably benign	0.22
R0466:Fbxw19	UTSW	9	109478649	missense	probably benign	0.32
R0513:Fbxw19	UTSW	9	109481553	splice site	probably null
R1538:Fbxw19	UTSW	9	109494988	missense	probably damaging	1.00
R1768:Fbxw19	UTSW	9	109494772	nonsense	probably null
R1869:Fbxw19	UTSW	9	109482032	missense	probably benign	0.11
R1933:Fbxw19	UTSW	9	109481650	missense	probably benign	0.20
R1960:Fbxw19	UTSW	9	109485936	missense	probably benign
R2288:Fbxw19	UTSW	9	109493568	missense	probably damaging	0.99
R2877:Fbxw19	UTSW	9	109485970	missense	probably damaging	1.00
R2878:Fbxw19	UTSW	9	109485970	missense	probably damaging	1.00
R4778:Fbxw19	UTSW	9	109494646	missense	probably damaging	1.00
R5192:Fbxw19	UTSW	9	109484428	missense	probably benign	0.01
R5533:Fbxw19	UTSW	9	109486065	missense	probably benign	0.00
R6107:Fbxw19	UTSW	9	109495766	missense	probably damaging	1.00
R6333:Fbxw19	UTSW	9	109494683	missense	probably benign	0.01
R6820:Fbxw19	UTSW	9	109482011	missense	probably benign	0.07
R7631:Fbxw19	UTSW	9	109482001	missense	probably damaging	1.00
R7651:Fbxw19	UTSW	9	109494646	missense	probably damaging	1.00
R8669:Fbxw19	UTSW	9	109484414	missense	probably benign	0.26
R8678:Fbxw19	UTSW	9	109483308	nonsense	probably null
R9121:Fbxw19	UTSW	9	109495822	missense	probably damaging	1.00
R9256:Fbxw19	UTSW	9	109481573	missense	probably damaging	0.99
R9324:Fbxw19	UTSW	9	109484372	missense	possibly damaging	0.57
R9393:Fbxw19	UTSW	9	109495805	missense	probably damaging	1.00
R9408:Fbxw19	UTSW	9	109486033	missense	probably benign
Z1176:Fbxw19	UTSW	9	109481582	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TCTTTCCTGACTGTAGGATGGC -3'
(R):5'- CCTCATTACTGGACTTGGAGAC -3'

Sequencing Primer
(F):5'- CCTGACTGTAGGATGGCTTTTC -3'
(R):5'- TCATTACTGGACTTGGAGACACAGTG -3'

Posted On

2016-07-06