Mutagenetix > Incidental Mutation

Incidental Mutation 'R8145:Fbxw15'

632758

Institutional Source

Beutler Lab

Gene Symbol

Fbxw15

Ensembl Gene

ENSMUSG00000074060

Gene Name

F-box and WD-40 domain protein 15

Synonyms

Fbxo12J

MMRRC Submission

067573-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

R8145 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

109381670-109397330 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 109384658 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 381 (C381S)

Ref Sequence

ENSEMBL: ENSMUSP00000058175 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056745] [ENSMUST00000198112] [ENSMUST00000198397]

AlphaFold

L7N1X6

Predicted Effect

probably benign
Transcript: ENSMUST00000056745
AA Change: C381S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000058175
Gene: ENSMUSG00000074060
AA Change: C381S

Domain	Start	End	E-Value	Type
FBOX	8	45	3.25e-4	SMART
SCOP:d1flga_	73	413	3e-7	SMART
Blast:WD40	137	176	5e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000198112

SMART Domains

Protein: ENSMUSP00000142894
Gene: ENSMUSG00000074060

Domain	Start	End	E-Value	Type
FBOX	8	45	2.1e-6	SMART
SCOP:d1tbga_	73	196	3e-5	SMART
Blast:WD40	84	123	1e-5	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000198397

SMART Domains

Protein: ENSMUSP00000143385
Gene: ENSMUSG00000074060

Domain	Start	End	E-Value	Type
FBOX	8	45	3.25e-4	SMART
SCOP:d1tbga_	116	240	1e-3	SMART
Blast:WD40	137	176	6e-6	BLAST

Coding Region Coverage

1x: 99.7%
3x: 99.5%
10x: 97.9%
20x: 90.4%

Validation Efficiency

100% (79/79)

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alg6	A	T	4: 99,634,564 (GRCm39)	D273V	probably damaging	Het
Ankk1	T	A	9: 49,327,097 (GRCm39)	H694L	possibly damaging	Het
Asb7	G	T	7: 66,309,696 (GRCm39)	N173K	probably benign	Het
Atp10b	A	T	11: 43,092,949 (GRCm39)	Q428L	probably damaging	Het
Bag3	A	G	7: 128,147,612 (GRCm39)	E409G	possibly damaging	Het
Bltp1	T	C	3: 37,052,416 (GRCm39)	S3039P	probably damaging	Het
Bpifb2	T	A	2: 153,733,232 (GRCm39)	V398E	probably damaging	Het
Btf3l4b	A	T	13: 96,217,649 (GRCm39)	D63E	probably benign	Het
Ccr6	T	C	17: 8,474,945 (GRCm39)	V50A	probably benign	Het
Cdcp3	G	T	7: 130,898,045 (GRCm39)	V2088L	unknown	Het
Cdx1	T	C	18: 61,152,995 (GRCm39)	N204D	probably damaging	Het
Ciao1	T	C	2: 127,087,726 (GRCm39)	D203G	possibly damaging	Het
Cldn7	A	T	11: 69,856,892 (GRCm39)	Y47F	possibly damaging	Het
Col6a1	A	T	10: 76,559,305 (GRCm39)	D110E	possibly damaging	Het
Cpne6	C	A	14: 55,752,025 (GRCm39)	Q261K	probably benign	Het
Crebbp	T	C	16: 3,946,389 (GRCm39)	T497A	probably benign	Het
Cyp2s1	A	G	7: 25,507,467 (GRCm39)		probably null	Het
Ddx42	A	T	11: 106,130,887 (GRCm39)	I454F	possibly damaging	Het
Ddx5	G	T	11: 106,672,911 (GRCm39)	A538E	probably benign	Het
Dnajb1	T	A	8: 84,336,944 (GRCm39)	V238D	probably damaging	Het
Dntt	A	G	19: 41,044,224 (GRCm39)	Y463C	probably damaging	Het
Eif4b	A	G	15: 102,001,423 (GRCm39)	T437A	unknown	Het
Eppk1	T	C	15: 75,990,900 (GRCm39)	T1994A	possibly damaging	Het
Fosl2	T	A	5: 32,310,412 (GRCm39)	V287D	probably damaging	Het
Gdpd4	A	G	7: 97,690,077 (GRCm39)	T590A	probably benign	Het
Gm49368	A	G	7: 127,712,487 (GRCm39)	E877G	probably null	Het
Grin2b	C	T	6: 135,709,497 (GRCm39)	A1350T	probably benign	Het
Gzmk	A	G	13: 113,308,430 (GRCm39)	L257P	probably damaging	Het
Has2	T	A	15: 56,545,175 (GRCm39)	K142N	probably benign	Het
Hectd1	T	C	12: 51,831,016 (GRCm39)	E944G	possibly damaging	Het
Hmcn1	T	C	1: 150,629,411 (GRCm39)	R949G	probably benign	Het
Hmcn2	A	G	2: 31,313,117 (GRCm39)	E3442G	probably damaging	Het
Irf9	T	A	14: 55,843,255 (GRCm39)	C152*	probably null	Het
Itga3	A	G	11: 94,943,290 (GRCm39)	W936R	probably damaging	Het
Klhl11	G	T	11: 100,354,740 (GRCm39)	D360E	probably damaging	Het
Lnx1	G	A	5: 74,846,060 (GRCm39)	T130I	probably benign	Het
Lrrc36	C	T	8: 106,170,396 (GRCm39)	P82L	probably damaging	Het
Map4k4	T	C	1: 40,039,694 (GRCm39)	C29R		Het
Mki67	T	C	7: 135,296,065 (GRCm39)	K2990E	probably benign	Het
Mnt	G	A	11: 74,733,799 (GRCm39)	A477T	unknown	Het
Mroh9	A	G	1: 162,890,096 (GRCm39)	S214P	probably benign	Het
Mrps18b	C	A	17: 36,225,293 (GRCm39)	R94L	possibly damaging	Het
Myh6	T	A	14: 55,191,382 (GRCm39)	I820F	probably benign	Het
Nphp3	A	G	9: 103,913,050 (GRCm39)	T943A	probably benign	Het
Or51a25	C	A	7: 102,372,937 (GRCm39)	L253F	probably damaging	Het
Or52b4i	A	G	7: 102,191,830 (GRCm39)	H229R	probably benign	Het
Papolb	T	C	5: 142,514,353 (GRCm39)	D430G	probably benign	Het
Pdzd2	T	C	15: 12,407,458 (GRCm39)	H334R	probably benign	Het
Pkd1l2	T	A	8: 117,781,742 (GRCm39)	M768L	probably benign	Het
Pklr	G	T	3: 89,052,795 (GRCm39)	R547L	probably benign	Het
Pla2g4a	T	C	1: 149,716,394 (GRCm39)	Y697C	probably benign	Het
Prkcd	T	C	14: 30,324,019 (GRCm39)	T435A	probably benign	Het
Rfx1	C	T	8: 84,800,657 (GRCm39)	P86L	probably benign	Het
Rnf19b	C	A	4: 128,977,862 (GRCm39)	A693D	probably benign	Het
Scn9a	A	G	2: 66,317,754 (GRCm39)	I1578T	probably damaging	Het
Slamf9	A	G	1: 172,303,942 (GRCm39)	S96G	probably benign	Het
Slc17a8	T	C	10: 89,412,233 (GRCm39)	D584G	probably benign	Het
Slc1a7	G	A	4: 107,869,473 (GRCm39)	V513M	probably benign	Het
Slc2a7	C	A	4: 150,252,818 (GRCm39)	T486K	probably damaging	Het
Slc6a20a	G	A	9: 123,466,065 (GRCm39)	A592V	probably damaging	Het
Spz1	T	C	13: 92,711,609 (GRCm39)	D289G	probably benign	Het
Sspo	G	A	6: 48,444,683 (GRCm39)	C2226Y	possibly damaging	Het
Taf4b	T	G	18: 14,963,085 (GRCm39)	D608E	probably damaging	Het
Tagap1	A	T	17: 7,223,526 (GRCm39)	I390N	probably damaging	Het
Tcp11l2	A	G	10: 84,444,480 (GRCm39)	N430D	probably damaging	Het
Thsd7b	T	C	1: 129,688,036 (GRCm39)	L649P	probably damaging	Het
Tmprss15	C	T	16: 78,757,473 (GRCm39)	G956R	probably damaging	Het
Tnc	G	T	4: 63,935,716 (GRCm39)	Q407K	probably benign	Het
Tti1	C	A	2: 157,849,509 (GRCm39)	E577*	probably null	Het
Vmn2r79	A	T	7: 86,686,862 (GRCm39)	M748L	probably benign	Het
Zbtb37	C	T	1: 160,847,654 (GRCm39)	R451Q	probably damaging	Het
Zfp1002	T	C	2: 150,096,455 (GRCm39)	K325E	probably benign	Het
Zfp566	A	T	7: 29,777,785 (GRCm39)	I132N	probably benign	Het
Zik1	C	T	7: 10,223,930 (GRCm39)	G389E	probably damaging	Het
Zzef1	A	T	11: 72,799,295 (GRCm39)	K2382*	probably null	Het

Other mutations in Fbxw15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02094:Fbxw15	APN	9	109,387,308 (GRCm39)	missense	possibly damaging	0.87
IGL02239:Fbxw15	APN	9	109,388,905 (GRCm39)	missense	probably benign	0.01
IGL02343:Fbxw15	APN	9	109,381,723 (GRCm39)	utr 3 prime	probably benign
IGL02748:Fbxw15	APN	9	109,387,278 (GRCm39)	missense	possibly damaging	0.66
IGL03206:Fbxw15	APN	9	109,394,430 (GRCm39)	missense	possibly damaging	0.90
IGL03370:Fbxw15	APN	9	109,384,219 (GRCm39)	missense	probably benign	0.00
lagging	UTSW	9	109,384,741 (GRCm39)	splice site	probably null
R0321:Fbxw15	UTSW	9	109,394,453 (GRCm39)	missense	probably benign	0.03
R0742:Fbxw15	UTSW	9	109,384,624 (GRCm39)	splice site	probably null
R1141:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1143:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1276:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1282:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1283:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1321:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1324:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1341:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1716:Fbxw15	UTSW	9	109,386,204 (GRCm39)	missense	probably benign	0.00
R1750:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1757:Fbxw15	UTSW	9	109,386,347 (GRCm39)	missense	probably damaging	0.99
R1765:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1799:Fbxw15	UTSW	9	109,387,314 (GRCm39)	missense	probably damaging	0.99
R1826:Fbxw15	UTSW	9	109,388,782 (GRCm39)	splice site	probably null
R1897:Fbxw15	UTSW	9	109,387,271 (GRCm39)	nonsense	probably null
R2237:Fbxw15	UTSW	9	109,384,303 (GRCm39)	missense	probably damaging	0.99
R2346:Fbxw15	UTSW	9	109,394,500 (GRCm39)	missense	probably damaging	1.00
R4391:Fbxw15	UTSW	9	109,397,300 (GRCm39)	start gained	probably benign
R4392:Fbxw15	UTSW	9	109,397,300 (GRCm39)	start gained	probably benign
R4812:Fbxw15	UTSW	9	109,388,990 (GRCm39)	missense	probably benign	0.01
R5198:Fbxw15	UTSW	9	109,387,242 (GRCm39)	missense	probably benign	0.00
R5278:Fbxw15	UTSW	9	109,384,752 (GRCm39)	missense	probably benign	0.03
R5541:Fbxw15	UTSW	9	109,394,498 (GRCm39)	missense	probably benign	0.23
R5899:Fbxw15	UTSW	9	109,384,741 (GRCm39)	splice site	probably null
R5975:Fbxw15	UTSW	9	109,384,320 (GRCm39)	missense	probably damaging	1.00
R6065:Fbxw15	UTSW	9	109,397,246 (GRCm39)	missense	probably damaging	1.00
R6285:Fbxw15	UTSW	9	109,386,234 (GRCm39)	missense	probably benign	0.09
R7357:Fbxw15	UTSW	9	109,387,308 (GRCm39)	missense	probably benign	0.28
R7781:Fbxw15	UTSW	9	109,386,330 (GRCm39)	missense	possibly damaging	0.71
R8182:Fbxw15	UTSW	9	109,384,778 (GRCm39)	missense	probably benign	0.00
R8272:Fbxw15	UTSW	9	109,388,828 (GRCm39)	missense	probably benign	0.18
R8713:Fbxw15	UTSW	9	109,384,667 (GRCm39)	missense	possibly damaging	0.93
R9069:Fbxw15	UTSW	9	109,394,468 (GRCm39)	nonsense	probably null
R9496:Fbxw15	UTSW	9	109,397,291 (GRCm39)	missense	probably benign	0.01
X0026:Fbxw15	UTSW	9	109,387,255 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AGGCTGGAGTCAATGTCAGATC -3'
(R):5'- TGGACTTGTCAGACCAATGGAC -3'

Sequencing Primer
(F):5'- TGCTCTGAGCCCATGTAAAG -3'
(R):5'- CTCTTTCAGACTAGCATGACAAGG -3'

Posted On

2020-06-30