Mutagenetix > Incidental Mutation

Incidental Mutation 'R0975:Fbxw14'

81077

Institutional Source

Beutler Lab

Gene Symbol

Fbxw14

Ensembl Gene

ENSMUSG00000105589

Gene Name

F-box and WD-40 domain protein 14

Synonyms

Fbxo12, E330009N23Rik, Fbx12

MMRRC Submission

039104-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.156) question?

Stock #

R0975 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

109099858-109116744 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 109100307 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Isoleucine at position 449 (N449I)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000112041] [ENSMUST00000198048] [ENSMUST00000198844]

AlphaFold

Q8C2Y5

Predicted Effect

probably benign
Transcript: ENSMUST00000066901
AA Change: N449I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000066613
Gene: ENSMUSG00000054087
AA Change: N449I

Domain	Start	End	E-Value	Type
FBOX	5	45	3.13e-6	SMART
SCOP:d1tbga_	114	249	4e-9	SMART
Blast:WD40	136	175	3e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000112041
AA Change: N396I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000107672
Gene: ENSMUSG00000105589
AA Change: N396I

Domain	Start	End	E-Value	Type
FBOX	5	45	3.13e-6	SMART
SCOP:d1tbga_	114	208	2e-3	SMART
Blast:WD40	136	175	4e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000198048

Predicted Effect

probably benign
Transcript: ENSMUST00000198844
AA Change: N449I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000143404
Gene: ENSMUSG00000105589
AA Change: N449I

Domain	Start	End	E-Value	Type
FBOX	5	45	3.13e-6	SMART
SCOP:d1tbga_	114	249	4e-9	SMART
Blast:WD40	136	175	3e-6	BLAST

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.5%
3x: 98.9%
10x: 97.6%
20x: 95.8%

Validation Efficiency

98% (52/53)

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam34l	A	G	8: 44,078,155 (GRCm39)	F690L	probably benign	Het
Ampd2	T	C	3: 107,984,437 (GRCm39)	Y464C	probably damaging	Het
Arap2	A	T	5: 62,888,229 (GRCm39)		probably benign	Het
Arhgap5	T	G	12: 52,563,927 (GRCm39)	N299K	possibly damaging	Het
Atl3	G	A	19: 7,498,500 (GRCm39)	W210*	probably null	Het
Bag1	T	C	4: 40,937,152 (GRCm39)	N320D	probably benign	Het
Ccdc39	T	C	3: 33,898,274 (GRCm39)	N24D	probably damaging	Het
Ccdc88b	G	A	19: 6,823,993 (GRCm39)	P1420L	probably damaging	Het
Cdr2	G	A	7: 120,557,614 (GRCm39)	P304S	probably benign	Het
Col20a1	A	T	2: 180,648,619 (GRCm39)	I969F	possibly damaging	Het
Coro1c	C	G	5: 114,020,182 (GRCm39)	R11P	probably damaging	Het
Cracd	T	C	5: 77,004,165 (GRCm39)		probably benign	Het
Cul7	T	A	17: 46,974,116 (GRCm39)	L1467H	probably damaging	Het
Cyp2c67	T	G	19: 39,597,622 (GRCm39)	K459Q	possibly damaging	Het
Cyp2c68	T	C	19: 39,691,802 (GRCm39)	T374A	possibly damaging	Het
Efcab6	T	A	15: 83,857,532 (GRCm39)	N289I	probably benign	Het
Elmo1	T	A	13: 20,435,307 (GRCm39)	I126N	probably damaging	Het
Esr2	C	T	12: 76,192,082 (GRCm39)	M315I	possibly damaging	Het
Frmpd1	C	T	4: 45,279,000 (GRCm39)	T575I	probably benign	Het
Gm14403	T	G	2: 177,201,217 (GRCm39)	N145K	probably damaging	Het
Gnl2	A	G	4: 124,942,171 (GRCm39)	D392G	probably damaging	Het
Hmcn1	A	C	1: 150,453,128 (GRCm39)	S5396A	probably benign	Het
Hoxd12	G	T	2: 74,506,278 (GRCm39)	R230L	probably damaging	Het
Khsrp	T	A	17: 57,334,066 (GRCm39)	D154V	possibly damaging	Het
Klhl28	C	T	12: 64,998,462 (GRCm39)	R344H	possibly damaging	Het
Klhl3	C	T	13: 58,161,677 (GRCm39)	V473M	possibly damaging	Het
Larp1b	A	G	3: 40,924,925 (GRCm39)	E134G	probably damaging	Het
Mcm9	G	A	10: 53,414,742 (GRCm39)	Q113*	probably null	Het
Mug1	A	T	6: 121,855,498 (GRCm39)	D944V	probably damaging	Het
Myh6	A	G	14: 55,190,826 (GRCm39)	S950P	probably damaging	Het
Nfix	G	A	8: 85,453,155 (GRCm39)	R300C	probably damaging	Het
Or1n1b	C	A	2: 36,780,562 (GRCm39)	M99I	possibly damaging	Het
Or5k14	T	A	16: 58,693,513 (GRCm39)		probably null	Het
Plcb4	T	C	2: 135,829,832 (GRCm39)		probably benign	Het
Pomt1	T	A	2: 32,143,907 (GRCm39)		probably null	Het
Prpf8	T	C	11: 75,399,500 (GRCm39)		probably benign	Het
Rad9b	C	T	5: 122,472,320 (GRCm39)		probably null	Het
Recql5	A	C	11: 115,814,082 (GRCm39)	D240E	probably damaging	Het
Sec31a	A	C	5: 100,543,763 (GRCm39)		probably null	Het
Slc5a4b	A	G	10: 75,917,241 (GRCm39)	V265A	probably benign	Het
Snx29	A	T	16: 11,165,735 (GRCm39)	D7V	possibly damaging	Het
Stk31	C	G	6: 49,400,343 (GRCm39)	D389E	probably damaging	Het
Tmeff2	T	C	1: 50,977,364 (GRCm39)		probably benign	Het
Tmem131	C	T	1: 36,893,966 (GRCm39)	A146T	probably damaging	Het
Tmem63c	T	A	12: 87,121,843 (GRCm39)		probably benign	Het
Tonsl	T	A	15: 76,523,132 (GRCm39)	D119V	probably damaging	Het
Trmt10a	G	A	3: 137,862,570 (GRCm39)	E287K	probably benign	Het
Vmn1r192	T	A	13: 22,371,633 (GRCm39)	M196L	probably damaging	Het
Vmn2r9	T	G	5: 108,991,169 (GRCm39)	T731P	probably damaging	Het
Wfdc6b	G	A	2: 164,455,705 (GRCm39)	M11I	probably damaging	Het
Ypel1	T	A	16: 16,925,077 (GRCm39)	T32S	probably benign	Het
Zfp827	A	G	8: 79,787,814 (GRCm39)	T327A	probably benign	Het

Other mutations in Fbxw14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01319:Fbxw14	APN	9	109,107,859 (GRCm39)	missense	probably damaging	1.00
IGL01351:Fbxw14	APN	9	109,103,640 (GRCm39)	missense	possibly damaging	0.47
IGL01654:Fbxw14	APN	9	109,115,648 (GRCm39)	splice site	probably benign
K3955:Fbxw14	UTSW	9	109,105,313 (GRCm39)	missense	possibly damaging	0.87
R0064:Fbxw14	UTSW	9	109,116,660 (GRCm39)	nonsense	probably null
R0133:Fbxw14	UTSW	9	109,103,647 (GRCm39)	missense	probably benign	0.02
R1124:Fbxw14	UTSW	9	109,105,236 (GRCm39)	missense	possibly damaging	0.48
R1782:Fbxw14	UTSW	9	109,107,759 (GRCm39)	missense	possibly damaging	0.94
R2118:Fbxw14	UTSW	9	109,103,692 (GRCm39)	splice site	probably benign
R3881:Fbxw14	UTSW	9	109,100,262 (GRCm39)	missense	possibly damaging	0.95
R4641:Fbxw14	UTSW	9	109,107,750 (GRCm39)	critical splice donor site	probably null
R4915:Fbxw14	UTSW	9	109,103,592 (GRCm39)	missense	possibly damaging	0.82
R4952:Fbxw14	UTSW	9	109,105,269 (GRCm39)	missense	probably benign	0.01
R6137:Fbxw14	UTSW	9	109,105,290 (GRCm39)	missense	probably damaging	1.00
R6187:Fbxw14	UTSW	9	109,105,332 (GRCm39)	missense	probably damaging	1.00
R6584:Fbxw14	UTSW	9	109,115,611 (GRCm39)	missense	possibly damaging	0.85
R7130:Fbxw14	UTSW	9	109,100,350 (GRCm39)	missense	probably benign	0.02
R7845:Fbxw14	UTSW	9	109,116,671 (GRCm39)	missense	probably damaging	1.00
R8049:Fbxw14	UTSW	9	109,105,211 (GRCm39)	missense	probably damaging	0.98
R8169:Fbxw14	UTSW	9	109,106,284 (GRCm39)	missense	probably benign	0.05
R8815:Fbxw14	UTSW	9	109,105,305 (GRCm39)	nonsense	probably null
R8816:Fbxw14	UTSW	9	109,105,305 (GRCm39)	nonsense	probably null
R8818:Fbxw14	UTSW	9	109,116,071 (GRCm39)	start gained	probably benign
R8958:Fbxw14	UTSW	9	109,107,810 (GRCm39)	missense	probably damaging	0.99
R8960:Fbxw14	UTSW	9	109,114,367 (GRCm39)	missense	possibly damaging	0.74
R9093:Fbxw14	UTSW	9	109,105,250 (GRCm39)	missense	probably benign
R9306:Fbxw14	UTSW	9	109,100,280 (GRCm39)	missense	probably benign	0.12
R9455:Fbxw14	UTSW	9	109,103,567 (GRCm39)	missense	probably benign	0.00
R9563:Fbxw14	UTSW	9	109,106,335 (GRCm39)	missense	probably benign	0.00
X0067:Fbxw14	UTSW	9	109,105,269 (GRCm39)	missense	probably benign	0.01
Z1177:Fbxw14	UTSW	9	109,105,314 (GRCm39)	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- GCAATGAAATGACAGATGTCACAGCAAA -3'
(R):5'- GTGGACACCTACACACATGACAACTAAG -3'

Sequencing Primer
(F):5'- tcttccatctgtttctgacttcc -3'
(R):5'- acactccatctctccagcc -3'

Posted On

2013-11-07