Mutagenetix > Incidental Mutation

Incidental Mutation 'R1666:Fbxl17'

187236

Institutional Source

Beutler Lab

Gene Symbol

Fbxl17

Ensembl Gene

ENSMUSG00000023965

Gene Name

F-box and leucine-rich repeat protein 17

Synonyms

6330576B01Rik, C130023C01Rik, Fbxo13, Fbx13

MMRRC Submission

039702-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.821) question?

Stock #

R1666 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

63364447-63807012 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 63692060 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000108459 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024761] [ENSMUST00000112840]

AlphaFold

Q9QZN1

Predicted Effect

probably null
Transcript: ENSMUST00000024761

SMART Domains

Protein: ENSMUSP00000024761
Gene: ENSMUSG00000023965

Domain	Start	End	E-Value	Type
low complexity region	17	36	N/A	INTRINSIC
low complexity region	76	89	N/A	INTRINSIC
low complexity region	103	138	N/A	INTRINSIC
low complexity region	180	193	N/A	INTRINSIC
low complexity region	214	245	N/A	INTRINSIC
low complexity region	246	270	N/A	INTRINSIC
FBOX	324	365	3.1e-8	SMART
LRR	359	384	4.6e-1	SMART
LRR	385	410	2e-1	SMART
LRR	411	436	8.5e-2	SMART
LRR	437	462	6.9e-4	SMART
LRR	463	488	1.3e-5	SMART
LRR	489	514	5.2e-2	SMART
LRR	515	539	2.9e-3	SMART
LRR	540	564	2e-1	SMART
low complexity region	567	580	N/A	INTRINSIC
LRR	591	615	8.4e-4	SMART
LRR	616	641	2.2e-1	SMART
LRR	642	667	6.3e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000090318

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000112839

Predicted Effect

probably null
Transcript: ENSMUST00000112840

SMART Domains

Protein: ENSMUSP00000108459
Gene: ENSMUSG00000023965

Domain	Start	End	E-Value	Type
LRR	8	33	1.2e1	SMART
LRR	34	58	6.57e-1	SMART
LRR	59	83	4.67e1	SMART
low complexity region	86	99	N/A	INTRINSIC
LRR	110	134	1.89e-1	SMART
LRR	135	160	5.25e1	SMART
LRR	161	186	1.47e2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000169134

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.7%
20x: 93.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the F-box protein family, such as FBXL17, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acvrl1	G	A	15: 101,035,458 (GRCm39)	R328H	probably damaging	Het
Afp	T	C	5: 90,652,927 (GRCm39)	S466P	probably damaging	Het
Arhgap45	A	G	10: 79,864,584 (GRCm39)	S879G	possibly damaging	Het
Asic1	A	G	15: 99,597,006 (GRCm39)	D556G	probably damaging	Het
Atp2a3	T	A	11: 72,869,633 (GRCm39)		probably null	Het
Brinp2	C	A	1: 158,074,128 (GRCm39)	E664D	probably damaging	Het
Cap2	C	A	13: 46,768,799 (GRCm39)	H147N	probably damaging	Het
Cd209f	G	A	8: 4,154,862 (GRCm39)	Q79*	probably null	Het
Chrna7	T	C	7: 62,861,890 (GRCm39)	Y54C	possibly damaging	Het
Clec1a	T	C	6: 129,413,967 (GRCm39)	D40G	probably benign	Het
Col11a1	A	G	3: 113,855,184 (GRCm39)	E148G	unknown	Het
Comp	A	T	8: 70,831,607 (GRCm39)		probably null	Het
Cpz	A	G	5: 35,665,460 (GRCm39)		probably null	Het
Cyfip1	T	A	7: 55,521,646 (GRCm39)	N13K	probably damaging	Het
Cyp2c50	A	T	19: 40,079,499 (GRCm39)	M198L	probably benign	Het
Deup1	A	T	9: 15,486,487 (GRCm39)	Y398N	possibly damaging	Het
Elapor1	A	G	3: 108,377,313 (GRCm39)	S434P	probably benign	Het
Epb41l4a	A	G	18: 34,054,962 (GRCm39)	L42P	probably damaging	Het
Exo1	T	C	1: 175,736,052 (GRCm39)	I812T	possibly damaging	Het
Fxn	A	G	19: 24,239,377 (GRCm39)	Y172H	probably damaging	Het
Gabra6	A	G	11: 42,208,461 (GRCm39)	S124P	probably damaging	Het
Gje1	C	A	10: 14,592,551 (GRCm39)	W77L	possibly damaging	Het
Glra1	A	G	11: 55,465,225 (GRCm39)	S23P	probably damaging	Het
Gm6811	T	C	17: 21,314,529 (GRCm39)		noncoding transcript	Het
Greb1l	T	A	18: 10,501,080 (GRCm39)		probably null	Het
Greb1l	T	C	18: 10,529,708 (GRCm39)		probably null	Het
Grm6	A	T	11: 50,750,711 (GRCm39)	I625F	probably damaging	Het
Guca1a	A	G	17: 47,711,167 (GRCm39)	F60L	probably damaging	Het
Hectd1	T	A	12: 51,800,607 (GRCm39)	E2070D	possibly damaging	Het
Itga5	G	A	15: 103,256,329 (GRCm39)	T910I	probably benign	Het
Kctd10	A	G	5: 114,507,051 (GRCm39)	V142A	probably benign	Het
Kif1c	C	T	11: 70,619,223 (GRCm39)	L953F	probably damaging	Het
Lmtk3	A	T	7: 45,443,588 (GRCm39)	D757V	probably benign	Het
Lpcat1	T	C	13: 73,658,242 (GRCm39)		probably null	Het
Lrrc30	A	T	17: 67,939,200 (GRCm39)	C127S	probably benign	Het
Mc4r	A	G	18: 66,992,480 (GRCm39)	L211P	probably damaging	Het
Mgat5b	T	A	11: 116,874,474 (GRCm39)	N635K	probably benign	Het
Mms19	A	T	19: 41,940,995 (GRCm39)	M443K	possibly damaging	Het
Mroh5	T	C	15: 73,659,754 (GRCm39)	N359S	probably benign	Het
Nlrc4	G	A	17: 74,752,901 (GRCm39)	T494M	probably damaging	Het
Ntf3	T	C	6: 126,079,401 (GRCm39)	D35G	possibly damaging	Het
Or5g25	A	T	2: 85,478,157 (GRCm39)	C169*	probably null	Het
Osbpl5	T	C	7: 143,262,776 (GRCm39)	H192R	probably damaging	Het
Parp4	A	T	14: 56,861,620 (GRCm39)	K984N	possibly damaging	Het
Pdgfra	G	A	5: 75,349,681 (GRCm39)	G892D	possibly damaging	Het
Pik3c2g	A	T	6: 139,612,634 (GRCm39)		probably benign	Het
Ppcdc	T	A	9: 57,321,998 (GRCm39)	M181L	possibly damaging	Het
Pramel7	G	A	2: 87,322,747 (GRCm39)	P6S	probably damaging	Het
Prkcz	G	T	4: 155,374,208 (GRCm39)	F69L	probably damaging	Het
Prkd1	G	A	12: 50,441,709 (GRCm39)	H277Y	probably damaging	Het
Ptgs2	A	G	1: 149,977,021 (GRCm39)	Y44C	probably damaging	Het
Rbck1	T	A	2: 152,158,819 (GRCm39)	S488C	probably damaging	Het
Rbl1	T	C	2: 157,001,654 (GRCm39)	Y878C	probably damaging	Het
Rbm6	G	A	9: 107,669,055 (GRCm39)	T619I	probably benign	Het
Rp1	A	G	1: 4,420,086 (GRCm39)	I342T	probably damaging	Het
Rpn2	C	T	2: 157,136,075 (GRCm39)	T161M	possibly damaging	Het
Rufy4	G	A	1: 74,186,837 (GRCm39)	V542I	probably benign	Het
Sema5b	C	T	16: 35,478,852 (GRCm39)	P559S	probably benign	Het
Serpinb3d	A	G	1: 107,008,481 (GRCm39)	V128A	probably benign	Het
Slc35f3	T	A	8: 127,115,960 (GRCm39)	S296T	probably damaging	Het
Slco1a8	T	A	6: 141,927,775 (GRCm39)		probably null	Het
Smarca2	A	G	19: 26,624,434 (GRCm39)	I365V	possibly damaging	Het
Spdya	T	A	17: 71,885,235 (GRCm39)	C230S	probably damaging	Het
Sv2b	G	A	7: 74,856,089 (GRCm39)	A67V	probably benign	Het
Tapbpl	A	G	6: 125,207,164 (GRCm39)	V175A	probably benign	Het
Tmt1a3	A	G	15: 100,233,099 (GRCm39)	I97V	probably benign	Het
Ttn	T	C	2: 76,642,095 (GRCm39)	T13373A	probably damaging	Het
Tubb5	A	T	17: 36,147,530 (GRCm39)	N52K	probably benign	Het
Tyr	T	A	7: 87,142,149 (GRCm39)	Y137F	probably damaging	Het
Unc45b	T	A	11: 82,808,565 (GRCm39)	I217N	probably benign	Het
Vmn1r202	A	T	13: 22,685,540 (GRCm39)	D292E	possibly damaging	Het
Vmn1r22	A	G	6: 57,877,704 (GRCm39)	M91T	probably benign	Het
Washc2	T	A	6: 116,200,215 (GRCm39)		probably null	Het
Zfp566	A	T	7: 29,777,901 (GRCm39)	H93Q	probably benign	Het
Zfp740	A	G	15: 102,116,753 (GRCm39)	D56G	probably damaging	Het
Zfp804b	A	C	5: 6,821,323 (GRCm39)	L580R	possibly damaging	Het
Zmiz2	T	G	11: 6,346,836 (GRCm39)	S148R	probably benign	Het
Zmym6	T	A	4: 127,016,652 (GRCm39)	I719N	probably damaging	Het
Zyx	T	A	6: 42,332,966 (GRCm39)	V372E	possibly damaging	Het

Other mutations in Fbxl17

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01420:Fbxl17	APN	17	63,692,047 (GRCm39)	missense	probably damaging	1.00
IGL02201:Fbxl17	APN	17	63,806,024 (GRCm39)	missense	probably damaging	1.00
IGL02256:Fbxl17	APN	17	63,806,085 (GRCm39)	missense	probably benign
IGL03408:Fbxl17	APN	17	63,387,541 (GRCm39)	nonsense	probably null
R0268:Fbxl17	UTSW	17	63,692,062 (GRCm39)	splice site	probably benign
R0269:Fbxl17	UTSW	17	63,691,987 (GRCm39)	missense	probably damaging	0.99
R0313:Fbxl17	UTSW	17	63,663,846 (GRCm39)	missense	probably damaging	1.00
R0315:Fbxl17	UTSW	17	63,663,846 (GRCm39)	missense	probably damaging	1.00
R0344:Fbxl17	UTSW	17	63,692,062 (GRCm39)	splice site	probably benign
R0356:Fbxl17	UTSW	17	63,663,846 (GRCm39)	missense	probably damaging	1.00
R0358:Fbxl17	UTSW	17	63,663,846 (GRCm39)	missense	probably damaging	1.00
R0553:Fbxl17	UTSW	17	63,663,846 (GRCm39)	missense	probably damaging	1.00
R0617:Fbxl17	UTSW	17	63,691,987 (GRCm39)	missense	probably damaging	0.99
R0629:Fbxl17	UTSW	17	63,778,409 (GRCm39)	missense	probably damaging	1.00
R1597:Fbxl17	UTSW	17	63,794,813 (GRCm39)	missense	probably damaging	1.00
R3001:Fbxl17	UTSW	17	63,532,072 (GRCm39)	missense	probably damaging	0.99
R3002:Fbxl17	UTSW	17	63,532,072 (GRCm39)	missense	probably damaging	0.99
R3121:Fbxl17	UTSW	17	63,778,419 (GRCm39)	missense	probably damaging	0.96
R3909:Fbxl17	UTSW	17	63,806,802 (GRCm39)	missense	possibly damaging	0.93
R4789:Fbxl17	UTSW	17	63,794,910 (GRCm39)	missense	probably benign	0.40
R6606:Fbxl17	UTSW	17	63,794,783 (GRCm39)	missense	probably damaging	0.97
R7153:Fbxl17	UTSW	17	63,367,346 (GRCm39)	missense	probably benign	0.09
R7722:Fbxl17	UTSW	17	63,663,823 (GRCm39)	missense	probably damaging	0.99
R7794:Fbxl17	UTSW	17	63,663,806 (GRCm39)	missense	probably damaging	0.97
R7841:Fbxl17	UTSW	17	63,794,820 (GRCm39)	missense	probably damaging	1.00
R8076:Fbxl17	UTSW	17	63,367,360 (GRCm39)	missense	probably damaging	0.99
R8178:Fbxl17	UTSW	17	63,794,967 (GRCm39)	splice site	probably null
R8338:Fbxl17	UTSW	17	63,663,753 (GRCm39)	missense	possibly damaging	0.93
R8873:Fbxl17	UTSW	17	63,691,971 (GRCm39)	missense	probably damaging	0.99
R9113:Fbxl17	UTSW	17	63,532,085 (GRCm39)	missense	probably benign	0.09
R9431:Fbxl17	UTSW	17	63,387,489 (GRCm39)	missense	probably damaging	1.00
R9444:Fbxl17	UTSW	17	63,778,455 (GRCm39)	missense	probably damaging	0.98
R9581:Fbxl17	UTSW	17	63,806,525 (GRCm39)	missense	probably benign
R9660:Fbxl17	UTSW	17	63,806,426 (GRCm39)	missense	probably benign	0.00
R9756:Fbxl17	UTSW	17	63,367,310 (GRCm39)	missense	probably damaging	0.98
X0019:Fbxl17	UTSW	17	63,367,378 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2014-05-09