Mutagenetix > Incidental Mutations

Incidental Mutation 'R7671:Fbxo15'

592191

Institutional Source

Beutler Lab

Gene Symbol

Fbxo15

Ensembl Gene

ENSMUSG00000034391

Gene Name

F-box protein 15

Synonyms

Fbx15, ecat3

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7671 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

84934782-84981472 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 84964153 bp

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 288 (H288Q)

Ref Sequence

ENSEMBL: ENSMUSP00000045925 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037718] [ENSMUST00000224467] [ENSMUST00000225015] [ENSMUST00000225445]

Predicted Effect

probably damaging
Transcript: ENSMUST00000037718
AA Change: H288Q

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000045925
Gene: ENSMUSG00000034391
AA Change: H288Q

Domain	Start	End	E-Value	Type
low complexity region	35	42	N/A	INTRINSIC
FBOX	46	86	3.4e-7	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000224467
AA Change: H243Q

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

Predicted Effect

probably benign
Transcript: ENSMUST00000225015

Predicted Effect

probably damaging
Transcript: ENSMUST00000225445
AA Change: H243Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

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 FBXO15, 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]
PHENOTYPE: Both male and female homozygous null mice develop normally and are fertile. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610009O20Rik	T	A	18: 38,259,925	I394N	probably damaging	Het
4930435E12Rik	C	T	16: 38,828,091	D219N	possibly damaging	Het
4932438A13Rik	T	C	3: 36,943,231	F1146L	probably damaging	Het
4933406M09Rik	T	C	1: 134,390,062	C191R	probably benign	Het
Akap13	C	A	7: 75,569,900	T17K	probably damaging	Het
Ankrd29	T	A	18: 12,260,986	K257I	probably damaging	Het
Bicc1	A	G	10: 70,957,167	L219P	probably benign	Het
Boc	C	T	16: 44,491,849	V617M		Het
Ccl8	A	G	11: 82,115,207		probably benign	Het
Col18a1	A	G	10: 77,085,383	L261P	unknown	Het
Col5a3	T	A	9: 20,775,086		probably null	Het
Cryba4	A	C	5: 112,248,173		probably null	Het
Csf2rb	A	G	15: 78,338,930	Y114C	probably damaging	Het
Ctif	T	C	18: 75,472,016	D484G	probably damaging	Het
Ctnnal1	A	G	4: 56,837,848	F261L	probably damaging	Het
Defb22	A	T	2: 152,486,030	N78K	unknown	Het
Efr3a	G	A	15: 65,837,434		probably null	Het
Elp4	G	T	2: 105,904,481	A3E	probably damaging	Het
Emilin2	A	G	17: 71,273,910	V607A	probably benign	Het
Epsti1	A	G	14: 77,904,490	Y2C	probably damaging	Het
Fam81b	A	C	13: 76,271,293	L46R	probably damaging	Het
Fam81b	G	T	13: 76,271,294	L46I	possibly damaging	Het
Gabrg1	T	A	5: 70,815,980	N77I	probably damaging	Het
Ganab	A	G	19: 8,912,852	Y715C	possibly damaging	Het
Hist3h2ba	T	C	11: 58,949,276	S113P	possibly damaging	Het
Iqgap2	T	C	13: 95,628,119	D1539G	probably damaging	Het
Kcp	T	C	6: 29,496,517	N633S	probably benign	Het
Krt6a	C	A	15: 101,690,543	S529I	unknown	Het
Leo1	A	G	9: 75,445,562	H129R	probably benign	Het
Lmf1	G	A	17: 25,579,349	V55M	possibly damaging	Het
Mcm9	A	G	10: 53,537,569	S472P	probably benign	Het
Med27	T	A	2: 29,377,938	V33D		Het
Mup15	C	T	4: 61,438,289	E80K	probably benign	Het
Myo18a	G	A	11: 77,859,420	R199H		Het
Nebl	T	A	2: 17,390,916	R558*	probably null	Het
Olfr1121	A	G	2: 87,372,269	T246A	probably damaging	Het
Olfr1252	A	T	2: 89,721,259	I284K	probably damaging	Het
Olfr1329	A	T	4: 118,916,986	H160Q	probably benign	Het
Olfr506	T	C	7: 108,612,991	I228T	probably damaging	Het
Olfr740	G	T	14: 50,453,885	V278L	probably benign	Het
Olfr815	T	C	10: 129,902,353	D119G	probably damaging	Het
Olfr890	A	T	9: 38,143,440	M97L	probably benign	Het
Pde11a	A	T	2: 76,215,353	F376I	possibly damaging	Het
Prima1	A	T	12: 103,235,661	C52S	probably damaging	Het
Pxn	G	A	5: 115,548,547	R366H	not run	Het
Sgce	T	C	6: 4,691,564	Y337C	probably damaging	Het
Slc25a10	T	A	11: 120,495,460	M130K	probably benign	Het
Slc29a2	A	T	19: 5,024,262	N5I	probably benign	Het
Slc35a1	A	T	4: 34,673,875	H150Q		Het
Slc5a4a	T	A	10: 76,147,550	V7D	unknown	Het
Stk17b	T	A	1: 53,766,000	D134V	probably damaging	Het
Thbs3	T	A	3: 89,216,707	S36T	probably benign	Het
Thsd4	A	G	9: 60,428,174	S152P	probably benign	Het
Tmem67	G	T	4: 12,063,698	H422N	probably benign	Het
Tram1	C	A	1: 13,589,644	V27F	probably damaging	Het
Trim14	A	G	4: 46,507,238	V326A	possibly damaging	Het

Other mutations in Fbxo15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00517:Fbxo15	APN	18	84959100	missense	probably damaging	1.00
IGL01375:Fbxo15	APN	18	84958279	missense	possibly damaging	0.64
IGL01730:Fbxo15	APN	18	84964174	missense	probably benign	0.38
IGL01807:Fbxo15	APN	18	84981381	utr 3 prime	probably benign
IGL02220:Fbxo15	APN	18	84964192	critical splice donor site	probably null
IGL02255:Fbxo15	APN	18	84964196	splice site	probably null
IGL02435:Fbxo15	APN	18	84959226	missense	probably damaging	0.97
IGL02546:Fbxo15	APN	18	84962722	critical splice donor site	probably null
IGL03099:Fbxo15	APN	18	84981213	missense	possibly damaging	0.87
R0346:Fbxo15	UTSW	18	84960221	critical splice donor site	probably null
R1606:Fbxo15	UTSW	18	84962620	missense	possibly damaging	0.93
R1671:Fbxo15	UTSW	18	84959106	missense	possibly damaging	0.73
R2113:Fbxo15	UTSW	18	84959105	missense	probably benign	0.00
R3962:Fbxo15	UTSW	18	84959247	missense	probably benign	0.02
R4064:Fbxo15	UTSW	18	84959118	missense	probably damaging	0.96
R5523:Fbxo15	UTSW	18	84960069	missense	probably damaging	1.00
R5931:Fbxo15	UTSW	18	84981125	missense	probably damaging	0.96
R6235:Fbxo15	UTSW	18	84980904	intron	probably benign
R6349:Fbxo15	UTSW	18	84964142	missense	probably benign	0.01
R6607:Fbxo15	UTSW	18	84959145	missense	possibly damaging	0.88
R7232:Fbxo15	UTSW	18	84962622	missense	probably damaging	1.00
R7325:Fbxo15	UTSW	18	84959118	missense	probably damaging	0.96
R7519:Fbxo15	UTSW	18	84964234	unclassified	probably benign
R8094:Fbxo15	UTSW	18	84965493	missense	probably benign	0.34
R8365:Fbxo15	UTSW	18	84962614	missense	probably damaging	1.00
X0022:Fbxo15	UTSW	18	84960119	missense	probably benign	0.00
Z1177:Fbxo15	UTSW	18	84958308	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TGGGTGAGTGGTCCAACATC -3'
(R):5'- AATGGCACCATGCTAACAGAAG -3'

Sequencing Primer
(F):5'- GGTGAGTGGTCCAACATCTTATACAC -3'
(R):5'- TGGCACCATGCTAACAGAAGAGATC -3'

Posted On

2019-11-12