Mutagenetix > Incidental Mutation

Incidental Mutation 'R1575:Fbxw21'

171111

Institutional Source

Beutler Lab

Gene Symbol

Fbxw21

Ensembl Gene

ENSMUSG00000047237

Gene Name

F-box and WD-40 domain protein 21

Synonyms

E330009P21Rik

MMRRC Submission

039613-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.062) question?

Stock #

R1575 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

108968522-108991090 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 108990984 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 25 (V25A)

Ref Sequence

ENSEMBL: ENSMUSP00000143200 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054925] [ENSMUST00000198076] [ENSMUST00000199540]

AlphaFold

Q8BI38

Predicted Effect

probably benign
Transcript: ENSMUST00000054925
AA Change: V25A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000056358
Gene: ENSMUSG00000047237
AA Change: V25A

Domain	Start	End	E-Value	Type
FBOX	5	45	1.46e-6	SMART
SCOP:d1tbga_	119	249	1e-7	SMART
Blast:WD40	137	176	1e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000198076
AA Change: V25A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000143095
Gene: ENSMUSG00000047237
AA Change: V25A

Domain	Start	End	E-Value	Type
FBOX	5	45	1.46e-6	SMART
SCOP:d1tbga_	119	249	9e-8	SMART
Blast:WD40	137	176	1e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000199540
AA Change: V25A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000143200
Gene: ENSMUSG00000047237
AA Change: V25A

Domain	Start	End	E-Value	Type
FBOX	5	45	9e-9	SMART

Meta Mutation Damage Score

0.1315

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 96.0%
20x: 91.5%

Validation Efficiency

100% (72/72)

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrl2	T	A	3: 148,558,398 (GRCm39)	T437S	probably benign	Het
Akna	A	G	4: 63,297,570 (GRCm39)	F828S	probably benign	Het
Alg9	G	T	9: 50,686,802 (GRCm39)	A40S	possibly damaging	Het
Alox8	T	A	11: 69,076,067 (GRCm39)	H628L	possibly damaging	Het
Aox3	T	C	1: 58,191,713 (GRCm39)	W422R	probably benign	Het
Atp13a4	T	C	16: 29,228,528 (GRCm39)	D984G	probably benign	Het
Bcam	T	C	7: 19,494,307 (GRCm39)	E363G	possibly damaging	Het
Cadps2	C	A	6: 23,429,217 (GRCm39)	V519F	probably damaging	Het
Calca	A	G	7: 114,234,396 (GRCm39)	Y18H	probably damaging	Het
Cd70	A	G	17: 57,453,364 (GRCm39)	I100T	probably damaging	Het
Cdk4	T	A	10: 126,900,520 (GRCm39)	H95Q	probably damaging	Het
Chchd1	T	A	14: 20,753,410 (GRCm39)	N11K	probably damaging	Het
Cma2	T	A	14: 56,210,272 (GRCm39)	N52K	probably damaging	Het
Cyp3a16	A	G	5: 145,373,267 (GRCm39)	V500A	probably benign	Het
Dicer1	A	G	12: 104,688,228 (GRCm39)		probably null	Het
Dnajc13	A	G	9: 104,034,037 (GRCm39)	S2206P	probably benign	Het
Dtl	T	C	1: 191,293,658 (GRCm39)		probably null	Het
Fam186b	T	C	15: 99,184,852 (GRCm39)	T24A	probably benign	Het
Gins1	T	C	2: 150,754,758 (GRCm39)	S45P	probably benign	Het
Gtpbp2	T	A	17: 46,476,869 (GRCm39)	V349D	probably damaging	Het
Hyal5	G	T	6: 24,876,792 (GRCm39)	D222Y	probably damaging	Het
Itgal	A	G	7: 126,900,060 (GRCm39)		probably null	Het
Klk14	A	G	7: 43,343,377 (GRCm39)		probably null	Het
Lama1	T	A	17: 68,117,404 (GRCm39)	L2518Q	possibly damaging	Het
Lrrc2	G	A	9: 110,808,555 (GRCm39)	G264D	probably benign	Het
Ltbp4	A	G	7: 27,022,245 (GRCm39)	S893P	probably damaging	Het
Mast4	G	A	13: 102,875,771 (GRCm39)	P1107L	probably damaging	Het
Mbd1	T	A	18: 74,408,490 (GRCm39)		probably null	Het
Naip2	A	T	13: 100,291,529 (GRCm39)	D1136E	probably benign	Het
Naip2	G	A	13: 100,291,537 (GRCm39)		probably benign	Het
Ncan	G	A	8: 70,562,848 (GRCm39)	T470I	probably benign	Het
Npy1r	A	T	8: 67,156,813 (GRCm39)	I78F	probably damaging	Het
Or10q1b	A	T	19: 13,682,889 (GRCm39)	M233L	probably benign	Het
Or8b52	G	A	9: 38,576,573 (GRCm39)	T189M	probably damaging	Het
Palb2	A	T	7: 121,710,061 (GRCm39)		probably null	Het
Pax3	T	C	1: 78,080,121 (GRCm39)	T422A	probably benign	Het
Pebp1	A	T	5: 117,424,229 (GRCm39)	D72E	possibly damaging	Het
Pnliprp1	A	T	19: 58,728,901 (GRCm39)	T363S	probably benign	Het
Rbm44	G	A	1: 91,084,565 (GRCm39)		probably null	Het
Rbm47	T	A	5: 66,182,358 (GRCm39)	Y425F	probably benign	Het
Robo3	G	T	9: 37,340,957 (GRCm39)	A83E	probably damaging	Het
Rrm1	A	G	7: 102,105,721 (GRCm39)	Y279C	probably damaging	Het
Rslcan18	A	T	13: 67,256,121 (GRCm39)		probably benign	Het
Scara5	C	A	14: 65,968,314 (GRCm39)	Q196K	probably benign	Het
Setd1b	C	T	5: 123,301,210 (GRCm39)		probably benign	Het
Siah1a	A	G	8: 87,451,869 (GRCm39)	F205S	probably damaging	Het
Smr2	AT	ATT	5: 88,256,683 (GRCm39)		probably null	Het
Ssu72	A	G	4: 155,815,814 (GRCm39)	D86G	probably benign	Het
St7	G	T	6: 17,886,110 (GRCm39)	K357N	probably damaging	Het
Sv2b	G	A	7: 74,797,425 (GRCm39)	T323I	probably damaging	Het
Syt1	T	C	10: 108,340,361 (GRCm39)	N319S	probably benign	Het
Tanc1	T	A	2: 59,621,995 (GRCm39)	F371L	probably damaging	Het
Tcf20	C	A	15: 82,739,693 (GRCm39)	G586V	probably benign	Het
Tg	T	C	15: 66,601,534 (GRCm39)		probably null	Het
Tyk2	A	T	9: 21,026,758 (GRCm39)	N620K	probably benign	Het
Ube2j1	T	A	4: 33,045,116 (GRCm39)	S130T	probably benign	Het
Ubr2	G	T	17: 47,243,418 (GRCm39)	P1696H	probably damaging	Het
Ubr5	A	T	15: 38,041,085 (GRCm39)	D266E	probably damaging	Het
Vipr2	A	G	12: 116,107,892 (GRCm39)	T426A	probably benign	Het
Vmn2r104	A	T	17: 20,262,477 (GRCm39)	W218R	probably damaging	Het
Vmn2r83	T	A	10: 79,314,956 (GRCm39)	N401K	probably damaging	Het
Vwf	A	G	6: 125,632,214 (GRCm39)	E82G	unknown	Het
Vwf	T	A	6: 125,640,534 (GRCm39)	Y2323*	probably null	Het
Wdr76	T	G	2: 121,359,402 (GRCm39)	V329G	probably damaging	Het
Zan	A	G	5: 137,460,214 (GRCm39)	C1226R	unknown	Het
Zbtb16	G	T	9: 48,743,572 (GRCm39)	Q247K	probably damaging	Het
Zfp541	T	C	7: 15,812,640 (GRCm39)	V431A	possibly damaging	Het

Other mutations in Fbxw21

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00679:Fbxw21	APN	9	108,991,032 (GRCm39)	missense	probably damaging	1.00
IGL00901:Fbxw21	APN	9	108,985,467 (GRCm39)	missense	probably benign	0.00
IGL01377:Fbxw21	APN	9	108,975,713 (GRCm39)	nonsense	probably null
IGL01941:Fbxw21	APN	9	108,977,224 (GRCm39)	missense	probably benign	0.07
IGL02491:Fbxw21	APN	9	108,972,887 (GRCm39)	missense	probably benign
IGL03163:Fbxw21	APN	9	108,974,552 (GRCm39)	missense	probably benign	0.01
IGL03377:Fbxw21	APN	9	108,968,597 (GRCm39)	missense	probably benign	0.01
R0148:Fbxw21	UTSW	9	108,977,085 (GRCm39)	critical splice donor site	probably null
R0328:Fbxw21	UTSW	9	108,975,653 (GRCm39)	missense	possibly damaging	0.52
R0909:Fbxw21	UTSW	9	108,985,476 (GRCm39)	missense	possibly damaging	0.84
R1506:Fbxw21	UTSW	9	108,977,257 (GRCm39)	missense	probably damaging	1.00
R1615:Fbxw21	UTSW	9	108,972,794 (GRCm39)	missense	probably damaging	1.00
R1719:Fbxw21	UTSW	9	108,977,242 (GRCm39)	missense	possibly damaging	0.85
R2415:Fbxw21	UTSW	9	108,985,469 (GRCm39)	missense	possibly damaging	0.71
R2424:Fbxw21	UTSW	9	108,986,587 (GRCm39)	nonsense	probably null
R2508:Fbxw21	UTSW	9	108,974,553 (GRCm39)	missense	probably benign	0.31
R2898:Fbxw21	UTSW	9	108,985,404 (GRCm39)	missense	possibly damaging	0.52
R2964:Fbxw21	UTSW	9	108,974,578 (GRCm39)	missense	probably benign	0.10
R2965:Fbxw21	UTSW	9	108,974,578 (GRCm39)	missense	probably benign	0.10
R2966:Fbxw21	UTSW	9	108,974,578 (GRCm39)	missense	probably benign	0.10
R4809:Fbxw21	UTSW	9	108,972,458 (GRCm39)	missense	probably damaging	1.00
R4911:Fbxw21	UTSW	9	108,974,731 (GRCm39)	missense	probably damaging	1.00
R5669:Fbxw21	UTSW	9	108,974,578 (GRCm39)	missense	probably benign	0.12
R5928:Fbxw21	UTSW	9	108,972,893 (GRCm39)	missense	possibly damaging	0.55
R6043:Fbxw21	UTSW	9	108,974,607 (GRCm39)	missense	possibly damaging	0.69
R6277:Fbxw21	UTSW	9	108,974,623 (GRCm39)	missense	possibly damaging	0.95
R6805:Fbxw21	UTSW	9	108,986,633 (GRCm39)	missense	probably damaging	1.00
R6944:Fbxw21	UTSW	9	108,986,603 (GRCm39)	missense	probably damaging	1.00
R7079:Fbxw21	UTSW	9	108,974,578 (GRCm39)	missense	probably benign	0.10
R7081:Fbxw21	UTSW	9	108,990,990 (GRCm39)	missense	probably damaging	1.00
R7744:Fbxw21	UTSW	9	108,986,720 (GRCm39)	missense	possibly damaging	0.81
R7774:Fbxw21	UTSW	9	108,972,908 (GRCm39)	missense	probably benign	0.00
R7980:Fbxw21	UTSW	9	108,985,639 (GRCm39)	splice site	probably null
R8043:Fbxw21	UTSW	9	108,975,694 (GRCm39)	missense	probably benign	0.01
R8260:Fbxw21	UTSW	9	108,975,614 (GRCm39)	critical splice donor site	probably null
R9142:Fbxw21	UTSW	9	108,985,413 (GRCm39)	missense	probably damaging	1.00
R9172:Fbxw21	UTSW	9	108,975,764 (GRCm39)	missense	probably benign	0.00
R9250:Fbxw21	UTSW	9	108,972,846 (GRCm39)	missense	probably benign	0.31
R9251:Fbxw21	UTSW	9	108,974,687 (GRCm39)	missense	probably damaging	1.00
R9294:Fbxw21	UTSW	9	108,972,830 (GRCm39)	missense	probably damaging	0.99
R9303:Fbxw21	UTSW	9	108,986,727 (GRCm39)	missense	probably benign
R9479:Fbxw21	UTSW	9	108,968,612 (GRCm39)	missense	probably benign	0.00
R9509:Fbxw21	UTSW	9	108,977,217 (GRCm39)	missense	possibly damaging	0.90
R9765:Fbxw21	UTSW	9	108,975,625 (GRCm39)	missense	possibly damaging	0.71
R9773:Fbxw21	UTSW	9	108,977,128 (GRCm39)	missense	possibly damaging	0.89
R9774:Fbxw21	UTSW	9	108,991,057 (GRCm39)	start codon destroyed	probably null	0.98
Z1088:Fbxw21	UTSW	9	108,974,605 (GRCm39)	missense	probably benign
Z1176:Fbxw21	UTSW	9	108,974,605 (GRCm39)	missense	probably benign
Z1177:Fbxw21	UTSW	9	108,974,605 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AGCTGAGTCCCGGAGATGCTAATG -3'
(R):5'- CCAGTCAAAGGCTGATGAGCTGTG -3'

Sequencing Primer
(F):5'- aagaaggagagaaggaaagaagg -3'
(R):5'- CTGTGGTTGGTAATCCTGCTAAATC -3'

Posted On

2014-04-13