Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01373:Fbxw24'

84076

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fbxw24

Ensembl Gene

ENSMUSG00000062275

Gene Name

F-box and WD-40 domain protein 24

Synonyms

Gm5162

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.061) question?

Stock #

IGL01373

Quality Score

Status

Chromosome

Chromosomal Location

109430184-109455125 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 109452701 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Aspartic acid at position 98 (G98D)

Ref Sequence

ENSEMBL: ENSMUSP00000073617 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073962]

AlphaFold

E9PXM9

Predicted Effect

probably damaging
Transcript: ENSMUST00000073962
AA Change: G98D

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000073617
Gene: ENSMUSG00000062275
AA Change: G98D

Domain	Start	End	E-Value	Type
FBOX	8	45	3.25e-4	SMART
SCOP:d1gxra_	87	227	8e-7	SMART
Blast:WD40	137	176	1e-6	BLAST

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsm4	C	T	7: 119,310,642 (GRCm39)	R510*	probably null	Het
Adamts12	A	T	15: 11,310,816 (GRCm39)	E1024D	probably benign	Het
Aff2	T	A	X: 68,911,335 (GRCm39)	D1239E	possibly damaging	Het
Agps	T	C	2: 75,683,128 (GRCm39)	V151A	probably benign	Het
Cables1	A	T	18: 12,021,821 (GRCm39)	R276S	probably damaging	Het
Cep72	A	G	13: 74,207,578 (GRCm39)	S64P	probably damaging	Het
Cmah	A	T	13: 24,614,532 (GRCm39)	D159V	probably damaging	Het
Cox6a1	C	A	5: 115,483,898 (GRCm39)		probably benign	Het
Cpxm1	T	C	2: 130,236,055 (GRCm39)	E369G	probably damaging	Het
Dnah6	A	G	6: 73,051,731 (GRCm39)	L3021P	probably benign	Het
Esyt1	T	C	10: 128,354,810 (GRCm39)	E530G	possibly damaging	Het
Fancd2	A	G	6: 113,530,713 (GRCm39)	I449V	probably benign	Het
Folh1	T	C	7: 86,395,350 (GRCm39)	I361V	probably benign	Het
Gpr19	T	A	6: 134,847,284 (GRCm39)	H41L	possibly damaging	Het
Kcnq4	A	G	4: 120,574,229 (GRCm39)	V143A	probably damaging	Het
Larp7-ps	A	G	4: 92,079,862 (GRCm39)	V42A	probably damaging	Het
Lmcd1	A	G	6: 112,287,586 (GRCm39)	I91V	probably benign	Het
Lpin3	G	T	2: 160,745,649 (GRCm39)	D651Y	probably damaging	Het
Ms4a6b	A	T	19: 11,506,871 (GRCm39)	H220L	possibly damaging	Het
Mxd4	G	A	5: 34,341,690 (GRCm39)		probably benign	Het
Nxnl2	T	C	13: 51,325,488 (GRCm39)	F44L	probably damaging	Het
Or11g2	T	A	14: 50,856,069 (GRCm39)	I130N	probably damaging	Het
Or2ag16	T	C	7: 106,351,653 (GRCm39)		probably benign	Het
Pcdhb20	A	T	18: 37,639,621 (GRCm39)	R716W	probably benign	Het
Pcx	T	A	19: 4,670,263 (GRCm39)		probably null	Het
Plekhf1	T	C	7: 37,921,221 (GRCm39)	T116A	probably benign	Het
Psmb2	G	T	4: 126,580,885 (GRCm39)	R93L	probably damaging	Het
Pstpip2	T	A	18: 77,922,916 (GRCm39)	L42*	probably null	Het
Ptpn22	A	T	3: 103,793,520 (GRCm39)	D557V	probably damaging	Het
Rbbp5	G	A	1: 132,420,339 (GRCm39)	V191I	probably benign	Het
Rgs1	T	A	1: 144,121,116 (GRCm39)	D185V	probably damaging	Het
Selenoh	A	G	2: 84,500,938 (GRCm39)		probably benign	Het
Slc6a5	C	T	7: 49,567,481 (GRCm39)	P312S	probably benign	Het
Snapc1	T	A	12: 74,011,454 (GRCm39)	M40K	probably benign	Het
Sptbn2	T	G	19: 4,796,000 (GRCm39)	Y1726*	probably null	Het
Syne2	T	C	12: 76,033,881 (GRCm39)	I3710T	probably damaging	Het
Tdrd9	G	A	12: 112,006,868 (GRCm39)	V911M	probably damaging	Het
Tex9	A	T	9: 72,388,036 (GRCm39)	D134E	possibly damaging	Het
Ttc41	G	T	10: 86,611,821 (GRCm39)	C1063F	possibly damaging	Het
Usp38	C	A	8: 81,716,647 (GRCm39)	A496S	possibly damaging	Het
Vmn2r13	T	A	5: 109,304,568 (GRCm39)	Y621F	probably damaging	Het
Vmn2r67	T	A	7: 84,785,834 (GRCm39)	M724L	probably benign	Het

Other mutations in Fbxw24

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01093:Fbxw24	APN	9	109,434,041 (GRCm39)	missense	probably benign	0.00
IGL01996:Fbxw24	APN	9	109,434,440 (GRCm39)	missense	possibly damaging	0.84
IGL02179:Fbxw24	APN	9	109,438,973 (GRCm39)	nonsense	probably null
IGL02718:Fbxw24	APN	9	109,453,858 (GRCm39)	missense	possibly damaging	0.55
IGL02936:Fbxw24	APN	9	109,454,026 (GRCm39)	splice site	probably null
IGL03010:Fbxw24	APN	9	109,452,678 (GRCm39)	missense	probably benign	0.07
IGL03350:Fbxw24	APN	9	109,436,081 (GRCm39)	missense	probably damaging	1.00
IGL03402:Fbxw24	APN	9	109,430,316 (GRCm39)	missense	probably damaging	1.00
R0140:Fbxw24	UTSW	9	109,434,482 (GRCm39)	missense	possibly damaging	0.73
R0718:Fbxw24	UTSW	9	109,452,577 (GRCm39)	splice site	probably benign
R1166:Fbxw24	UTSW	9	109,436,066 (GRCm39)	missense	probably benign	0.00
R1550:Fbxw24	UTSW	9	109,436,112 (GRCm39)	missense	probably benign	0.00
R1950:Fbxw24	UTSW	9	109,434,481 (GRCm39)	missense	probably benign	0.02
R1986:Fbxw24	UTSW	9	109,436,124 (GRCm39)	missense	probably damaging	0.97
R2244:Fbxw24	UTSW	9	109,434,117 (GRCm39)	missense	possibly damaging	0.66
R3683:Fbxw24	UTSW	9	109,437,110 (GRCm39)	missense	possibly damaging	0.51
R4324:Fbxw24	UTSW	9	109,434,013 (GRCm39)	critical splice donor site	probably null
R4387:Fbxw24	UTSW	9	109,439,053 (GRCm39)	missense	probably damaging	1.00
R4409:Fbxw24	UTSW	9	109,437,256 (GRCm39)	missense	probably damaging	1.00
R4410:Fbxw24	UTSW	9	109,437,256 (GRCm39)	missense	probably damaging	1.00
R4803:Fbxw24	UTSW	9	109,453,910 (GRCm39)	missense	probably benign	0.02
R5571:Fbxw24	UTSW	9	109,436,066 (GRCm39)	missense	probably benign	0.00
R6042:Fbxw24	UTSW	9	109,436,079 (GRCm39)	missense	probably benign	0.09
R6523:Fbxw24	UTSW	9	109,434,048 (GRCm39)	nonsense	probably null
R6799:Fbxw24	UTSW	9	109,453,998 (GRCm39)	missense	probably damaging	1.00
R7122:Fbxw24	UTSW	9	109,430,328 (GRCm39)	missense	probably benign	0.03
R7239:Fbxw24	UTSW	9	109,434,598 (GRCm39)	missense	possibly damaging	0.71
R7405:Fbxw24	UTSW	9	109,436,136 (GRCm39)	missense	possibly damaging	0.46
R7705:Fbxw24	UTSW	9	109,437,516 (GRCm39)	splice site	probably null
R8536:Fbxw24	UTSW	9	109,452,599 (GRCm39)	missense	probably damaging	1.00
R8873:Fbxw24	UTSW	9	109,453,996 (GRCm39)	missense	probably damaging	1.00
R9332:Fbxw24	UTSW	9	109,452,681 (GRCm39)	missense	probably damaging	1.00
R9430:Fbxw24	UTSW	9	109,439,038 (GRCm39)	missense	probably damaging	0.99

Posted On

2013-11-11