Mutagenetix > Incidental Mutation

Incidental Mutation 'R0137:Fmnl3'

60930

Institutional Source

Beutler Lab

Gene Symbol

Fmnl3

Ensembl Gene

ENSMUSG00000023008

Gene Name

formin-like 3

Synonyms

2700073B04Rik, Wbp3

MMRRC Submission

038422-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.772) question?

Stock #

R0137 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

99215106-99268363 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

G to C at 99220619 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000113094 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081224] [ENSMUST00000088233] [ENSMUST00000120633]

AlphaFold

Q6ZPF4

Predicted Effect

probably benign
Transcript: ENSMUST00000081224

SMART Domains

Protein: ENSMUSP00000079984
Gene: ENSMUSG00000023008

Domain	Start	End	E-Value	Type
Drf_GBD	26	227	2.99e-88	SMART
Drf_FH3	230	421	6.1e-71	SMART
low complexity region	448	497	N/A	INTRINSIC
FH2	510	944	9.85e-141	SMART
low complexity region	960	975	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000088233

SMART Domains

Protein: ENSMUSP00000085566
Gene: ENSMUSG00000023008

Domain	Start	End	E-Value	Type
Drf_GBD	26	278	3.91e-92	SMART
Drf_FH3	281	472	6.1e-71	SMART
low complexity region	499	548	N/A	INTRINSIC
FH2	561	995	9.85e-141	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000120633

SMART Domains

Protein: ENSMUSP00000113094
Gene: ENSMUSG00000023008

Domain	Start	End	E-Value	Type
Drf_GBD	26	278	3.91e-92	SMART
Drf_FH3	281	472	6.1e-71	SMART
low complexity region	499	548	N/A	INTRINSIC
FH2	561	995	9.85e-141	SMART
low complexity region	1011	1026	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139767

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 96.1%
20x: 91.8%

Validation Efficiency

95% (94/99)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a formin homology 2 domain and has high sequence identity to the mouse Wbp3 protein. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

Allele List at MGI

All alleles(2) : Targeted, other(2)

Other mutations in this stock

Total: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
6430548M08Rik	A	T	8: 120,878,115 (GRCm39)	H190L	possibly damaging	Het
Adap1	A	G	5: 139,278,976 (GRCm39)		probably benign	Het
Adgra3	C	T	5: 50,121,182 (GRCm39)		probably benign	Het
Adgre5	A	T	8: 84,451,527 (GRCm39)	V527E	probably damaging	Het
Anapc5	A	T	5: 122,938,695 (GRCm39)	Y360N	probably damaging	Het
Angptl6	C	A	9: 20,789,683 (GRCm39)	A70S	probably benign	Het
Ankdd1a	C	A	9: 65,417,610 (GRCm39)	K137N	probably null	Het
Ccdc170	T	C	10: 4,496,950 (GRCm39)		probably benign	Het
Ccdc51	A	G	9: 108,920,698 (GRCm39)	E195G	probably damaging	Het
Cdc37	A	T	9: 21,053,426 (GRCm39)	C204S	possibly damaging	Het
Cfap36	T	C	11: 29,172,431 (GRCm39)		probably benign	Het
Col6a2	C	A	10: 76,432,259 (GRCm39)	G965C	probably damaging	Het
Csn1s2a	G	A	5: 87,926,826 (GRCm39)	S53N	possibly damaging	Het
Dab2ip	T	C	2: 35,582,388 (GRCm39)		probably null	Het
Dhx58	A	G	11: 100,587,823 (GRCm39)	V578A	probably damaging	Het
Diaph1	G	T	18: 38,024,902 (GRCm39)	Q520K	unknown	Het
Eefsec	C	A	6: 88,274,631 (GRCm39)	K444N	probably benign	Het
Eftud2	A	T	11: 102,759,443 (GRCm39)	H153Q	possibly damaging	Het
Eif5b	T	G	1: 38,058,324 (GRCm39)	S209A	probably benign	Het
Exosc2	T	A	2: 31,562,497 (GRCm39)	Y46N	probably damaging	Het
F2	C	T	2: 91,456,075 (GRCm39)	G562D	probably damaging	Het
Fgf23	G	A	6: 127,057,128 (GRCm39)	G148D	probably damaging	Het
Fstl5	G	A	3: 76,614,786 (GRCm39)	G179R	probably damaging	Het
Garre1	A	T	7: 33,938,644 (GRCm39)	W246R	probably damaging	Het
Gart	T	A	16: 91,422,282 (GRCm39)	Q745L	probably benign	Het
Gmeb1	T	A	4: 131,959,419 (GRCm39)	M212L	probably benign	Het
Gpaa1	T	C	15: 76,218,981 (GRCm39)	Y548H	probably damaging	Het
Gpatch1	T	C	7: 34,986,667 (GRCm39)	E763G	probably damaging	Het
Grm8	T	A	6: 27,762,389 (GRCm39)	I279F	probably damaging	Het
Hcls1	T	A	16: 36,771,536 (GRCm39)	H147Q	probably damaging	Het
Hpcal1	A	C	12: 17,836,389 (GRCm39)	D73A	probably damaging	Het
Il22ra1	T	C	4: 135,478,317 (GRCm39)	S463P	probably benign	Het
Itgbl1	G	A	14: 124,078,098 (GRCm39)		probably null	Het
Izumo3	G	T	4: 92,035,437 (GRCm39)		probably benign	Het
Kcna5	A	T	6: 126,510,346 (GRCm39)	L594Q	probably damaging	Het
Kif13a	A	T	13: 46,918,079 (GRCm39)	D409E	probably benign	Het
Kif9	A	T	9: 110,314,106 (GRCm39)	I39F	probably damaging	Het
Klri2	C	T	6: 129,709,171 (GRCm39)	R227H	possibly damaging	Het
Lamc3	G	A	2: 31,798,628 (GRCm39)	G445S	probably damaging	Het
Lctl	A	G	9: 64,024,980 (GRCm39)		probably benign	Het
Lrp4	T	C	2: 91,325,327 (GRCm39)	L1384P	probably damaging	Het
Mcm9	G	A	10: 53,439,526 (GRCm39)	S549L	possibly damaging	Het
Ms4a15	G	A	19: 10,956,697 (GRCm39)		probably benign	Het
Mtor	T	C	4: 148,555,081 (GRCm39)	V901A	possibly damaging	Het
Nckap1l	A	T	15: 103,390,391 (GRCm39)	I721F	probably benign	Het
Nemp2	T	C	1: 52,684,588 (GRCm39)	V298A	probably benign	Het
Npc1l1	T	A	11: 6,178,148 (GRCm39)	K421*	probably null	Het
Npr1	C	T	3: 90,363,244 (GRCm39)	V879M	probably damaging	Het
Odad4	A	G	11: 100,454,394 (GRCm39)	E393G	probably damaging	Het
Or2ad1	A	G	13: 21,326,336 (GRCm39)	V297A	possibly damaging	Het
Or51q1c	A	G	7: 103,652,709 (GRCm39)	T82A	probably benign	Het
Osgin1	A	T	8: 120,169,219 (GRCm39)	I39F	possibly damaging	Het
Phip	G	C	9: 82,809,244 (GRCm39)		probably null	Het
Pkdrej	G	T	15: 85,705,768 (GRCm39)	P56Q	possibly damaging	Het
Plcxd2	A	G	16: 45,800,889 (GRCm39)	Y112H	probably damaging	Het
Plekha1	C	T	7: 130,499,176 (GRCm39)	T155M	probably damaging	Het
Prkdc	T	C	16: 15,558,196 (GRCm39)		probably null	Het
Prss1	A	G	6: 41,439,495 (GRCm39)	H76R	probably damaging	Het
Psg23	T	C	7: 18,348,558 (GRCm39)	D83G	probably benign	Het
Ptprd	T	A	4: 76,055,140 (GRCm39)	Q196L	probably benign	Het
Ranbp3l	A	T	15: 9,063,067 (GRCm39)	H292L	probably damaging	Het
Ranbp6	T	C	19: 29,787,097 (GRCm39)	E1085G	probably benign	Het
Rccd1	A	G	7: 79,970,326 (GRCm39)	V97A	possibly damaging	Het
Rchy1	T	C	5: 92,105,458 (GRCm39)	S48G	probably benign	Het
Rnmt	G	A	18: 68,446,771 (GRCm39)	M265I	probably benign	Het
Robo3	A	T	9: 37,336,640 (GRCm39)	M376K	probably benign	Het
Rrp12	T	C	19: 41,862,289 (GRCm39)	D898G	probably benign	Het
Scg3	A	T	9: 75,570,462 (GRCm39)		probably benign	Het
Sec31b	A	T	19: 44,522,821 (GRCm39)	M57K	probably damaging	Het
Slc17a6	A	C	7: 51,315,892 (GRCm39)	I387L	probably benign	Het
Speer4a1	T	A	5: 26,240,982 (GRCm39)	Q170L	possibly damaging	Het
Srsf9	A	G	5: 115,470,260 (GRCm39)	D146G	possibly damaging	Het
Ss18	A	G	18: 14,788,200 (GRCm39)	M90T	probably damaging	Het
Syna	A	T	5: 134,588,314 (GRCm39)	F212I	possibly damaging	Het
Tex54	A	G	19: 8,718,221 (GRCm39)		probably benign	Het
Thsd1	A	G	8: 22,733,055 (GRCm39)	H34R	probably damaging	Het
Tmem143	T	C	7: 45,547,086 (GRCm39)	I84T	probably benign	Het
Trim50	T	C	5: 135,395,487 (GRCm39)	V281A	probably damaging	Het
Trp53i11	C	A	2: 93,029,696 (GRCm39)		probably benign	Het
Ttll4	C	T	1: 74,718,851 (GRCm39)	T234I	possibly damaging	Het
Ttyh1	A	T	7: 4,127,719 (GRCm39)	I136F	possibly damaging	Het
Ube2f	T	C	1: 91,189,976 (GRCm39)		probably benign	Het
Vcl	T	A	14: 21,037,083 (GRCm39)	L227*	probably null	Het
Vmn1r222	A	C	13: 23,416,974 (GRCm39)	C80G	probably damaging	Het
Vps13b	G	T	15: 35,926,365 (GRCm39)	A3889S	probably benign	Het
Vps8	T	C	16: 21,323,136 (GRCm39)		probably benign	Het
Zbtb44	A	G	9: 30,978,006 (GRCm39)	Y422C	probably damaging	Het
Zfp180	A	G	7: 23,805,158 (GRCm39)	S526G	possibly damaging	Het
Zfp518a	A	C	19: 40,904,310 (GRCm39)	E1413A	probably damaging	Het
Zfp629	T	A	7: 127,210,858 (GRCm39)	Y317F	probably damaging	Het
Zfp804b	T	C	5: 6,820,534 (GRCm39)	E843G	probably benign	Het

Other mutations in Fmnl3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00648:Fmnl3	APN	15	99,220,551 (GRCm39)	missense	probably damaging	1.00
IGL00672:Fmnl3	APN	15	99,223,562 (GRCm39)	missense	probably damaging	1.00
IGL00727:Fmnl3	APN	15	99,220,551 (GRCm39)	missense	probably damaging	1.00
IGL00754:Fmnl3	APN	15	99,220,551 (GRCm39)	missense	probably damaging	1.00
IGL00927:Fmnl3	APN	15	99,235,509 (GRCm39)	critical splice donor site	probably null
IGL02376:Fmnl3	APN	15	99,216,844 (GRCm39)	missense	possibly damaging	0.51
IGL02607:Fmnl3	APN	15	99,222,653 (GRCm39)	missense	probably damaging	1.00
IGL03323:Fmnl3	APN	15	99,219,162 (GRCm39)	missense	probably damaging	1.00
C9142:Fmnl3	UTSW	15	99,235,508 (GRCm39)	splice site	probably null
PIT4280001:Fmnl3	UTSW	15	99,219,134 (GRCm39)	critical splice donor site	probably null
R0003:Fmnl3	UTSW	15	99,219,013 (GRCm39)	missense	probably damaging	0.99
R0003:Fmnl3	UTSW	15	99,219,013 (GRCm39)	missense	probably damaging	0.99
R0116:Fmnl3	UTSW	15	99,220,619 (GRCm39)	splice site	probably benign
R0117:Fmnl3	UTSW	15	99,220,619 (GRCm39)	splice site	probably benign
R0138:Fmnl3	UTSW	15	99,220,619 (GRCm39)	splice site	probably benign
R0701:Fmnl3	UTSW	15	99,219,188 (GRCm39)	missense	probably damaging	0.99
R2338:Fmnl3	UTSW	15	99,268,108 (GRCm39)	missense	probably benign	0.01
R3729:Fmnl3	UTSW	15	99,219,745 (GRCm39)	missense	probably damaging	0.99
R4707:Fmnl3	UTSW	15	99,221,362 (GRCm39)	missense	probably benign	0.00
R5346:Fmnl3	UTSW	15	99,229,871 (GRCm39)	missense	probably damaging	1.00
R5655:Fmnl3	UTSW	15	99,219,743 (GRCm39)	missense	probably damaging	0.99
R5916:Fmnl3	UTSW	15	99,219,709 (GRCm39)	missense	probably damaging	0.99
R5951:Fmnl3	UTSW	15	99,223,791 (GRCm39)	missense	probably damaging	1.00
R5954:Fmnl3	UTSW	15	99,223,791 (GRCm39)	missense	probably damaging	1.00
R5957:Fmnl3	UTSW	15	99,223,791 (GRCm39)	missense	probably damaging	1.00
R6334:Fmnl3	UTSW	15	99,235,534 (GRCm39)	missense	probably damaging	1.00
R6891:Fmnl3	UTSW	15	99,223,754 (GRCm39)	missense	probably damaging	1.00
R7182:Fmnl3	UTSW	15	99,219,663 (GRCm39)	missense	probably damaging	0.99
R7423:Fmnl3	UTSW	15	99,227,281 (GRCm39)	missense	probably damaging	0.99
R7952:Fmnl3	UTSW	15	99,220,518 (GRCm39)	missense	probably damaging	0.97
R7977:Fmnl3	UTSW	15	99,225,979 (GRCm39)	missense	possibly damaging	0.89
R7987:Fmnl3	UTSW	15	99,225,979 (GRCm39)	missense	possibly damaging	0.89
R8749:Fmnl3	UTSW	15	99,219,322 (GRCm39)	missense	possibly damaging	0.88
R9397:Fmnl3	UTSW	15	99,225,938 (GRCm39)	critical splice donor site	probably null
R9598:Fmnl3	UTSW	15	99,223,210 (GRCm39)	missense	probably damaging	1.00
X0009:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0010:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0011:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0012:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0014:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0017:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0021:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0023:Fmnl3	UTSW	15	99,223,165 (GRCm39)	missense	probably damaging	1.00
X0023:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0028:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0033:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0060:Fmnl3	UTSW	15	99,217,919 (GRCm39)	missense	possibly damaging	0.69
X0064:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00
X0067:Fmnl3	UTSW	15	99,220,208 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGGCTCTAAAGTCATCCCAGTCTCC -3'
(R):5'- AACTTGACCAGAGCTTCCATAGCAC -3'

Sequencing Primer
(F):5'- CACTGAAGACAGTGCCATTGATC -3'
(R):5'- ACTCTTCTCTGGGTCTCAAAGG -3'

Posted On

2013-07-24