Mutagenetix > Incidental Mutation

Incidental Mutation 'R4648:Vil1'

350452

Institutional Source

Beutler Lab

Gene Symbol

Vil1

Ensembl Gene

ENSMUSG00000026175

Gene Name

villin 1

Synonyms

Villin

MMRRC Submission

041909-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.371) question?

Stock #

R4648 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

74448543-74474719 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 74471457 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Threonine at position 746 (M746T)

Ref Sequence

ENSEMBL: ENSMUSP00000027366 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027366] [ENSMUST00000044260]

AlphaFold

Q62468

Predicted Effect

probably benign
Transcript: ENSMUST00000027366
AA Change: M746T

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000027366
Gene: ENSMUSG00000026175
AA Change: M746T

Domain	Start	End	E-Value	Type
GEL	17	114	2.93e-29	SMART
GEL	135	229	1.33e-18	SMART
GEL	251	349	5.85e-29	SMART
GEL	398	495	1.44e-28	SMART
GEL	515	601	7.31e-30	SMART
GEL	620	714	1.36e-29	SMART
VHP	792	827	1.77e-14	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000044260

SMART Domains

Protein: ENSMUSP00000035445
Gene: ENSMUSG00000033364

Domain	Start	End	E-Value	Type
Pfam:UCH_N	1	105	5.1e-47	PFAM
low complexity region	182	200	N/A	INTRINSIC
Pfam:UCH_1	341	645	3.4e-16	PFAM
UIM	704	723	1.33e1	SMART
UIM	806	825	1.04e-1	SMART
UIM	828	847	2.11e-2	SMART
low complexity region	893	909	N/A	INTRINSIC

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.5%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a family of calcium-regulated actin-binding proteins. This protein represents a dominant part of the brush border cytoskeleton which functions in the capping, severing, and bundling of actin filaments. Two mRNAs of 2.7 kb and 3.5 kb have been observed; they result from utilization of alternate poly-adenylation signals present in the terminal exon. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mutants do not exhibit gross abnormalities or apparent defects of microvilli morphogenesis, however in one line, an increased sensitivity to colitis induced by dextran sulfate was observed. [provided by MGI curators]

Allele List at MGI

All alleles(8) : Targeted(4) Gene trapped(4)

Other mutations in this stock

Total: 85 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700031F05Rik	G	T	X: 101,904,515 (GRCm39)	N132K	possibly damaging	Het
2010315B03Rik	T	A	9: 124,056,228 (GRCm39)	Y232F	probably benign	Het
2310079G19Rik	T	C	16: 88,424,255 (GRCm39)	S79G	probably benign	Het
4930568D16Rik	T	A	2: 35,244,458 (GRCm39)	Y298F	probably damaging	Het
Alpk2	A	G	18: 65,482,953 (GRCm39)	F352L	probably damaging	Het
Angpt1	T	A	15: 42,539,580 (GRCm39)	Y93F	probably benign	Het
Ankrd33b	T	C	15: 31,325,170 (GRCm39)	*129W	probably null	Het
Atp5pf	T	C	16: 84,625,343 (GRCm39)	M87V	probably benign	Het
Atp8b3	A	G	10: 80,361,457 (GRCm39)	S822P	possibly damaging	Het
Bbs10	A	G	10: 111,136,995 (GRCm39)	K703E	probably benign	Het
Bbs2	A	T	8: 94,807,507 (GRCm39)	V429E	probably damaging	Het
Bccip	C	T	7: 133,316,628 (GRCm39)	L83F	probably damaging	Het
Brd9	G	A	13: 74,088,895 (GRCm39)	V198I	probably benign	Het
C1galt1c1	A	T	X: 37,720,349 (GRCm39)	S216T	probably benign	Het
Calhm1	A	G	19: 47,132,240 (GRCm39)	L125P	probably damaging	Het
Ccdc110	A	T	8: 46,395,705 (GRCm39)	Q532L	possibly damaging	Het
Cdh19	G	A	1: 110,852,907 (GRCm39)	L343F	probably benign	Het
Cep350	A	G	1: 155,778,344 (GRCm39)	S1653P	possibly damaging	Het
Cmtm4	A	G	8: 105,082,952 (GRCm39)	I135T	possibly damaging	Het
Cmya5	A	G	13: 93,230,336 (GRCm39)	L1584P	possibly damaging	Het
Crocc2	G	A	1: 93,096,516 (GRCm39)	V24M	possibly damaging	Het
Crp	A	G	1: 172,525,704 (GRCm39)	M1V	probably null	Het
Csmd1	G	A	8: 16,048,788 (GRCm39)	Q2305*	probably null	Het
Cyp2c38	T	A	19: 39,449,132 (GRCm39)	I74F	probably benign	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Dcaf1	A	T	9: 106,742,876 (GRCm39)		probably benign	Het
Dhx16	C	G	17: 36,196,527 (GRCm39)	A565G	probably benign	Het
Dock7	C	A	4: 98,857,881 (GRCm39)	E1448*	probably null	Het
Dpf2	C	T	19: 5,957,109 (GRCm39)	R38H	probably damaging	Het
E030030I06Rik	T	A	10: 22,024,744 (GRCm39)	R56S	unknown	Het
Etnk1	A	G	6: 143,141,000 (GRCm39)	Y248C	probably damaging	Het
Ext1	A	G	15: 52,953,383 (GRCm39)	S494P	possibly damaging	Het
Gk2	T	C	5: 97,603,579 (GRCm39)	S420G	probably benign	Het
Gm26596	T	C	10: 112,765,064 (GRCm39)		probably benign	Het
Gm5414	G	T	15: 101,536,543 (GRCm39)	N27K	possibly damaging	Het
Gskip	A	G	12: 105,664,988 (GRCm39)	D9G	probably benign	Het
H2-K2	T	A	17: 34,194,989 (GRCm39)		noncoding transcript	Het
Hk1	T	G	10: 62,140,558 (GRCm39)	S105R	probably benign	Het
Hmg20b	T	A	10: 81,184,416 (GRCm39)	Q129L	probably damaging	Het
Idnk	A	G	13: 58,310,683 (GRCm39)	D67G	probably benign	Het
Igfbp5	G	T	1: 72,903,222 (GRCm39)	H118N	probably benign	Het
Irf4	A	T	13: 30,947,580 (GRCm39)	Y427F	probably benign	Het
Khdc3	A	G	9: 73,009,868 (GRCm39)	E26G	possibly damaging	Het
Kif7	T	C	7: 79,358,939 (GRCm39)	D512G	probably damaging	Het
Lamb3	T	A	1: 193,013,665 (GRCm39)	I513N	probably damaging	Het
Lipo3	A	G	19: 33,760,860 (GRCm39)	L174P	probably damaging	Het
Lnx1	C	T	5: 74,771,457 (GRCm39)	V350I	probably benign	Het
Map3k21	A	G	8: 126,668,850 (GRCm39)	D812G	probably benign	Het
Mast2	G	T	4: 116,172,036 (GRCm39)	Y637*	probably null	Het
Matn2	T	C	15: 34,428,679 (GRCm39)	I681T	probably damaging	Het
Med18	A	T	4: 132,190,274 (GRCm39)	V37D	possibly damaging	Het
Mip	T	A	10: 128,062,922 (GRCm39)	H122Q	probably benign	Het
Mmp13	A	T	9: 7,274,233 (GRCm39)	D180V	probably damaging	Het
Mpg	C	A	11: 32,180,034 (GRCm39)	C187*	probably null	Het
Mtmr14	A	G	6: 113,237,567 (GRCm39)	E256G	probably benign	Het
Myo7b	C	T	18: 32,100,178 (GRCm39)		probably null	Het
Nhsl3	G	T	4: 129,115,733 (GRCm39)	T977K	probably benign	Het
Nmt1	T	A	11: 102,954,743 (GRCm39)	V425D	probably damaging	Het
Nynrin	T	A	14: 56,110,351 (GRCm39)	Y1819*	probably null	Het
Or10ak16	A	G	4: 118,751,147 (GRCm39)	N289S	possibly damaging	Het
Or4c107	T	A	2: 88,789,556 (GRCm39)	F249I	probably damaging	Het
Or5i1	T	C	2: 87,613,565 (GRCm39)	V227A	possibly damaging	Het
Otof	T	C	5: 30,540,914 (GRCm39)	E875G	possibly damaging	Het
Paqr3	T	A	5: 97,256,069 (GRCm39)	R102*	probably null	Het
Phc1	T	C	6: 122,298,872 (GRCm39)	I699V	possibly damaging	Het
Prkdc	T	G	16: 15,634,638 (GRCm39)	D3594E	probably benign	Het
Pstpip1	A	T	9: 56,032,502 (GRCm39)	D246V	probably damaging	Het
Rbm46	A	T	3: 82,771,765 (GRCm39)	D283E	probably benign	Het
Ror2	A	T	13: 53,439,536 (GRCm39)	C9*	probably null	Het
Setd1b	C	T	5: 123,286,175 (GRCm39)	A407V	unknown	Het
Slc26a4	T	G	12: 31,590,525 (GRCm39)	D376A	possibly damaging	Het
Smarcad1	A	G	6: 65,044,073 (GRCm39)	E215G	probably benign	Het
Spag16	G	A	1: 69,866,194 (GRCm39)	R11Q	probably null	Het
Sult1d1	T	A	5: 87,713,954 (GRCm39)	Q30L	probably benign	Het
Tbc1d5	A	G	17: 51,043,251 (GRCm39)	C746R	probably benign	Het
Tdh	A	G	14: 63,731,205 (GRCm39)	L323P	possibly damaging	Het
Tet2	A	T	3: 133,193,843 (GRCm39)	M197K	probably benign	Het
Tnn	T	C	1: 159,973,612 (GRCm39)	M252V	probably benign	Het
Trdn	G	T	10: 33,071,977 (GRCm39)	E215*	probably null	Het
Trem1	G	A	17: 48,551,590 (GRCm39)	V84I	probably benign	Het
Tspan5	T	C	3: 138,604,076 (GRCm39)	F154L	probably damaging	Het
Usp45	A	G	4: 21,825,044 (GRCm39)	R647G	probably benign	Het
Usp50	T	A	2: 126,619,953 (GRCm39)	I120F	probably damaging	Het
Washc4	T	A	10: 83,410,407 (GRCm39)	M665K	possibly damaging	Het
Zfp750	T	C	11: 121,402,706 (GRCm39)	T681A	probably benign	Het

Other mutations in Vil1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00162:Vil1	APN	1	74,463,034 (GRCm39)	missense	probably damaging	1.00
IGL00703:Vil1	APN	1	74,463,119 (GRCm39)	missense	possibly damaging	0.61
IGL01011:Vil1	APN	1	74,474,046 (GRCm39)	splice site	probably null
IGL01314:Vil1	APN	1	74,467,397 (GRCm39)	missense	probably damaging	1.00
IGL01772:Vil1	APN	1	74,454,278 (GRCm39)	missense	probably benign
IGL02378:Vil1	APN	1	74,469,850 (GRCm39)	splice site	probably null
IGL02517:Vil1	APN	1	74,465,851 (GRCm39)	missense	probably benign	0.43
IGL02955:Vil1	APN	1	74,457,682 (GRCm39)	missense	probably benign	0.10
IGL03036:Vil1	APN	1	74,458,771 (GRCm39)	missense	probably damaging	1.00
PIT4362001:Vil1	UTSW	1	74,460,542 (GRCm39)	missense	probably damaging	1.00
R0104:Vil1	UTSW	1	74,457,525 (GRCm39)	missense	probably benign	0.44
R0241:Vil1	UTSW	1	74,465,853 (GRCm39)	missense	probably damaging	1.00
R0241:Vil1	UTSW	1	74,465,853 (GRCm39)	missense	probably damaging	1.00
R0496:Vil1	UTSW	1	74,460,499 (GRCm39)	missense	possibly damaging	0.88
R1329:Vil1	UTSW	1	74,466,717 (GRCm39)	missense	probably benign	0.00
R1824:Vil1	UTSW	1	74,457,606 (GRCm39)	missense	probably benign	0.00
R1916:Vil1	UTSW	1	74,457,684 (GRCm39)	missense	probably benign
R2188:Vil1	UTSW	1	74,466,724 (GRCm39)	missense	probably benign	0.22
R2216:Vil1	UTSW	1	74,464,838 (GRCm39)	missense	probably benign	0.05
R3808:Vil1	UTSW	1	74,466,772 (GRCm39)	missense	probably benign
R3939:Vil1	UTSW	1	74,471,574 (GRCm39)	missense	probably benign	0.09
R4288:Vil1	UTSW	1	74,457,684 (GRCm39)	missense	probably benign
R4748:Vil1	UTSW	1	74,460,425 (GRCm39)	missense	probably damaging	1.00
R5333:Vil1	UTSW	1	74,471,549 (GRCm39)	missense	probably benign
R5429:Vil1	UTSW	1	74,471,490 (GRCm39)	missense	probably benign	0.05
R5973:Vil1	UTSW	1	74,455,192 (GRCm39)	missense	possibly damaging	0.93
R6007:Vil1	UTSW	1	74,459,026 (GRCm39)	missense	probably damaging	1.00
R6247:Vil1	UTSW	1	74,471,498 (GRCm39)	missense	probably benign
R6306:Vil1	UTSW	1	74,460,470 (GRCm39)	missense	possibly damaging	0.90
R6989:Vil1	UTSW	1	74,463,113 (GRCm39)	missense	probably damaging	0.99
R7112:Vil1	UTSW	1	74,455,161 (GRCm39)	missense	probably damaging	1.00
R7320:Vil1	UTSW	1	74,457,603 (GRCm39)	missense	probably damaging	1.00
R7481:Vil1	UTSW	1	74,459,058 (GRCm39)	missense	probably damaging	1.00
R7553:Vil1	UTSW	1	74,465,891 (GRCm39)	critical splice donor site	probably null
R7709:Vil1	UTSW	1	74,465,754 (GRCm39)	missense	probably benign	0.39
R7791:Vil1	UTSW	1	74,467,295 (GRCm39)	missense	probably damaging	1.00
R8159:Vil1	UTSW	1	74,463,136 (GRCm39)	missense	probably benign	0.00
R8190:Vil1	UTSW	1	74,474,052 (GRCm39)	nonsense	probably null
R9650:Vil1	UTSW	1	74,464,775 (GRCm39)	missense	probably benign	0.32
R9679:Vil1	UTSW	1	74,469,833 (GRCm39)	missense	probably benign	0.00
R9734:Vil1	UTSW	1	74,454,309 (GRCm39)	missense	possibly damaging	0.46
Z1176:Vil1	UTSW	1	74,467,391 (GRCm39)	missense	probably damaging	0.98
Z1177:Vil1	UTSW	1	74,460,589 (GRCm39)	missense	probably benign
Z1177:Vil1	UTSW	1	74,454,291 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AACTGACTTAGGCCAGTTGC -3'
(R):5'- ATGGACCAGACCTTGTCCTG -3'

Sequencing Primer
(F):5'- CTAGGCTATTAGCTTTTGGGTCCAAC -3'
(R):5'- AGACCTTGTCCTGCTTGTG -3'

Posted On

2015-10-08