Mutagenetix > Incidental Mutation

Incidental Mutation 'R4594:Mx2'

344294

Institutional Source

Beutler Lab

Gene Symbol

Mx2

Ensembl Gene

ENSMUSG00000023341

Gene Name

MX dynamin-like GTPase 2

Synonyms

Mx-2

MMRRC Submission

041810-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.178) question?

Stock #

R4594 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

97337281-97362101 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to A at 97348632 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 268 (Y268*)

Ref Sequence

ENSEMBL: ENSMUSP00000140229 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024112] [ENSMUST00000188251] [ENSMUST00000190447]

AlphaFold

Q9WVP9

Predicted Effect

probably null
Transcript: ENSMUST00000024112
AA Change: Y268*

SMART Domains

Protein: ENSMUSP00000024112
Gene: ENSMUSG00000023341
AA Change: Y268*

Domain	Start	End	E-Value	Type
DYNc	39	282	2.71e-135	SMART
Blast:DYNc	426	539	4e-17	BLAST
GED	562	653	9.88e-30	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000188251
AA Change: Y268*

SMART Domains

Protein: ENSMUSP00000141038
Gene: ENSMUSG00000023341
AA Change: Y268*

Domain	Start	End	E-Value	Type
DYNc	39	282	1.3e-137	SMART
low complexity region	592	603	N/A	INTRINSIC
low complexity region	619	637	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190097

Predicted Effect

probably null
Transcript: ENSMUST00000190447
AA Change: Y268*

SMART Domains

Protein: ENSMUSP00000140229
Gene: ENSMUSG00000023341
AA Change: Y268*

Domain	Start	End	E-Value	Type
DYNc	39	282	1.3e-137	SMART

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.7%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700109H08Rik	A	G	5: 3,625,754 (GRCm39)	T64A	probably damaging	Het
4933427I04Rik	A	T	4: 123,754,331 (GRCm39)	T82S	possibly damaging	Het
Adamts15	A	T	9: 30,832,743 (GRCm39)	I264N	probably damaging	Het
Alpk1	G	A	3: 127,477,203 (GRCm39)	A285V	probably damaging	Het
Auh	T	C	13: 53,067,002 (GRCm39)		probably benign	Het
Cacna2d3	A	G	14: 28,704,303 (GRCm39)	F826S	probably benign	Het
Ccdc54	G	T	16: 50,410,380 (GRCm39)	Y295*	probably null	Het
Ctnna3	G	A	10: 64,421,858 (GRCm39)	V551I	probably benign	Het
Diaph3	C	T	14: 87,223,473 (GRCm39)	C347Y	probably damaging	Het
Dnajb5	A	G	4: 42,950,842 (GRCm39)		probably benign	Het
Dscam	A	T	16: 96,519,196 (GRCm39)	I847K	possibly damaging	Het
Fam8a1	T	C	13: 46,824,742 (GRCm39)	F243S	probably damaging	Het
Fat2	T	C	11: 55,175,578 (GRCm39)	I1712V	possibly damaging	Het
Fgfr1	T	C	8: 26,063,852 (GRCm39)	V793A	probably damaging	Het
Got2	T	C	8: 96,598,814 (GRCm39)	E196G	probably benign	Het
Gsk3b	G	A	16: 37,991,063 (GRCm39)	C107Y	possibly damaging	Het
H2-M5	T	C	17: 37,298,697 (GRCm39)	T250A	possibly damaging	Het
Il17f	T	A	1: 20,848,026 (GRCm39)	T151S	probably damaging	Het
Ints12	A	G	3: 132,814,629 (GRCm39)	N279D	probably benign	Het
Kcnd3	C	T	3: 105,566,082 (GRCm39)	A421V	probably damaging	Het
Kynu	T	A	2: 43,569,902 (GRCm39)	S395T	probably benign	Het
Llgl1	C	T	11: 60,597,147 (GRCm39)	T226I	probably benign	Het
Mael	T	A	1: 166,063,056 (GRCm39)	Q132L	probably damaging	Het
Mcpt1	A	T	14: 56,256,109 (GRCm39)	R49S	probably benign	Het
Meioc	G	T	11: 102,564,992 (GRCm39)	G203C	probably damaging	Het
Mfsd4b1	A	G	10: 39,883,313 (GRCm39)	S46P	probably benign	Het
Muc6	G	T	7: 141,218,685 (GRCm39)	T1996N	possibly damaging	Het
Myom1	A	G	17: 71,407,069 (GRCm39)	D1064G	possibly damaging	Het
Nek11	A	G	9: 105,270,046 (GRCm39)		probably null	Het
Nfe2	A	G	15: 103,157,232 (GRCm39)	L253S	probably damaging	Het
Nup205	T	C	6: 35,173,424 (GRCm39)	I478T	probably benign	Het
Nxpe2	T	C	9: 48,230,782 (GRCm39)	D529G	probably damaging	Het
Oard1	T	C	17: 48,722,267 (GRCm39)	S88P	possibly damaging	Het
Or11g25	A	G	14: 50,723,619 (GRCm39)	R235G	probably benign	Het
Or2p2	C	T	13: 21,256,692 (GRCm39)	V260I	probably benign	Het
Or4n4	G	A	14: 50,519,140 (GRCm39)	T190I	probably benign	Het
Or51k1	T	C	7: 103,661,624 (GRCm39)	D95G	probably benign	Het
Or52e5	T	C	7: 104,718,797 (GRCm39)	V41A	probably benign	Het
Or6k6	G	T	1: 173,944,886 (GRCm39)	T232N	probably damaging	Het
Or8b1	A	C	9: 38,400,057 (GRCm39)	H244P	probably damaging	Het
Osgin1	C	T	8: 120,171,992 (GRCm39)	T262I	possibly damaging	Het
Plcb4	A	T	2: 135,844,519 (GRCm39)	M146L	probably damaging	Het
Prkdc	A	T	16: 15,585,830 (GRCm39)	E2456V	possibly damaging	Het
Ptk2	G	A	15: 73,078,045 (GRCm39)	A1004V	probably damaging	Het
Rab15	G	A	12: 76,847,445 (GRCm39)		probably benign	Het
Rad51ap2	T	C	12: 11,507,881 (GRCm39)	V601A	probably benign	Het
Rasef	T	A	4: 73,698,626 (GRCm39)	I12F	possibly damaging	Het
Rdh14	T	A	12: 10,444,567 (GRCm39)	N139K	probably damaging	Het
Rexo2	A	T	9: 48,391,717 (GRCm39)	V46E	probably damaging	Het
Rskr	T	A	11: 78,182,473 (GRCm39)	V94D	possibly damaging	Het
Slmap	A	T	14: 26,186,772 (GRCm39)	L68H	probably damaging	Het
Speer3	C	G	5: 13,846,394 (GRCm39)	A238G	possibly damaging	Het
Tmem132e	T	C	11: 82,325,894 (GRCm39)	I206T	possibly damaging	Het
Trappc8	A	T	18: 20,970,005 (GRCm39)	V995E	probably benign	Het
Vmn2r12	A	C	5: 109,234,301 (GRCm39)	I637S	probably damaging	Het
Vmn2r124	T	C	17: 18,294,231 (GRCm39)	F773L	probably damaging	Het
Vmn2r99	A	T	17: 19,613,924 (GRCm39)	D548V	probably damaging	Het
Wdr81	T	C	11: 75,336,620 (GRCm39)	N1590D	probably benign	Het
Zbtb6	A	T	2: 37,319,054 (GRCm39)	N291K	possibly damaging	Het
Zfp119a	G	A	17: 56,173,325 (GRCm39)	R173C	probably benign	Het
Zmynd15	T	C	11: 70,355,008 (GRCm39)	L335P	probably damaging	Het

Other mutations in Mx2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00421:Mx2	APN	16	97,345,678 (GRCm39)	missense	probably damaging	0.99
IGL01111:Mx2	APN	16	97,359,919 (GRCm39)	missense	probably benign
IGL02103:Mx2	APN	16	97,345,795 (GRCm39)	missense	probably damaging	1.00
IGL02678:Mx2	APN	16	97,357,320 (GRCm39)	critical splice donor site	probably null
IGL03166:Mx2	APN	16	97,347,990 (GRCm39)	missense	probably damaging	1.00
IGL03323:Mx2	APN	16	97,347,575 (GRCm39)	missense	probably damaging	0.99
R0254:Mx2	UTSW	16	97,357,295 (GRCm39)	missense	probably benign
R0699:Mx2	UTSW	16	97,345,753 (GRCm39)	missense	probably damaging	1.00
R1180:Mx2	UTSW	16	97,357,209 (GRCm39)	missense	probably damaging	1.00
R1702:Mx2	UTSW	16	97,359,883 (GRCm39)	missense	probably benign
R1762:Mx2	UTSW	16	97,339,903 (GRCm39)	missense	probably benign	0.09
R1922:Mx2	UTSW	16	97,361,551 (GRCm39)	missense	probably benign	0.05
R2049:Mx2	UTSW	16	97,339,903 (GRCm39)	missense	probably benign	0.09
R2141:Mx2	UTSW	16	97,339,903 (GRCm39)	missense	probably benign	0.09
R2142:Mx2	UTSW	16	97,339,903 (GRCm39)	missense	probably benign	0.09
R3010:Mx2	UTSW	16	97,347,999 (GRCm39)	missense	possibly damaging	0.85
R4079:Mx2	UTSW	16	97,357,236 (GRCm39)	missense	probably damaging	0.98
R4553:Mx2	UTSW	16	97,353,205 (GRCm39)	missense	possibly damaging	0.52
R5211:Mx2	UTSW	16	97,348,633 (GRCm39)	missense	probably damaging	1.00
R5785:Mx2	UTSW	16	97,339,904 (GRCm39)	missense	possibly damaging	0.90
R6091:Mx2	UTSW	16	97,347,635 (GRCm39)	missense	probably damaging	1.00
R7250:Mx2	UTSW	16	97,348,664 (GRCm39)	missense	probably damaging	0.99
R7485:Mx2	UTSW	16	97,346,918 (GRCm39)	missense	probably benign	0.11
R7793:Mx2	UTSW	16	97,348,083 (GRCm39)	missense	probably damaging	1.00
R7816:Mx2	UTSW	16	97,346,812 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATCATGTCTGCCTCAGCCAAG -3'
(R):5'- TCATCCTCAGGCTGTTGCAC -3'

Sequencing Primer
(F):5'- GGATGAGATCCTGGTGGCC -3'
(R):5'- TCAGGCTGTTGCACACACAC -3'

Posted On

2015-09-25