Mutagenetix > Incidental Mutation

Incidental Mutation 'R7090:Mtss2'

550157

Institutional Source

Beutler Lab

Gene Symbol

Mtss2

Ensembl Gene

ENSMUSG00000033763

Gene Name

MTSS I-BAR domain containing 2

Synonyms

Mtss1l, ABBA

MMRRC Submission

045184-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7090 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

111448108-111468032 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 111456656 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 242 (V242E)

Ref Sequence

ENSEMBL: ENSMUSP00000050211 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052457] [ENSMUST00000144041]

AlphaFold

Q6P9S0

Predicted Effect

probably damaging
Transcript: ENSMUST00000052457
AA Change: V242E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000050211
Gene: ENSMUSG00000033763
AA Change: V242E

Domain	Start	End	E-Value	Type
Pfam:IMD	15	236	8.1e-108	PFAM
low complexity region	252	274	N/A	INTRINSIC
low complexity region	284	295	N/A	INTRINSIC
low complexity region	312	330	N/A	INTRINSIC
low complexity region	368	386	N/A	INTRINSIC
low complexity region	429	442	N/A	INTRINSIC
low complexity region	546	562	N/A	INTRINSIC
low complexity region	668	690	N/A	INTRINSIC

Predicted Effect

SMART Domains

Protein: ENSMUSP00000116518
Gene: ENSMUSG00000033763
AA Change: V127E

Domain	Start	End	E-Value	Type
Pfam:IMD	1	122	1e-56	PFAM
low complexity region	138	179	N/A	INTRINSIC
low complexity region	202	213	N/A	INTRINSIC
low complexity region	230	248	N/A	INTRINSIC
low complexity region	286	304	N/A	INTRINSIC
low complexity region	347	360	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000144041
AA Change: V180E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000115220
Gene: ENSMUSG00000033763
AA Change: V180E

Domain	Start	End	E-Value	Type
Pfam:IMD	1	174	3.6e-72	PFAM
low complexity region	190	212	N/A	INTRINSIC
low complexity region	222	233	N/A	INTRINSIC
low complexity region	250	268	N/A	INTRINSIC
low complexity region	306	324	N/A	INTRINSIC
low complexity region	367	380	N/A	INTRINSIC
low complexity region	484	500	N/A	INTRINSIC
low complexity region	606	628	N/A	INTRINSIC

Predicted Effect

SMART Domains

Protein: ENSMUSP00000119495
Gene: ENSMUSG00000033763
AA Change: V131E

Domain	Start	End	E-Value	Type
Pfam:IMD	1	126	2.5e-59	PFAM
low complexity region	142	183	N/A	INTRINSIC
low complexity region	206	217	N/A	INTRINSIC
low complexity region	239	249	N/A	INTRINSIC

Meta Mutation Damage Score

0.5527

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Calm3	A	T	7: 16,651,004 (GRCm39)	Y139*	probably null	Het
Ccdc27	T	C	4: 154,112,523 (GRCm39)	N584S	probably benign	Het
Cdh24	C	G	14: 54,876,964 (GRCm39)	G13A	probably damaging	Het
Chd8	T	C	14: 52,452,677 (GRCm39)	K1281E	probably damaging	Het
Clasp1	G	T	1: 118,409,816 (GRCm39)	G4C	probably benign	Het
Cul9	G	T	17: 46,811,765 (GRCm39)	P2488T	probably damaging	Het
Daam2	A	G	17: 49,789,973 (GRCm39)	V428A	probably damaging	Het
Dcaf8	A	G	1: 172,016,535 (GRCm39)	S441G	probably damaging	Het
Dchs2	A	G	3: 83,255,581 (GRCm39)	T2426A	probably benign	Het
Dnai3	C	A	3: 145,746,582 (GRCm39)	K881N	possibly damaging	Het
Dpys	A	G	15: 39,690,279 (GRCm39)	V358A	probably damaging	Het
Efhd1	A	G	1: 87,217,219 (GRCm39)	D112G	probably damaging	Het
Exoc1	T	C	5: 76,714,800 (GRCm39)	S120P	unknown	Het
Fyco1	A	G	9: 123,626,784 (GRCm39)	L1309S	probably damaging	Het
Gm14403	A	G	2: 177,201,114 (GRCm39)	N111S	possibly damaging	Het
Gm5901	A	G	7: 105,026,555 (GRCm39)	T108A	probably benign	Het
Idh2	TCCCAGG	T	7: 79,748,079 (GRCm39)		probably benign	Het
Itgb5	T	G	16: 33,705,464 (GRCm39)	D251E	probably damaging	Het
Kcnk15	T	C	2: 163,700,637 (GRCm39)	V292A	probably benign	Het
Kdm2a	A	T	19: 4,369,169 (GRCm39)	Y1149N	probably damaging	Het
Kdm3a	T	C	6: 71,572,529 (GRCm39)	T1011A	possibly damaging	Het
Krt35	A	T	11: 99,986,498 (GRCm39)		probably null	Het
Lipn	T	A	19: 34,049,180 (GRCm39)	D115E	possibly damaging	Het
Lpin3	T	G	2: 160,738,672 (GRCm39)	L208R	probably damaging	Het
Ltf	C	A	9: 110,855,048 (GRCm39)	Q354K	probably benign	Het
Marf1	C	A	16: 13,929,566 (GRCm39)	C1680F	possibly damaging	Het
Myo7b	T	C	18: 32,131,765 (GRCm39)	Y477C	probably damaging	Het
Nbn	T	A	4: 15,981,350 (GRCm39)	S481T	probably benign	Het
Ncoa2	A	G	1: 13,257,062 (GRCm39)	Y146H	probably damaging	Het
Ntng1	A	T	3: 109,842,496 (GRCm39)	C92*	probably null	Het
Or10ad1b	C	T	15: 98,125,083 (GRCm39)	V150I	probably benign	Het
Or2n1b	G	A	17: 38,460,385 (GRCm39)	G302D	probably benign	Het
Or8k18	T	A	2: 86,085,420 (GRCm39)	N206Y	probably damaging	Het
Or8k31-ps1	T	C	2: 86,356,471 (GRCm39)	I17V	probably benign	Het
Os9	A	T	10: 126,935,547 (GRCm39)	S308T	probably benign	Het
Otx2	T	A	14: 48,896,192 (GRCm39)	T289S	probably benign	Het
Pakap	C	T	4: 57,648,042 (GRCm39)	A60V	probably benign	Het
Pigg	A	G	5: 108,484,378 (GRCm39)	T675A	possibly damaging	Het
Pink1	C	T	4: 138,042,912 (GRCm39)	E461K	probably damaging	Het
Pip5k1a	A	G	3: 94,967,809 (GRCm39)	S543P	possibly damaging	Het
Prkaa1	A	G	15: 5,206,611 (GRCm39)	T454A	probably benign	Het
Ptk2	G	A	15: 73,093,658 (GRCm39)	P854S	possibly damaging	Het
Rab31	C	T	17: 66,005,012 (GRCm39)	V83I	possibly damaging	Het
Rabggtb	G	T	3: 153,615,986 (GRCm39)	D117E	probably benign	Het
Rbl1	T	C	2: 156,994,820 (GRCm39)	H951R	probably benign	Het
Sapcd2	A	G	2: 25,266,091 (GRCm39)	S314G	probably benign	Het
Septin4	T	C	11: 87,475,264 (GRCm39)	L164P	probably damaging	Het
Shroom1	A	G	11: 53,356,760 (GRCm39)	E541G	probably damaging	Het
Slc26a7	C	A	4: 14,565,460 (GRCm39)	G208*	probably null	Het
Smco2	A	G	6: 146,772,711 (GRCm39)	I304M	probably damaging	Het
Spg7	T	C	8: 123,818,491 (GRCm39)		probably null	Het
Spocd1	T	C	4: 129,847,691 (GRCm39)	F552L		Het
St6galnac2	T	C	11: 116,568,461 (GRCm39)	D334G	probably damaging	Het
Sub1	A	G	15: 11,986,572 (GRCm39)	S92P	probably benign	Het
Syne2	T	C	12: 75,989,125 (GRCm39)	F1829L	probably benign	Het
Tdrd1	T	C	19: 56,839,833 (GRCm39)	V631A	probably benign	Het
Tdrd9	T	C	12: 111,958,904 (GRCm39)	S113P	probably benign	Het
Tgfbrap1	A	C	1: 43,110,725 (GRCm39)	V260G	probably damaging	Het
Tyw3	G	C	3: 154,299,426 (GRCm39)	S94R	probably benign	Het
Urb2	T	C	8: 124,757,338 (GRCm39)	V1015A	probably benign	Het
Usp5	A	G	6: 124,806,357 (GRCm39)	M1T	probably null	Het
Utrn	T	C	10: 12,560,260 (GRCm39)	D1343G	possibly damaging	Het
Vmn2r56	T	C	7: 12,449,254 (GRCm39)	Y328C	probably damaging	Het
Vmn2r99	A	T	17: 19,613,972 (GRCm39)	E564V	possibly damaging	Het
Zc3h8	T	C	2: 128,777,241 (GRCm39)	T133A	possibly damaging	Het

Other mutations in Mtss2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02124:Mtss2	APN	8	111,464,256 (GRCm39)	missense	probably damaging	1.00
R0620:Mtss2	UTSW	8	111,464,580 (GRCm39)	missense	probably damaging	0.98
R0685:Mtss2	UTSW	8	111,454,029 (GRCm39)	critical splice donor site	probably null
R2082:Mtss2	UTSW	8	111,452,889 (GRCm39)	critical splice donor site	probably null
R2149:Mtss2	UTSW	8	111,453,015 (GRCm39)	missense	possibly damaging	0.58
R2266:Mtss2	UTSW	8	111,455,362 (GRCm39)	missense	possibly damaging	0.80
R2267:Mtss2	UTSW	8	111,455,362 (GRCm39)	missense	possibly damaging	0.80
R2269:Mtss2	UTSW	8	111,455,362 (GRCm39)	missense	possibly damaging	0.80
R2378:Mtss2	UTSW	8	111,464,981 (GRCm39)	missense	probably damaging	1.00
R3756:Mtss2	UTSW	8	111,456,692 (GRCm39)	missense	probably damaging	1.00
R4005:Mtss2	UTSW	8	111,465,673 (GRCm39)	frame shift	probably null
R4552:Mtss2	UTSW	8	111,465,137 (GRCm39)	missense	probably damaging	1.00
R4553:Mtss2	UTSW	8	111,465,137 (GRCm39)	missense	probably damaging	1.00
R4849:Mtss2	UTSW	8	111,452,875 (GRCm39)	missense	possibly damaging	0.92
R5212:Mtss2	UTSW	8	111,455,850 (GRCm39)	missense	probably damaging	1.00
R6294:Mtss2	UTSW	8	111,453,960 (GRCm39)	missense	possibly damaging	0.89
R6336:Mtss2	UTSW	8	111,458,796 (GRCm39)	missense	probably damaging	1.00
R7580:Mtss2	UTSW	8	111,464,268 (GRCm39)	missense	possibly damaging	0.95
R7581:Mtss2	UTSW	8	111,452,845 (GRCm39)	missense	possibly damaging	0.92
R7810:Mtss2	UTSW	8	111,452,833 (GRCm39)	missense	probably damaging	0.99
R8497:Mtss2	UTSW	8	111,465,222 (GRCm39)	missense	possibly damaging	0.95
R9033:Mtss2	UTSW	8	111,465,651 (GRCm39)	missense	probably damaging	1.00
R9596:Mtss2	UTSW	8	111,458,689 (GRCm39)	missense
R9640:Mtss2	UTSW	8	111,464,575 (GRCm39)	missense	probably benign	0.00
R9796:Mtss2	UTSW	8	111,456,753 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- AGCCCATGTTTAAAAGAAGGCTG -3'
(R):5'- CCAATGTGTGCACCCGTATC -3'

Sequencing Primer
(F):5'- CCATGTTTAAAAGAAGGCTGAAGTTG -3'
(R):5'- CACCCGTATCTCCTATATGTGAGAAG -3'

Posted On

2019-05-15