Mutagenetix > Incidental Mutation

Incidental Mutation 'R5567:Mxra8'

436906

Institutional Source

Beutler Lab

Gene Symbol

Mxra8

Ensembl Gene

ENSMUSG00000029070

Gene Name

matrix-remodelling associated 8

Synonyms

1200013A08Rik, Asp3, limitrin, DICAM

MMRRC Submission

043124-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5567 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

155924137-155928545 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 155925465 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Threonine at position 58 (M58T)

Ref Sequence

ENSEMBL: ENSMUSP00000030947 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030947] [ENSMUST00000141883]

AlphaFold

Q9DBV4

Predicted Effect

probably damaging
Transcript: ENSMUST00000030947
AA Change: M58T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000030947
Gene: ENSMUSG00000029070
AA Change: M58T

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
IG	38	156	6.16e-4	SMART
IG	170	291	9.71e-2	SMART
transmembrane domain	340	362	N/A	INTRINSIC
low complexity region	371	384	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000097740

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126487

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132142

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133592

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141766

Predicted Effect

probably damaging
Transcript: ENSMUST00000141883
AA Change: M55T

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000114929
Gene: ENSMUSG00000029070
AA Change: M55T

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
IG	35	153	6.16e-4	SMART
IG	167	288	9.71e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143886

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.6%
20x: 96.0%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Phenotypic analysis of mice homozygous for a gene trap allele indicates this mutation has no notable phenotype in any parameter tested in a high-throughput screen. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aak1	C	T	6: 86,932,150 (GRCm39)	Q374*	probably null	Het
Adam19	A	G	11: 46,027,077 (GRCm39)	D570G	probably damaging	Het
Aqr	G	A	2: 113,979,451 (GRCm39)	T328M	probably damaging	Het
Bltp3b	T	A	10: 89,644,383 (GRCm39)	M29K	probably benign	Het
Boc	G	A	16: 44,313,187 (GRCm39)	T559I	probably damaging	Het
Cadps	A	T	14: 12,473,497 (GRCm38)	I876N	possibly damaging	Het
Cdh9	A	G	15: 16,855,930 (GRCm39)	T657A	probably damaging	Het
Cep104	T	C	4: 154,086,734 (GRCm39)	S794P	possibly damaging	Het
Cep72	T	C	13: 74,188,260 (GRCm39)	Q211R	probably benign	Het
Coq6	T	A	12: 84,415,413 (GRCm39)	D145E	probably benign	Het
Crym	T	C	7: 119,801,116 (GRCm39)	E11G	probably benign	Het
Csmd3	A	T	15: 47,508,864 (GRCm39)	M2907K	possibly damaging	Het
Cspg4	A	C	9: 56,793,932 (GRCm39)	I556L	probably benign	Het
Cwf19l2	T	A	9: 3,456,831 (GRCm39)	D721E	probably damaging	Het
Defb36	T	A	2: 152,454,503 (GRCm39)	V54E	probably damaging	Het
Dlg5	C	A	14: 24,242,981 (GRCm39)	E55*	probably null	Het
Dna2	G	T	10: 62,802,452 (GRCm39)	A857S	possibly damaging	Het
E330034G19Rik	A	G	14: 24,346,892 (GRCm39)	K60E	possibly damaging	Het
Eps8l2	G	A	7: 140,934,920 (GRCm39)	R76Q	possibly damaging	Het
Fbxl18	A	G	5: 142,881,022 (GRCm39)		probably benign	Het
Flnc	T	A	6: 29,444,044 (GRCm39)	C619*	probably null	Het
Ftcd	A	G	10: 76,423,967 (GRCm39)	K503E	probably benign	Het
Gbp2b	C	T	3: 142,317,126 (GRCm39)	A494V	possibly damaging	Het
Gfral	C	T	9: 76,115,900 (GRCm39)	A25T	probably benign	Het
Gins2	T	A	8: 121,315,684 (GRCm39)	D24V	possibly damaging	Het
Gm10985	T	C	3: 53,752,683 (GRCm39)	I22T	probably damaging	Het
Golga4	T	A	9: 118,387,251 (GRCm39)	S1458T	probably damaging	Het
Gpatch1	T	C	7: 35,006,640 (GRCm39)	K176R	probably damaging	Het
Gsto1	T	C	19: 47,846,338 (GRCm39)	W62R	probably damaging	Het
Gtf2h3	C	T	5: 124,722,360 (GRCm39)	T121I	probably benign	Het
Gxylt1	A	G	15: 93,152,180 (GRCm39)		probably null	Het
Hs6st1	C	T	1: 36,142,719 (GRCm39)	P218L	probably benign	Het
Itpr3	C	T	17: 27,322,880 (GRCm39)	T1119M	possibly damaging	Het
Kif5c	A	G	2: 49,620,211 (GRCm39)	D226G	possibly damaging	Het
Klk1b1	T	A	7: 43,620,593 (GRCm39)	S228T	probably damaging	Het
Krt1	A	G	15: 101,755,340 (GRCm39)	F473S	probably benign	Het
Large1	A	G	8: 73,564,081 (GRCm39)	S562P	possibly damaging	Het
Lpxn	T	A	19: 12,810,023 (GRCm39)	M265K	possibly damaging	Het
Lrriq1	G	A	10: 103,006,457 (GRCm39)	P1223S	possibly damaging	Het
Map3k9	A	G	12: 81,778,798 (GRCm39)	L505P	possibly damaging	Het
Morn2	A	G	17: 80,604,709 (GRCm39)	D128G	probably damaging	Het
Msl2	A	G	9: 100,978,936 (GRCm39)	K437E	possibly damaging	Het
Msr1	T	C	8: 40,064,760 (GRCm39)	I305V	probably benign	Het
Muc4	A	G	16: 32,598,066 (GRCm39)	E3237G	possibly damaging	Het
Myo16	A	G	8: 10,372,676 (GRCm39)	D125G	probably damaging	Het
Myom2	A	G	8: 15,152,546 (GRCm39)	Q631R	probably benign	Het
Nlrp1b	T	A	11: 71,072,229 (GRCm39)	H538L	probably benign	Het
Nme3	T	A	17: 25,115,823 (GRCm39)		probably null	Het
Nop2	T	C	6: 125,110,726 (GRCm39)	S68P	probably benign	Het
Nploc4	C	T	11: 120,275,440 (GRCm39)	V499M	probably benign	Het
Nub1	A	G	5: 24,913,814 (GRCm39)	E565G	possibly damaging	Het
Or1e19	C	T	11: 73,316,272 (GRCm39)	C179Y	probably damaging	Het
Or6e1	A	G	14: 54,519,825 (GRCm39)	F176L	probably damaging	Het
Or7e168	A	G	9: 19,719,674 (GRCm39)	D20G	probably damaging	Het
Or9g3	G	A	2: 85,589,994 (GRCm39)	S242F	probably damaging	Het
Parl	A	G	16: 20,101,762 (GRCm39)	M90T	probably damaging	Het
Pelo	T	C	13: 115,226,152 (GRCm39)	I102V	probably benign	Het
Pigt	T	A	2: 164,343,482 (GRCm39)	Y319*	probably null	Het
Plb1	A	G	5: 32,521,543 (GRCm39)	T1465A	unknown	Het
Plxna4	T	C	6: 32,134,915 (GRCm39)	N1763D	possibly damaging	Het
Pmpca	A	G	2: 26,280,553 (GRCm39)	E133G	probably damaging	Het
Pus7l	G	A	15: 94,425,746 (GRCm39)	P552S	probably benign	Het
Qsox2	A	G	2: 26,115,230 (GRCm39)	M1T	probably null	Het
Ralb	C	T	1: 119,411,265 (GRCm39)	V25I	probably damaging	Het
Rbbp6	A	G	7: 122,601,057 (GRCm39)		probably benign	Het
Rnf43	A	G	11: 87,618,271 (GRCm39)	E187G	probably damaging	Het
Rpl31	C	T	1: 39,409,108 (GRCm39)	R41C	probably benign	Het
Scap	A	G	9: 110,206,712 (GRCm39)	S386G	probably damaging	Het
Skint10	T	C	4: 112,573,067 (GRCm39)	Y243C	probably damaging	Het
Stpg2	A	G	3: 139,125,547 (GRCm39)	T447A	probably benign	Het
Tas1r1	G	A	4: 152,122,782 (GRCm39)	A21V	probably damaging	Het
Tas2r122	C	T	6: 132,688,335 (GRCm39)	G186E	probably benign	Het
Tenm4	C	A	7: 96,545,416 (GRCm39)	Y2477*	probably null	Het
Them7	A	G	2: 105,209,153 (GRCm39)	T158A	probably benign	Het
Tmcc2	A	C	1: 132,285,543 (GRCm39)	S608A	probably benign	Het
Ttc41	T	C	10: 86,596,784 (GRCm39)		probably null	Het
Ttk	T	A	9: 83,744,588 (GRCm39)	N593K	possibly damaging	Het
Tulp1	A	G	17: 28,578,172 (GRCm39)	V289A	possibly damaging	Het
Unc93a2	T	C	17: 7,631,202 (GRCm39)	T456A	probably benign	Het
Usp34	A	C	11: 23,438,336 (GRCm39)	Q278P	probably damaging	Het
Vmn2r78	T	A	7: 86,570,737 (GRCm39)	D418E	probably benign	Het
Vmn2r90	C	T	17: 17,932,336 (GRCm39)	A81V	probably damaging	Het
Xpc	T	A	6: 91,475,117 (GRCm39)	N636I	probably damaging	Het
Zfp563	A	T	17: 33,308,431 (GRCm39)		probably benign	Het

Other mutations in Mxra8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00235:Mxra8	APN	4	155,927,020 (GRCm39)	missense	probably benign	0.06
IGL01871:Mxra8	APN	4	155,927,258 (GRCm39)	missense	probably benign
IGL02900:Mxra8	APN	4	155,925,668 (GRCm39)	splice site	probably null
IGL02900:Mxra8	APN	4	155,925,576 (GRCm39)	missense	possibly damaging	0.52
Buffet	UTSW	4	155,927,593 (GRCm39)	missense	possibly damaging	0.89
R0206:Mxra8	UTSW	4	155,927,053 (GRCm39)	missense	probably damaging	0.97
R0206:Mxra8	UTSW	4	155,927,053 (GRCm39)	missense	probably damaging	0.97
R0513:Mxra8	UTSW	4	155,926,190 (GRCm39)	missense	probably benign	0.00
R1318:Mxra8	UTSW	4	155,925,956 (GRCm39)	missense	probably damaging	1.00
R1414:Mxra8	UTSW	4	155,925,464 (GRCm39)	missense	probably damaging	0.99
R1775:Mxra8	UTSW	4	155,927,531 (GRCm39)	missense	probably damaging	1.00
R2473:Mxra8	UTSW	4	155,926,500 (GRCm39)	missense	probably damaging	0.99
R4270:Mxra8	UTSW	4	155,925,594 (GRCm39)	missense	probably damaging	0.96
R4519:Mxra8	UTSW	4	155,927,440 (GRCm39)	critical splice donor site	probably null
R4844:Mxra8	UTSW	4	155,927,151 (GRCm39)	missense	probably benign	0.19
R4849:Mxra8	UTSW	4	155,925,331 (GRCm39)	intron	probably benign
R4912:Mxra8	UTSW	4	155,925,361 (GRCm39)	splice site	probably null
R4929:Mxra8	UTSW	4	155,927,118 (GRCm39)	missense	probably damaging	1.00
R5665:Mxra8	UTSW	4	155,927,378 (GRCm39)	missense	probably benign	0.01
R5913:Mxra8	UTSW	4	155,927,760 (GRCm39)	critical splice acceptor site	probably null
R6250:Mxra8	UTSW	4	155,925,546 (GRCm39)	missense	possibly damaging	0.95
R6857:Mxra8	UTSW	4	155,927,593 (GRCm39)	missense	possibly damaging	0.89
R7142:Mxra8	UTSW	4	155,927,519 (GRCm39)	missense	probably benign	0.23
R7658:Mxra8	UTSW	4	155,927,420 (GRCm39)	missense	probably benign	0.04
R7842:Mxra8	UTSW	4	155,927,367 (GRCm39)	missense	probably damaging	1.00
R8182:Mxra8	UTSW	4	155,925,589 (GRCm39)	nonsense	probably null
R8679:Mxra8	UTSW	4	155,927,122 (GRCm39)	missense	probably damaging	1.00
R9803:Mxra8	UTSW	4	155,924,282 (GRCm39)	start gained	probably benign

Predicted Primers

PCR Primer
(F):5'- TGTCCTCAGGTCAGTATCCC -3'
(R):5'- AAGTTGCCGTCGTGGAAAGC -3'

Sequencing Primer
(F):5'- AGTATCCCCTATCCAGCTGTGGG -3'
(R):5'- CCGTCGTGGAAAGCAGAAG -3'

Posted On

2016-10-24