Mutagenetix > Incidental Mutation

Incidental Mutation 'R1413:Mpp7'

159725

Institutional Source

Beutler Lab

Gene Symbol

Mpp7

Ensembl Gene

ENSMUSG00000057440

Gene Name

membrane protein, palmitoylated 7 (MAGUK p55 subfamily member 7)

Synonyms

2810038M04Rik, LOC381166, 5430426E14Rik, 1110068J02Rik

MMRRC Submission

039469-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.131) question?

Stock #

R1413 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

7347959-7626866 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 7350977 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Cysteine at position 573 (W573C)

Ref Sequence

ENSEMBL: ENSMUSP00000111535 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000115869]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000115869
AA Change: W573C

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

SMART Domains

Protein: ENSMUSP00000111535
Gene: ENSMUSG00000057440
AA Change: W573C

Domain	Start	End	E-Value	Type
L27	10	68	7.05e-14	SMART
L27	72	125	3.72e-13	SMART
PDZ	147	220	3.8e-15	SMART
SH3	231	297	1.4e-11	SMART
low complexity region	317	328	N/A	INTRINSIC
GuKc	367	563	4.01e-65	SMART

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.7%
20x: 91.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the p55 Stardust family of membrane-associated guanylate kinase (MAGUK) proteins, which function in the establishment of epithelial cell polarity. This family member forms a complex with the polarity protein DLG1 (discs, large homolog 1) and facilitates epithelial cell polarity and tight junction formation. Polymorphisms in this gene are associated with variations in site-specific bone mineral density (BMD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc9	T	C	6: 142,573,245 (GRCm39)	N1051D	possibly damaging	Het
Abcc9	A	G	6: 142,536,222 (GRCm39)	V1504A	probably damaging	Het
Actr6	A	T	10: 89,564,019 (GRCm39)	Y84*	probably null	Het
Adgrl3	T	C	5: 81,841,366 (GRCm39)	Y816H	probably damaging	Het
Ahcyl2	T	C	6: 29,768,586 (GRCm39)		probably benign	Het
Amd1	A	T	10: 40,166,404 (GRCm39)	C157*	probably null	Het
Ank1	G	A	8: 23,609,393 (GRCm39)	E1362K	probably damaging	Het
Atp10b	A	G	11: 43,121,391 (GRCm39)	Q1018R	probably benign	Het
Atp1a2	G	A	1: 172,106,911 (GRCm39)	T803I	probably damaging	Het
Atr	T	G	9: 95,814,495 (GRCm39)	L2064R	probably damaging	Het
Bmp3	T	A	5: 99,020,264 (GRCm39)	L229Q	probably damaging	Het
Ccl25	A	G	8: 4,403,892 (GRCm39)	*54W	probably null	Het
Cdc45	A	T	16: 18,627,491 (GRCm39)	N111K	possibly damaging	Het
Cfap61	T	A	2: 145,805,363 (GRCm39)	S154T	probably benign	Het
Cyp2c37	T	A	19: 39,982,542 (GRCm39)	S127T	probably benign	Het
Cyp4f40	T	A	17: 32,892,913 (GRCm39)	D309E	probably benign	Het
D6Ertd527e	A	G	6: 87,088,335 (GRCm39)	D166G	unknown	Het
Dmbt1	T	A	7: 130,651,944 (GRCm39)	D395E	probably damaging	Het
Dnah5	A	G	15: 28,370,555 (GRCm39)	S2832G	probably benign	Het
Dync1h1	G	A	12: 110,602,943 (GRCm39)	E2195K	probably benign	Het
Fah	T	C	7: 84,242,420 (GRCm39)	D296G	probably damaging	Het
Fam83g	A	G	11: 61,593,504 (GRCm39)	N346S	probably damaging	Het
Fgl1	T	A	8: 41,644,638 (GRCm39)	T289S	possibly damaging	Het
Fmo1	A	C	1: 162,661,431 (GRCm39)	L284R	probably damaging	Het
Frem3	T	A	8: 81,395,430 (GRCm39)	M1819K	probably benign	Het
Fsip2	T	A	2: 82,818,762 (GRCm39)	L4832M	possibly damaging	Het
Fut1	T	C	7: 45,268,852 (GRCm39)	W269R	probably damaging	Het
Ggnbp2	A	G	11: 84,723,955 (GRCm39)	Y638H	probably damaging	Het
Gp2	T	A	7: 119,050,853 (GRCm39)	I293F	probably benign	Het
Gpi1	T	C	7: 33,929,580 (GRCm39)	N20S	probably benign	Het
Gxylt1	C	T	15: 93,152,273 (GRCm39)	R222H	probably damaging	Het
Hemgn	T	C	4: 46,396,091 (GRCm39)	K382E	possibly damaging	Het
Hook3	T	A	8: 26,528,134 (GRCm39)	E585D	probably damaging	Het
Irf6	G	A	1: 192,851,613 (GRCm39)	M401I	probably benign	Het
Jmjd1c	A	G	10: 67,085,529 (GRCm39)	T2259A	probably damaging	Het
Lactb	T	A	9: 66,878,201 (GRCm39)	R209S	probably damaging	Het
Lonp2	A	G	8: 87,368,212 (GRCm39)	D342G	probably damaging	Het
Mmachc	T	C	4: 116,563,194 (GRCm39)	S54G	probably damaging	Het
Or13e8	T	A	4: 43,697,011 (GRCm39)	H54L	possibly damaging	Het
Or5w1b	T	A	2: 87,476,182 (GRCm39)	Y95F	probably benign	Het
Or6b2b	A	T	1: 92,418,610 (GRCm39)	I289N	probably damaging	Het
Pappa2	A	T	1: 158,764,124 (GRCm39)	D462E	probably benign	Het
Pcdh12	A	T	18: 38,416,496 (GRCm39)	F210I	probably damaging	Het
Ppp1r12c	A	G	7: 4,487,443 (GRCm39)		probably null	Het
Prkce	T	A	17: 86,803,446 (GRCm39)	D448E	possibly damaging	Het
Ptprb	C	A	10: 116,175,584 (GRCm39)	T1193K	probably damaging	Het
Qrfpr	T	A	3: 36,236,809 (GRCm39)	E197D	possibly damaging	Het
Rusc2	T	A	4: 43,416,568 (GRCm39)	C625S	probably benign	Het
Shcbp1	T	G	8: 4,791,968 (GRCm39)		probably null	Het
Snrnp40	C	G	4: 130,271,836 (GRCm39)		probably null	Het
Spag5	T	A	11: 78,196,143 (GRCm39)	C449*	probably null	Het
Stpg3	T	C	2: 25,103,862 (GRCm39)	D158G	probably damaging	Het
Sycp2	T	C	2: 177,989,590 (GRCm39)	Y1423C	probably benign	Het
Tiprl	C	T	1: 165,043,359 (GRCm39)	E256K	possibly damaging	Het
Tmem132c	T	A	5: 127,640,631 (GRCm39)	V934D	probably damaging	Het
Topors	A	G	4: 40,261,982 (GRCm39)	V434A	probably benign	Het
Usp11	A	G	X: 20,584,946 (GRCm39)	Y731C	probably damaging	Het
Vmn2r58	T	A	7: 41,513,387 (GRCm39)	I419L	probably benign	Het
Wfs1	C	A	5: 37,139,422 (GRCm39)	R72L	possibly damaging	Het
Zan	T	C	5: 137,426,201 (GRCm39)	D2525G	unknown	Het
Zfp280c	A	G	X: 47,652,715 (GRCm39)	V285A	probably benign	Het
Zfp511	T	A	7: 139,617,528 (GRCm39)	F177I	probably damaging	Het
Zfp964	A	G	8: 70,115,720 (GRCm39)	M107V	unknown	Het
Zmynd11	A	G	13: 9,760,256 (GRCm39)	Y122H	probably damaging	Het

Other mutations in Mpp7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00938:Mpp7	APN	18	7,353,297 (GRCm39)	missense	probably benign	0.00
IGL01575:Mpp7	APN	18	7,403,365 (GRCm39)	splice site	probably benign
IGL02973:Mpp7	APN	18	7,403,297 (GRCm39)	missense	probably damaging	1.00
IGL02985:Mpp7	APN	18	7,461,637 (GRCm39)	critical splice donor site	probably null
IGL03224:Mpp7	APN	18	7,403,269 (GRCm39)	missense	probably benign	0.28
IGL03248:Mpp7	APN	18	7,403,269 (GRCm39)	missense	probably benign	0.28
R0040:Mpp7	UTSW	18	7,403,180 (GRCm39)	splice site	probably benign
R0089:Mpp7	UTSW	18	7,439,555 (GRCm39)	splice site	probably benign
R1634:Mpp7	UTSW	18	7,350,984 (GRCm39)	missense	possibly damaging	0.63
R1859:Mpp7	UTSW	18	7,350,967 (GRCm39)	makesense	probably null
R2379:Mpp7	UTSW	18	7,403,345 (GRCm39)	nonsense	probably null
R2869:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R2869:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R2871:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R2871:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R3008:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R3009:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R3010:Mpp7	UTSW	18	7,461,678 (GRCm39)	missense	possibly damaging	0.76
R3782:Mpp7	UTSW	18	7,351,085 (GRCm39)	missense	probably damaging	0.99
R3980:Mpp7	UTSW	18	7,444,062 (GRCm39)	missense	probably benign	0.23
R4574:Mpp7	UTSW	18	7,353,228 (GRCm39)	missense	probably benign	0.02
R4772:Mpp7	UTSW	18	7,379,983 (GRCm39)	splice site	probably null
R5066:Mpp7	UTSW	18	7,513,002 (GRCm39)	missense	possibly damaging	0.95
R5437:Mpp7	UTSW	18	7,458,930 (GRCm39)	critical splice donor site	probably null
R5451:Mpp7	UTSW	18	7,442,855 (GRCm39)	missense	probably null	0.95
R5578:Mpp7	UTSW	18	7,355,101 (GRCm39)	missense	probably benign
R5651:Mpp7	UTSW	18	7,355,016 (GRCm39)	critical splice donor site	probably null
R5787:Mpp7	UTSW	18	7,461,682 (GRCm39)	missense	probably benign
R6979:Mpp7	UTSW	18	7,355,049 (GRCm39)	missense	possibly damaging	0.64
R6984:Mpp7	UTSW	18	7,441,623 (GRCm39)	missense	probably damaging	1.00
R7448:Mpp7	UTSW	18	7,351,079 (GRCm39)	missense	probably damaging	0.98
R7517:Mpp7	UTSW	18	7,440,183 (GRCm39)	nonsense	probably null
R8278:Mpp7	UTSW	18	7,444,025 (GRCm39)	missense	probably benign
R8373:Mpp7	UTSW	18	7,444,096 (GRCm39)	missense	probably damaging	1.00
R8676:Mpp7	UTSW	18	7,440,430 (GRCm39)	critical splice donor site	probably null
R9206:Mpp7	UTSW	18	7,403,327 (GRCm39)	missense	probably benign	0.12
R9208:Mpp7	UTSW	18	7,403,327 (GRCm39)	missense	probably benign	0.12
R9439:Mpp7	UTSW	18	7,461,692 (GRCm39)	nonsense	probably null
R9790:Mpp7	UTSW	18	7,355,049 (GRCm39)	missense	probably benign	0.07
R9791:Mpp7	UTSW	18	7,355,049 (GRCm39)	missense	probably benign	0.07
X0028:Mpp7	UTSW	18	7,403,273 (GRCm39)	missense	probably benign	0.04
Z1177:Mpp7	UTSW	18	7,355,062 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TGAGCCCAAGTGAGGCATGAAC -3'
(R):5'- GCAATGTGTCCATGCAATCGTGAG -3'

Sequencing Primer
(F):5'- GGCATGAACTTTGATACCTACTGC -3'
(R):5'- ACCCTGAAGGGAGTTCAGC -3'

Posted On

2014-03-14