Mutagenetix > Incidental Mutation

Incidental Mutation 'R6980:Megf11'

543780

Institutional Source

Beutler Lab

Gene Symbol

Megf11

Ensembl Gene

ENSMUSG00000036466

Gene Name

multiple EGF-like-domains 11

Synonyms

2410080H04Rik

MMRRC Submission

045088-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.129) question?

Stock #

R6980 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

64292908-64616487 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 64613132 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 1016 (E1016G)

Ref Sequence

ENSEMBL: ENSMUSP00000128672 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000068967] [ENSMUST00000093829] [ENSMUST00000118485] [ENSMUST00000164113]

AlphaFold

Q80T91

Predicted Effect

probably damaging
Transcript: ENSMUST00000068967
AA Change: E1059G

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

SMART Domains

Protein: ENSMUSP00000065353
Gene: ENSMUSG00000036466
AA Change: E1059G

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
low complexity region	74	84	N/A	INTRINSIC
EGF	101	129	1.85e0	SMART
EGF_Lam	145	184	9.55e-3	SMART
EGF_Lam	188	227	2e-5	SMART
EGF	226	258	5.57e-4	SMART
EGF_Lam	274	313	1.26e-2	SMART
EGF_Lam	317	357	2.52e-2	SMART
EGF_Lam	361	402	4.16e-3	SMART
EGF	401	433	6.21e-2	SMART
EGF	444	476	4.1e-2	SMART
EGF	487	519	7.02e-1	SMART
EGF_Lam	535	574	1.43e-1	SMART
EGF_Lam	578	617	5.04e-2	SMART
EGF	616	650	8.52e0	SMART
EGF	661	693	9.41e-2	SMART
EGF	704	736	8.52e0	SMART
EGF_Lam	752	791	2.99e-4	SMART
EGF	790	822	1.14e0	SMART
transmembrane domain	848	870	N/A	INTRINSIC
low complexity region	895	909	N/A	INTRINSIC
low complexity region	1022	1037	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000093829

SMART Domains

Protein: ENSMUSP00000091349
Gene: ENSMUSG00000036466

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
low complexity region	74	84	N/A	INTRINSIC
EGF_Lam	114	153	9.55e-3	SMART
EGF_Lam	157	196	2e-5	SMART
EGF	195	227	5.57e-4	SMART
EGF_Lam	243	282	1.26e-2	SMART
EGF_Lam	286	326	2.52e-2	SMART
EGF_Lam	330	371	4.16e-3	SMART
EGF	370	402	6.21e-2	SMART
EGF	413	445	4.1e-2	SMART
EGF	456	488	7.02e-1	SMART
EGF_Lam	504	543	1.43e-1	SMART
EGF_Lam	547	586	5.04e-2	SMART
EGF	585	619	8.52e0	SMART
EGF	630	662	9.41e-2	SMART
EGF_Lam	678	717	2.99e-4	SMART
EGF	716	748	1.14e0	SMART
transmembrane domain	774	796	N/A	INTRINSIC
low complexity region	821	835	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000118485
AA Change: E963G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000114035
Gene: ENSMUSG00000036466
AA Change: E963G

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
low complexity region	74	84	N/A	INTRINSIC
EGF	101	129	1.85e0	SMART
EGF_Lam	145	184	9.55e-3	SMART
EGF_Lam	188	227	2e-5	SMART
EGF	226	258	5.57e-4	SMART
EGF_Lam	274	313	1.26e-2	SMART
EGF_Lam	317	357	2.52e-2	SMART
EGF_Lam	361	402	4.16e-3	SMART
EGF	401	433	6.21e-2	SMART
EGF	444	476	4.1e-2	SMART
EGF	487	519	7.02e-1	SMART
EGF_Lam	535	574	1.43e-1	SMART
EGF_Lam	578	617	5.04e-2	SMART
EGF	616	650	8.52e0	SMART
EGF	661	693	9.41e-2	SMART
EGF	704	736	8.52e0	SMART
EGF_Lam	752	791	2.99e-4	SMART
EGF	790	822	1.14e0	SMART
transmembrane domain	848	870	N/A	INTRINSIC
low complexity region	926	941	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000164113
AA Change: E1016G

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

SMART Domains

Protein: ENSMUSP00000128672
Gene: ENSMUSG00000036466
AA Change: E1016G

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
low complexity region	74	84	N/A	INTRINSIC
EGF	101	129	1.85e0	SMART
EGF_Lam	145	184	9.55e-3	SMART
EGF_Lam	188	227	2e-5	SMART
EGF	226	258	5.57e-4	SMART
EGF_Lam	274	313	1.26e-2	SMART
EGF_Lam	317	357	2.52e-2	SMART
EGF_Lam	361	402	4.16e-3	SMART
EGF	401	433	6.21e-2	SMART
EGF	444	476	4.1e-2	SMART
EGF	487	519	7.02e-1	SMART
EGF_Lam	535	574	1.43e-1	SMART
EGF_Lam	578	617	5.04e-2	SMART
EGF	616	650	8.52e0	SMART
EGF	661	693	9.41e-2	SMART
EGF_Lam	709	748	2.99e-4	SMART
EGF	747	779	1.14e0	SMART
transmembrane domain	805	827	N/A	INTRINSIC
low complexity region	852	866	N/A	INTRINSIC
low complexity region	979	994	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted allele exhibit abnormal spacing of horizontal cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 88 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca2	C	A	2: 25,330,878 (GRCm39)	R1189S	possibly damaging	Het
Abcf2	T	C	5: 24,770,970 (GRCm39)	Q594R	probably benign	Het
Abhd18	G	A	3: 40,888,215 (GRCm39)	S353N	probably benign	Het
Adrb1	G	T	19: 56,712,046 (GRCm39)	A415S	probably benign	Het
Art2b	T	C	7: 101,229,680 (GRCm39)	N73S	probably benign	Het
BC028528	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	3: 95,795,448 (GRCm39)		probably benign	Het
BC028528	CACTGGTTCTGTGGT	CACTGGTTCTGTGGTTACTGGTTCTGTGGT	3: 95,795,480 (GRCm39)		probably benign	Het
BC028528	ACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC	ACTGGTTCTGTGGTCTCTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC	3: 95,795,451 (GRCm39)		probably benign	Het
Cacna1a	A	G	8: 85,338,914 (GRCm39)	M1753V	possibly damaging	Het
Cbx8	A	T	11: 118,930,287 (GRCm39)	I102N	possibly damaging	Het
Ccdc178	T	A	18: 22,238,620 (GRCm39)	E332D	probably benign	Het
Cdhr17	T	A	5: 17,031,944 (GRCm39)	V533D	possibly damaging	Het
Cfap74	G	A	4: 155,550,809 (GRCm39)		probably benign	Het
Chat	A	T	14: 32,146,111 (GRCm39)	M354K	probably benign	Het
Cmas	A	G	6: 142,702,526 (GRCm39)	T10A	probably damaging	Het
Cyb561d1	A	T	3: 108,107,475 (GRCm39)	L51H	probably benign	Het
D030056L22Rik	A	T	19: 18,694,629 (GRCm39)	N128I	probably damaging	Het
D130043K22Rik	G	T	13: 25,048,764 (GRCm39)	A423S	probably damaging	Het
Dnah14	T	C	1: 181,475,795 (GRCm39)	I1349T	probably benign	Het
Dnajb3	T	G	1: 88,132,736 (GRCm39)	D222A	probably damaging	Het
Dtx1	T	C	5: 120,819,422 (GRCm39)	E592G	probably damaging	Het
Dzank1	C	T	2: 144,332,056 (GRCm39)	G427R	possibly damaging	Het
E130308A19Rik	A	C	4: 59,719,991 (GRCm39)	K508Q	probably damaging	Het
Eif4e1b	T	A	13: 54,931,916 (GRCm39)		probably null	Het
Ell2	A	G	13: 75,904,495 (GRCm39)	M159V	probably null	Het
Eml4	G	A	17: 83,758,446 (GRCm39)	V377I	probably benign	Het
Fryl	A	T	5: 73,207,773 (GRCm39)	S2466T	probably benign	Het
Gfpt1	C	A	6: 87,054,071 (GRCm39)	T426K	probably damaging	Het
Gm49355	T	C	14: 12,307,173 (GRCm38)		probably benign	Het
Gm5114	T	C	7: 39,058,624 (GRCm39)	I332V	probably benign	Het
Gpr15	T	A	16: 58,539,105 (GRCm39)		probably benign	Het
Gpr179	T	C	11: 97,225,684 (GRCm39)	E2157G	probably benign	Het
Gramd4	A	G	15: 86,016,170 (GRCm39)	N482S	probably benign	Het
Hfm1	A	T	5: 107,028,343 (GRCm39)	I829K	probably benign	Het
Hydin	A	T	8: 111,139,916 (GRCm39)	E728D	possibly damaging	Het
Ifngr2	T	A	16: 91,356,895 (GRCm39)	V143E	probably damaging	Het
Ift172	T	C	5: 31,414,730 (GRCm39)	D1390G	probably benign	Het
Kdf1	A	T	4: 133,256,138 (GRCm39)	D285V	probably damaging	Het
Mast4	C	T	13: 102,941,155 (GRCm39)	V301I	probably damaging	Het
Mdn1	G	A	4: 32,726,942 (GRCm39)		probably null	Het
Mixl1	G	A	1: 180,524,453 (GRCm39)	A42V	possibly damaging	Het
Mpp2	A	G	11: 101,950,154 (GRCm39)	W567R	probably damaging	Het
Mrgpra6	A	G	7: 46,838,697 (GRCm39)	L136P	probably damaging	Het
Mroh7	T	A	4: 106,557,434 (GRCm39)	I759L	probably benign	Het
Nrxn2	A	G	19: 6,500,609 (GRCm39)	D277G	probably benign	Het
Nup210l	A	T	3: 90,027,234 (GRCm39)	K205N	probably benign	Het
Or4g17	A	G	2: 111,209,620 (GRCm39)	I92V	possibly damaging	Het
Or4p4b-ps1	A	G	2: 88,453,939 (GRCm39)	*97W	probably null	Het
Or52e19b	T	C	7: 103,032,303 (GRCm39)	E302G	probably benign	Het
Or5al6	A	T	2: 85,976,681 (GRCm39)	Y132*	probably null	Het
Oxnad1	C	T	14: 31,807,576 (GRCm39)		probably benign	Het
Pamr1	C	T	2: 102,472,549 (GRCm39)	T616I	probably benign	Het
Pcdhgb5	C	T	18: 37,866,592 (GRCm39)	H796Y	possibly damaging	Het
Pdlim7	G	T	13: 55,656,041 (GRCm39)	D126E	probably benign	Het
Pfdn2	C	T	1: 171,185,465 (GRCm39)		probably benign	Het
Piezo2	T	A	18: 63,216,032 (GRCm39)		probably null	Het
Pms2	A	T	5: 143,848,842 (GRCm39)	I43L	probably benign	Het
Prex2	T	A	1: 11,232,487 (GRCm39)	S851R	probably benign	Het
Ptpn4	T	A	1: 119,671,151 (GRCm39)	E202D	possibly damaging	Het
Rnf40	T	A	7: 127,193,849 (GRCm39)	V455E	probably damaging	Het
Rp1l1	A	G	14: 64,266,169 (GRCm39)	N585S	probably benign	Het
Rrp12	A	G	19: 41,878,582 (GRCm39)	S188P	probably damaging	Het
Rsbn1l	T	A	5: 21,101,482 (GRCm39)	H686L	probably benign	Het
Runx2	C	T	17: 45,046,203 (GRCm39)	V107I	possibly damaging	Het
Rusc2	A	G	4: 43,422,846 (GRCm39)	I994M	probably benign	Het
Ryr1	T	A	7: 28,808,812 (GRCm39)	D420V	probably benign	Het
Sash1	T	C	10: 8,605,612 (GRCm39)	Q926R	probably benign	Het
Scgb3a2	T	A	18: 43,897,499 (GRCm39)	I6N	probably damaging	Het
Sdc3	T	A	4: 130,544,233 (GRCm39)		probably benign	Het
Sik2	A	G	9: 50,808,755 (GRCm39)	V658A	probably benign	Het
Slc25a39	A	G	11: 102,296,601 (GRCm39)	V81A	probably damaging	Het
Snai2	T	A	16: 14,526,113 (GRCm39)	S255T	possibly damaging	Het
Sorbs1	A	T	19: 40,316,060 (GRCm39)	Y371*	probably null	Het
Spata31d1b	A	T	13: 59,863,236 (GRCm39)	H128L	probably benign	Het
Spdl1	A	T	11: 34,721,706 (GRCm39)	M1K	probably null	Het
Tgm3	T	A	2: 129,868,697 (GRCm39)	N211K	probably benign	Het
Tmem116	T	C	5: 121,606,050 (GRCm39)		probably null	Het
Tmem132e	T	A	11: 82,329,212 (GRCm39)		probably null	Het
Tmem53	T	C	4: 117,125,705 (GRCm39)	C251R	probably damaging	Het
Trcg1	A	C	9: 57,152,856 (GRCm39)	D551A	probably damaging	Het
Trp63	T	A	16: 25,620,843 (GRCm39)	F12I	probably benign	Het
Ttn	C	T	2: 76,709,401 (GRCm39)		probably null	Het
Tubgcp4	T	C	2: 121,025,946 (GRCm39)	V596A	probably benign	Het
Ugt2a3	A	C	5: 87,473,491 (GRCm39)	H475Q	probably damaging	Het
Unc79	G	A	12: 103,025,759 (GRCm39)	R382K	probably damaging	Het
Vmn2r58	T	C	7: 41,513,662 (GRCm39)	H327R	possibly damaging	Het
Vmn2r7	G	A	3: 64,623,987 (GRCm39)	T111I	possibly damaging	Het
Zfp318	T	A	17: 46,708,138 (GRCm39)	Y399N	probably damaging	Het

Other mutations in Megf11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00979:Megf11	APN	9	64,416,009 (GRCm39)	missense	probably damaging	1.00
IGL01285:Megf11	APN	9	64,567,728 (GRCm39)	missense	probably damaging	1.00
IGL01309:Megf11	APN	9	64,588,698 (GRCm39)	missense	probably benign	0.01
IGL01953:Megf11	APN	9	64,597,370 (GRCm39)	missense	probably damaging	1.00
IGL02341:Megf11	APN	9	64,451,902 (GRCm39)	missense	probably damaging	1.00
IGL02407:Megf11	APN	9	64,587,531 (GRCm39)	missense	probably damaging	1.00
IGL02621:Megf11	APN	9	64,601,214 (GRCm39)	missense	probably benign	0.07
R0277:Megf11	UTSW	9	64,598,632 (GRCm39)	critical splice donor site	probably null
R0386:Megf11	UTSW	9	64,547,360 (GRCm39)	missense	probably damaging	1.00
R1354:Megf11	UTSW	9	64,560,459 (GRCm39)	missense	probably benign	0.00
R1709:Megf11	UTSW	9	64,602,694 (GRCm39)	missense	probably damaging	1.00
R1865:Megf11	UTSW	9	64,587,581 (GRCm39)	missense	probably benign	0.39
R1895:Megf11	UTSW	9	64,586,558 (GRCm39)	missense	probably damaging	1.00
R1946:Megf11	UTSW	9	64,586,558 (GRCm39)	missense	probably damaging	1.00
R2221:Megf11	UTSW	9	64,567,713 (GRCm39)	missense	possibly damaging	0.63
R2223:Megf11	UTSW	9	64,567,713 (GRCm39)	missense	possibly damaging	0.63
R3552:Megf11	UTSW	9	64,602,745 (GRCm39)	missense	possibly damaging	0.75
R4641:Megf11	UTSW	9	64,597,407 (GRCm39)	missense	possibly damaging	0.93
R4746:Megf11	UTSW	9	64,416,027 (GRCm39)	missense	probably damaging	1.00
R5594:Megf11	UTSW	9	64,593,755 (GRCm39)	missense	probably damaging	1.00
R5716:Megf11	UTSW	9	64,413,392 (GRCm39)	missense	possibly damaging	0.72
R5898:Megf11	UTSW	9	64,593,246 (GRCm39)	missense	probably damaging	1.00
R5960:Megf11	UTSW	9	64,567,731 (GRCm39)	missense	probably benign	0.00
R6372:Megf11	UTSW	9	64,613,907 (GRCm39)	missense	probably damaging	1.00
R6811:Megf11	UTSW	9	64,451,923 (GRCm39)	missense	probably damaging	0.99
R6868:Megf11	UTSW	9	64,587,591 (GRCm39)	missense	probably damaging	1.00
R6984:Megf11	UTSW	9	64,593,734 (GRCm39)	missense	probably benign
R7155:Megf11	UTSW	9	64,555,233 (GRCm39)	missense	probably null	1.00
R7638:Megf11	UTSW	9	64,586,535 (GRCm39)	missense	probably damaging	0.96
R7643:Megf11	UTSW	9	64,613,914 (GRCm39)	missense	probably damaging	1.00
R7688:Megf11	UTSW	9	64,599,146 (GRCm39)	missense	possibly damaging	0.92
R7840:Megf11	UTSW	9	64,602,709 (GRCm39)	missense	possibly damaging	0.94
R8744:Megf11	UTSW	9	64,451,970 (GRCm39)	critical splice donor site	probably null
R8799:Megf11	UTSW	9	64,588,673 (GRCm39)	missense	probably benign	0.05
R9383:Megf11	UTSW	9	64,545,732 (GRCm39)	missense	probably damaging	1.00
R9493:Megf11	UTSW	9	64,547,376 (GRCm39)	missense	probably damaging	1.00
R9797:Megf11	UTSW	9	64,545,591 (GRCm39)	missense	possibly damaging	0.83
V5088:Megf11	UTSW	9	64,597,351 (GRCm39)	nonsense	probably null
V5622:Megf11	UTSW	9	64,597,351 (GRCm39)	nonsense	probably null
V5622:Megf11	UTSW	9	64,597,351 (GRCm39)	nonsense	probably null
Z1088:Megf11	UTSW	9	64,567,758 (GRCm39)	missense	probably damaging	1.00
Z1177:Megf11	UTSW	9	64,587,608 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AATGAATCCTATGTCCTTGCTTGTC -3'
(R):5'- GGCAACCCTGAGACAAAGTTTC -3'

Sequencing Primer
(F):5'- ATGTCCTTGCTTGTCCTAAGAAATC -3'
(R):5'- CTGAGACAAAGTTTCTCCTCAGG -3'

Posted On

2019-05-13