Mutagenetix > Incidental Mutation

Incidental Mutation 'R1470:Megf6'

197926

Institutional Source

Beutler Lab

Gene Symbol

Megf6

Ensembl Gene

ENSMUSG00000057751

Gene Name

multiple EGF-like-domains 6

Synonyms

2600001P17Rik, Egfl3

MMRRC Submission

039523-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1470 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

154170730-154275713 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

C to T at 154252419 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000121641 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030897] [ENSMUST00000152159]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000030897

SMART Domains

Protein: ENSMUSP00000030897
Gene: ENSMUSG00000057751

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
EGF_CA	122	162	1.54e-6	SMART
EGF_CA	163	203	2.08e-12	SMART
EGF	207	245	5.4e-2	SMART
EGF	249	286	2.39e-3	SMART
EGF_CA	287	327	4.96e-10	SMART
EGF	336	373	1.64e-1	SMART
EGF	377	413	1.99e1	SMART
EGF_CA	414	454	7.4e-9	SMART
EGF	521	554	4.26e0	SMART
EGF_Lam	570	609	1.19e-3	SMART
EGF_like	613	652	5.29e-1	SMART
EGF	642	685	2.2e1	SMART
EGF_Lam	656	697	1.04e-3	SMART
EGF	687	730	1.59e1	SMART
EGF_like	701	742	2.27e0	SMART
EGF_Lam	746	784	1.33e-1	SMART
EGF	783	816	2.85e-1	SMART
EGF_Lam	832	871	3.88e-3	SMART
EGF_Lam	875	915	3.25e-5	SMART
EGF	914	946	4.7e-2	SMART
EGF_like	962	1001	1.69e-1	SMART
EGF	1000	1032	7.02e-1	SMART
EGF_Lam	1048	1087	3.1e-2	SMART
EGF	1077	1118	7.53e-1	SMART
EGF_like	1091	1130	5.59e-1	SMART
EGF	1129	1161	5.04e-2	SMART
EGF_Lam	1177	1216	2.94e-3	SMART
EGF	1206	1248	1.87e1	SMART
EGF_Lam	1220	1260	3.1e-2	SMART
EGF	1259	1291	1.73e0	SMART
EGF	1302	1334	6.55e-1	SMART
EGF	1345	1377	4.39e-2	SMART
EGF_Lam	1393	1432	7.64e-2	SMART
EGF_Lam	1436	1475	2.64e-5	SMART
EGF_like	1465	1506	4.2e1	SMART
EGF_Lam	1479	1518	1.19e-3	SMART
EGF	1517	1549	1.84e1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000152159

SMART Domains

Protein: ENSMUSP00000121641
Gene: ENSMUSG00000057751

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
EGF_CA	55	95	2.08e-12	SMART
EGF	99	137	5.4e-2	SMART
EGF	141	178	2.39e-3	SMART
EGF_CA	179	219	4.96e-10	SMART
EGF	228	265	1.64e-1	SMART
EGF	269	305	1.99e1	SMART
EGF_CA	306	346	7.4e-9	SMART
EGF	413	446	4.26e0	SMART
EGF_Lam	462	501	1.19e-3	SMART
EGF_like	505	544	5.29e-1	SMART
EGF	534	577	2.2e1	SMART
EGF_Lam	548	589	1.04e-3	SMART
EGF	579	622	1.59e1	SMART
EGF_like	593	634	2.27e0	SMART
EGF_Lam	638	676	1.33e-1	SMART
EGF	675	708	2.85e-1	SMART
EGF_Lam	724	763	3.88e-3	SMART
EGF_Lam	767	807	3.25e-5	SMART
EGF	806	838	4.7e-2	SMART
EGF_Lam	854	893	2.56e-3	SMART
EGF	892	924	2.02e-1	SMART
EGF	935	967	7.13e-2	SMART
EGF	978	1010	1.73e0	SMART
EGF	1021	1053	6.55e-1	SMART
EGF	1064	1096	4.39e-2	SMART
EGF	1107	1139	4.97e-1	SMART
EGF	1159	1191	1.84e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183595

Coding Region Coverage

1x: 97.5%
3x: 97.0%
10x: 95.5%
20x: 93.0%

Validation Efficiency

97% (125/129)

Allele List at MGI

Other mutations in this stock

Total: 142 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930415O20Rik	T	C	15: 98,585,261		probably benign	Het
4932438A13Rik	T	C	3: 36,998,331	M3060T	probably benign	Het
Aak1	T	A	6: 86,967,355	S749T	unknown	Het
Abcb4	A	T	5: 8,940,968	I843F	probably damaging	Het
Abcb6	A	T	1: 75,172,679		probably benign	Het
AC161516.2	G	T	5: 67,946,397		probably benign	Het
AC238840.1	A	T	7: 38,767,953		noncoding transcript	Het
Actr8	T	A	14: 29,986,969	H244Q	possibly damaging	Het
Acyp2	A	G	11: 30,506,452		probably benign	Het
Adgrv1	A	G	13: 81,382,298	Y5886H	probably benign	Het
Afap1	C	T	5: 35,961,737		probably benign	Het
Agk	T	A	6: 40,386,817	W244R	probably damaging	Het
Akirin1	T	A	4: 123,738,090		probably benign	Het
Ankrd11	C	A	8: 122,899,724	V161L	probably damaging	Het
Arap3	T	C	18: 37,989,196		probably null	Het
Arhgap29	A	G	3: 121,992,319		probably benign	Het
Armc3	A	G	2: 19,238,736	M88V	probably benign	Het
Atp13a5	G	T	16: 29,349,015	P109T	probably benign	Het
Avpr1b	T	A	1: 131,600,585	V282D	probably damaging	Het
Baz2b	T	C	2: 59,978,546	K120E	possibly damaging	Het
Cacna1a	T	A	8: 84,514,950		probably benign	Het
Cacng6	G	A	7: 3,424,888	C76Y	probably damaging	Het
Cactin	G	T	10: 81,323,151	E279*	probably null	Het
Car9	A	G	4: 43,510,222	Y268C	probably damaging	Het
Ccdc146	T	A	5: 21,319,566	I263F	probably damaging	Het
Cdc16	A	T	8: 13,758,992		probably benign	Het
Cdh16	T	G	8: 104,618,371	S429R	probably benign	Het
Cep250	A	G	2: 155,991,075	E1639G	probably damaging	Het
Ces1d	A	T	8: 93,195,021	V38D	possibly damaging	Het
Chd1	A	T	17: 15,726,283	Q97L	possibly damaging	Het
Ciita	G	A	16: 10,514,468	D898N	possibly damaging	Het
Clstn1	A	G	4: 149,634,722	N336S	possibly damaging	Het
Cntnap5a	A	G	1: 116,259,519	D607G	probably damaging	Het
Col1a2	G	A	6: 4,518,822		probably benign	Het
Col20a1	C	T	2: 180,994,960	H245Y	probably benign	Het
Coq8b	A	T	7: 27,252,309	T399S	probably benign	Het
Cpn2	A	G	16: 30,260,185	S233P	probably benign	Het
Cryz	G	A	3: 154,606,476	G70D	probably damaging	Het
Csmd1	G	T	8: 16,157,204		probably benign	Het
Def6	T	A	17: 28,225,982	D451E	possibly damaging	Het
Dnah8	T	A	17: 30,747,277	C2480*	probably null	Het
Dnah9	T	C	11: 65,927,822	N3230S	probably benign	Het
Dyrk4	G	T	6: 126,916,374	S15*	probably null	Het
Erc1	T	C	6: 119,694,602	R917G	probably damaging	Het
Fgd2	T	A	17: 29,374,108		probably benign	Het
Frem3	G	T	8: 80,611,191	V38L	probably benign	Het
Gas2l3	T	C	10: 89,413,934	I441V	probably benign	Het
Gm14393	T	A	2: 175,063,981	Y6F	probably damaging	Het
Gm1527	A	G	3: 28,915,268	K256E	possibly damaging	Het
Gtf2ird1	T	A	5: 134,395,802		probably null	Het
Hmces	C	A	6: 87,936,139	T292K	probably benign	Het
Hpse2	G	A	19: 43,388,253	S20L	probably benign	Het
Ikbke	A	T	1: 131,276,487	V23E	probably null	Het
Ino80	A	T	2: 119,379,649	V1387E	probably damaging	Het
Islr	G	T	9: 58,157,306	A306D	probably damaging	Het
Jakmip1	G	A	5: 37,100,838	G276D	probably damaging	Het
Jchain	A	G	5: 88,526,120	V55A	probably benign	Het
Kalrn	T	C	16: 34,187,471	K1350E	probably damaging	Het
Kansl1l	T	C	1: 66,801,997	Q48R	possibly damaging	Het
Kmt5a	T	C	5: 124,447,271	L23P	probably damaging	Het
Lrba	C	T	3: 86,737,142	H381Y	probably damaging	Het
Lrch3	T	C	16: 32,988,495		probably benign	Het
Lrrc32	T	C	7: 98,499,357	V448A	probably benign	Het
Mapkbp1	T	C	2: 120,017,820	M617T	probably damaging	Het
Mfap1a	T	C	2: 121,502,801	M50V	probably benign	Het
Mgam	G	T	6: 40,759,128	A854S	probably damaging	Het
Myh3	A	C	11: 67,098,059		probably benign	Het
Myo18b	C	A	5: 112,693,033	R2298L	probably damaging	Het
Myo1h	T	A	5: 114,319,704	M92K	probably damaging	Het
Nfkbib	T	C	7: 28,762,022		probably null	Het
Nlrp2	T	A	7: 5,300,951	T192S	probably benign	Het
Nr2f1	A	T	13: 78,198,165	Y137N	possibly damaging	Het
Nup98	T	A	7: 102,147,306	D841V	probably damaging	Het
Nvl	A	G	1: 181,139,262	V59A	probably damaging	Het
Ogdhl	C	A	14: 32,346,788	N948K	probably damaging	Het
Olfr530	A	G	7: 140,373,113	S166P	probably benign	Het
Olfr538	A	G	7: 140,574,749	T199A	probably benign	Het
Olfr578	A	C	7: 102,984,323	Y280*	probably null	Het
Olfr743	T	C	14: 50,533,702	S97P	possibly damaging	Het
Orc2	A	C	1: 58,481,158		probably benign	Het
Osgin1	G	A	8: 119,444,965	R166H	probably damaging	Het
Palb2	A	T	7: 122,107,523	F741I	probably benign	Het
Palb2	G	T	7: 122,107,524	Y740*	probably null	Het
Parvb	G	A	15: 84,271,252	G46D	probably damaging	Het
Parvb	G	A	15: 84,271,308	D65N	probably benign	Het
Pcsk2	A	T	2: 143,546,518	K10*	probably null	Het
Pde3a	C	T	6: 141,466,206	A502V	probably benign	Het
Pfas	T	C	11: 68,991,359	I893V	probably benign	Het
Pla2g4a	A	T	1: 149,840,720	D663E	probably damaging	Het
Prickle2	G	A	6: 92,458,602	P6L	probably damaging	Het
Prx	T	A	7: 27,517,601	M648K	probably benign	Het
Ptpn21	T	C	12: 98,688,476	N744S	probably benign	Het
Ptprq	C	T	10: 107,718,574	V97M	probably damaging	Het
Pvr	T	C	7: 19,918,624	E122G	possibly damaging	Het
Racgap1	T	C	15: 99,639,775	K15E	probably damaging	Het
Rock1	C	T	18: 10,136,091		probably null	Het
Rorc	T	A	3: 94,397,302	Y331*	probably null	Het
Rpl37	T	C	15: 5,118,614	V91A	probably benign	Het
Rrp36	T	A	17: 46,672,380	K103*	probably null	Het
Ryr3	T	A	2: 112,653,007	M4142L	probably benign	Het
Sash1	A	T	10: 8,789,593	L125H	probably damaging	Het
Scn5a	T	C	9: 119,536,475	M369V	possibly damaging	Het
Siglec1	A	T	2: 131,070,387	N1678K	probably benign	Het
Slc15a5	A	T	6: 138,072,994	V141E	probably benign	Het
Slc43a1	T	C	2: 84,859,676		probably benign	Het
Slc8a3	A	T	12: 81,199,710	H856Q	probably benign	Het
Sptlc2	T	A	12: 87,355,640	M171L	probably benign	Het
Srcap	T	A	7: 127,559,727		probably benign	Het
St6gal2	A	G	17: 55,490,943	D310G	probably damaging	Het
Susd2	T	A	10: 75,638,054	D689V	probably damaging	Het
Suz12	A	T	11: 80,019,732	E303V	possibly damaging	Het
Taldo1	C	A	7: 141,398,587	T150K	probably damaging	Het
Tex14	T	C	11: 87,549,529		probably benign	Het
Tg	T	A	15: 66,849,463	F274I	possibly damaging	Het
Tmem151b	T	C	17: 45,545,737	D259G	probably damaging	Het
Tmem179	G	T	12: 112,501,854	H64Q	probably benign	Het
Tmem236	A	G	2: 14,218,921	T174A	probably benign	Het
Tmtc1	T	A	6: 148,305,985		probably benign	Het
Tnc	A	T	4: 63,966,574	N1821K	probably damaging	Het
Tnfrsf11a	A	G	1: 105,825,048	N261S	probably damaging	Het
Traf6	G	T	2: 101,696,649		probably benign	Het
Trank1	C	A	9: 111,343,232	F96L	possibly damaging	Het
Trim56	T	A	5: 137,113,163	I500F	probably damaging	Het
Ttc30b	G	T	2: 75,937,811	S199R	probably benign	Het
Ttll5	A	G	12: 85,879,394	I321V	possibly damaging	Het
Ttn	C	A	2: 76,778,023	W17852L	probably damaging	Het
Twnk	G	A	19: 45,009,381	V450M	probably damaging	Het
Uba52	A	G	8: 70,509,556	I127T	possibly damaging	Het
Ubr4	T	A	4: 139,421,226		probably null	Het
Uggt1	A	T	1: 36,176,796	M130K	probably benign	Het
Ulk4	T	A	9: 121,081,656	T1101S	probably benign	Het
Urb1	A	G	16: 90,752,014	S2269P	probably benign	Het
Ush2a	G	T	1: 188,400,206	R875L	probably benign	Het
Usp9y	T	A	Y: 1,332,471	H1624L	probably benign	Homo
Vipr1	T	C	9: 121,665,520	L308S	possibly damaging	Het
Vps50	G	A	6: 3,517,777		probably benign	Het
Xdh	T	G	17: 73,891,112	K1260T	probably damaging	Het
Yipf4	A	G	17: 74,493,968	I94V	probably benign	Het
Zfhx4	A	G	3: 5,413,146	*3582W	probably null	Het
Zfp58	T	C	13: 67,492,025	N116D	possibly damaging	Het
Zfp750	C	A	11: 121,511,993	R643L	probably benign	Het
Znfx1	A	G	2: 167,042,587	V51A	possibly damaging	Het

Other mutations in Megf6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01122:Megf6	APN	4	154253807	missense	probably damaging	1.00
IGL01410:Megf6	APN	4	154252563	critical splice donor site	probably null
IGL01512:Megf6	APN	4	154262583	missense	possibly damaging	0.64
IGL01824:Megf6	APN	4	154252234	missense	probably damaging	1.00
IGL02172:Megf6	APN	4	154270692	missense	probably damaging	1.00
IGL02727:Megf6	APN	4	154253149	splice site	probably null
IGL02966:Megf6	APN	4	154253777	missense	probably damaging	1.00
Didactic	UTSW	4	154254587	missense	probably damaging	1.00
R0118:Megf6	UTSW	4	154254641	missense	probably damaging	0.99
R0220:Megf6	UTSW	4	154258215	missense	probably damaging	1.00
R0347:Megf6	UTSW	4	154254635	missense	possibly damaging	0.90
R0383:Megf6	UTSW	4	154265326	missense	probably benign	0.01
R0417:Megf6	UTSW	4	154267967	missense	probably benign	0.06
R0526:Megf6	UTSW	4	154258941	missense	probably benign
R0528:Megf6	UTSW	4	154259173	missense	probably benign	0.04
R0928:Megf6	UTSW	4	154177047	missense	probably damaging	1.00
R1311:Megf6	UTSW	4	154263782	splice site	probably null
R1458:Megf6	UTSW	4	154177121	missense	probably benign	0.39
R1476:Megf6	UTSW	4	154177121	missense	probably benign	0.39
R1479:Megf6	UTSW	4	154177121	missense	probably benign	0.39
R1624:Megf6	UTSW	4	154177121	missense	probably benign	0.39
R1626:Megf6	UTSW	4	154177121	missense	probably benign	0.39
R1638:Megf6	UTSW	4	154262510	splice site	probably benign
R1777:Megf6	UTSW	4	154270690	nonsense	probably null
R1831:Megf6	UTSW	4	154270677	missense	probably benign	0.00
R1944:Megf6	UTSW	4	154256066	missense	possibly damaging	0.75
R1984:Megf6	UTSW	4	154267667	missense	probably damaging	1.00
R2109:Megf6	UTSW	4	154177121	missense	probably benign	0.39
R2448:Megf6	UTSW	4	154266645	splice site	probably null
R2880:Megf6	UTSW	4	154252549	missense	probably damaging	1.00
R4032:Megf6	UTSW	4	154177093	nonsense	probably null
R4058:Megf6	UTSW	4	154242532	splice site	probably benign
R4672:Megf6	UTSW	4	154249452	missense	probably damaging	0.99
R4688:Megf6	UTSW	4	154253814	missense	probably damaging	0.99
R4752:Megf6	UTSW	4	154252438	missense	probably damaging	1.00
R4863:Megf6	UTSW	4	154254281	critical splice donor site	probably null
R4909:Megf6	UTSW	4	154265391	missense	probably damaging	1.00
R4942:Megf6	UTSW	4	154253820	missense	probably damaging	1.00
R4981:Megf6	UTSW	4	154267450	missense	possibly damaging	0.95
R4990:Megf6	UTSW	4	154267226	missense	possibly damaging	0.94
R5001:Megf6	UTSW	4	154268060	missense	probably damaging	1.00
R5189:Megf6	UTSW	4	154252523	missense	probably benign	0.31
R5210:Megf6	UTSW	4	154269816	intron	probably benign
R5220:Megf6	UTSW	4	154253838	critical splice donor site	probably null
R5250:Megf6	UTSW	4	154256010	missense	possibly damaging	0.65
R5697:Megf6	UTSW	4	154258229	missense	probably null	0.15
R5808:Megf6	UTSW	4	154267662	missense	probably benign
R5916:Megf6	UTSW	4	154249425	critical splice acceptor site	probably null
R6054:Megf6	UTSW	4	154263179	missense	probably benign	0.06
R6075:Megf6	UTSW	4	154262599	nonsense	probably null
R6515:Megf6	UTSW	4	154258919	missense	possibly damaging	0.84
R6599:Megf6	UTSW	4	154258087	splice site	probably null
R6811:Megf6	UTSW	4	154252161	missense	probably damaging	1.00
R6925:Megf6	UTSW	4	154254587	missense	probably damaging	1.00
R7023:Megf6	UTSW	4	154254145	missense	possibly damaging	0.95
R7117:Megf6	UTSW	4	154258922	missense	possibly damaging	0.78
R7163:Megf6	UTSW	4	154267441	missense	probably damaging	0.98
R7345:Megf6	UTSW	4	154267315	missense	probably benign
R7580:Megf6	UTSW	4	154270744	nonsense	probably null
R7649:Megf6	UTSW	4	154265085	missense	probably damaging	0.96
R7702:Megf6	UTSW	4	154270470	missense	probably benign	0.00
R8010:Megf6	UTSW	4	154270507	missense	probably benign	0.13
R8175:Megf6	UTSW	4	154268619	nonsense	probably null
R8231:Megf6	UTSW	4	154252518	missense	probably damaging	1.00
R8436:Megf6	UTSW	4	154265192	missense	probably damaging	1.00
R8460:Megf6	UTSW	4	154266177	nonsense	probably null
R8738:Megf6	UTSW	4	154267979	missense	probably benign
R8854:Megf6	UTSW	4	154268012	missense	probably damaging	1.00
R8896:Megf6	UTSW	4	154242403	missense	probably damaging	0.99
R9098:Megf6	UTSW	4	154269703	missense	probably damaging	0.99
R9147:Megf6	UTSW	4	154254673	missense	probably benign	0.18
R9148:Megf6	UTSW	4	154254673	missense	probably benign	0.18
R9161:Megf6	UTSW	4	154267715	missense	probably benign	0.44
R9355:Megf6	UTSW	4	154253825	missense	probably damaging	1.00
R9386:Megf6	UTSW	4	154256077	missense	probably damaging	1.00
R9404:Megf6	UTSW	4	154263768	missense
R9469:Megf6	UTSW	4	154250912	missense	probably damaging	1.00
R9472:Megf6	UTSW	4	154249453	missense	probably damaging	1.00
R9777:Megf6	UTSW	4	154259160	missense	probably damaging	1.00
Z1177:Megf6	UTSW	4	154237826	missense	probably benign	0.12
Z1177:Megf6	UTSW	4	154250849	missense	probably damaging	1.00
Z1177:Megf6	UTSW	4	154267681	missense	possibly damaging	0.48
Z1177:Megf6	UTSW	4	154267682	missense	probably damaging	0.99
Z1177:Megf6	UTSW	4	154267747	nonsense	probably null
Z1177:Megf6	UTSW	4	154269741	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TGCAGATGTGGACGAATGTGCC -3'
(R):5'- TGCTGATGCTGACTCTTGTCAACTC -3'

Sequencing Primer
(F):5'- TGTCACGCAGGCTATGAG -3'
(R):5'- GAGGAGACTTCTAAGCCATAGCAC -3'

Posted On

2014-05-23