Mutagenetix > Incidental Mutation

Incidental Mutation 'R0390:Mon2'

31623

Institutional Source

Beutler Lab

Gene Symbol

Mon2

Ensembl Gene

ENSMUSG00000034602

Gene Name

MON2 homolog, regulator of endosome to Golgi trafficking

Synonyms

2610528O22Rik, SF21

MMRRC Submission

038596-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.931) question?

Stock #

R0390 (G1)

Quality Score

193

Status

Validated

Chromosome

Chromosomal Location

122992060-123076505 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 123007021 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 1501 (D1501G)

Ref Sequence

ENSEMBL: ENSMUSP00000131052 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037557] [ENSMUST00000073792] [ENSMUST00000170935]

AlphaFold

Q80TL7

Predicted Effect

probably null
Transcript: ENSMUST00000037557
AA Change: D1500G

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000037568
Gene: ENSMUSG00000034602
AA Change: D1500G

Domain	Start	End	E-Value	Type
low complexity region	119	138	N/A	INTRINSIC
low complexity region	164	176	N/A	INTRINSIC
Pfam:Sec7_N	208	294	6.5e-16	PFAM
Pfam:Sec7_N	299	385	2.6e-16	PFAM
low complexity region	405	438	N/A	INTRINSIC
low complexity region	558	575	N/A	INTRINSIC
low complexity region	615	627	N/A	INTRINSIC
Pfam:DUF1981	844	929	2.4e-21	PFAM
low complexity region	984	1001	N/A	INTRINSIC
low complexity region	1182	1193	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000073792
AA Change: D1507G

PolyPhen 2 Score 0.052 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000073462
Gene: ENSMUSG00000034602
AA Change: D1507G

Domain	Start	End	E-Value	Type
Pfam:DCB	8	184	3e-72	PFAM
Pfam:Sec7_N	211	384	3.1e-58	PFAM
low complexity region	405	438	N/A	INTRINSIC
low complexity region	558	575	N/A	INTRINSIC
low complexity region	615	627	N/A	INTRINSIC
Pfam:DUF1981	848	929	6.6e-20	PFAM
Pfam:Mon2_C	932	1706	N/A	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000170935
AA Change: D1501G

PolyPhen 2 Score 0.052 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000131052
Gene: ENSMUSG00000034602
AA Change: D1501G

Domain	Start	End	E-Value	Type
low complexity region	119	138	N/A	INTRINSIC
low complexity region	164	176	N/A	INTRINSIC
Pfam:Sec7_N	208	294	6.5e-16	PFAM
Pfam:Sec7_N	299	385	2.6e-16	PFAM
low complexity region	405	438	N/A	INTRINSIC
low complexity region	559	576	N/A	INTRINSIC
low complexity region	616	628	N/A	INTRINSIC
Pfam:DUF1981	845	930	8.1e-22	PFAM
low complexity region	985	1002	N/A	INTRINSIC
low complexity region	1183	1194	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218735

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222536

Meta Mutation Damage Score

0.6121

Coding Region Coverage

1x: 99.1%
3x: 98.1%
10x: 95.9%
20x: 92.0%

Validation Efficiency

98% (110/112)

Allele List at MGI

Other mutations in this stock

Total: 110 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A730017C20Rik	T	A	18: 59,075,688	V136E	probably damaging	Het
Adam18	C	T	8: 24,674,054	G38R	probably benign	Het
Ap2m1	T	C	16: 20,541,099	M183T	probably damaging	Het
Apob	A	T	12: 7,988,678	I364F	probably damaging	Het
Arl6	A	T	16: 59,622,421		probably benign	Het
Cand2	A	G	6: 115,774,653	M15V	possibly damaging	Het
Cbl	A	G	9: 44,201,005	F131S	probably damaging	Het
Ccdc151	T	A	9: 21,991,708	H442L	probably benign	Het
Ccdc74a	A	G	16: 17,650,476	S321G	probably benign	Het
Cdc14b	T	C	13: 64,210,192		probably benign	Het
Cep152	T	C	2: 125,576,869		probably benign	Het
Cep290	A	G	10: 100,508,758	E479G	probably benign	Het
Chrm2	T	G	6: 36,524,111	I301R	probably benign	Het
Clec2e	A	G	6: 129,093,468	W197R	probably damaging	Het
Cnot10	G	T	9: 114,629,150	S96*	probably null	Het
Col19a1	A	G	1: 24,289,655		probably benign	Het
Csmd2	T	C	4: 128,133,673		probably benign	Het
Cthrc1	A	T	15: 39,086,764	*172L	probably null	Het
Cul9	A	T	17: 46,528,589	I821N	probably benign	Het
Daam1	G	C	12: 71,975,304		probably benign	Het
Dhx58	A	T	11: 100,699,264	I398N	probably damaging	Het
Dip2b	T	A	15: 100,193,913	H844Q	probably damaging	Het
Dmac2	A	G	7: 25,621,029	D50G	probably damaging	Het
Dmxl1	C	A	18: 49,879,362	Q1529K	probably benign	Het
Dtna	C	T	18: 23,597,501	P315L	probably damaging	Het
Ep300	T	C	15: 81,640,116	S1382P	unknown	Het
Fat2	A	T	11: 55,310,777	N490K	probably damaging	Het
Flg2	T	A	3: 93,200,355		probably benign	Het
Gm13084	T	A	4: 143,811,699	D234V	probably benign	Het
Gpatch1	T	C	7: 35,281,381		probably benign	Het
Grin2a	C	A	16: 9,579,585	K879N	possibly damaging	Het
Hacd3	A	C	9: 65,001,022	I164S	possibly damaging	Het
Hinfp	A	C	9: 44,298,948	C197G	probably damaging	Het
Hsd17b12	T	C	2: 94,114,990		probably benign	Het
Hsd3b1	A	T	3: 98,853,039	L212Q	probably damaging	Het
Ifrd1	C	T	12: 40,214,094		probably null	Het
Igf2bp2	A	G	16: 22,081,801	F129L	possibly damaging	Het
Kirrel3	T	A	9: 35,020,163	I409N	probably damaging	Het
Klhdc10	T	C	6: 30,447,412	I204T	probably damaging	Het
Kpna6	A	T	4: 129,657,804	S65R	possibly damaging	Het
Lama3	A	T	18: 12,407,563	D308V	probably benign	Het
Larp4b	T	A	13: 9,158,107		probably null	Het
Lgr6	C	T	1: 134,994,010	A199T	probably damaging	Het
Lyzl1	A	T	18: 4,169,175	T11S	probably benign	Het
Man1c1	A	G	4: 134,578,315	L366P	probably damaging	Het
Mef2a	A	G	7: 67,251,724	M100T	probably damaging	Het
Mettl13	G	A	1: 162,538,889	H474Y	possibly damaging	Het
Mmp3	A	G	9: 7,451,320	D352G	probably benign	Het
Mns1	T	C	9: 72,452,804	I412T	probably damaging	Het
Mylk	G	T	16: 34,875,620	G242W	probably damaging	Het
Nav1	T	C	1: 135,449,966	D1715G	possibly damaging	Het
Nckap1l	T	C	15: 103,453,883	S2P	probably damaging	Het
Nek3	A	T	8: 22,128,729		probably benign	Het
Nfrkb	A	G	9: 31,388,897		probably benign	Het
Nlrp4d	T	C	7: 10,388,778	D53G	probably benign	Het
Nol8	T	C	13: 49,662,152	S561P	probably damaging	Het
Nuf2	A	C	1: 169,525,297		probably benign	Het
Ofcc1	T	A	13: 40,015,313	D866V	possibly damaging	Het
Olfr195	A	G	16: 59,149,299	I150V	probably benign	Het
Optn	A	G	2: 5,046,195	L125P	probably benign	Het
Otoa	T	A	7: 121,131,341	F588Y	probably benign	Het
Pappa	T	A	4: 65,351,613		probably null	Het
Pde5a	T	G	3: 122,835,583	C635W	probably damaging	Het
Pdgfb	A	T	15: 80,003,419		probably null	Het
Pih1d2	T	A	9: 50,621,046	C135S	probably damaging	Het
Plcg1	G	T	2: 160,752,366	C361F	probably damaging	Het
Ppp4r4	T	C	12: 103,601,360		probably benign	Het
Prdm10	G	A	9: 31,349,268		probably null	Het
Prex2	T	A	1: 11,089,706		probably null	Het
Prss56	T	G	1: 87,184,730		probably null	Het
Prtg	A	G	9: 72,844,958	K209E	probably benign	Het
Ptprc	G	A	1: 138,122,575	T36I	possibly damaging	Het
Rasgrp4	A	G	7: 29,145,860	Y302C	probably damaging	Het
Rb1cc1	T	A	1: 6,248,634	M759K	probably damaging	Het
Rbm15b	T	A	9: 106,885,998	M324L	probably benign	Het
Rcbtb2	T	C	14: 73,178,547	V500A	probably damaging	Het
Rgs6	A	G	12: 83,133,677	K434R	probably damaging	Het
Rims1	C	T	1: 22,596,526	A125T	possibly damaging	Het
Robo3	A	G	9: 37,422,177	V746A	probably benign	Het
Rtl1	C	T	12: 109,591,386	E1340K	unknown	Het
Sacs	G	A	14: 61,205,640	D1712N	possibly damaging	Het
Samd4b	G	A	7: 28,403,977	P19S	probably benign	Het
Samhd1	T	C	2: 157,114,231	Y347C	probably damaging	Het
Sema6d	T	A	2: 124,658,490	I393N	probably damaging	Het
Sigmar1	C	T	4: 41,741,243	A4T	probably benign	Het
Skint9	C	A	4: 112,389,179	L245F	probably benign	Het
Slc35f5	T	C	1: 125,585,095	L372P	probably damaging	Het
Smc1b	A	T	15: 85,066,277	I1182N	probably damaging	Het
Smyd3	A	G	1: 178,957,573		probably benign	Het
Sptlc1	T	C	13: 53,337,612	D417G	probably benign	Het
Sv2c	T	C	13: 96,088,708	N31S	probably benign	Het
Tjp1	T	C	7: 65,314,990	D811G	probably damaging	Het
Top2b	A	G	14: 16,418,442	T1221A	probably benign	Het
Tph2	T	C	10: 115,174,109	D182G	probably damaging	Het
Traf6	C	T	2: 101,688,588	Q141*	probably null	Het
Ttn	T	C	2: 76,756,931	D21574G	probably damaging	Het
Uba2	T	A	7: 34,151,021	N367I	probably benign	Het
Ube2b	T	C	11: 51,988,602		probably benign	Het
Ubr5	G	T	15: 38,030,672	L426I	probably benign	Het
Ugt2a2	T	A	5: 87,464,148	H301L	probably benign	Het
Upf2	T	A	2: 6,018,894		probably benign	Het
Utrn	T	C	10: 12,710,060	D991G	probably benign	Het
Vmn2r25	T	C	6: 123,823,181	D734G	probably damaging	Het
Vmn2r68	T	A	7: 85,233,249		probably benign	Het
Vmn2r68	C	G	7: 85,233,258		probably null	Het
Vwf	T	A	6: 125,626,361	Y891*	probably null	Het
Wwox	C	T	8: 114,706,278	T228I	probably benign	Het
Zer1	C	T	2: 30,108,213		probably benign	Het
Zfp180	C	T	7: 24,104,707	H184Y	possibly damaging	Het
Zfp68	A	T	5: 138,607,225	Y279N	probably benign	Het

Other mutations in Mon2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00497:Mon2	APN	10	123026299	missense	probably damaging	1.00
IGL01072:Mon2	APN	10	123010539	nonsense	probably null
IGL02080:Mon2	APN	10	123052190	missense	probably damaging	0.98
IGL02157:Mon2	APN	10	123013472	missense	probably damaging	1.00
IGL02419:Mon2	APN	10	123016447	missense	probably benign	0.05
IGL02498:Mon2	APN	10	123034330	missense	probably benign	0.00
IGL02638:Mon2	APN	10	123023939	missense	probably damaging	1.00
IGL02664:Mon2	APN	10	123009496	splice site	probably benign
IGL02690:Mon2	APN	10	123009627	missense	possibly damaging	0.67
IGL02878:Mon2	APN	10	123006991	missense	probably benign	0.09
IGL03092:Mon2	APN	10	123018100	missense	probably damaging	1.00
IGL03103:Mon2	APN	10	123030103	splice site	probably benign
IGL03208:Mon2	APN	10	123018069	splice site	probably benign
R0010:Mon2	UTSW	10	123032694	missense	probably damaging	1.00
R0016:Mon2	UTSW	10	123035546	missense	probably damaging	0.96
R0016:Mon2	UTSW	10	123035546	missense	probably damaging	0.96
R0027:Mon2	UTSW	10	123036048	missense	possibly damaging	0.66
R0027:Mon2	UTSW	10	123036048	missense	possibly damaging	0.66
R0145:Mon2	UTSW	10	123013512	missense	possibly damaging	0.94
R0481:Mon2	UTSW	10	123013396	missense	possibly damaging	0.94
R0513:Mon2	UTSW	10	123038610	missense	probably damaging	1.00
R0599:Mon2	UTSW	10	123026065	splice site	probably benign
R1226:Mon2	UTSW	10	123002819	missense	probably benign	0.17
R1548:Mon2	UTSW	10	123036007	splice site	probably benign
R1598:Mon2	UTSW	10	123016396	missense	probably damaging	1.00
R1650:Mon2	UTSW	10	122995777	missense	probably benign	0.45
R1687:Mon2	UTSW	10	123026124	missense	probably damaging	0.98
R1721:Mon2	UTSW	10	123031097	missense	probably damaging	0.98
R1768:Mon2	UTSW	10	123013763	missense	probably benign	0.00
R1827:Mon2	UTSW	10	123046311	missense	probably damaging	0.97
R1879:Mon2	UTSW	10	123002885	missense	probably damaging	1.00
R1954:Mon2	UTSW	10	123038483	missense	probably damaging	1.00
R1955:Mon2	UTSW	10	123038483	missense	probably damaging	1.00
R1968:Mon2	UTSW	10	123009565	missense	probably damaging	1.00
R2060:Mon2	UTSW	10	122995776	missense	probably damaging	1.00
R2160:Mon2	UTSW	10	123075929	nonsense	probably null
R2165:Mon2	UTSW	10	123042364	splice site	probably null
R3737:Mon2	UTSW	10	123013375	missense	probably damaging	1.00
R3814:Mon2	UTSW	10	123013565	missense	probably damaging	0.98
R4058:Mon2	UTSW	10	123002819	missense	probably benign	0.17
R4091:Mon2	UTSW	10	123038510	missense	probably damaging	1.00
R4214:Mon2	UTSW	10	123016492	missense	probably benign	0.03
R4354:Mon2	UTSW	10	123026983	missense	probably benign	0.02
R4422:Mon2	UTSW	10	123042982	missense	probably damaging	1.00
R4505:Mon2	UTSW	10	123009589	missense	probably damaging	0.99
R4791:Mon2	UTSW	10	123006057	missense	probably benign	0.01
R4797:Mon2	UTSW	10	123016517	missense	probably benign	0.45
R4944:Mon2	UTSW	10	123038459	critical splice donor site	probably null
R4982:Mon2	UTSW	10	122995789	missense	probably damaging	1.00
R5298:Mon2	UTSW	10	123010606	missense	probably benign
R5503:Mon2	UTSW	10	123032645	missense	possibly damaging	0.54
R5653:Mon2	UTSW	10	123026094	missense	probably damaging	0.96
R5687:Mon2	UTSW	10	123008239	missense	probably damaging	0.99
R5838:Mon2	UTSW	10	123010492	critical splice donor site	probably null
R6108:Mon2	UTSW	10	123032695	missense	probably benign	0.00
R6182:Mon2	UTSW	10	123038659	splice site	probably null
R6355:Mon2	UTSW	10	123022920	missense	possibly damaging	0.58
R6358:Mon2	UTSW	10	123013504	missense	probably damaging	0.98
R6548:Mon2	UTSW	10	123036093	missense	probably damaging	1.00
R6557:Mon2	UTSW	10	123016402	missense	probably damaging	1.00
R6649:Mon2	UTSW	10	123038480	missense	possibly damaging	0.46
R7140:Mon2	UTSW	10	123035453	missense	probably benign	0.00
R7303:Mon2	UTSW	10	123038459	critical splice donor site	probably null
R7317:Mon2	UTSW	10	123013946	missense	probably damaging	0.97
R7355:Mon2	UTSW	10	123009516	missense	probably benign
R7508:Mon2	UTSW	10	123023939	missense	probably damaging	1.00
R7509:Mon2	UTSW	10	123032552	missense	probably benign
R7647:Mon2	UTSW	10	123006026	missense	probably benign
R7720:Mon2	UTSW	10	123032588	missense	probably benign	0.00
R7799:Mon2	UTSW	10	123042331	missense	probably benign	0.41
R7801:Mon2	UTSW	10	123059186	critical splice donor site	probably null
R7823:Mon2	UTSW	10	123032654	missense	probably damaging	1.00
R7985:Mon2	UTSW	10	123016308	missense	probably damaging	1.00
R8310:Mon2	UTSW	10	123002783	missense	probably damaging	1.00
R8810:Mon2	UTSW	10	123009611	missense	possibly damaging	0.94
R8825:Mon2	UTSW	10	123013871	missense	probably benign	0.00
R8937:Mon2	UTSW	10	123059205	missense	probably benign
R8978:Mon2	UTSW	10	123035564	nonsense	probably null
R9011:Mon2	UTSW	10	123026308	missense	possibly damaging	0.95
R9213:Mon2	UTSW	10	123036111	nonsense	probably null
R9358:Mon2	UTSW	10	123032547	missense	probably benign	0.00
R9630:Mon2	UTSW	10	123038510	missense	probably damaging	1.00
X0022:Mon2	UTSW	10	123006102	missense	probably benign	0.07

Predicted Primers

PCR Primer
(F):5'- AAGGTTCCGCAAAGCTGTCCTC -3'
(R):5'- AGATGTTCAGCTCAAGATTGCTCCG -3'

Sequencing Primer
(F):5'- cacacacacacacacacag -3'
(R):5'- GCTCAAGATTGCTCCGAGTATTTAAC -3'

Posted On

2013-04-24