Mutagenetix > Incidental Mutation

Incidental Mutation 'R2051:Ago1'

226403

Institutional Source

Beutler Lab

Gene Symbol

Ago1

Ensembl Gene

ENSMUSG00000041530

Gene Name

argonaute RISC catalytic subunit 1

Synonyms

Eif2c1, argonaute 1

MMRRC Submission

040058-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.810) question?

Stock #

R2051 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

126328805-126362376 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 126354246 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 188 (H188R)

Ref Sequence

ENSEMBL: ENSMUSP00000095498 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000097888] [ENSMUST00000176315]

AlphaFold

Q8CJG1

Predicted Effect

probably benign
Transcript: ENSMUST00000097888
AA Change: H188R

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000095498
Gene: ENSMUSG00000041530
AA Change: H188R

Domain	Start	End	E-Value	Type
Pfam:ArgoN	26	164	2.3e-26	PFAM
DUF1785	173	225	3.48e-25	SMART
PAZ	233	368	1.41e-5	SMART
Pfam:ArgoL2	373	418	3.6e-18	PFAM
Pfam:ArgoMid	427	509	7.6e-37	PFAM
Piwi	515	816	4.16e-131	SMART
Blast:Piwi	823	849	3e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000127800

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149425

Predicted Effect

probably benign
Transcript: ENSMUST00000176315

SMART Domains

Protein: ENSMUSP00000134871
Gene: ENSMUSG00000041530

Domain	Start	End	E-Value	Type
Pfam:PAZ	1	62	4.1e-23	PFAM
Piwi	211	512	4.16e-131	SMART
Blast:Piwi	519	545	2e-6	BLAST

Coding Region Coverage

1x: 99.1%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a member of the argonaute family of proteins, which associate with small RNAs and have important roles in RNA interference (RNAi) and RNA silencing. This protein binds to microRNAs (miRNAs) or small interfering RNAs (siRNAs) and represses translation of mRNAs that are complementary to them. It is also involved in transcriptional gene silencing (TGS) of promoter regions that are complementary to bound short antigene RNAs (agRNAs), as well as in the degradation of miRNA-bound mRNA targets. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target, and that its mRNA could give rise to an additional C-terminally extended isoform by use of an alternative in-frame translation termination codon. [provided by RefSeq, Nov 2015]
PHENOTYPE: Mice homozygous for a conditional allele activated in keratinocytes exhibit no abnormal phenotype. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700123K08Rik	G	A	5: 138,562,447 (GRCm39)	T98M	probably damaging	Het
4932414N04Rik	G	T	2: 68,541,392 (GRCm39)	K10N	possibly damaging	Het
Aadat	T	A	8: 60,960,173 (GRCm39)	S40T	probably benign	Het
Abca13	A	G	11: 9,278,098 (GRCm39)	I3093V	probably benign	Het
Acacb	A	T	5: 114,383,951 (GRCm39)	Q2160L	probably damaging	Het
Acp6	G	T	3: 97,075,333 (GRCm39)	S189I	probably benign	Het
Actr5	A	T	2: 158,474,213 (GRCm39)	M339L	probably benign	Het
Adcy1	A	T	11: 7,111,885 (GRCm39)	K917*	probably null	Het
Adgrg5	C	T	8: 95,668,695 (GRCm39)	R504C	probably benign	Het
Akap9	T	A	5: 4,025,685 (GRCm39)	C23*	probably null	Het
Ank3	T	C	10: 69,733,920 (GRCm39)	I728T	probably damaging	Het
Ankrd50	A	G	3: 38,508,642 (GRCm39)	S1242P	probably benign	Het
Arhgap29	G	A	3: 121,775,509 (GRCm39)	R84H	probably benign	Het
Arhgef10	A	G	8: 14,995,320 (GRCm39)	D7G	probably null	Het
Arid4b	A	G	13: 14,362,230 (GRCm39)	E898G	probably damaging	Het
Atrnl1	A	G	19: 57,680,281 (GRCm39)	N727S	probably benign	Het
Baalc	G	T	15: 38,796,629 (GRCm39)		probably benign	Het
Cdc25c	G	C	18: 34,871,292 (GRCm39)	L275V	probably damaging	Het
Chpf2	G	T	5: 24,796,274 (GRCm39)	V407L	probably benign	Het
Chrnb3	C	A	8: 27,876,839 (GRCm39)	N84K	probably damaging	Het
Cnot1	A	G	8: 96,451,221 (GRCm39)	F2171L	possibly damaging	Het
Csmd3	C	T	15: 48,485,389 (GRCm39)		probably null	Het
Cux1	T	A	5: 136,361,512 (GRCm39)	Q138L	probably damaging	Het
Cyp2c65	A	G	19: 39,070,675 (GRCm39)	N286S	probably benign	Het
Dclre1b	T	C	3: 103,716,356 (GRCm39)	S17G	possibly damaging	Het
Dlgap5	A	G	14: 47,648,941 (GRCm39)	S221P	probably benign	Het
Dnah1	T	G	14: 31,001,080 (GRCm39)	T2422P	probably damaging	Het
Enpp1	A	G	10: 24,587,702 (GRCm39)		probably null	Het
Erbb2	T	C	11: 98,310,998 (GRCm39)	C53R	probably damaging	Het
Exoc8	A	G	8: 125,622,219 (GRCm39)	V716A	probably benign	Het
Fam193a	T	A	5: 34,619,494 (GRCm39)	D766E	probably benign	Het
Fbxo43	C	A	15: 36,162,278 (GRCm39)	G310W	probably damaging	Het
Fcgbp	C	T	7: 27,819,785 (GRCm39)	T2504I	probably damaging	Het
Fnbp4	C	T	2: 90,587,876 (GRCm39)	P418L	probably benign	Het
Gjd2	T	C	2: 113,841,539 (GRCm39)	T313A	probably damaging	Het
Gm12695	T	A	4: 96,658,008 (GRCm39)	R54W	probably damaging	Het
Gm128	T	C	3: 95,148,051 (GRCm39)	D81G	possibly damaging	Het
Gm21834	A	G	17: 58,048,763 (GRCm39)	V151A	possibly damaging	Het
Grhl1	T	A	12: 24,636,151 (GRCm39)		probably null	Het
Hcn1	C	T	13: 118,112,619 (GRCm39)	T861I	probably damaging	Het
Herc6	C	A	6: 57,602,961 (GRCm39)	Q547K	probably benign	Het
Iqgap3	T	C	3: 88,027,474 (GRCm39)	L699P	probably damaging	Het
Kank4	T	C	4: 98,668,339 (GRCm39)	D36G	probably damaging	Het
Kcnk5	A	T	14: 20,192,277 (GRCm39)	S295T	probably damaging	Het
Krt18	T	C	15: 101,937,935 (GRCm39)	V144A	probably benign	Het
Krtap9-5	A	G	11: 99,840,030 (GRCm39)	I244V	unknown	Het
Leng1	T	G	7: 3,668,400 (GRCm39)	N16T	probably damaging	Het
Lss	A	G	10: 76,367,712 (GRCm39)	K15E	possibly damaging	Het
Mastl	G	T	2: 23,022,836 (GRCm39)	A629E	possibly damaging	Het
Mavs	G	C	2: 131,082,370 (GRCm39)	A85P	possibly damaging	Het
Nav3	T	C	10: 109,660,536 (GRCm39)	D678G	probably damaging	Het
Nsd3	T	G	8: 26,181,116 (GRCm39)	S906A	probably damaging	Het
Nsfl1c	A	G	2: 151,345,002 (GRCm39)	N118S	probably damaging	Het
Nup205	T	A	6: 35,207,451 (GRCm39)	M1501K	probably benign	Het
Or4p7	C	T	2: 88,221,882 (GRCm39)	T97M	possibly damaging	Het
Or6n1	T	A	1: 173,916,785 (GRCm39)	Y60N	possibly damaging	Het
Pax8	A	G	2: 24,326,520 (GRCm39)	S281P	probably benign	Het
Pds5b	T	G	5: 150,671,655 (GRCm39)	I433R	probably damaging	Het
Peg3	T	C	7: 6,715,720 (GRCm39)	N117D	probably damaging	Het
Pfkm	A	T	15: 98,029,573 (GRCm39)	D728V	probably benign	Het
Phkb	T	C	8: 86,776,450 (GRCm39)		probably null	Het
Pkp4	T	C	2: 59,165,248 (GRCm39)	V704A	probably benign	Het
Ppfia2	T	A	10: 106,673,160 (GRCm39)	S501T	probably damaging	Het
Ptpru	T	C	4: 131,546,398 (GRCm39)	E284G	possibly damaging	Het
Ror1	C	T	4: 100,265,065 (GRCm39)	R180*	probably null	Het
Ryr3	T	A	2: 112,586,986 (GRCm39)	Y2666F	probably damaging	Het
Sec23a	C	A	12: 59,037,754 (GRCm39)		probably null	Het
Sertad3	C	T	7: 27,175,694 (GRCm39)	Q43*	probably null	Het
Setd2	C	T	9: 110,379,958 (GRCm39)	H1258Y	probably benign	Het
Sharpin	A	G	15: 76,232,407 (GRCm39)	S177P	probably benign	Het
Skap1	T	C	11: 96,432,289 (GRCm39)	F86S	possibly damaging	Het
Slc8a2	T	C	7: 15,874,940 (GRCm39)	I396T	probably damaging	Het
Slc9a2	T	C	1: 40,765,597 (GRCm39)	F329S	probably damaging	Het
Slx4ip	C	T	2: 136,908,125 (GRCm39)	L161F	possibly damaging	Het
Sox4	A	G	13: 29,136,764 (GRCm39)	S81P	probably damaging	Het
Ssc4d	G	T	5: 135,999,118 (GRCm39)	S28R	probably benign	Het
St8sia2	C	T	7: 73,592,950 (GRCm39)	G369S	possibly damaging	Het
Swt1	T	C	1: 151,248,081 (GRCm39)	Y836C	probably damaging	Het
Taar7d	A	G	10: 23,903,904 (GRCm39)	D262G	probably benign	Het
Taar8b	T	A	10: 23,967,212 (GRCm39)	L327F	probably benign	Het
Tars1	A	T	15: 11,393,280 (GRCm39)	L138*	probably null	Het
Tbcd	A	T	11: 121,344,496 (GRCm39)	D75V	probably damaging	Het
Tesc	A	G	5: 118,184,394 (GRCm39)	I25V	probably damaging	Het
Tmem132e	G	T	11: 82,331,264 (GRCm39)	S407I	probably damaging	Het
Tmem50b	C	A	16: 91,377,180 (GRCm39)	A95S	possibly damaging	Het
Tnr	T	C	1: 159,719,603 (GRCm39)	I960T	probably benign	Het
Tns2	C	T	15: 102,017,369 (GRCm39)	R281C	probably damaging	Het
Tpcn1	G	C	5: 120,681,453 (GRCm39)	P532A	probably damaging	Het
Tpsb2	T	C	17: 25,585,539 (GRCm39)		probably benign	Het
Triobp	C	A	15: 78,888,740 (GRCm39)	H1948Q	probably damaging	Het
Tshb	T	C	3: 102,684,857 (GRCm39)	I116V	probably benign	Het
Ttc13	A	T	8: 125,398,950 (GRCm39)		probably null	Het
Usp34	A	T	11: 23,414,468 (GRCm39)	T2804S	probably damaging	Het
Vmn2r18	A	T	5: 151,486,016 (GRCm39)	C493S	possibly damaging	Het
Vmn2r2	T	C	3: 64,024,766 (GRCm39)	K605R	possibly damaging	Het
Vmn2r37	T	C	7: 9,220,792 (GRCm39)	Y357C	probably damaging	Het
Zc3h6	T	G	2: 128,857,538 (GRCm39)	S686A	possibly damaging	Het
Zfp608	G	A	18: 55,121,386 (GRCm39)	P67L	probably benign	Het
Zyg11a	T	C	4: 108,049,244 (GRCm39)		probably benign	Het

Other mutations in Ago1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01377:Ago1	APN	4	126,353,610 (GRCm39)	missense	probably damaging	0.98
IGL02578:Ago1	APN	4	126,333,324 (GRCm39)	missense	probably benign	0.12
IGL02709:Ago1	APN	4	126,347,433 (GRCm39)	nonsense	probably null
IGL02810:Ago1	APN	4	126,336,886 (GRCm39)	missense	probably benign	0.00
IGL03037:Ago1	APN	4	126,355,587 (GRCm39)	missense	probably benign	0.00
IGL03091:Ago1	APN	4	126,352,982 (GRCm39)	missense	probably damaging	0.98
IGL03100:Ago1	APN	4	126,336,964 (GRCm39)	missense	probably benign	0.08
IGL03121:Ago1	APN	4	126,353,796 (GRCm39)	missense	probably benign	0.00
R0195:Ago1	UTSW	4	126,357,484 (GRCm39)	missense	probably benign	0.01
R0244:Ago1	UTSW	4	126,357,499 (GRCm39)	missense	possibly damaging	0.94
R0309:Ago1	UTSW	4	126,336,959 (GRCm39)	missense	probably benign	0.06
R0514:Ago1	UTSW	4	126,333,388 (GRCm39)	missense	probably benign
R0557:Ago1	UTSW	4	126,353,817 (GRCm39)	missense	probably benign	0.00
R1104:Ago1	UTSW	4	126,347,426 (GRCm39)	missense	probably damaging	0.99
R1553:Ago1	UTSW	4	126,334,194 (GRCm39)	missense	probably damaging	0.99
R1624:Ago1	UTSW	4	126,357,534 (GRCm39)	missense	probably damaging	0.97
R1851:Ago1	UTSW	4	126,333,788 (GRCm39)	missense	probably benign	0.00
R1867:Ago1	UTSW	4	126,335,029 (GRCm39)	missense	probably damaging	0.98
R2001:Ago1	UTSW	4	126,348,187 (GRCm39)	missense	probably null	0.36
R2057:Ago1	UTSW	4	126,337,021 (GRCm39)	missense	probably damaging	0.98
R2105:Ago1	UTSW	4	126,355,581 (GRCm39)	missense	probably benign	0.30
R2117:Ago1	UTSW	4	126,357,650 (GRCm39)	splice site	probably null
R2256:Ago1	UTSW	4	126,335,704 (GRCm39)	missense	possibly damaging	0.80
R2272:Ago1	UTSW	4	126,347,443 (GRCm39)	missense	probably benign	0.01
R2517:Ago1	UTSW	4	126,333,732 (GRCm39)	nonsense	probably null
R2850:Ago1	UTSW	4	126,336,868 (GRCm39)	splice site	probably benign
R2993:Ago1	UTSW	4	126,333,839 (GRCm39)	splice site	probably benign
R3746:Ago1	UTSW	4	126,354,837 (GRCm39)	missense	probably benign
R3747:Ago1	UTSW	4	126,354,837 (GRCm39)	missense	probably benign
R3750:Ago1	UTSW	4	126,354,837 (GRCm39)	missense	probably benign
R4600:Ago1	UTSW	4	126,354,185 (GRCm39)	missense	probably benign	0.37
R4934:Ago1	UTSW	4	126,342,652 (GRCm39)	missense	possibly damaging	0.56
R4983:Ago1	UTSW	4	126,347,447 (GRCm39)	missense	probably damaging	0.99
R5086:Ago1	UTSW	4	126,347,397 (GRCm39)	missense	probably benign	0.01
R5132:Ago1	UTSW	4	126,355,516 (GRCm39)	missense	probably benign	0.01
R5239:Ago1	UTSW	4	126,335,008 (GRCm39)	missense	probably damaging	1.00
R5609:Ago1	UTSW	4	126,354,830 (GRCm39)	missense	possibly damaging	0.80
R5705:Ago1	UTSW	4	126,342,587 (GRCm39)	missense	probably benign	0.01
R5980:Ago1	UTSW	4	126,354,362 (GRCm39)	unclassified	probably benign
R6036:Ago1	UTSW	4	126,337,021 (GRCm39)	missense	probably damaging	0.98
R6036:Ago1	UTSW	4	126,337,021 (GRCm39)	missense	probably damaging	0.98
R6398:Ago1	UTSW	4	126,342,601 (GRCm39)	missense	probably benign	0.26
R6505:Ago1	UTSW	4	126,357,628 (GRCm39)	missense	probably benign	0.00
R6545:Ago1	UTSW	4	126,348,145 (GRCm39)	missense	possibly damaging	0.74
R6944:Ago1	UTSW	4	126,354,215 (GRCm39)	missense	possibly damaging	0.78
R7041:Ago1	UTSW	4	126,357,499 (GRCm39)	missense	possibly damaging	0.94
R7490:Ago1	UTSW	4	126,333,298 (GRCm39)	makesense	probably null
R7496:Ago1	UTSW	4	126,355,545 (GRCm39)	missense	probably benign	0.20
R7575:Ago1	UTSW	4	126,347,701 (GRCm39)	missense	probably benign	0.12
R7625:Ago1	UTSW	4	126,337,022 (GRCm39)	missense	probably benign	0.18
R7988:Ago1	UTSW	4	126,354,210 (GRCm39)	missense	probably damaging	1.00
R8041:Ago1	UTSW	4	126,335,729 (GRCm39)	missense	probably damaging	1.00
R8073:Ago1	UTSW	4	126,337,019 (GRCm39)	missense	probably benign	0.04
R8086:Ago1	UTSW	4	126,354,774 (GRCm39)	missense	probably benign
R8127:Ago1	UTSW	4	126,348,214 (GRCm39)	missense	possibly damaging	0.95
R8772:Ago1	UTSW	4	126,354,316 (GRCm39)	unclassified	probably benign
R8878:Ago1	UTSW	4	126,357,516 (GRCm39)	missense	probably benign	0.35
R8989:Ago1	UTSW	4	126,357,583 (GRCm39)	missense	probably benign	0.01
R9140:Ago1	UTSW	4	126,336,977 (GRCm39)	missense	probably benign
X0025:Ago1	UTSW	4	126,336,908 (GRCm39)	missense	possibly damaging	0.47
Z1177:Ago1	UTSW	4	126,347,449 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGGTAGGGATAGCATGGCTC -3'
(R):5'- AGATGGTTAGACCCCTGGCC -3'

Sequencing Primer
(F):5'- AGCATGGCTCAGATTCTTTCAG -3'
(R):5'- AGGTCAGTCTTACTATTGGCCCAAG -3'

Posted On

2014-09-17