Mutagenetix > Incidental Mutation

Incidental Mutation 'R2256:Ago1'

243339

Institutional Source

Beutler Lab

Gene Symbol

Ago1

Ensembl Gene

ENSMUSG00000041530

Gene Name

argonaute RISC catalytic subunit 1

Synonyms

Eif2c1, argonaute 1

MMRRC Submission

040256-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.748) question?

Stock #

R2256 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

126435012-126468583 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 126441911 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 669 (V669A)

Ref Sequence

ENSEMBL: ENSMUSP00000095498 (fasta)

Gene Model

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

AlphaFold

Q8CJG1

Predicted Effect

possibly damaging
Transcript: ENSMUST00000097888
AA Change: V669A

PolyPhen 2 Score 0.796 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000095498
Gene: ENSMUSG00000041530
AA Change: V669A

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: ENSMUST00000156533

Predicted Effect

probably benign
Transcript: ENSMUST00000176315
AA Change: V365A

PolyPhen 2 Score 0.306 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000134871
Gene: ENSMUSG00000041530
AA Change: V365A

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

Meta Mutation Damage Score

0.8223

Coding Region Coverage

1x: 99.3%
3x: 98.8%
10x: 97.7%
20x: 96.3%

Validation Efficiency

98% (97/99)

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: 98 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001C19Rik	AC	A	17: 47,433,423 (GRCm38)		probably benign	Het
4931409K22Rik	C	T	5: 24,552,040 (GRCm38)		probably benign	Het
6720489N17Rik	A	T	13: 62,607,396 (GRCm38)	I36N	probably benign	Het
Abcb4	T	C	5: 8,958,431 (GRCm38)	S1200P	probably damaging	Het
Acadsb	A	G	7: 131,443,653 (GRCm38)	Y438C	probably benign	Het
Acp7	A	C	7: 28,614,413 (GRCm38)	W399G	probably damaging	Het
Actr3b	A	G	5: 25,822,405 (GRCm38)	T113A	possibly damaging	Het
Adgrv1	T	C	13: 81,506,140 (GRCm38)	D2204G	probably benign	Het
Ang5	T	A	14: 43,962,521 (GRCm38)	L14Q	probably null	Het
Aoc1	T	C	6: 48,906,440 (GRCm38)	Y417H	possibly damaging	Het
Arhgap32	T	C	9: 32,247,497 (GRCm38)	I186T	probably damaging	Het
Atf2	A	T	2: 73,845,511 (GRCm38)		probably null	Het
Atg4a	A	G	X: 140,990,235 (GRCm38)	I91V	probably benign	Het
Atp7b	T	G	8: 21,998,266 (GRCm38)	T1102P	probably damaging	Het
Bend5	A	C	4: 111,431,010 (GRCm38)		probably benign	Het
Camkk2	T	C	5: 122,746,335 (GRCm38)	D341G	probably damaging	Het
Cast	T	A	13: 74,739,905 (GRCm38)	I208L	probably damaging	Het
Ccdc141	A	T	2: 77,132,262 (GRCm38)	W113R	probably damaging	Het
Cdk14	T	A	5: 4,888,924 (GRCm38)	M433L	probably benign	Het
Cel	A	G	2: 28,561,192 (GRCm38)	F51S	probably damaging	Het
Cenpc1	A	G	5: 86,016,203 (GRCm38)	L853S	probably damaging	Het
Cep162	C	A	9: 87,206,914 (GRCm38)	D972Y	probably damaging	Het
Clasrp	A	G	7: 19,586,585 (GRCm38)		probably benign	Het
Cntnap5c	T	A	17: 58,330,315 (GRCm38)	N1062K	probably benign	Het
Col3a1	A	G	1: 45,321,632 (GRCm38)	D74G	unknown	Het
Copb1	T	A	7: 114,253,875 (GRCm38)	D29V	possibly damaging	Het
Cox6a1	C	T	5: 115,348,848 (GRCm38)	E35K	possibly damaging	Het
Cyp2b9	G	A	7: 26,173,605 (GRCm38)		probably null	Het
Ddx46	A	G	13: 55,647,708 (GRCm38)	K177E	possibly damaging	Het
Dmbt1	T	C	7: 131,090,494 (GRCm38)	F823L	probably benign	Het
Drc7	A	T	8: 95,075,009 (GRCm38)	H666L	probably benign	Het
Fam228a	T	C	12: 4,737,775 (GRCm38)		probably benign	Het
Fam71e2	T	A	7: 4,771,021 (GRCm38)	M31L	probably benign	Het
Fam83e	A	T	7: 45,728,770 (GRCm38)	K406M	possibly damaging	Het
Fam83e	A	T	7: 45,728,769 (GRCm38)	K406*	probably null	Het
Fam90a1a	T	A	8: 21,963,517 (GRCm38)	L296Q	possibly damaging	Het
Fat1	A	G	8: 44,950,371 (GRCm38)	Y53C	probably damaging	Het
Fhdc1	T	C	3: 84,446,046 (GRCm38)	E624G	probably benign	Het
Fryl	T	A	5: 73,072,844 (GRCm38)	N1657Y	possibly damaging	Het
Fsip2	T	A	2: 82,962,751 (GRCm38)	D417E	probably benign	Het
Greb1l	A	G	18: 10,503,307 (GRCm38)	M453V	possibly damaging	Het
Gtf2b	A	G	3: 142,781,424 (GRCm38)	D207G	probably benign	Het
Has3	C	A	8: 106,874,256 (GRCm38)	L117I	probably damaging	Het
Jmjd1c	T	A	10: 67,225,294 (GRCm38)	I1142N	probably damaging	Het
Lipt2	C	T	7: 100,159,394 (GRCm38)	T38I	probably benign	Het
Magea2	A	T	X: 155,027,859 (GRCm38)	L243Q	probably damaging	Het
Mast4	A	T	13: 102,735,751 (GRCm38)	C2178S	possibly damaging	Het
Mctp2	A	G	7: 72,185,820 (GRCm38)	L543P	probably damaging	Het
Mphosph9	C	T	5: 124,283,659 (GRCm38)	V740I	probably benign	Het
Mut	A	T	17: 40,956,319 (GRCm38)	I595F	probably benign	Het
Myo1e	G	A	9: 70,378,373 (GRCm38)		probably null	Het
Nlrc4	A	G	17: 74,445,630 (GRCm38)	I586T	probably damaging	Het
Nom1	T	A	5: 29,437,752 (GRCm38)	V417D	probably damaging	Het
Nphs1	A	T	7: 30,467,992 (GRCm38)	I782F	possibly damaging	Het
Numa1	A	G	7: 102,000,791 (GRCm38)	E1243G	probably damaging	Het
Olfr1000	T	A	2: 85,608,463 (GRCm38)	Y149F	possibly damaging	Het
Olfr1254	T	C	2: 89,788,470 (GRCm38)	H294R	probably benign	Het
Olfr1290	T	C	2: 111,489,978 (GRCm38)	Y60C	probably damaging	Het
Olfr474	A	T	7: 107,955,037 (GRCm38)	Y132F	probably damaging	Het
Olfr676	A	G	7: 105,035,819 (GRCm38)	Y207C	probably benign	Het
Orai2	C	T	5: 136,161,600 (GRCm38)	V52I	probably damaging	Het
Osbpl5	A	G	7: 143,709,094 (GRCm38)	C186R	probably damaging	Het
Osbpl6	A	G	2: 76,584,474 (GRCm38)	E403G	probably damaging	Het
Padi4	G	A	4: 140,759,940 (GRCm38)	T217I	possibly damaging	Het
Parm1	C	T	5: 91,594,121 (GRCm38)	T116I	possibly damaging	Het
Pde4dip	T	A	3: 97,718,184 (GRCm38)	Q1366L	probably damaging	Het
Phgdh	T	C	3: 98,328,291 (GRCm38)	K108E	probably benign	Het
Pold1	T	C	7: 44,533,799 (GRCm38)		probably null	Het
Ppp1r37	G	T	7: 19,562,018 (GRCm38)		probably benign	Het
Sdk2	T	C	11: 113,830,794 (GRCm38)	N1332S	probably benign	Het
Sema6d	A	G	2: 124,664,150 (GRCm38)	D626G	probably damaging	Het
Skiv2l2	A	T	13: 112,876,512 (GRCm38)	M890K	probably damaging	Het
Slc18b1	A	G	10: 23,810,922 (GRCm38)	N212S	probably benign	Het
Slc2a9	T	C	5: 38,453,199 (GRCm38)	T86A	probably damaging	Het
Slco1a6	A	T	6: 142,091,016 (GRCm38)	M555K	probably benign	Het
Sntg2	C	T	12: 30,236,688 (GRCm38)	W302*	probably null	Het
Spata22	T	A	11: 73,340,475 (GRCm38)	M185K	possibly damaging	Het
Stk35	T	A	2: 129,810,507 (GRCm38)	Y309*	probably null	Het
Taar8c	A	G	10: 24,101,071 (GRCm38)	V281A	probably benign	Het
Thoc1	C	A	18: 9,993,466 (GRCm38)	D608E	possibly damaging	Het
Tmem121b	A	G	6: 120,492,071 (GRCm38)	Y562H	probably damaging	Het
Tmem121b	A	T	6: 120,492,069 (GRCm38)	Y562*	probably null	Het
Tmtc4	A	T	14: 122,941,408 (GRCm38)	I449N	probably benign	Het
Tmub1	G	A	5: 24,447,177 (GRCm38)		probably benign	Het
Tmub1	C	A	5: 24,446,924 (GRCm38)	G14V	possibly damaging	Het
Tshz2	A	G	2: 169,886,477 (GRCm38)	T529A	probably damaging	Het
Ugdh	A	T	5: 65,417,115 (GRCm38)		probably benign	Het
Usp25	A	G	16: 77,113,794 (GRCm38)	K913E	probably benign	Het
Vgf	A	G	5: 137,031,547 (GRCm38)		probably benign	Het
Vmn2r19	T	A	6: 123,329,886 (GRCm38)	F451Y	probably benign	Het
Vmn2r59	A	T	7: 42,012,245 (GRCm38)	C715*	probably null	Het
Vps9d1	C	A	8: 123,245,121 (GRCm38)	A582S	probably benign	Het
Xbp1	T	G	11: 5,524,841 (GRCm38)	H247Q	probably damaging	Het
Zfp319	A	T	8: 95,328,501 (GRCm38)	M358K	possibly damaging	Het
Zfp438	A	T	18: 5,213,508 (GRCm38)	N483K	probably damaging	Het
Zfp518b	T	C	5: 38,671,636 (GRCm38)	N1009D	possibly damaging	Het
Zfp644	A	T	5: 106,635,845 (GRCm38)	H945Q	probably damaging	Het
Zgrf1	T	A	3: 127,561,997 (GRCm38)	S291T	probably benign	Het

Other mutations in Ago1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01377:Ago1	APN	4	126,459,817 (GRCm38)	missense	probably damaging	0.98
IGL02578:Ago1	APN	4	126,439,531 (GRCm38)	missense	probably benign	0.12
IGL02709:Ago1	APN	4	126,453,640 (GRCm38)	nonsense	probably null
IGL02810:Ago1	APN	4	126,443,093 (GRCm38)	missense	probably benign	0.00
IGL03037:Ago1	APN	4	126,461,794 (GRCm38)	missense	probably benign	0.00
IGL03091:Ago1	APN	4	126,459,189 (GRCm38)	missense	probably damaging	0.98
IGL03100:Ago1	APN	4	126,443,171 (GRCm38)	missense	probably benign	0.08
IGL03121:Ago1	APN	4	126,460,003 (GRCm38)	missense	probably benign	0.00
R0195:Ago1	UTSW	4	126,463,691 (GRCm38)	missense	probably benign	0.01
R0244:Ago1	UTSW	4	126,463,706 (GRCm38)	missense	possibly damaging	0.94
R0309:Ago1	UTSW	4	126,443,166 (GRCm38)	missense	probably benign	0.06
R0514:Ago1	UTSW	4	126,439,595 (GRCm38)	missense	probably benign
R0557:Ago1	UTSW	4	126,460,024 (GRCm38)	missense	probably benign	0.00
R1104:Ago1	UTSW	4	126,453,633 (GRCm38)	missense	probably damaging	0.99
R1553:Ago1	UTSW	4	126,440,401 (GRCm38)	missense	probably damaging	0.99
R1624:Ago1	UTSW	4	126,463,741 (GRCm38)	missense	probably damaging	0.97
R1851:Ago1	UTSW	4	126,439,995 (GRCm38)	missense	probably benign	0.00
R1867:Ago1	UTSW	4	126,441,236 (GRCm38)	missense	probably damaging	0.98
R2001:Ago1	UTSW	4	126,454,394 (GRCm38)	missense	probably null	0.36
R2051:Ago1	UTSW	4	126,460,453 (GRCm38)	missense	probably benign	0.01
R2057:Ago1	UTSW	4	126,443,228 (GRCm38)	missense	probably damaging	0.98
R2105:Ago1	UTSW	4	126,461,788 (GRCm38)	missense	probably benign	0.30
R2117:Ago1	UTSW	4	126,463,857 (GRCm38)	splice site	probably null
R2272:Ago1	UTSW	4	126,453,650 (GRCm38)	missense	probably benign	0.01
R2517:Ago1	UTSW	4	126,439,939 (GRCm38)	nonsense	probably null
R2850:Ago1	UTSW	4	126,443,075 (GRCm38)	splice site	probably benign
R2993:Ago1	UTSW	4	126,440,046 (GRCm38)	splice site	probably benign
R3746:Ago1	UTSW	4	126,461,044 (GRCm38)	missense	probably benign
R3747:Ago1	UTSW	4	126,461,044 (GRCm38)	missense	probably benign
R3750:Ago1	UTSW	4	126,461,044 (GRCm38)	missense	probably benign
R4600:Ago1	UTSW	4	126,460,392 (GRCm38)	missense	probably benign	0.37
R4934:Ago1	UTSW	4	126,448,859 (GRCm38)	missense	possibly damaging	0.56
R4983:Ago1	UTSW	4	126,453,654 (GRCm38)	missense	probably damaging	0.99
R5086:Ago1	UTSW	4	126,453,604 (GRCm38)	missense	probably benign	0.01
R5132:Ago1	UTSW	4	126,461,723 (GRCm38)	missense	probably benign	0.01
R5239:Ago1	UTSW	4	126,441,215 (GRCm38)	missense	probably damaging	1.00
R5609:Ago1	UTSW	4	126,461,037 (GRCm38)	missense	possibly damaging	0.80
R5705:Ago1	UTSW	4	126,448,794 (GRCm38)	missense	probably benign	0.01
R5980:Ago1	UTSW	4	126,460,569 (GRCm38)	unclassified	probably benign
R6036:Ago1	UTSW	4	126,443,228 (GRCm38)	missense	probably damaging	0.98
R6036:Ago1	UTSW	4	126,443,228 (GRCm38)	missense	probably damaging	0.98
R6398:Ago1	UTSW	4	126,448,808 (GRCm38)	missense	probably benign	0.26
R6505:Ago1	UTSW	4	126,463,835 (GRCm38)	missense	probably benign	0.00
R6545:Ago1	UTSW	4	126,454,352 (GRCm38)	missense	possibly damaging	0.74
R6944:Ago1	UTSW	4	126,460,422 (GRCm38)	missense	possibly damaging	0.78
R7041:Ago1	UTSW	4	126,463,706 (GRCm38)	missense	possibly damaging	0.94
R7490:Ago1	UTSW	4	126,439,505 (GRCm38)	makesense	probably null
R7496:Ago1	UTSW	4	126,461,752 (GRCm38)	missense	probably benign	0.20
R7575:Ago1	UTSW	4	126,453,908 (GRCm38)	missense	probably benign	0.12
R7625:Ago1	UTSW	4	126,443,229 (GRCm38)	missense	probably benign	0.18
R7988:Ago1	UTSW	4	126,460,417 (GRCm38)	missense	probably damaging	1.00
R8041:Ago1	UTSW	4	126,441,936 (GRCm38)	missense	probably damaging	1.00
R8073:Ago1	UTSW	4	126,443,226 (GRCm38)	missense	probably benign	0.04
R8086:Ago1	UTSW	4	126,460,981 (GRCm38)	missense	probably benign
R8127:Ago1	UTSW	4	126,454,421 (GRCm38)	missense	possibly damaging	0.95
R8772:Ago1	UTSW	4	126,460,523 (GRCm38)	unclassified	probably benign
R8878:Ago1	UTSW	4	126,463,723 (GRCm38)	missense	probably benign	0.35
R8989:Ago1	UTSW	4	126,463,790 (GRCm38)	missense	probably benign	0.01
R9140:Ago1	UTSW	4	126,443,184 (GRCm38)	missense	probably benign
X0025:Ago1	UTSW	4	126,443,115 (GRCm38)	missense	possibly damaging	0.47
Z1177:Ago1	UTSW	4	126,453,656 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACTGAGAACTGTGTGCTGAAAC -3'
(R):5'- CCTCAGACCCCTTACTTGAGAG -3'

Sequencing Primer
(F):5'- CTGTGTGCTGAAACAAAAGTCC -3'
(R):5'- GACCCCTTACTTGAGAGCAAAGG -3'

Posted On

2014-10-16