AGO3 (argonaute RISC catalytic component 3) - Rat Genome Database

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Gene: AGO3 (argonaute RISC catalytic component 3) Homo sapiens
Analyze
Symbol: AGO3
Name: argonaute RISC catalytic component 3
RGD ID: 1319350
HGNC Page HGNC:18421
Description: Enables RNA binding activity and endoribonuclease activity, cleaving miRNA-paired mRNA. Involved in RNA secondary structure unwinding; negative regulation of gene expression; and regulation of stem cell proliferation. Located in cytoplasmic ribonucleoprotein granule; cytosol; and nucleoplasm. Part of RISC complex and RISC-loading complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: argonaute 3; argonaute 3, RISC catalytic component; argonaute3; eIF-2C 3; eIF2C 3; EIF2C3; eukaryotic translation initiation factor 2C, 3; FLJ12765; hAgo3; MGC86946; protein argonaute-3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38135,930,718 - 36,072,500 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl135,930,718 - 36,072,500 (+)EnsemblGRCh38hg38GRCh38
GRCh37136,396,706 - 36,538,101 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36136,169,359 - 36,294,650 (+)NCBINCBI36Build 36hg18NCBI36
Celera134,671,200 - 34,796,478 (+)NCBICelera
Cytogenetic Map1p34.3NCBI
HuRef134,513,684 - 34,638,740 (+)NCBIHuRef
CHM1_1136,513,064 - 36,638,399 (+)NCBICHM1_1
T2T-CHM13v2.0135,793,433 - 35,935,374 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Argonaute proteins at a glance. Ender C and Meister G, J Cell Sci. 2010 Jun 1;123(Pt 11):1819-23.
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10997877   PMID:12414724   PMID:12477932   PMID:12526743   PMID:12906857   PMID:14702039   PMID:15260970   PMID:16196087   PMID:18187620   PMID:18771919   PMID:19167051   PMID:19324964  
PMID:19383768   PMID:19393748   PMID:19470757   PMID:19946888   PMID:19966796   PMID:21145461   PMID:21634124   PMID:21873635   PMID:21906983   PMID:21963094   PMID:21988832   PMID:22474261  
PMID:22658674   PMID:22681889   PMID:22795694   PMID:22915799   PMID:23064648   PMID:23665583   PMID:23748378   PMID:24100239   PMID:24778252   PMID:26186194   PMID:26318153   PMID:26496610  
PMID:26673895   PMID:26831064   PMID:27542412   PMID:28330616   PMID:28514442   PMID:28683311   PMID:28718761   PMID:28813667   PMID:29040713   PMID:29395067   PMID:29507755   PMID:29568061  
PMID:30997501   PMID:31343991   PMID:31586073   PMID:31753913   PMID:33122430   PMID:33444963   PMID:33845483   PMID:33961781   PMID:34244482   PMID:34709727   PMID:35013218   PMID:35140242  
PMID:35156780   PMID:35271311   PMID:35803934   PMID:35819319   PMID:36215168   PMID:36232890   PMID:36244648   PMID:36736316   PMID:37827155   PMID:38172120  


Genomics

Comparative Map Data
AGO3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38135,930,718 - 36,072,500 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl135,930,718 - 36,072,500 (+)EnsemblGRCh38hg38GRCh38
GRCh37136,396,706 - 36,538,101 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36136,169,359 - 36,294,650 (+)NCBINCBI36Build 36hg18NCBI36
Celera134,671,200 - 34,796,478 (+)NCBICelera
Cytogenetic Map1p34.3NCBI
HuRef134,513,684 - 34,638,740 (+)NCBIHuRef
CHM1_1136,513,064 - 36,638,399 (+)NCBICHM1_1
T2T-CHM13v2.0135,793,433 - 35,935,374 (+)NCBIT2T-CHM13v2.0
Ago3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394126,220,797 - 126,323,360 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4126,225,497 - 126,323,349 (-)EnsemblGRCm39 Ensembl
GRCm384126,326,994 - 126,431,670 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4126,331,704 - 126,429,556 (-)EnsemblGRCm38mm10GRCm38
MGSCv374126,017,922 - 126,106,786 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364125,847,689 - 125,931,698 (-)NCBIMGSCv36mm8
Celera4124,677,462 - 124,766,345 (-)NCBICelera
Cytogenetic Map4D2.2NCBI
cM Map460.39NCBI
Ago3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85143,913,957 - 143,998,746 (-)NCBIGRCr8
mRatBN7.25138,632,367 - 138,714,230 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5138,639,569 - 138,714,230 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5141,339,497 - 141,411,826 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05143,109,506 - 143,181,823 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05143,110,283 - 143,182,600 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05144,355,792 - 144,436,509 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5144,364,269 - 144,436,509 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05148,131,514 - 148,203,725 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45145,713,438 - 145,779,165 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.15145,722,862 - 145,796,791 (-)NCBI
Celera5137,138,867 - 137,210,660 (-)NCBICelera
Cytogenetic Map5q36NCBI
Ago3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545213,977,481 - 14,094,259 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495545213,977,487 - 14,108,729 (+)NCBIChiLan1.0ChiLan1.0
AGO3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21190,774,637 - 190,916,632 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11189,897,430 - 190,038,609 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0135,196,371 - 35,322,220 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1136,371,926 - 36,497,190 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl136,372,221 - 36,497,190 (+)Ensemblpanpan1.1panPan2
AGO3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1156,133,303 - 6,253,032 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl156,145,895 - 6,253,085 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha156,376,188 - 6,496,197 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0156,268,985 - 6,389,129 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl156,281,474 - 6,502,020 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1156,121,863 - 6,242,128 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0156,190,183 - 6,310,872 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0156,205,177 - 6,325,232 (-)NCBIUU_Cfam_GSD_1.0
LOC103225123
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12096,784,226 - 96,923,183 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2096,801,900 - 96,923,148 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603319,802,930 - 19,942,329 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ago3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476418,948,484 - 19,052,523 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476418,948,469 - 19,078,247 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in AGO3
30 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p34.3(chr1:34753938-36055310)x1 copy number loss See cases [RCV000137966] Chr1:34753938..36055310 [GRCh38]
Chr1:35219539..36520911 [GRCh37]
Chr1:34992126..36293498 [NCBI36]
Chr1:1p34.3
likely pathogenic
GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3 copy number gain See cases [RCV000138891] Chr1:24381206..41401517 [GRCh38]
Chr1:24707696..41886350 [GRCh37]
Chr1:24580283..41658937 [NCBI36]
Chr1:1p36.11-34.2
pathogenic
GRCh38/hg38 1p34.3(chr1:35934217-36821999)x4 copy number gain See cases [RCV000138892] Chr1:35934217..36821999 [GRCh38]
Chr1:36399818..37287600 [GRCh37]
Chr1:36172405..37060187 [NCBI36]
Chr1:1p34.3
likely pathogenic
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12
likely benign
GRCh37/hg19 1p34.3(chr1:34830287-36945093)x1 copy number loss See cases [RCV000448022] Chr1:34830287..36945093 [GRCh37]
Chr1:1p34.3
pathogenic
GRCh37/hg19 1p34.3(chr1:35950860-36465764)x1 copy number loss See cases [RCV000448765] Chr1:35950860..36465764 [GRCh37]
Chr1:1p34.3
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_024852.4(AGO3):c.1357G>T (p.Ala453Ser) single nucleotide variant Inborn genetic diseases [RCV003299473] Chr1:36013999 [GRCh38]
Chr1:36479600 [GRCh37]
Chr1:1p34.3
uncertain significance
NC_000001.10:g.(?_33241563)_(46663513_?)dup duplication Charcot-Marie-Tooth disease dominant intermediate C [RCV000708276] Chr1:33241563..46663513 [GRCh37]
Chr1:1p35.1-34.1
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p35.2-34.3(chr1:31562164-37421958)x3 copy number gain not provided [RCV000748949] Chr1:31562164..37421958 [GRCh37]
Chr1:1p35.2-34.3
pathogenic
NM_024852.4(AGO3):c.1959A>G (p.Gln653=) single nucleotide variant not provided [RCV000973804] Chr1:36039906 [GRCh38]
Chr1:36505507 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.1660A>G (p.Ile554Val) single nucleotide variant not provided [RCV000900420] Chr1:36034242 [GRCh38]
Chr1:36499843 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.2577C>T (p.Phe859=) single nucleotide variant not provided [RCV000968520] Chr1:36055739 [GRCh38]
Chr1:36521340 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.1257C>G (p.Leu419=) single nucleotide variant not provided [RCV000914598] Chr1:36013737 [GRCh38]
Chr1:36479338 [GRCh37]
Chr1:1p34.3
likely benign
NM_024852.4(AGO3):c.429G>C (p.Arg143=) single nucleotide variant not provided [RCV000923291] Chr1:35972140 [GRCh38]
Chr1:36437741 [GRCh37]
Chr1:1p34.3
likely benign
GRCh37/hg19 1p35.1-34.3(chr1:32859415-36454915) copy number loss not provided [RCV000767772] Chr1:32859415..36454915 [GRCh37]
Chr1:1p35.1-34.3
pathogenic
NM_024852.4(AGO3):c.2343G>A (p.Gln781=) single nucleotide variant not provided [RCV000961277] Chr1:36055014 [GRCh38]
Chr1:36520615 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.510G>A (p.Leu170=) single nucleotide variant not provided [RCV000897698] Chr1:35972221 [GRCh38]
Chr1:36437822 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.1002A>G (p.Glu334=) single nucleotide variant not provided [RCV000893539] Chr1:36009017 [GRCh38]
Chr1:36474618 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.1751+10G>A single nucleotide variant not provided [RCV000930181] Chr1:36034343 [GRCh38]
Chr1:36499944 [GRCh37]
Chr1:1p34.3
likely benign
NM_024852.4(AGO3):c.1572G>A (p.Pro524=) single nucleotide variant not provided [RCV000961880] Chr1:36027279 [GRCh38]
Chr1:36492880 [GRCh37]
Chr1:1p34.3
benign
NM_024852.4(AGO3):c.930G>A (p.Ala310=) single nucleotide variant not provided [RCV000893501] Chr1:36008945 [GRCh38]
Chr1:36474546 [GRCh37]
Chr1:1p34.3
likely benign
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1
uncertain significance
NM_024852.4(AGO3):c.435G>A (p.Leu145=) single nucleotide variant not provided [RCV000980300] Chr1:35972146 [GRCh38]
Chr1:36437747 [GRCh37]
Chr1:1p34.3
likely benign
GRCh37/hg19 1p34.3(chr1:36496921-36829945)x3 copy number gain not provided [RCV000847964] Chr1:36496921..36829945 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.1209G>A (p.Arg403=) single nucleotide variant not provided [RCV000954366] Chr1:36013689 [GRCh38]
Chr1:36479290 [GRCh37]
Chr1:1p34.3
benign|likely benign
NM_024852.4(AGO3):c.2520A>G (p.Pro840=) single nucleotide variant not provided [RCV000932920] Chr1:36055682 [GRCh38]
Chr1:36521283 [GRCh37]
Chr1:1p34.3
likely benign
NM_024852.4(AGO3):c.1803T>C (p.His601=) single nucleotide variant not provided [RCV000890503] Chr1:36036228 [GRCh38]
Chr1:36501829 [GRCh37]
Chr1:1p34.3
likely benign
NM_024852.4(AGO3):c.684A>G (p.Ala228=) single nucleotide variant not provided [RCV000934464] Chr1:36004366 [GRCh38]
Chr1:36469967 [GRCh37]
Chr1:1p34.3
likely benign
NM_024852.4(AGO3):c.673T>C (p.Phe225Leu) single nucleotide variant not provided [RCV001280747] Chr1:36004355 [GRCh38]
Chr1:36469956 [GRCh37]
Chr1:1p34.3
uncertain significance
NC_000001.10:g.(?_33241563)_(46663513_?)dup duplication Charcot-Marie-Tooth disease, dominant intermediate C [RCV001308684] Chr1:33241563..46663513 [GRCh37]
Chr1:1p35.1-34.1
uncertain significance
NM_024852.4(AGO3):c.1475T>C (p.Phe492Ser) single nucleotide variant not specified [RCV002246950] Chr1:36027182 [GRCh38]
Chr1:36492783 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.1738G>C (p.Val580Leu) single nucleotide variant Inborn genetic diseases [RCV003293474] Chr1:36034320 [GRCh38]
Chr1:36499921 [GRCh37]
Chr1:1p34.3
uncertain significance
GRCh37/hg19 1p35.1-33(chr1:33285582-47891811) copy number gain not specified [RCV002052781] Chr1:33285582..47891811 [GRCh37]
Chr1:1p35.1-33
pathogenic
GRCh37/hg19 1p34.3(chr1:35950860-36635695) copy number gain not specified [RCV002053225] Chr1:35950860..36635695 [GRCh37]
Chr1:1p34.3
uncertain significance
GRCh37/hg19 1p34.3(chr1:36041366-39112237) copy number loss not specified [RCV002053236] Chr1:36041366..39112237 [GRCh37]
Chr1:1p34.3
uncertain significance
GRCh37/hg19 1p34.3(chr1:35950860-36465764) copy number loss not specified [RCV002053205] Chr1:35950860..36465764 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.1076A>G (p.Asp359Gly) single nucleotide variant not specified [RCV002246949] Chr1:36009521 [GRCh38]
Chr1:36475122 [GRCh37]
Chr1:1p34.3
uncertain significance
GRCh37/hg19 1p34.3(chr1:35104233-37357913)x1 copy number loss not provided [RCV002474552] Chr1:35104233..37357913 [GRCh37]
Chr1:1p34.3
pathogenic
NM_024852.4(AGO3):c.1427G>A (p.Arg476His) single nucleotide variant Inborn genetic diseases [RCV003308467] Chr1:36027134 [GRCh38]
Chr1:36492735 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.298G>A (p.Val100Met) single nucleotide variant Inborn genetic diseases [RCV002751734] Chr1:35967061 [GRCh38]
Chr1:36432662 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.439G>A (p.Glu147Lys) single nucleotide variant Inborn genetic diseases [RCV002783603] Chr1:35972150 [GRCh38]
Chr1:36437751 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.287A>G (p.Asn96Ser) single nucleotide variant Inborn genetic diseases [RCV002983790] Chr1:35967050 [GRCh38]
Chr1:36432651 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.1171A>G (p.Thr391Ala) single nucleotide variant Inborn genetic diseases [RCV002802876] Chr1:36013651 [GRCh38]
Chr1:36479252 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.36G>C (p.Gln12His) single nucleotide variant Inborn genetic diseases [RCV002900823] Chr1:35945708 [GRCh38]
Chr1:36411309 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.622C>T (p.Arg208Trp) single nucleotide variant Inborn genetic diseases [RCV002747639] Chr1:35973475 [GRCh38]
Chr1:36439076 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.1187A>G (p.Gln396Arg) single nucleotide variant Inborn genetic diseases [RCV003263710] Chr1:36013667 [GRCh38]
Chr1:36479268 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.2321G>C (p.Cys774Ser) single nucleotide variant Inborn genetic diseases [RCV003362649] Chr1:36054992 [GRCh38]
Chr1:36520593 [GRCh37]
Chr1:1p34.3
uncertain significance
Single allele inversion Bilateral polymicrogyria [RCV003459046] Chr1:33246132..61045156 [GRCh38]
Chr1:1p35.1-31.3
likely pathogenic
NM_024852.4(AGO3):c.1773A>G (p.Pro591=) single nucleotide variant not provided [RCV003406336] Chr1:36036198 [GRCh38]
Chr1:36501799 [GRCh37]
Chr1:1p34.3
likely benign
NM_024852.4(AGO3):c.1277G>A (p.Arg426Gln) single nucleotide variant AGO3-related condition [RCV003399536] Chr1:36013919 [GRCh38]
Chr1:36479520 [GRCh37]
Chr1:1p34.3
uncertain significance
NM_024852.4(AGO3):c.1013C>T (p.Thr338Ile) single nucleotide variant AGO3-related condition [RCV003414442] Chr1:36009028 [GRCh38]
Chr1:36474629 [GRCh37]
Chr1:1p34.3
uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR129-1hsa-miR-129-5pMirecordsexternal_infoNANA18189265
MIR129-2hsa-miR-129-5pMirecordsexternal_infoNANA18189265

Predicted Target Of
Summary Value
Count of predictions:7087
Count of miRNA genes:1352
Interacting mature miRNAs:1818
Transcripts:ENST00000246314, ENST00000324350, ENST00000373191, ENST00000397828, ENST00000471099, ENST00000491443
Prediction methods:Microtar, Miranda, Pita, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH102469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37136,521,893 - 36,522,017UniSTSGRCh37
Build 36136,294,480 - 36,294,604RGDNCBI36
Celera134,796,308 - 34,796,432RGD
Cytogenetic Map1p34UniSTS
HuRef134,638,570 - 34,638,694UniSTS
GeneMap99-GB4 RH Map1109.71UniSTS
SHGC-141728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37136,424,325 - 36,424,621UniSTSGRCh37
Build 36136,196,912 - 36,197,208RGDNCBI36
Celera134,698,750 - 34,699,046RGD
Cytogenetic Map1p34UniSTS
HuRef134,541,101 - 34,541,397UniSTS
TNG Radiation Hybrid Map117189.0UniSTS
SHGC-74579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37136,521,426 - 36,521,644UniSTSGRCh37
Build 36136,294,013 - 36,294,231RGDNCBI36
Celera134,795,841 - 34,796,059RGD
Cytogenetic Map1p34UniSTS
HuRef134,638,103 - 34,638,321UniSTS
TNG Radiation Hybrid Map117235.0UniSTS
GeneMap99-GB4 RH Map1109.53UniSTS
NCBI RH Map1234.3UniSTS
SHGC-74570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37136,394,918 - 36,395,157UniSTSGRCh37
Build 36136,167,505 - 36,167,744RGDNCBI36
Celera134,669,346 - 34,669,585RGD
Cytogenetic Map1p34UniSTS
HuRef134,511,919 - 34,512,158UniSTS
TNG Radiation Hybrid Map117153.0UniSTS
GeneMap99-GB4 RH Map1108.11UniSTS
NCBI RH Map1230.0UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 21 5 149 118 74 31 283 22 81 69 4 64
Low 2417 2815 1573 620 1704 461 4280 2124 3439 394 1379 1544 175 1 1200 2723 5 2
Below cutoff 1 171 4 4 129 4 2 42 12 3 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_024852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_177422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005270575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005270576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011540879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011540882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047448134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054334825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA251146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027796 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL138787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL139286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC066888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF438817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF979526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX104163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000246314   ⟹   ENSP00000246314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl135,931,258 - 36,056,462 (+)Ensembl
RefSeq Acc Id: ENST00000324350   ⟹   ENSP00000317425
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl135,930,718 - 35,983,409 (+)Ensembl
RefSeq Acc Id: ENST00000373191   ⟹   ENSP00000362287
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl135,931,105 - 36,072,500 (+)Ensembl
RefSeq Acc Id: ENST00000397828   ⟹   ENSP00000380928
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl135,931,082 - 35,982,652 (+)Ensembl
RefSeq Acc Id: ENST00000471099
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl136,043,264 - 36,055,262 (+)Ensembl
RefSeq Acc Id: ENST00000491443
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl135,966,955 - 35,973,592 (+)Ensembl
RefSeq Acc Id: ENST00000634486   ⟹   ENSP00000489286
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl135,931,095 - 36,056,239 (+)Ensembl
RefSeq Acc Id: NM_024852   ⟹   NP_079128
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,931,105 - 36,072,500 (+)NCBI
GRCh37136,396,364 - 36,522,360 (+)NCBI
Build 36136,169,359 - 36,294,650 (+)NCBI Archive
Celera134,671,200 - 34,796,478 (+)RGD
HuRef134,513,684 - 34,638,740 (+)ENTREZGENE
CHM1_1136,513,064 - 36,638,399 (+)NCBI
T2T-CHM13v2.0135,793,999 - 35,935,374 (+)NCBI
Sequence:
RefSeq Acc Id: NM_177422   ⟹   NP_803171
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,931,105 - 36,072,500 (+)NCBI
GRCh37136,396,364 - 36,522,360 (+)NCBI
Build 36136,169,359 - 36,294,650 (+)NCBI Archive
Celera134,671,200 - 34,796,478 (+)RGD
HuRef134,513,684 - 34,638,740 (+)ENTREZGENE
CHM1_1136,513,064 - 36,638,399 (+)NCBI
T2T-CHM13v2.0135,793,999 - 35,935,374 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005270575   ⟹   XP_005270632
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,930,718 - 36,072,500 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005270576   ⟹   XP_005270633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38136,004,482 - 36,072,500 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011540879   ⟹   XP_011539181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,931,408 - 36,072,500 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000523   ⟹   XP_016856012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,930,718 - 36,072,500 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000524   ⟹   XP_016856013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,983,544 - 36,072,500 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017000526   ⟹   XP_016856015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,982,658 - 36,072,500 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047448134   ⟹   XP_047304090
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,983,544 - 36,072,500 (+)NCBI
RefSeq Acc Id: XM_054334819   ⟹   XP_054190794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,793,433 - 35,935,374 (+)NCBI
RefSeq Acc Id: XM_054334820   ⟹   XP_054190795
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,793,615 - 35,935,374 (+)NCBI
RefSeq Acc Id: XM_054334821   ⟹   XP_054190796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,794,508 - 35,935,374 (+)NCBI
RefSeq Acc Id: XM_054334822   ⟹   XP_054190797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,846,428 - 35,935,374 (+)NCBI
RefSeq Acc Id: XM_054334823   ⟹   XP_054190798
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,846,428 - 35,935,374 (+)NCBI
RefSeq Acc Id: XM_054334824   ⟹   XP_054190799
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,845,542 - 35,935,374 (+)NCBI
RefSeq Acc Id: XM_054334825   ⟹   XP_054190800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0135,867,369 - 35,935,374 (+)NCBI
Protein Sequences
Protein RefSeqs NP_079128 (Get FASTA)   NCBI Sequence Viewer  
  NP_803171 (Get FASTA)   NCBI Sequence Viewer  
  XP_005270632 (Get FASTA)   NCBI Sequence Viewer  
  XP_005270633 (Get FASTA)   NCBI Sequence Viewer  
  XP_011539181 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856012 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856013 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856015 (Get FASTA)   NCBI Sequence Viewer  
  XP_047304090 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190794 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190795 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190796 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190797 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190798 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190799 (Get FASTA)   NCBI Sequence Viewer  
  XP_054190800 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH66888 (Get FASTA)   NCBI Sequence Viewer  
  BAB14262 (Get FASTA)   NCBI Sequence Viewer  
  BAB55374 (Get FASTA)   NCBI Sequence Viewer  
  BAF85559 (Get FASTA)   NCBI Sequence Viewer  
  BAG63629 (Get FASTA)   NCBI Sequence Viewer  
  BAG64857 (Get FASTA)   NCBI Sequence Viewer  
  EAX07394 (Get FASTA)   NCBI Sequence Viewer  
  EAX07395 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000246314
  ENSP00000246314.6
  ENSP00000317425.5
  ENSP00000362287
  ENSP00000362287.3
  ENSP00000380928.2
  ENSP00000489286.1
GenBank Protein Q9H9G7 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_079128   ⟸   NM_024852
- Peptide Label: isoform a
- UniProtKB: Q5TA55 (UniProtKB/Swiss-Prot),   B1ALI0 (UniProtKB/Swiss-Prot),   Q9H1U6 (UniProtKB/Swiss-Prot),   Q9H9G7 (UniProtKB/Swiss-Prot),   A8KA05 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_803171   ⟸   NM_177422
- Peptide Label: isoform b
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005270632   ⟸   XM_005270575
- Peptide Label: isoform X1
- UniProtKB: Q5TA55 (UniProtKB/Swiss-Prot),   B1ALI0 (UniProtKB/Swiss-Prot),   Q9H1U6 (UniProtKB/Swiss-Prot),   Q9H9G7 (UniProtKB/Swiss-Prot),   A8KA05 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005270633   ⟸   XM_005270576
- Peptide Label: isoform X4
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011539181   ⟸   XM_011540879
- Peptide Label: isoform X2
- UniProtKB: A8KA05 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856012   ⟸   XM_017000523
- Peptide Label: isoform X1
- UniProtKB: Q5TA55 (UniProtKB/Swiss-Prot),   B1ALI0 (UniProtKB/Swiss-Prot),   Q9H1U6 (UniProtKB/Swiss-Prot),   Q9H9G7 (UniProtKB/Swiss-Prot),   A8KA05 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856015   ⟸   XM_017000526
- Peptide Label: isoform X3
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856013   ⟸   XM_017000524
- Peptide Label: isoform X3
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000489286   ⟸   ENST00000634486
RefSeq Acc Id: ENSP00000362287   ⟸   ENST00000373191
RefSeq Acc Id: ENSP00000317425   ⟸   ENST00000324350
RefSeq Acc Id: ENSP00000246314   ⟸   ENST00000246314
RefSeq Acc Id: ENSP00000380928   ⟸   ENST00000397828
RefSeq Acc Id: XP_047304090   ⟸   XM_047448134
- Peptide Label: isoform X3
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190794   ⟸   XM_054334819
- Peptide Label: isoform X1
- UniProtKB: Q9H9G7 (UniProtKB/Swiss-Prot),   Q5TA55 (UniProtKB/Swiss-Prot),   B1ALI0 (UniProtKB/Swiss-Prot),   Q9H1U6 (UniProtKB/Swiss-Prot),   A8KA05 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190795   ⟸   XM_054334820
- Peptide Label: isoform X1
- UniProtKB: Q9H9G7 (UniProtKB/Swiss-Prot),   Q5TA55 (UniProtKB/Swiss-Prot),   B1ALI0 (UniProtKB/Swiss-Prot),   Q9H1U6 (UniProtKB/Swiss-Prot),   A8KA05 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190796   ⟸   XM_054334821
- Peptide Label: isoform X2
- UniProtKB: A8KA05 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190799   ⟸   XM_054334824
- Peptide Label: isoform X3
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190798   ⟸   XM_054334823
- Peptide Label: isoform X3
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190797   ⟸   XM_054334822
- Peptide Label: isoform X3
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054190800   ⟸   XM_054334825
- Peptide Label: isoform X4
- UniProtKB: B4E1P5 (UniProtKB/TrEMBL)
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H9G7-F1-model_v2 AlphaFold Q9H9G7 1-860 view protein structure

Promoters
RGD ID:6854960
Promoter ID:EPDNEW_H645
Type:initiation region
Name:AGO3_2
Description:argonaute 3, RISC catalytic component
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H646  EPDNEW_H647  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,930,718 - 35,930,778EPDNEW
RGD ID:6854962
Promoter ID:EPDNEW_H646
Type:initiation region
Name:AGO3_1
Description:argonaute 3, RISC catalytic component
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H645  EPDNEW_H647  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,931,252 - 35,931,312EPDNEW
RGD ID:6854964
Promoter ID:EPDNEW_H647
Type:multiple initiation site
Name:AGO3_3
Description:argonaute 3, RISC catalytic component
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H645  EPDNEW_H646  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38135,947,406 - 35,947,466EPDNEW
RGD ID:6785113
Promoter ID:HG_KWN:1990
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000324350,   ENST00000397828,   NM_177422,   OTTHUMT00000019831,   UC001BZO.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36136,168,536 - 36,169,432 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:18421 AgrOrtholog
COSMIC AGO3 COSMIC
Ensembl Genes ENSG00000126070 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000246314 ENTREZGENE
  ENST00000246314.10 UniProtKB/Swiss-Prot
  ENST00000324350.9 UniProtKB/TrEMBL
  ENST00000373191 ENTREZGENE
  ENST00000373191.9 UniProtKB/Swiss-Prot
  ENST00000397828.3 UniProtKB/TrEMBL
  ENST00000634486.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.420.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.2300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  paz domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000126070 GTEx
HGNC ID HGNC:18421 ENTREZGENE
Human Proteome Map AGO3 Human Proteome Map
InterPro AGO3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ArgoL1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ArgoL2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Argonaute_Mid_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Argonaute_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAZ_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAZ_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Piwi UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Piwi_ago-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RNaseH-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RNaseH_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:192669 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 192669 ENTREZGENE
OMIM 607355 OMIM
PANTHER EUKARYOTIC TRANSLATION INITIATION FACTOR 2C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN ARGONAUTE-3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam ArgoL1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ArgoL2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ArgoMid UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ArgoN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Piwi UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38329 PharmGKB
PROSITE PAZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PIWI UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DUF1785 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Piwi UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF101690 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF53098 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0U1RR19_HUMAN UniProtKB/TrEMBL
  A8KA05 ENTREZGENE, UniProtKB/TrEMBL
  AGO3_HUMAN UniProtKB/Swiss-Prot
  B1ALI0 ENTREZGENE
  B4E1P5 ENTREZGENE, UniProtKB/TrEMBL
  Q5TA55 ENTREZGENE
  Q5TA56_HUMAN UniProtKB/TrEMBL
  Q9H1U6 ENTREZGENE
  Q9H9G7 ENTREZGENE
UniProt Secondary B1ALI0 UniProtKB/Swiss-Prot
  Q5TA55 UniProtKB/Swiss-Prot
  Q9H1U6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-11-29 AGO3  argonaute RISC catalytic component 3    argonaute 3, RISC catalytic component  Symbol and/or name change 5135510 APPROVED
2015-12-01 AGO3  argonaute 3, RISC catalytic component    argonaute RISC catalytic component 3  Symbol and/or name change 5135510 APPROVED
2013-02-20 AGO3  argonaute RISC catalytic component 3  EIF2C3  eukaryotic translation initiation factor 2C, 3  Symbol and/or name change 5135510 APPROVED
2011-09-01 EIF2C3  eukaryotic translation initiation factor 2C, 3  EIF2C3  eukaryotic translation initiation factor 2C, 3  Symbol and/or name change 5135510 APPROVED