AGO2 - argonaute RISC catalytic component 2 Gene

Also Known as PPD; Q10; CASC7; EIF2C2; LESKRES; LINC00980

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 27161

About AGO2

Cytogenetic location: 8q24.3 Genomic coordinates (GRCh38): 8:140,520,156-140,642,313 (from NCBI)

This gene has 10 transcripts (splice variants), 211 orthologues, 3 paralogues and is associated with 2 phenotypes. Ubiquitous expression in skin (RPKM 3.3), ovary (RPKM 3.3) and 25 other tissues.

Summary

This gene encodes a member of the Argonaute family of proteins which play a role in RNA interference. The encoded protein is highly basic, and contains a PAZ domain and a PIWI domain. It may interact with dicer1 and play a role in short-interfering-RNA-mediated gene silencing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

AGO2 Products (2)

mRNA Protein Name
NM_001164623.3 NP_001158095.1 protein argonaute-2 isoform 2
NM_012154.5 NP_036286.2 protein argonaute-2 isoform 1
Molecular Function GO Annotation Evidence References Source
enables RNA 7-methylguanosine cap binding IDA
IDA: Inferred from direct assay
17524464 GOA
enables RNA endonuclease activity IDA
IDA: Inferred from direct assay
18178619 GOA
enables RNA polymerase II complex binding IDA
IDA: Inferred from direct assay
25336585 GOA
enables core promoter sequence-specific DNA binding IMP
IMP: Inferred from mutant phenotype
25336585 GOA
enables double-stranded RNA binding IDA
IDA: Inferred from direct assay
19966796 GOA
enables endoribonuclease activity, cleaving miRNA-paired mRNA IDA
IDA: Inferred from direct assay
15260970 GOA
enables endoribonuclease activity, cleaving miRNA-paired mRNA IMP
IMP: Inferred from mutant phenotype
22795694 GOA
enables endoribonuclease activity, cleaving siRNA-paired mRNA IDA
IDA: Inferred from direct assay
15260970 GOA
enables mRNA 3'-UTR AU-rich region binding IDA
IDA: Inferred from direct assay
17382880 GOA
enables mRNA cap binding IDA
IDA: Inferred from direct assay
17524464 GOA
enables mRNA cap binding IPI
IPI: Inferred from physical interaction
23409027 GOA
enables miRNA binding IDA
IDA: Inferred from direct assay
15260970 GOA
enables miRNA binding IPI
IPI: Inferred from physical interaction
31012336 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
14749716 GOA
contributes to siRNA binding IDA
IDA: Inferred from direct assay
15973356 GOA
enables siRNA binding IDA
IDA: Inferred from direct assay
17495927 GOA
enables single-stranded RNA binding IDA
IDA: Inferred from direct assay
19966796 GOA
Biological Process GO Annotation Evidence References Source
involved in P-body assembly IDA
IDA: Inferred from direct assay
31400113 GOA
involved in RISC complex assembly IDA
IDA: Inferred from direct assay
19701182 GOA
involved in RNA secondary structure unwinding IDA
IDA: Inferred from direct assay
19966796 GOA
involved in RNA secondary structure unwinding IMP
IMP: Inferred from mutant phenotype
22795694 GOA
involved in miRNA processing IDA
IDA: Inferred from direct assay
19966796 GOA
involved in miRNA-mediated gene silencing by inhibition of translation IDA
IDA: Inferred from direct assay
17671087 GOA
involved in miRNA-mediated gene silencing by inhibition of translation IMP
IMP: Inferred from mutant phenotype
18771919 GOA
involved in miRNA-mediated gene silencing by mRNA destabilization IDA
IDA: Inferred from direct assay
15260970 GOA
involved in miRNA-mediated gene silencing by mRNA destabilization IMP
IMP: Inferred from mutant phenotype
18771919 GOA
involved in negative regulation of translational initiation IDA
IDA: Inferred from direct assay
17524464 GOA
involved in positive regulation of angiogenesis IDA
IDA: Inferred from direct assay
27208409 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
25336585 GOA
involved in positive regulation of translation IDA
IDA: Inferred from direct assay
17382880 GOA
involved in positive regulation of trophoblast cell migration IMP
IMP: Inferred from mutant phenotype
27208409 GOA
involved in pre-miRNA processing IDA
IDA: Inferred from direct assay
16424907 GOA
involved in regulation of synapse maturation IDA
IDA: Inferred from direct assay
29735530 GOA
involved in regulation of synapse maturation IMP
IMP: Inferred from mutant phenotype
29735530 GOA
involved in siRNA processing IDA
IDA: Inferred from direct assay
23661684 GOA
involved in siRNA-mediated gene silencing by mRNA destabilization IDA
IDA: Inferred from direct assay
15260970 GOA
involved in siRNA-mediated gene silencing by mRNA destabilization IMP
IMP: Inferred from mutant phenotype
22795694 GOA
Cellular Component GO Annotation Evidence References Source
located in P-body IDA
IDA: Inferred from direct assay
20616046 GOA
part of RISC complex IDA
IDA: Inferred from direct assay
15260970 GOA
part of RISC complex IGI
IGI: Inferred from genetic interaction
31012336 GOA
part of RISC complex IPI
IPI: Inferred from physical interaction
19826008 GOA
part of RISC-loading complex IDA
IDA: Inferred from direct assay
15973356 GOA
part of RISC-loading complex IPI
IPI: Inferred from physical interaction
23661684 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
15260970 GOA
located in extracellular exosome IDA
IDA: Inferred from direct assay
28159509 GOA
is active in glutamatergic synapse IDA
IDA: Inferred from direct assay
29735530 GOA
is active in glutamatergic synapse IMP
IMP: Inferred from mutant phenotype
29735530 GOA
located in nucleus IDA
IDA: Inferred from direct assay
23985560 GOA
is active in postsynapse IDA
IDA: Inferred from direct assay
29735530 GOA
is active in postsynapse IMP
IMP: Inferred from mutant phenotype
29735530 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

AGO2 Protein Structure

ArgoL1

ArgoL1: Argonaute linker 1 domain (175 - 227)

PAZ

PAZ: PAZ domain (235 - 370)

Piwi

Piwi: Piwi domain (518 - 817)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 859 a.a.
Protein Preferred Names Protein Names

protein argonaute-2

  • PAZ Piwi domain protein

AGO2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
AGO2 Q9UKV8 MTDH Homo sapiens Q86UE4 24981741
Intra
AGO2 Q9UKV8 FKBP4 Homo sapiens Q02790 23741051
Intra
AGO2 Q9UKV8 FKBP4 Homo sapiens Q02790 23741051
Intra
AGO2 Q9UKV8 PTGES3 Homo sapiens Q15185 23741051
Intra
AGO2 Q9UKV8 PTGES3 Homo sapiens Q15185 23741051
Intra
AGO2 Q9UKV8 DMWD Homo sapiens G5E9A7 32814053
Intra
AGO2 Q9UKV8 DMWD Homo sapiens G5E9A7 32814053
Intra
AGO2 Q9UKV8 DMWD Homo sapiens G5E9A7 32814053
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 19955415
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1
GMS
19820710
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 23636329
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 18178619
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1
GMS
18178619
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 19820710
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1
EM
19820710
Intra
AGO2 Q9UKV8 CNOT7 Homo sapiens Q9UIV1 19716330
Intra
AGO2 Q9UKV8 PLEKHA7 Homo sapiens Q6IQ23 28877994
Intra
AGO2 Q9UKV8 PLEKHA7 Homo sapiens Q6IQ23
PLA
28877994
Intra
AGO2 Q9UKV8 PLEKHA7 Homo sapiens Q6IQ23 28877994
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 19324964
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 35271311
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28683311
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 19716330
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7
IF
19324964
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 23090477
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28683311
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28683311
Intra
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28877994
Intra
AGO2 Q9UKV8 ZMAT3 Homo sapiens Q9HA38 23085987
Intra
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
Intra
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
Intra
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
Intra
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4
PLA
28683311
Intra
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
Intra
AGO2 Q9UKV8 RACK1 Homo sapiens P63244 21525958
Intra
AGO2 Q9UKV8 EGFR Homo sapiens P00533 23636329
Intra
AGO2 Q9UKV8 EGFR Homo sapiens P00533 23636329
Intra
AGO2 Q9UKV8 EGFR Homo sapiens P00533 23636329
Intra
AGO2 Q9UKV8 FGFR3 Homo sapiens P22607 32814053
Intra
AGO2 Q9UKV8 FGFR3 Homo sapiens P22607 32814053
Intra
AGO2 Q9UKV8 FGFR3 Homo sapiens P22607 32814053
Intra
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 28683311
Intra
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 16756390
Intra
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 28683311
Intra
AGO2 Q9UKV8 DDX6 Homo sapiens P26196
PLA
28683311
Intra
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 16756390
Intra
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 28683311
Intra
AGO2 Q9UKV8 IPO8 Homo sapiens O15397 17932509
Intra
AGO2 Q9UKV8 IPO8 Homo sapiens O15397 19167051
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 19716330
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 23622242
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 26496610
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 23741051
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3
GMS
23622242
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 14749716
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 33961781
Intra
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 17932509
Intra
AGO2 Q9UKV8 RB1 Homo sapiens P06400 22366686
Intra
AGO2 Q9UKV8 SPRED1 Homo sapiens Q7Z699 32814053
Intra
AGO2 Q9UKV8 SPRED1 Homo sapiens Q7Z699 32814053
Intra
AGO2 Q9UKV8 SPRED1 Homo sapiens Q7Z699 32814053
Intra
AGO2 Q9UKV8 AGO1 Homo sapiens Q9UL18 16756390
Intra
AGO2 Q9UKV8 AGO1 Homo sapiens Q9UL18 35271311
Intra
AGO2 Q9UKV8 AGO1 Homo sapiens Q9UL18 16756390
Intra
AGO2 Q9UKV8 LRRK2 Homo sapiens Q5S007 20671708
Intra
AGO2 Q9UKV8 GNL3 Homo sapiens Q9BVP2 24550003
Intra
AGO2 Q9UKV8 GNL3 Homo sapiens Q9BVP2 17932509
Intra
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 21981923
Intra
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 35271311
Intra
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 19383768
Intra
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 19383768
Intra
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 19838187
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9-2 19383768
Intra
AGO2 Q9UKV8 PRKRA Homo sapiens O75569 16424907
Intra
AGO2 Q9UKV8 EIF4EBP1 Homo sapiens Q13541 20671708
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 17932509
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 19383768
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 19838187
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 35271311
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 19716330
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 24043833
Intra
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9
FPS
24043833
Intra
AGO2 Q9UKV8 PRNP Homo sapiens P04156 22484317
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 19716330
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 23622242
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633
GMS
19820710
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 18178619
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633
GMS
18178619
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 17932509
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 19820710
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 23636329
Intra
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633
EM
19820710
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant AGO2 Proteins

Cat. No. Product Name Accession Purity
HY-P72835 AGO2/Argonaute-2 Protein, Human (sf9, His) Q9UKV8 (M1-A859) ≥ 90%, as determined by reducing SDS-PAGE.

AGO2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80441 Argonaute 2 Antibody (YA612) WB, ICC/IF, IHC-P, FC, IP Human, Mouse
HY-P80546 Argonaute 2 Antibody WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat
HY-P86098 Argonaute 2 Antibody (YA5790) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Lessel-Kreienkamp Syndrome
  • LESKRES

Non-Specific Syndromic Intellectual Disability
  • Complex Neurodevelopmental Disorder

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Eunuchism
Patau Syndrome
  • Trisomy 13

  • Complete Trisomy 13 Syndrome

  • Trisomy 13 Syndrome

  • D1 Trisomy

  • Patau'S Syndrome

  • Complete Trisomy 13

  • Chromosome 13, Trisomy 13 Complete

  • D Trisomy Syndrome

  • Bartholin-Patau Syndrome

  • Chromosome 13 Duplication

  • D1 Trisomy Syndrome

  • D>1< Trisomy Syndrome

  • Patau

  • Chromosome 13 Trisomy

  • Abnormal Autosomes 13

Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • X-Linked Intellectual Disability And Macroorchidism

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Orofaciodigital Syndrome Viii
  • Edwards Syndrome

  • Trisomy 18

  • Complete Trisomy 18 Syndrome

  • OFD8

  • Orofaciodigital Syndrome 8

  • Trisomy 18 Syndrome

  • Oral-Facial-Digital Syndrome With Hypoplastic Epiglottis

  • E3 Trisomy

  • Oral-Facial-Digital Syndrome Type 8

  • Orofaciodigital Syndrome Type 8

  • Ofds Viii

  • Oral-Facial-Digital Syndrome, Type Viii

  • Ofd Syndrome 8

  • Ofds 8

  • Oral Facial Digital Syndrome 8

  • Oral Facial Digital Syndrome Type 8

  • 18 Trisomy

  • Chromosome 18 Trisomy

  • Trisomy 16-18

  • Trisomy E

  • Trisomy E Syndrome

  • Chromosome 18 Duplication

  • Oral-Facial-Digital Syndrome, Edwards Type

  • Orofaciodigital Syndrome, Edwards Type

  • Chromosome 18, Trisomy

  • Cleft Lip/Palate With Abnormal Thumbs And Microcephaly

  • Trisomy 18 Chromosome

  • Abnormal Autosomes 18

Male Infertility
  • Infertility, Male

  • Infertility Male

  • Male Sterility

  • Absolute Infertility

Malaria
  • Malaria, Susceptibility To

  • Malaria, Resistance To

  • Malaria, Cerebral

  • Cerebral Malaria

  • Malaria, Severe, Susceptibility To

  • Malaria, Severe, Resistance To

  • Malaria, Cerebral, Susceptibility To

  • Induced Malaria

  • Malaria, Vivax, Protection Against

  • Malaria, Severe

  • Malaria, Cerebral, Reduced Risk Of

  • Malaria, Protection Against

  • Resistance To Malaria Due To G6pd Deficiency

  • Malaria Due To G6pd Deficiency

  • Malarial Encephalitis

  • CM

  • Malaria Cerebral

  • Susceptibility To Malaria

  • Acute Pernicious Fever

  • Aestivo-Autumnal Fever

  • Aestivo Autumnal Malaria

  • Chagres Fever

  • Continued Malaria Fever

  • Estivo-Autumnal Fever

  • Estivo-Autumnal Malaria

  • Estivo-Autumnal Malarial Fever

  • Falciparum Fever

  • Malignant Tertian Fever

  • Malignant Tertian Malaria

  • Pernicious Intermittent Fever

  • Pernicious Malaria

  • Quotidian Malaria

  • Subtertian Fever

  • Subtertian Malaria Fever

  • Subtertian Malignant Tertian Malaria

  • Tropical Malaria

  • Algid Malaria

  • Bilious Haemoglobinuric Fever

  • Black Water Fever

  • Blackwater Fever

  • Malarial Blackwater Fever

  • Severe Malarial Falciparum

  • West African Fever

  • Malarial Haematinuria

  • Haemoglobinuric Fever

  • Haemoglobinuric Malaria

  • Severe Plasmodium Falciparum Malaria

  • Malarial Haemoglobinuria

  • Malarial Haematuria

  • Falciparum Malaria [Malignant Tertian]

  • Malaria Tropica

  • Malarial Shock

  • Chagres Virus Disease

  • Malignant Malaria

  • Mtm - [Malignant Tertian Malaria]

  • Tm -[Malignant Tertian Malaria]

  • Panama Fever

  • St - [Subtertian Malaria]

  • Malarial Quotidian

  • Benign Tertian Malaria

  • Tertian Ague

  • Vivax Fever

  • Plasmodium Vivax Malaria Nos

  • Btm - [Benign Tertian Malaria]

  • Bt - [Benign Tertian Malaria]

  • Vivax Malaria

  • Benign Tertian Vivax Malaria

  • Tertian Malaria

  • Quartan Malaria

  • Quartan Ague

  • Quartan Fever

  • Plasmodium Malariae Malaria Nos

  • Quartan Malarial

  • Malaria By Plasmodium Malariae

  • Malariae Malaria

  • Ovale Tertian Malaria

  • Plasmodium Ovale Fever

  • Malaria Fever By Plasmodium Ovale

  • Ovale Malaria

  • Malaria By Plasmodium Ovale

  • Malarial Ovale

  • Marsh Fever

  • Remittent Congestive Fever

  • Coastal Fever

  • Remittent Gastric Fever

  • Miasmatic Fever

  • Congestive Remittent Fever

  • Intermittent Fever

  • Jungle Fever

  • Paludism

  • Cameroon Fever

  • Ague

  • Corsican Fever

  • Intermittent Bilious Fever

  • Disease Due To Plasmodiidae

  • Malarial Fever

  • Plasmodiosis

  • Remittent Fever

  • Roman Fever

  • Malaria Fever Nos

  • Malaria Nos

  • Paludal Fever

  • Clinically Diagnosed Malaria

  • Clinically Diagnosed Malaria Without Parasitological Confirmation

  • Congestive Fever

  • Malarial Cachexia

  • Marsh Cachexia

  • Paludal Cachexia

  • Recurrent Malaria

  • Remittent Malaria

Cervical Non-Keratinizing Squamous Cell Carcinoma
Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus AGO2 RGD RGD:621255
Mus musculus AGO2 MGD MGI:2446632
Felis catus AGO2 VGNC VGNC:81639
Canis familiaris AGO2 VGNC VGNC:37707
Bos taurus AGO2 VGNC VGNC:50167
Macaca mulatta AGO2 VGNC VGNC:81347
Others AGO2 NCBI