1. Gene
  2. AGO2 - argonaute RISC catalytic component 2 Gene

AGO2 - argonaute RISC catalytic component 2 Gene

中文名称:argonaute RISC 催化组分 2

种属: Homo sapiens

同用名: PPD; Q10; CASC7; EIF2C2; LESKRES; LINC00980

基因 ID: 27161 | 基因类型: protein coding

关于 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.

功能概要

该基因编码在 RNA 干扰中发挥作用的 Argonaute 蛋白家族成员。编码的蛋白质是高度碱性的,包含一个 PAZ 结构域和一个 PIWI 结构域。它可能与 dicer1 相互作用并在短干扰 RNA 介导的基因沉默中发挥作用。已发现该基因编码不同异构体的多个转录变体。[RefSeq 提供,2009 年 9 月]

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 基因产物(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
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables RNA 7-methylguanosine cap binding IDA
IDA: 通过直接分析推断
17524464 GOA
enables RNA endonuclease activity IDA
IDA: 通过直接分析推断
18178619 GOA
enables RNA polymerase II complex binding IDA
IDA: 通过直接分析推断
25336585 GOA
enables core promoter sequence-specific DNA binding IMP
IMP: 通过突变表型推断
25336585 GOA
enables double-stranded RNA binding IDA
IDA: 通过直接分析推断
19966796 GOA
enables endoribonuclease activity, cleaving miRNA-paired mRNA IDA
IDA: 通过直接分析推断
15260970 GOA
enables endoribonuclease activity, cleaving miRNA-paired mRNA IMP
IMP: 通过突变表型推断
22795694 GOA
enables endoribonuclease activity, cleaving siRNA-paired mRNA IDA
IDA: 通过直接分析推断
15260970 GOA
enables mRNA 3'-UTR AU-rich region binding IDA
IDA: 通过直接分析推断
17382880 GOA
enables mRNA cap binding IDA
IDA: 通过直接分析推断
17524464 GOA
enables mRNA cap binding IPI
IPI: 通过物理相互作用推断
23409027 GOA
enables miRNA binding IDA
IDA: 通过直接分析推断
15260970 GOA
enables miRNA binding IPI
IPI: 通过物理相互作用推断
31012336 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
14749716 GOA
contributes to siRNA binding IDA
IDA: 通过直接分析推断
15973356 GOA
enables siRNA binding IDA
IDA: 通过直接分析推断
17495927 GOA
enables single-stranded RNA binding IDA
IDA: 通过直接分析推断
19966796 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in P-body assembly IDA
IDA: 通过直接分析推断
31400113 GOA
involved in RISC complex assembly IDA
IDA: 通过直接分析推断
19701182 GOA
involved in RNA secondary structure unwinding IDA
IDA: 通过直接分析推断
19966796 GOA
involved in RNA secondary structure unwinding IMP
IMP: 通过突变表型推断
22795694 GOA
involved in miRNA processing IDA
IDA: 通过直接分析推断
19966796 GOA
involved in miRNA-mediated gene silencing by inhibition of translation IDA
IDA: 通过直接分析推断
17671087 GOA
involved in miRNA-mediated gene silencing by inhibition of translation IMP
IMP: 通过突变表型推断
18771919 GOA
involved in miRNA-mediated gene silencing by mRNA destabilization IDA
IDA: 通过直接分析推断
15260970 GOA
involved in miRNA-mediated gene silencing by mRNA destabilization IMP
IMP: 通过突变表型推断
18771919 GOA
involved in negative regulation of translational initiation IDA
IDA: 通过直接分析推断
17524464 GOA
involved in positive regulation of angiogenesis IDA
IDA: 通过直接分析推断
27208409 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: 通过突变表型推断
25336585 GOA
involved in positive regulation of translation IDA
IDA: 通过直接分析推断
17382880 GOA
involved in positive regulation of trophoblast cell migration IMP
IMP: 通过突变表型推断
27208409 GOA
involved in pre-miRNA processing IDA
IDA: 通过直接分析推断
16424907 GOA
involved in regulation of synapse maturation IDA
IDA: 通过直接分析推断
29735530 GOA
involved in regulation of synapse maturation IMP
IMP: 通过突变表型推断
29735530 GOA
involved in siRNA processing IDA
IDA: 通过直接分析推断
23661684 GOA
involved in siRNA-mediated gene silencing by mRNA destabilization IDA
IDA: 通过直接分析推断
15260970 GOA
involved in siRNA-mediated gene silencing by mRNA destabilization IMP
IMP: 通过突变表型推断
22795694 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in P-body IDA
IDA: 通过直接分析推断
20616046 GOA
part of RISC complex IDA
IDA: 通过直接分析推断
15260970 GOA
part of RISC complex IGI
IGI: 通过遗传相互作用推断
31012336 GOA
part of RISC complex IPI
IPI: 通过物理相互作用推断
19826008 GOA
part of RISC-loading complex IDA
IDA: 通过直接分析推断
15973356 GOA
part of RISC-loading complex IPI
IPI: 通过物理相互作用推断
23661684 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
15260970 GOA
located in extracellular exosome IDA
IDA: 通过直接分析推断
28159509 GOA
is active in glutamatergic synapse IDA
IDA: 通过直接分析推断
29735530 GOA
is active in glutamatergic synapse IMP
IMP: 通过突变表型推断
29735530 GOA
located in nucleus IDA
IDA: 通过直接分析推断
23985560 GOA
is active in postsynapse IDA
IDA: 通过直接分析推断
29735530 GOA
is active in postsynapse IMP
IMP: 通过突变表型推断
29735530 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

AGO2 蛋白结构

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.
蛋白主名 其他名称

protein argonaute-2

PAZ Piwi domain protein

AGO2 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
AGO2 Q9UKV8 MTDH Homo sapiens Q86UE4 24981741
种属内
AGO2 Q9UKV8 FKBP4 Homo sapiens Q02790 23741051
种属内
AGO2 Q9UKV8 FKBP4 Homo sapiens Q02790 23741051
种属内
AGO2 Q9UKV8 PTGES3 Homo sapiens Q15185 23741051
种属内
AGO2 Q9UKV8 PTGES3 Homo sapiens Q15185 23741051
种属内
AGO2 Q9UKV8 DMWD Homo sapiens G5E9A7 32814053
种属内
AGO2 Q9UKV8 DMWD Homo sapiens G5E9A7 32814053
种属内
AGO2 Q9UKV8 DMWD Homo sapiens G5E9A7 32814053
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 19955415
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1
GMS
19820710
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 23636329
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 18178619
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1
GMS
18178619
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1 19820710
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3-1
EM
19820710
种属内
AGO2 Q9UKV8 CNOT7 Homo sapiens Q9UIV1 19716330
种属内
AGO2 Q9UKV8 PLEKHA7 Homo sapiens Q6IQ23 28877994
种属内
AGO2 Q9UKV8 PLEKHA7 Homo sapiens Q6IQ23
PLA
28877994
种属内
AGO2 Q9UKV8 PLEKHA7 Homo sapiens Q6IQ23 28877994
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 19324964
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 35271311
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28683311
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 19716330
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7
IF
19324964
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 23090477
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28683311
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28683311
种属内
AGO2 Q9UKV8 TNRC6A Homo sapiens Q8NDV7 28877994
种属内
AGO2 Q9UKV8 ZMAT3 Homo sapiens Q9HA38 23085987
种属内
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
种属内
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
种属内
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
种属内
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4
PLA
28683311
种属内
AGO2 Q9UKV8 LIMD1 Homo sapiens Q9UGP4 28683311
种属内
AGO2 Q9UKV8 RACK1 Homo sapiens P63244 21525958
种属内
AGO2 Q9UKV8 EGFR Homo sapiens P00533 23636329
种属内
AGO2 Q9UKV8 EGFR Homo sapiens P00533 23636329
种属内
AGO2 Q9UKV8 EGFR Homo sapiens P00533 23636329
种属内
AGO2 Q9UKV8 FGFR3 Homo sapiens P22607 32814053
种属内
AGO2 Q9UKV8 FGFR3 Homo sapiens P22607 32814053
种属内
AGO2 Q9UKV8 FGFR3 Homo sapiens P22607 32814053
种属内
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 28683311
种属内
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 16756390
种属内
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 28683311
种属内
AGO2 Q9UKV8 DDX6 Homo sapiens P26196
PLA
28683311
种属内
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 16756390
种属内
AGO2 Q9UKV8 DDX6 Homo sapiens P26196 28683311
种属内
AGO2 Q9UKV8 IPO8 Homo sapiens O15397 17932509
种属内
AGO2 Q9UKV8 IPO8 Homo sapiens O15397 19167051
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 19716330
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 23622242
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 26496610
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 23741051
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3
GMS
23622242
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 14749716
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 33961781
种属内
AGO2 Q9UKV8 DICER1 Homo sapiens Q9UPY3 17932509
种属内
AGO2 Q9UKV8 RB1 Homo sapiens P06400 22366686
种属内
AGO2 Q9UKV8 SPRED1 Homo sapiens Q7Z699 32814053
种属内
AGO2 Q9UKV8 SPRED1 Homo sapiens Q7Z699 32814053
种属内
AGO2 Q9UKV8 SPRED1 Homo sapiens Q7Z699 32814053
种属内
AGO2 Q9UKV8 AGO1 Homo sapiens Q9UL18 16756390
种属内
AGO2 Q9UKV8 AGO1 Homo sapiens Q9UL18 35271311
种属内
AGO2 Q9UKV8 AGO1 Homo sapiens Q9UL18 16756390
种属内
AGO2 Q9UKV8 LRRK2 Homo sapiens Q5S007 20671708
种属内
AGO2 Q9UKV8 GNL3 Homo sapiens Q9BVP2 24550003
种属内
AGO2 Q9UKV8 GNL3 Homo sapiens Q9BVP2 17932509
种属内
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 21981923
种属内
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 35271311
种属内
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 19383768
种属内
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 19383768
种属内
AGO2 Q9UKV8 TNRC6C Homo sapiens Q9HCJ0 19838187
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9-2 19383768
种属内
AGO2 Q9UKV8 PRKRA Homo sapiens O75569 16424907
种属内
AGO2 Q9UKV8 EIF4EBP1 Homo sapiens Q13541 20671708
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 17932509
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 19383768
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 19838187
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 35271311
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 19716330
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9 24043833
种属内
AGO2 Q9UKV8 TNRC6B Homo sapiens Q9UPQ9
FPS
24043833
种属内
AGO2 Q9UKV8 PRNP Homo sapiens P04156 22484317
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 19716330
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 23622242
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633
GMS
19820710
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 18178619
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633
GMS
18178619
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 17932509
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 19820710
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633 23636329
种属内
AGO2 Q9UKV8 TARBP2 Homo sapiens Q15633
EM
19820710
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 AGO2 蛋白

目录号 产品名 蛋白编号 纯度
HY-P72835 AGO2/Argonaute-2 Protein, Human (sf9, His) Q9UKV8 (M1-A859) ≥95%

AGO2 抗体

目录号 产品名 应用 反应物种
HY-P80546 Argonaute 2 Antibody WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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