1. Gene
  2. LMO2 - LIM domain only 2 Gene

LMO2 - LIM domain only 2 Gene

中文名称:仅 LIM 域 2

种属: Homo sapiens

同用名: TTG2; LMO-2; RBTN2; RHOM2; RBTNL1

基因 ID: 4005 | 基因类型: protein coding

关于 LMO2

Cytogenetic location: 11p13 Genomic coordinates (GRCh38): 11:33,858,576-33,892,076 (from NCBI)

This gene has 6 transcripts (splice variants), 193 orthologues, 20 paralogues and is associated with 51 phenotypes. Broad expression in bone marrow (RPKM 14.3), lymph node (RPKM 11.4) and 24 other tissues.

功能概要

LMO2 编码卵黄囊红细胞生成所需的富含半胱氨酸的两个 LIM 结构域蛋白。 LMO2 蛋白在造血发育中具有核心和关键作用,并且高度保守。 LMO2 转录起始位点位于 11p13 T 细胞易位簇 (11p13 ttc) 下游约 25 kb 处,此处发生许多 T 细胞急性淋巴细胞白血病特异性易位。可变剪接导致编码不同异构体的多个转录变体。[RefSeq 提供,2008 年 11 月]

LMO2 encodes a cysteine-rich, two LIM-domain protein that is required for yolk sac erythropoiesis. The LMO2 protein has a central and crucial role in hematopoietic development and is highly conserved. The LMO2 transcription start site is located approximately 25 kb downstream from the 11p13 T-cell translocation cluster (11p13 ttc), where a number T-cell acute lymphoblastic leukemia-specific translocations occur. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Nov 2008]

LMO2 基因产物(3)

mRNA Protein Name
NM_001142315.2 NP_001135787.1 rhombotin-2 isoform 2
NM_001142316.2 NP_001135788.1 rhombotin-2 isoform 2
NM_005574.4 NP_005565.2 rhombotin-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 polymerase II-specific DNA-binding transcription factor binding IPI
IPI: 通过物理相互作用推断
16314316 GOA
enables bHLH transcription factor binding IPI
IPI: 通过物理相互作用推断
16314316 GOA
enables identical protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16189514 GOA
enables transcription coactivator activity IDA
IDA: 通过直接分析推断
16314316 GOA
enables transcription coregulator binding IPI
IPI: 通过物理相互作用推断
16314316 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: 通过直接分析推断
16314316 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of transcription regulator complex IDA
IDA: 通过直接分析推断
16314316 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

LMO2 蛋白结构

LIM

LIM: LIM domain (30 - 88)

LIM

LIM: LIM domain (94 - 150)

  • 0
  • 100
  • 158 a.a.
蛋白主名 其他名称

rhombotin-2

LIM domain only protein 2

LMO2 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
Intra LMO2 P25791 MAPRE1 Homo sapiens Q15691
Y2H Array
25416956
Intra LMO2 P25791 MAPRE1 Homo sapiens Q15691
Validated Y2H
25416956
Intra LMO2 P25791 KRT40 Homo sapiens Q6A162
Y2H Prey Pooling
25416956
Intra LMO2 P25791 KRT40 Homo sapiens Q6A162
Validated Y2H
25416956
Intra LMO2 P25791 KRTAP10-7 Homo sapiens P60409
Validated Y2H
25416956
Intra LMO2 P25791 KRTAP10-7 Homo sapiens P60409
Y2H Array
25416956
Intra LMO2 P25791 KRTAP10-7 Homo sapiens P60409
Y2H Prey Pooling
25416956
Intra LMO2 P25791 ADAMTSL4 Homo sapiens Q6UY14-3
Validated Y2H
25416956
Intra LMO2 P25791 TFPT Homo sapiens P0C1Z6-2
Validated Y2H
25416956
Intra LMO2 P25791 NUTM1 Homo sapiens Q86Y26
Y2H Prey Pooling
25416956
Intra LMO2 P25791 MBIP Homo sapiens Q9NS73-5
Y2H Array
25416956
Intra LMO2 P25791 MAGEA8 Homo sapiens P43361
Y2H Array
25416956
Intra LMO2 P25791 MAGEA8 Homo sapiens P43361
Validated Y2H
25416956
Intra LMO2 P25791 IFT43 Homo sapiens Q96FT9
Validated Y2H
25416956
Intra LMO2 P25791 CLHC1 Homo sapiens Q8NHS4
Y2H Prey Pooling
25416956
Intra LMO2 P25791 CLHC1 Homo sapiens Q8NHS4
Y2H Array
25416956
Intra LMO2 P25791 TRIM54 Homo sapiens Q9BYV2
Y2H Prey Pooling
25416956
Intra LMO2 P25791 SSX2IP Homo sapiens Q9Y2D8
Y2H Array
25416956
Intra LMO2 P25791 SSX2IP Homo sapiens Q9Y2D8
Validated Y2H
25416956
Intra LMO2 P25791 N4BP2L2 Homo sapiens Q92802
Validated Y2H
25416956
Intra LMO2 P25791 N4BP2L2 Homo sapiens Q92802
Y2H Array
25416956
Intra LMO2 P25791 N4BP2L2 Homo sapiens Q92802
Y2H Prey Pooling
25416956
Intra LMO2 P25791 BLZF1 Homo sapiens Q9H2G9
Y2H Prey Pooling
25416956
Intra LMO2 P25791 BLZF1 Homo sapiens Q9H2G9
Validated Y2H
25416956
Intra LMO2 P25791 CMTM5 Homo sapiens Q96DZ9
Y2H Prey Pooling
25416956
Intra LMO2 P25791 TUFT1 Homo sapiens Q9NNX1
Y2H Prey Pooling
25416956
Intra LMO2 P25791 TUFT1 Homo sapiens Q9NNX1
Validated Y2H
25416956
Intra LMO2 P25791 TUFT1 Homo sapiens Q9NNX1
Y2H Array
25416956
Intra LMO2 P25791 REL Homo sapiens Q04864
Y2H Prey Pooling
25416956
Intra LMO2 P25791 SKP1 Homo sapiens P63208
Y2H Array
25416956
Intra LMO2 P25791 SKP1 Homo sapiens P63208
Y2H Prey Pooling
25416956
Intra LMO2 P25791 SKP1 Homo sapiens P63208
Validated Y2H
25416956
Intra LMO2 P25791 SOX5 Homo sapiens P35711
Y2H Prey Pooling
25416956
Intra LMO2 P25791 SOX5 Homo sapiens P35711
Y2H Array
25416956
Intra LMO2 P25791 HNRNPC Homo sapiens P07910
Y2H Prey Pooling
25416956
Intra LMO2 P25791 HNRNPC Homo sapiens P07910
Validated Y2H
25416956
Intra LMO2 P25791 PRKG1 Homo sapiens Q13976
Y2H Array
31515488
Intra LMO2 P25791 PRKG1 Homo sapiens Q13976
Validated Y2H
25416956
Intra LMO2 P25791 PRKG1 Homo sapiens Q13976
Y2H Array
25416956
Intra LMO2 P25791 SAXO1 Homo sapiens Q8IYX7
Y2H Array
31515488
Intra LMO2 P25791 SAXO1 Homo sapiens Q8IYX7
Y2H Prey Pooling
25416956
Intra LMO2 P25791 GRB2 Homo sapiens P62993
Validated Y2H
25416956
Intra LMO2 P25791 GRB2 Homo sapiens P62993
Y2H Array
25416956
Intra LMO2 P25791 STAT3 Homo sapiens P40763
Validated Y2H
25416956
Intra LMO2 P25791 GOLGA2 Homo sapiens Q08379
Validated Y2H
25416956
Intra LMO2 P25791 GOLGA2 Homo sapiens Q08379
Y2H Array
25416956
Intra LMO2 P25791 LDB1 Homo sapiens Q86U70
Anti Tag CoIP
33961781
Intra LMO2 P25791 LDB1 Homo sapiens Q86U70
Y2H Prey Pooling
25416956
Intra LMO2 P25791 LDB1 Homo sapiens Q86U70
Y2H
21988832
Intra LMO2 P25791 ZNF24 Homo sapiens P17028
Y2H Array
31515488
Intra LMO2 P25791 ZNF24 Homo sapiens P17028
Validated Y2H
25416956
Intra LMO2 P25791 ZFP64 Homo sapiens Q9NTW7
Validated Y2H
25416956
Intra LMO2 P25791 ZFP64 Homo sapiens Q9NTW7
Y2H Prey Pooling
25416956
Intra LMO2 P25791 DRAP1 Homo sapiens Q14919
Y2H Array
25416956
Intra LMO2 P25791 PHC2 Homo sapiens Q8IXK0
Validated Y2H
25416956
Intra LMO2 P25791 PHC2 Homo sapiens Q8IXK0
Y2H
21516116
Intra LMO2 P25791 TLE5 Homo sapiens Q08117
Y2H Prey Pooling
25416956
Intra LMO2 P25791 TLE5 Homo sapiens Q08117
Validated Y2H
25416956
Intra LMO2 P25791 MAPRE3 Homo sapiens Q9UPY8
Y2H
21516116
Intra LMO2 P25791 MAPRE3 Homo sapiens Q9UPY8
Y2H Pooling
16189514
Intra LMO2 P25791 MAPRE3 Homo sapiens Q9UPY8
Validated Y2H
25416956
Intra LMO2 P25791 RINT1 Homo sapiens Q6NUQ1
Y2H Array
25416956
Intra LMO2 P25791 RINT1 Homo sapiens Q6NUQ1
Y2H Prey Pooling
25416956
Intra LMO2 P25791 RINT1 Homo sapiens Q6NUQ1
Y2H Array
31515488
Intra LMO2 P25791 RELA Homo sapiens Q04206
Pull Down
21988832
Intra LMO2 P25791 RELA Homo sapiens Q04206
Confocal
21988832
Intra LMO2 P25791 KRT15 Homo sapiens P19012
Validated Y2H
25416956
Intra LMO2 P25791 CALCOCO2 Homo sapiens Q13137
Validated Y2H
25416956
Intra LMO2 P25791 MAPRE2 Homo sapiens Q15555
Y2H Pooling
16189514
Intra LMO2 P25791 MAPRE2 Homo sapiens Q15555
Y2H Array
31515488
Intra LMO2 P25791 MAPRE2 Homo sapiens Q15555
Validated Y2H
25416956
Intra LMO2 P25791 MAPRE2 Homo sapiens Q15555
Anti Tag CoIP
33961781
Intra LMO2 P25791 MAPRE2 Homo sapiens Q15555
Y2H Prey Pooling
25416956
Intra LMO2 P25791 TRIM23 Homo sapiens P36406
Validated Y2H
25416956
Intra LMO2 P25791 NIF3L1 Homo sapiens Q9GZT8
Y2H Prey Pooling
25416956
Intra LMO2 P25791 LZTS2 Homo sapiens Q9BRK4
Y2H Prey Pooling
25416956
Intra LMO2 P25791 LZTS2 Homo sapiens Q9BRK4
Validated Y2H
25416956
Intra LMO2 P25791 FHL3 Homo sapiens Q13643
Validated Y2H
25416956
Intra LMO2 P25791 FHL3 Homo sapiens Q13643
Y2H Array
25416956
Intra LMO2 P25791 AGTRAP Homo sapiens Q6RW13
Y2H Array
25416956
Intra LMO2 P25791 CBY2 Homo sapiens Q8NA61
Y2H Array
25416956
Intra LMO2 P25791 CBY2 Homo sapiens Q8NA61
Validated Y2H
25416956
Intra LMO2 P25791 MTUS2 Homo sapiens Q5JR59
Y2H Prey Pooling
25416956
Intra LMO2 P25791 MTUS2 Homo sapiens Q5JR59
Validated Y2H
25416956
Intra LMO2 P25791 ABI2 Homo sapiens Q9NYB9
Y2H Array
29892012
Intra LMO2 P25791 ABI2 Homo sapiens Q9NYB9
Validated Y2H
25416956
Intra LMO2 P25791 GFAP Homo sapiens P14136
Validated Y2H
25416956
Intra LMO2 P25791 GFAP Homo sapiens P14136
Y2H Array
25416956
Intra LMO2 P25791 BANP Homo sapiens Q8N9N5
Validated Y2H
25416956
Intra LMO2 P25791 AIMP2 Homo sapiens Q13155
Validated Y2H
25416956
Intra LMO2 P25791 AIMP2 Homo sapiens Q13155
Y2H Array
25416956
Intra LMO2 P25791 AIMP2 Homo sapiens Q13155
Y2H Prey Pooling
25416956
Intra LMO2 P25791 HOOK1 Homo sapiens Q9UJC3
Validated Y2H
25416956
Intra LMO2 P25791 HOOK1 Homo sapiens Q9UJC3
Y2H Prey Pooling
25416956
Intra LMO2 P25791 MRFAP1L1 Homo sapiens Q96HT8
Y2H Prey Pooling
25416956
Intra LMO2 P25791 IHO1 Homo sapiens Q8IYA8
Y2H Prey Pooling
25416956
Intra LMO2 P25791 ROCK1 Homo sapiens Q13464
Y2H Prey Pooling
25416956
Intra LMO2 P25791 ROCK1 Homo sapiens Q13464
Y2H Array
25416956
Intra LMO2 P25791 NOTCH2NLA Homo sapiens Q7Z3S9
Y2H Prey Pooling
25416956
Intra LMO2 P25791 NOTCH2NLA Homo sapiens Q7Z3S9
Y2H Array
25416956
Intra LMO2 P25791 NOTCH2NLA Homo sapiens Q7Z3S9
Validated Y2H
25416956
Intra LMO2 P25791 C1orf94 Homo sapiens Q6P1W5
Validated Y2H
25416956
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Severe Combined Immunodeficiency, X-Linked

X-Linked Severe Combined Immunodeficiency

SCIDX1

XSCID

Scidx

X-Linked Scid

X-Scid

Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, Nk Cell-Negative

Scid, X-Linked

Immunodeficiency 4

Imd4

Gamma Chain Deficiency

Scid-X1

X-Linked Combined Immunodeficiency Diseases

Thymic Epithelial Hypoplasia

Severe Combined Immunodeficiency T- B+ Due To Gamma Chain Deficiency

Severe Combined Immunodeficiency T- B+, X-Linked

Il2rg Scid, T- B+ Nk-

T-B+ Severe Combined Immunodeficiency Due To Gamma Chain Deficiency

T-B+ Scid Due To Gamma Chain Deficiency

T-B+ Severe Combined Immunodeficiency, X-Linked

Severe Combined Immunodeficiency X-Linked T-Cell-Negative/B-Cell-Positive/Nk-Cell-Negative

Agammaglobulinemia Swiss Type

Scid X-Linked

Severe Combined Immunodeficiency X-Linked T Cell-Negative/B Cell-Positive/Nk Cell-Negative

Severe Combined Immunodeficiency X-Linked T-Cell Negative/B-Cell Positive/Nk-Cell Negative

Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency

T-Cell Acute Lymphoblastic Leukemia

T-Cell Leukemia

Acute T Cell Leukemia

Precursor T Lymphoblastic Leukemia

Precursor T-Lymphoblastic Lymphoma/Leukemia

T Acute Lymphoblastic Leukemia

T-Cell Acute Lymphocytic Leukaemia

T-Cell Lymphoblastic Leukemia/Lymphoma

Leukemia T-Cell

Leukemia, T-Cell

Leukemia, Acute, Lymphoblastic, T-Cell

Leukemia, T-Cell Acute Lymphoblastic

Leukemia, Acute T-Cell

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Precursor T-Cell Lymphoblastic Lymphoma

Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

Lymphoblastic Lymphoma

Lymphoma, Lymphoblastic

Lymphoma Lymphoblastic

Precursor Cell Lymphoblastic Lymphoma

Precursor Cell Lymphoblastic Leukemia Lymphoma

Leukemia

Leukemias

Leukaemia, Unspecified, Without Mention Of Remission

Aleukemic Leukaemia

Chronic Leukaemia

Subacute Leukaemia

Leukaemia Disorder

Leukaemia Nos

Severe Combined Immunodeficiency

Scid

Severe Combined Immunodeficiency Disease

Combined T And B Cell Inborn Immunodeficiency

Immunodeficiency, Severe Combined

Scid - [Severe Combined Immunodeficiencies]

Combined Immunodeficiency

Combined T Cell And B Cell Immunodeficiency

Congenital Combined Immunodeficiency

Syndrome With Combined Immunodeficiency

Combined T And B Cell Immunodeficiency

Combined Immunity Deficiency

Combined Immunodeficiency Syndrome

Combined T-Cell And B-Cell Immunodeficiency

Lymphopenic Agammaglobulinaemia

Granulomatous Disease, Chronic, X-Linked

CGDX

Chronic Granulomatous Disease, X-Linked

X-Linked Chronic Granulomatous Disease

Cgd

Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked

Cdgx

X-Linked Chronic Cytochrome B-Negative Granulomatous Disease

Chronic Granulomatous Disease Cytochrome B-Negative X-Linked

Chronic Granulomatous Disease Cytochrome B-Positive X-Linked

Granulomatous Disease, Chronic, X-Linked, Variant

Adenosine Deaminase Deficiency

Ada Deficiency

Ada-Scid

Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency

Adenosine Deaminase Deficient Severe Combined Immunodeficiency

Scid Due To Ada Deficiency

Severe Combined Immunodeficiency Due To Ada Deficiency

Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency

Ada

Scid Due To Adenosine Deaminase Deficiency

Precursor T-Cell Acute Lymphoblastic Leukemia

T-All

Precursor T-Cell Acute Lymphoblastic Leukemia/Lymphoma

Precursor T-Cell Acute Lymphocytic Leukemia

Precursor T-Cell Acute Lymphocytic Leukemia/Lymphoma

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Adult T-Cell Lymphoma/Leukemia

Phagocyte Bactericidal Dysfunction

Phagocytic Dysfunction

Childhood T-Cell Acute Lymphoblastic Leukemia

T-Cell Childhood Acute Lymphoblastic Leukemia

Childhood Precursor T-Lymphoblastic Lymphoma/Leukemia

T-Cell Childhood Acute Lymphocytic Leukemia

Childhood T Lymphoblastic Leukemia/Lymphoma

Ureteral Lymphoma

Lymphoma Of Ureter

Ureter Lymphoma

Nodal Marginal Zone Lymphoma

Mucosa-Associated Lymphoid Tissue Lymphoma

Monocytoid B-Cell Lymphoma

High-Grade B-Cell Lymphoma Double-Hit/Triple-Hit

Hgbl-Dh/Th

High Grade B-Cell Lymphoma With Myc And Bcl2 Or Bcl6 Rearrangements

High Grade B-Cell Lymphoma With Myc And/ Or Bcl2 And/Or Bcl6 Rearrangement

Purine-Pyrimidine Metabolic Disorder

Inborn Errors Of Purine-Pyrimidine Metabolism

Disorder Of Purine Or Pyrimidine Metabolism

Chronic Granulomatous Disease

Cgd

Granulomatous Disease, Chronic

Autosomal Recessive Chronic Granulomatous Disease

X-Linked Chronic Granulomatous Disease

Bridges-Good Syndrome

Congenital Dysphagocytosis

Quie Syndrome

Chronic Septic Granulomatosis

Chronic Granulomatous Disorder

Granulomatous Disease Chronic

Granulomatous Disease, Chronic, X-Linked

Leukemia, Acute Lymphoblastic

Acute Lymphoblastic Leukemia

ALL

Acute Lymphocytic Leukemia

Leukemia, Acute Lymphocytic, Susceptibility To, 1

Acute Lymphoblastic Leukaemia

Precursor Lymphoblastic Lymphoma/Leukemia

Precursor Lymphoid Neoplasm

Leukemia, Acute Lymphoblastic, Susceptibility To

B-Cell Acute Lymphoblastic Leukemia

Leukemia, Acute Lymphocytic 1

Acute Lymphocytic Leukaemia

Acute Lymphoblastic Leukemia/Lymphoma

All1

Childhood Acute Lymphoblastic Leukemia

Leukemia Acute Lymphoblastic 1

Leukemia Acute Lymphoblastic B-Hyperdiploid

Leukemia Acute Lymphocytic

Leukemia Acute Lymphocytic 1

Leukemia B-Cell Acute Lymphoblastic

Leukemia T-Cell Acute Lymphoblastic

Leukemia, Acute Lymphoblastic, 3

ALL3

Lymphoblastic Leukemia Acute

Leukemia, Acute, Lymphoblastic

Precursor Cell Lymphoblastic Leukemia Lymphoma

Leukemia, Lymphocytic, Acute, L1

Leukemia, Acute Lymphoblastic, Susceptibility To, 3

Thrombocytopenia

Low Platelet Count

Low Platelets

Decreased Platelets

Platelet Dysfunction Nos

Metachromatic Leukodystrophy

Arylsulfatase A Deficiency

MLD

Arsa Deficiency

Sulfatide Lipidosis

Metachromatic Leukoencephalopathy

Cerebral Sclerosis, Diffuse, Metachromatic Form

Cerebroside Sulfatase Deficiency

Leukodystrophy, Metachromatic

Pseudoarylsulfatase A Deficiency

Leukodystrophy Metachromatic

Sulfatidosis

Metachromatic Leukodystrophy, Late Infantile

Metachromatic Leukodystrophy Variant

Deficiency Of Cerebroside-Sulfatase

Scholz Cerebral Sclerosis

Sulfatide Lipoidosis

Cerebral Sclerosis Diffuse Metachromatic Form

Arylsulfatase A Deficiency Disease

Cerebroside Sulphatase Deficiency Disease

Greenfield Disease

Metachromatic Leukodystrophy, Adult

Metachromatic Leukodystrophy, Juvenile

Leukodystrophy Metachromatic Adult

Leukodystrophy Metachromatic Juvenile

Leukodystrophy Metachromatic Late Infantile

Metachromatic Leukodystrophy, Adult Type

Metachromatic Leukodystrophy, Juvenile Type

Metachromatic Leukodystrophy, Infant

Greenfield'S Disease

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

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 LMO2 RGD RGD:1307101
Mus musculus LMO2 MGD MGI:102811
Felis catus LMO2 VGNC VGNC:82023
Bos taurus LMO2 VGNC VGNC:30934
Macaca mulatta LMO2 VGNC VGNC:74431