LMO2 - LIM domain only 2 Gene

Also Known as TTG2; LMO-2; RBTN2; RHOM2; RBTNL1

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 4005

About 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.

Summary

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 Products (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
Molecular Function GO Annotation Evidence 参考文献 由来
enables RNA polymerase II-specific DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
16314316 GOA
enables bHLH transcription factor binding IPI
IPI: Inferred from physical interaction
16314316 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
16314316 GOA
enables transcription coregulator binding IPI
IPI: Inferred from physical interaction
16314316 GOA
Biological Process GO Annotation Evidence 参考文献 由来
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
16314316 GOA
Cellular Component GO Annotation Evidence 参考文献 由来
part of transcription regulator complex IDA
IDA: Inferred from direct assay
16314316 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

LMO2 Protein Structure

LIM

LIM: LIM domain (30 - 88)

LIM

LIM: LIM domain (94 - 150)

  • 0
  • 100
  • 158 a.a.
Protein Preferred Names Protein Names

rhombotin-2

  • LIM domain only protein 2

LMO2 Protein-protein interaction Information

Type
タンパク質名 Protein ID Interactor Interactor Species Interactor ID Detection Method 参考文献
Intra
LMO2 P25791 MAPRE1 Homo sapiens Q15691 25416956
Intra
LMO2 P25791 MAPRE1 Homo sapiens Q15691 25416956
Intra
LMO2 P25791 KRT40 Homo sapiens Q6A162 25416956
Intra
LMO2 P25791 KRT40 Homo sapiens Q6A162 25416956
Intra
LMO2 P25791 KRTAP10-7 Homo sapiens P60409 25416956
Intra
LMO2 P25791 KRTAP10-7 Homo sapiens P60409 25416956
Intra
LMO2 P25791 KRTAP10-7 Homo sapiens P60409 25416956
Intra
LMO2 P25791 ADAMTSL4 Homo sapiens Q6UY14-3 25416956
Intra
LMO2 P25791 TFPT Homo sapiens P0C1Z6-2 25416956
Intra
LMO2 P25791 NUTM1 Homo sapiens Q86Y26 25416956
Intra
LMO2 P25791 MBIP Homo sapiens Q9NS73-5 25416956
Intra
LMO2 P25791 MAGEA8 Homo sapiens P43361 25416956
Intra
LMO2 P25791 MAGEA8 Homo sapiens P43361 25416956
Intra
LMO2 P25791 IFT43 Homo sapiens Q96FT9 25416956
Intra
LMO2 P25791 CLHC1 Homo sapiens Q8NHS4 25416956
Intra
LMO2 P25791 CLHC1 Homo sapiens Q8NHS4 25416956
Intra
LMO2 P25791 TRIM54 Homo sapiens Q9BYV2 25416956
Intra
LMO2 P25791 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
LMO2 P25791 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
LMO2 P25791 N4BP2L2 Homo sapiens Q92802 25416956
Intra
LMO2 P25791 N4BP2L2 Homo sapiens Q92802 25416956
Intra
LMO2 P25791 N4BP2L2 Homo sapiens Q92802 25416956
Intra
LMO2 P25791 BLZF1 Homo sapiens Q9H2G9 25416956
Intra
LMO2 P25791 BLZF1 Homo sapiens Q9H2G9 25416956
Intra
LMO2 P25791 CMTM5 Homo sapiens Q96DZ9 25416956
Intra
LMO2 P25791 TUFT1 Homo sapiens Q9NNX1 25416956
Intra
LMO2 P25791 TUFT1 Homo sapiens Q9NNX1 25416956
Intra
LMO2 P25791 TUFT1 Homo sapiens Q9NNX1 25416956
Intra
LMO2 P25791 REL Homo sapiens Q04864 25416956
Intra
LMO2 P25791 SKP1 Homo sapiens P63208 25416956
Intra
LMO2 P25791 SKP1 Homo sapiens P63208 25416956
Intra
LMO2 P25791 SKP1 Homo sapiens P63208 25416956
Intra
LMO2 P25791 SOX5 Homo sapiens P35711 25416956
Intra
LMO2 P25791 SOX5 Homo sapiens P35711 25416956
Intra
LMO2 P25791 HNRNPC Homo sapiens P07910 25416956
Intra
LMO2 P25791 HNRNPC Homo sapiens P07910 25416956
Intra
LMO2 P25791 PRKG1 Homo sapiens Q13976 31515488
Intra
LMO2 P25791 PRKG1 Homo sapiens Q13976 25416956
Intra
LMO2 P25791 PRKG1 Homo sapiens Q13976 25416956
Intra
LMO2 P25791 SAXO1 Homo sapiens Q8IYX7 31515488
Intra
LMO2 P25791 SAXO1 Homo sapiens Q8IYX7 25416956
Intra
LMO2 P25791 GRB2 Homo sapiens P62993 25416956
Intra
LMO2 P25791 GRB2 Homo sapiens P62993 25416956
Intra
LMO2 P25791 STAT3 Homo sapiens P40763 25416956
Intra
LMO2 P25791 GOLGA2 Homo sapiens Q08379 25416956
Intra
LMO2 P25791 GOLGA2 Homo sapiens Q08379 25416956
Intra
LMO2 P25791 LDB1 Homo sapiens Q86U70 33961781
Intra
LMO2 P25791 LDB1 Homo sapiens Q86U70 25416956
Intra
LMO2 P25791 LDB1 Homo sapiens Q86U70
Y2H
21988832
Intra
LMO2 P25791 ZNF24 Homo sapiens P17028 31515488
Intra
LMO2 P25791 ZNF24 Homo sapiens P17028 25416956
Intra
LMO2 P25791 ZFP64 Homo sapiens Q9NTW7 25416956
Intra
LMO2 P25791 ZFP64 Homo sapiens Q9NTW7 25416956
Intra
LMO2 P25791 DRAP1 Homo sapiens Q14919 25416956
Intra
LMO2 P25791 PHC2 Homo sapiens Q8IXK0 25416956
Intra
LMO2 P25791 PHC2 Homo sapiens Q8IXK0
Y2H
21516116
Intra
LMO2 P25791 TLE5 Homo sapiens Q08117 25416956
Intra
LMO2 P25791 TLE5 Homo sapiens Q08117 25416956
Intra
LMO2 P25791 MAPRE3 Homo sapiens Q9UPY8
Y2H
21516116
Intra
LMO2 P25791 MAPRE3 Homo sapiens Q9UPY8 16189514
Intra
LMO2 P25791 MAPRE3 Homo sapiens Q9UPY8 25416956
Intra
LMO2 P25791 RINT1 Homo sapiens Q6NUQ1 25416956
Intra
LMO2 P25791 RINT1 Homo sapiens Q6NUQ1 25416956
Intra
LMO2 P25791 RINT1 Homo sapiens Q6NUQ1 31515488
Intra
LMO2 P25791 RELA Homo sapiens Q04206 21988832
Intra
LMO2 P25791 RELA Homo sapiens Q04206 21988832
Intra
LMO2 P25791 KRT15 Homo sapiens P19012 25416956
Intra
LMO2 P25791 CALCOCO2 Homo sapiens Q13137 25416956
Intra
LMO2 P25791 MAPRE2 Homo sapiens Q15555 16189514
Intra
LMO2 P25791 MAPRE2 Homo sapiens Q15555 31515488
Intra
LMO2 P25791 MAPRE2 Homo sapiens Q15555 25416956
Intra
LMO2 P25791 MAPRE2 Homo sapiens Q15555 33961781
Intra
LMO2 P25791 MAPRE2 Homo sapiens Q15555 25416956
Intra
LMO2 P25791 TRIM23 Homo sapiens P36406 25416956
Intra
LMO2 P25791 NIF3L1 Homo sapiens Q9GZT8 25416956
Intra
LMO2 P25791 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
LMO2 P25791 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
LMO2 P25791 FHL3 Homo sapiens Q13643 25416956
Intra
LMO2 P25791 FHL3 Homo sapiens Q13643 25416956
Intra
LMO2 P25791 AGTRAP Homo sapiens Q6RW13 25416956
Intra
LMO2 P25791 CBY2 Homo sapiens Q8NA61 25416956
Intra
LMO2 P25791 CBY2 Homo sapiens Q8NA61 25416956
Intra
LMO2 P25791 MTUS2 Homo sapiens Q5JR59 25416956
Intra
LMO2 P25791 MTUS2 Homo sapiens Q5JR59 25416956
Intra
LMO2 P25791 ABI2 Homo sapiens Q9NYB9 29892012
Intra
LMO2 P25791 ABI2 Homo sapiens Q9NYB9 25416956
Intra
LMO2 P25791 GFAP Homo sapiens P14136 25416956
Intra
LMO2 P25791 GFAP Homo sapiens P14136 25416956
Intra
LMO2 P25791 BANP Homo sapiens Q8N9N5 25416956
Intra
LMO2 P25791 AIMP2 Homo sapiens Q13155 25416956
Intra
LMO2 P25791 AIMP2 Homo sapiens Q13155 25416956
Intra
LMO2 P25791 AIMP2 Homo sapiens Q13155 25416956
Intra
LMO2 P25791 HOOK1 Homo sapiens Q9UJC3 25416956
Intra
LMO2 P25791 HOOK1 Homo sapiens Q9UJC3 25416956
Intra
LMO2 P25791 MRFAP1L1 Homo sapiens Q96HT8 25416956
Intra
LMO2 P25791 IHO1 Homo sapiens Q8IYA8 25416956
Intra
LMO2 P25791 ROCK1 Homo sapiens Q13464 25416956
Intra
LMO2 P25791 ROCK1 Homo sapiens Q13464 25416956
Intra
LMO2 P25791 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
LMO2 P25791 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
LMO2 P25791 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
LMO2 P25791 C1orf94 Homo sapiens Q6P1W5 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

LMO2 抗体

製品番号 製品名 アプリケーション 反応性
HY-P81528 LMO2 Antibody (YA1273) IHC-P Human
HY-P81528A LMO2 Antibody (YA1273)(PBS only) IHC-P Human

関連疾患

Diseases Alias
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

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

生物種 Symbol 由来 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
Others LMO2 NCBI