LMO1


Summary: This locus encodes a transcriptional regulator that contains two cysteine-rich LIM domains but lacks a DNA-binding domain. LIM domains may play a role in protein interactions; thus the encoded protein may regulate transcription by competitively binding to specific DNA-binding transcription factors. Alterations at this locus have been associated with acute lymphoblastic T-cell leukemia. Chromosomal rearrangements have been observed between this locus and at least two loci, the delta subunit of the T-cell antigen receptor gene and the LIM domain binding 1 gene. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2012].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:186921
PHARMGKB IDPA30407
Map Location11p15.4

Gene Categories:

CLINICALLY ACTIONABLE

GO terms in LMO1


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Term Type
Evidence Type
GO Term ID
GO Des.
BP IEA GO:0000122 negative regulation of transcription by RNA polymerase II
BP IMP GO:0045944 positive regulation of transcription by RNA polymerase II
BP IEA GO:0046013 regulation of T cell homeostatic proliferation
BP TAS GO:1902036 regulation of hematopoietic stem cell differentiation
CC ISS GO:0005634 nucleus
CC TAS GO:0005654 nucleoplasm
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Gene expression in normal tissue: LMO1

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in LMO1


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Database
Pathway ID
Pathway Des.
reactome R-HSA-212436 Generic Transcription Pathway
reactome R-HSA-73857 RNA Polymerase II Transcription
reactome R-HSA-74160 Gene expression (Transcription)
reactome R-HSA-8878171 Transcriptional regulation by RUNX1
reactome R-HSA-8939236 RUNX1 regulates transcription of genes involved in differentiation of HSCs
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD219 Bax channel blocker 3
iGMDRD193 Fqi1 3
iGMDRD446 LY 2183240 3
iGMDRD435 BI-2536 6
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in LMO1

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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