Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4004
Gene name Gene Name - the full gene name approved by the HGNC.
LIM domain only 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LMO1
Synonyms (NCBI Gene) Gene synonyms aliases
RBTN1, RHOM1, TTG1
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.4
Summary Summary of gene provided in NCBI Entrez Gene.
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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1111866 hsa-miR-181a CLIP-seq
MIRT1111867 hsa-miR-181b CLIP-seq
MIRT1111868 hsa-miR-181c CLIP-seq
MIRT1111869 hsa-miR-181d CLIP-seq
MIRT1111870 hsa-miR-3163 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
ARX Unknown 23771350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0003713 Function Transcription coactivator activity IBA
GO:0005515 Function Protein binding IPI 21516116, 25416956, 27107012, 31515488, 32296183, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
186921 6641 ENSG00000166407
Protein
UniProt ID P25800
Protein name Rhombotin-1 (Cysteine-rich protein TTG-1) (LIM domain only protein 1) (LMO-1) (T-cell translocation protein 1)
Protein function May be involved in gene regulation within neural lineage cells potentially by direct DNA binding or by binding to other transcription factors.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00412 LIM 24 82 LIM domain Domain
PF00412 LIM 88 146 LIM domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed mainly in the central nervous. Low level of expression in other tissues including thymus. {ECO:0000269|PubMed:2052354}.
Sequence
Sequence length 156
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RUNX1 regulates transcription of genes involved in differentiation of HSCs
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes N/A N/A GWAS
Neuroblastoma Neuroblastoma N/A N/A GWAS
Restless Legs Syndrome Restless legs syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adrenal Gland Neoplasms Associate 27009839
Ataxia Telangiectasia Associate 12086890
Breast Neoplasms Associate 40076569
Carcinogenesis Associate 21124317, 33870932
Colorectal Neoplasms Associate 24845030
Leukemia Associate 7957052
Lung Neoplasms Stimulate 33870932
Neoplasms Stimulate 24845030
Neoplasms Associate 28260788, 29695398, 30194082, 33870932
Neuroblastoma Associate 21124317, 21436895, 23222812, 25312269, 26030754, 27009839, 29695398, 30194082, 31819055, 33870932