Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55885
Gene name Gene Name - the full gene name approved by the HGNC.
LIM domain only 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LMO3
Synonyms (NCBI Gene) Gene synonyms aliases
RBTN3, RBTNL2, RHOM3, Rhom-3
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12p12.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the rhombotin family of cysteine-rich LIM domain oncogenes. This gene is predominantly expressed in the brain. Related family members, LMO1 and LMO2 on chromosome 11, have been reported to be involved in chromos
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017853 hsa-miR-335-5p Microarray 18185580
MIRT1111879 hsa-miR-1226 CLIP-seq
MIRT1111880 hsa-miR-1236 CLIP-seq
MIRT1111881 hsa-miR-1305 CLIP-seq
MIRT1111882 hsa-miR-141 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
NKX2-1 Unknown 23322301
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003713 Function Transcription coactivator activity IBA
GO:0005515 Function Protein binding IPI 16189514, 20211142, 25416956, 27107012, 31515488, 32296183, 32814053, 33961781
GO:0005634 Component Nucleus IBA
GO:0005737 Component Cytoplasm IDA 23823477
GO:0035360 Process Positive regulation of peroxisome proliferator activated receptor signaling pathway IDA 23823477
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
180386 6643 ENSG00000048540
Protein
UniProt ID Q8TAP4
Protein name LIM domain only protein 3 (LMO-3) (Neuronal-specific transcription factor DAT1) (Rhombotin-3)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00412 LIM 13 71 LIM domain Domain
PF00412 LIM 77 134 LIM domain Domain
Sequence
Sequence length 145
Interactions View interactions
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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 Mild age-related type 2 diabetes N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Tourette Syndrome Tourette syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 35854639
Adenocarcinoma of Lung Associate 23322301
Adenoma Oxyphilic Associate 28986304
Carcinogenesis Associate 33980985
Carcinoma Basal Cell Inhibit 38366633
Carcinoma Hepatocellular Associate 30219064
Carcinoma Pancreatic Ductal Associate 38366633
Carcinoma Squamous Cell Associate 22011669
Carcinoma Squamous Cell Inhibit 38366633
Endometrial Neoplasms Associate 36581816