Gene data
LMO7- Name
- LIM domain 7
- Type
- protein-coding
- Position
- 75,620,434–75,859,870 (+)
- Aliases
- FBX20, FBXO20, LMO7b, LOMP
- Ensembl
- ENSG00000136153
- RefSeq RNA
- NM_001306080.2, NM_001330583.1, NM_001366632.2, NM_001366633.2, NM_001366634.2
- RefSeq protein
- NP_001293009.1, NP_001317512.1, NP_001353561.1, NP_001353562.1, NP_001353563.1
This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain, and may be involved in protein-protein interactions. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, however, the full-length nature of some variants is not known. [provided by RefSeq, Jan 2009].
Gene Ontology
Biological process
Molecular function
Pathways
Adherens junction - Homo sapiens (human)Adaptive Immune SystemDiseaseImmune SystemMetabolism of proteinsDiseases of signal transduction by growth factor receptors and second messengersPost-translational protein modificationNeddylationSignaling by ALK in cancerSignaling by ALK fusions and activated point mutants
via MyGene.info
Gene · Ensembl
LIM domain 7
- Symbol
- LMO7
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 13:75,620,434-75,859,870
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 83924
- genetic association
- type-1 diabetes
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/4008
- genomic end
- 76434004
- genomic start
- 76194570
- chromosome
- human chromosome 13
- cytogenetic location
- 13q22.2
via Wikidata · CC0