Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4008
Gene name Gene Name - the full gene name approved by the HGNC.
LIM domain 7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LMO7
Synonyms (NCBI Gene) Gene synonyms aliases
FBX20, FBXO20, LMO7b, LOMP
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q22.2
Summary Summary of gene provided in NCBI Entrez Gene.
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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT027702 hsa-miR-98-5p Microarray 19088304
MIRT031907 hsa-miR-16-5p Proteomics 18668040
MIRT732828 hsa-miR-30a-3p Immunofluorescence, Luciferase reporter assay, RNA-seq, Western blotting 33397440
MIRT732828 hsa-miR-30a-3p Immunofluorescence, Luciferase reporter assay, RNA-seq, Western blotting 33397440
MIRT1111953 hsa-miR-1252 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
SRF Unknown 21670154
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000151 Component Ubiquitin ligase complex NAS 10531035
GO:0004842 Function Ubiquitin-protein transferase activity NAS 10531035
GO:0005515 Function Protein binding IPI 15161933, 30429017, 35271311
GO:0005634 Component Nucleus IDA 17067998
GO:0005634 Component Nucleus TAS 9826547
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604362 6646 ENSG00000136153
Protein
UniProt ID Q8WWI1
Protein name LIM domain only protein 7 (LMO-7) (F-box only protein 20) (LOMP)
PDB 2EAQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00307 CH 71 179 Calponin homology (CH) domain Domain
PF15949 DUF4757 294 375 Domain of unknown function (DUF4757) Family
PF15949 DUF4757 635 787 Domain of unknown function (DUF4757) Family
PF00595 PDZ 1043 1119 PDZ domain Domain
PF00412 LIM 1614 1676 LIM domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Isoform 2 and isoform 4 are predominantly expressed in brain. {ECO:0000269|PubMed:11935316, ECO:0000269|PubMed:9826547}.
Sequence
MKKIRICHIFTFYSWMSYDVLFQRTELGALEIWRQLICAHVCICVGWLYLRDRVCSKKDI
ILRTEQNSGRTILIKAVTEKNFETKDFRASLENGVLLCDLINKLKPGVIKKINRLSTPIA
GLDNINVFLKACEQIGLKEAQLFHPGDLQDLSNRVTVKQEETDRRVKNVLITLYWLGRK
A
QSNPYYNGPHLNLKAFENLLGQALTKALEDSSFLKRSGRDSGYGDIWCPERGEFLAPPRH
HKREDSFESLDSLGSRSLTSCSSDITLRGGREGFESDTDSEFTFKMQDYNKDDMSYRRIS
AVEPKTALPFNRFLPNKSRQPSYVPAPLRKKKPDKHEDNRRSWASPVYTEADGTFSSNQR
RIWGTNVENWPTVQG
TSKSSCYLEEEKAKTRSIPNIVKDDLYVRKLSPVMPNPGNAFDQF
LPKCWTPEDVNWKRIKRETYKPWYKEFQGFSQFLLLQALQTYSDDILSSETHTKIDPTSG
PRLITRRKNLSYAPGYRRDDLEMAALDPDLENDDFFVRKTGVFHANPYVLRAFEDFRKFS
EQDDSVERDIILQCREGELVLPDLEKDDMIVRRIPAQKKEVPLSGAPDRYHPVPFPEPWT
LPPEIQAKFLCVFERTCPSKEKSNSCRILVPSYRQKKDDMLTRKIQSWKLGTTVPPISFT
PGPCSEADLKRWEAIREASRLRHKKRLMVERLFQKIYGENGSKSMSDVSAEDVQNLRQLR
YEEMQKIKSQLKEQDQKWQDDLAKWKDRRKSYTSDLQKKKEEREEIEKQALEKSKRSSKT
FKEMLQD
RESQNQKSTVPSRRRMYSFDDVLEEGKRPPTMTVSEASYQSERVEEKGATYPS
EIPKEDSTTFAKREDRVTTEIQLPSQSPVEEQSPASLSSLRSRSTQMESTRVSASLPRSY
RKTDTVRLTSVVTPRPFGSQTRGISSLPRSYTMDDAWKYNGDVEDIKRTPNNVVSTPAPS
PDASQLASSLSSQKEVAATEEDVTRLPSPTSPFSSLSQDQAATSKATLSSTSGLDLMSES
GEGEISPQREVSRSQDQFSDMRISINQTPGKSLDFGFTIKWDIPGIFVASVEAGSPAEFS
QLQVDDEIIAINNTKFSYNDSKEWEEAMAKAQETGHLVM
DVRRYGKAGSPETKWIDATSG
IYNSEKSSNLSVTTDFSESLQSSNIESKEINGIHDESNAFESKASESISLKNLKRRSQFF
EQGSSDSVVPDLPVPTISAPSRWVWDQEEERKRQERWQKEQDRLLQEKYQREQEKLREEW
QRAKQEAERENSKYLDEELMVLSSNSMSLTTREPSLATWEATWSEGSKSSDREGTRAGEE
ERRQPQEEVVHEDQGKKPQDQLVIERERKWEQQLQEEQEQKRLQAEAEEQKRPAEEQKRQ
AEIERETSVRIYQYRRPVDSYDIPKTEEASSGFLPGDRNKSRSTTELDDYSTNKNGNNKY
LDQIGNMTSSQRRSKKEQVPSGAELERQQILQEMRKRTPLHNDNSWIRQRSASVNKEPVS
LPGIMRRGESLDNLDSPRSNSWRQPPWLNQPTGFYASSSVQDFSRPPPQLVSTSNRAYMR
NPSSSVPPPSAGSVKTSTTGVATTQSPTPRSHSPSASQSGSQLRNRSVSGKRICSYCNNI
LGKGAAMIIESLGLCYHLHCFKCVACECDLGGSSSGAEVRIRNHQLYCNDCYLRFK
SGRP
TAM
Sequence length 1683
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
Astrocytoma Astrocytoma N/A N/A GWAS
Glaucoma Glaucoma N/A N/A GWAS
Glioblastoma Glioblastoma N/A N/A GWAS
Hemorrhoids Hemorrhoids N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Bardet Biedl Syndrome Associate 28800606
Breast Neoplasms Associate 21670154
Carcinoma Pancreatic Ductal Stimulate 35046938
Ciliopathies Associate 28800606
Dry Eye Syndromes Associate 30312344
Encephalitis Tick Borne Associate 31122248
Glaucoma Associate 29449654
Glaucoma Open Angle Associate 29449654
LEOPARD Syndrome Associate 21179469
Lung Neoplasms Associate 28026121