Gene Gene information from NCBI Gene database.
Entrez ID 4008
Gene name LIM domain 7
Gene symbol LMO7
Synonyms (NCBI Gene)
FBX20FBXO20LMO7bLOMP
Chromosome 13
Chromosome location 13q22.2
Summary 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.
73
miRTarBase ID miRNA Experiments Reference
MIRT027702 hsa-miR-98-5p Microarray 19088304
MIRT031907 hsa-miR-16-5p Proteomics 18668040
MIRT732828 hsa-miR-30a-3p ImmunofluorescenceLuciferase reporter assayRNA-seqWestern blotting 33397440
MIRT732828 hsa-miR-30a-3p ImmunofluorescenceLuciferase reporter assayRNA-seqWestern blotting 33397440
MIRT1111953 hsa-miR-1252 CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
SRF Unknown 21670154
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604362 6646 ENSG00000136153
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
14
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Bladder exstrophy-epispadias-cloacal extrophy complex Uncertain significance rs768883595 RCV003389437
LMO7-related disorder Uncertain significance; Likely benign; Benign rs146636938, rs372046266, rs2544545358, rs962289502, rs2548688696, rs751906309, rs146713281, rs534973931, rs144089219, rs370670178, rs182908547 RCV003963762
RCV003412012
RCV003406024
RCV003421125
RCV003909263
RCV003973950
RCV003913898
RCV003952041
RCV003969067
RCV003966888
RCV003915851
Lung cancer Uncertain significance rs201965259 RCV005937547
Associations from Text MiningDisease 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