Gene Gene information from NCBI Gene database.
Entrez ID 338645
Gene name Leucine zipper protein 2
Gene symbol LUZP2
Synonyms (NCBI Gene)
KFSP2566PRO6246
Chromosome 11
Chromosome location 11p14.3
Summary This gene encodes a leucine zipper protein. This protein is deleted in some patients with Wilms tumor-Aniridia-Genitourinary anomalies-mental Retardation (WAGR) syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct
miRNA miRNA information provided by mirtarbase database.
236
miRTarBase ID miRNA Experiments Reference
MIRT690016 hsa-miR-4768-3p HITS-CLIP 23313552
MIRT690015 hsa-miR-4459 HITS-CLIP 23313552
MIRT690014 hsa-miR-4433a-3p HITS-CLIP 23313552
MIRT690013 hsa-miR-6849-3p HITS-CLIP 23313552
MIRT690012 hsa-miR-544b HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608178 23206 ENSG00000187398
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86TE4
Protein name Leucine zipper protein 2
Family and domains
Sequence
MKFSPAHYLLPLLPALVLSTRQDYEELEKQLKEVFKERSTILRQLTKTSRELDGIKVNLQ
SLKNDEQSAKTDVQKLLELGQKQREEMKSLQEALQNQLKETSEKAEKHQATINFLKTEVE
RKSKMIRDLQNENKSLKNKLLSGNKLCGIHAEESKKIQAQLKELRYGKKDLLFKAQQLTD
LEQKLAVAKNELEKAALDRESQMKAMKETVQLCLTSVFRDQPPPPLSLITSNPTRMLLPP
RNIASKLPDAAAKSKPQQSASGNNESSQVESTKEGNPSTTACDSQDEGRPCSMKHKESPP
SNATAETEPIPQKLQMPPCSECEVKKAPEKPLTSFEGMAAREEKIL
Sequence length 346
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
22
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ASPHYXIA NEONATORUM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 22881374, 29747637
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Carcinoma Non Small Cell Lung Associate 36056349
★☆☆☆☆
Found in Text Mining only
Infarction Middle Cerebral Artery Associate 29747637
★☆☆☆☆
Found in Text Mining only
Lymphoma Non Hodgkin Associate 32695826
★☆☆☆☆
Found in Text Mining only
Neoplasm Metastasis Associate 36056349
★☆☆☆☆
Found in Text Mining only
Neoplasms Stimulate 27221037
★☆☆☆☆
Found in Text Mining only
Neoplasms Inhibit 32695826
★☆☆☆☆
Found in Text Mining only
Obesity Associate 25772781
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Associate 36124532, 37245085
★☆☆☆☆
Found in Text Mining only