Gene Gene information from NCBI Gene database.
Entrez ID 55692
Gene name LUC7 like
Gene symbol LUC7L
Synonyms (NCBI Gene)
LUC7B1Luc7SR+89hLuc7B1
Chromosome 16
Chromosome location 16p13.3
Summary The LUC7L gene may represent a mammalian heterochromatic gene, encoding a putative RNA-binding protein similar to the yeast Luc7p subunit of the U1 snRNP splicing complex that is normally required for 5-prime splice site selection (Tufarelli et al., 2001
miRNA miRNA information provided by mirtarbase database.
59
miRTarBase ID miRNA Experiments Reference
MIRT028863 hsa-miR-26b-5p Microarray 19088304
MIRT031469 hsa-miR-16-5p Proteomics 18668040
MIRT556403 hsa-miR-4695-5p PAR-CLIP 21572407
MIRT556402 hsa-miR-10b-3p PAR-CLIP 21572407
MIRT556401 hsa-miR-4768-3p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0003729 Function MRNA binding IBA
GO:0003729 Function MRNA binding IEA
GO:0005515 Function Protein binding IPI 22365833, 23602568, 32296183, 32707033, 32814053, 33961781
GO:0005685 Component U1 snRNP IBA
GO:0005685 Component U1 snRNP IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607782 6723 ENSG00000007392
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NQ29
Protein name Putative RNA-binding protein Luc7-like 1 (Putative SR protein LUC7B1) (SR+89)
Protein function May bind to RNA via its Arg/Ser-rich domain.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03194 LUC7 5 250 LUC7 N_terminus Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:11170747}.
Sequence
Sequence length 371
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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
ANEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONNECTIVE TISSUE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
FAMILIAL HEMOLYTIC ANEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
alpha-Thalassemia alpha Thalassemia BEFREE 12730694
★☆☆☆☆
Found in Text Mining only
alpha^+^ Thalassemia alpha Thalassemia BEFREE 12730694
★☆☆☆☆
Found in Text Mining only
Anemia Anemia BEFREE 12730694
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Prostatic Neoplasms Prostatic neoplasm Pubtator 37143720 Associate
★☆☆☆☆
Found in Text Mining only
Thalassemia Thalassemia Pubtator 28381876 Associate
★☆☆☆☆
Found in Text Mining only