Gene Gene information from NCBI Gene database.
Entrez ID 79782
Gene name Leucine rich repeat containing 31
Gene symbol LRRC31
Synonyms (NCBI Gene)
HEL-S-293
Chromosome 3
Chromosome location 3q26.2
miRNA miRNA information provided by mirtarbase database.
42
miRTarBase ID miRNA Experiments Reference
MIRT707462 hsa-miR-5580-3p HITS-CLIP 21572407
MIRT551418 hsa-miR-5011-5p HITS-CLIP 21572407
MIRT551417 hsa-miR-656-3p HITS-CLIP 21572407
MIRT551416 hsa-miR-511-3p HITS-CLIP 21572407
MIRT551415 hsa-miR-6504-3p HITS-CLIP 21572407
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620925 26261 ENSG00000114248
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UY01
Protein name Leucine-rich repeat-containing protein 31
Family and domains
Sequence
MSQTRKKTSSEGETKPQTSTVNKFLRGSNAESRKEDNDLKTSDSQPSDWIQKTATSETAK
PLSSEMEWRSSMEKNEHFLQKLGKKAVNKCLDLNNCGLTTADMKEMVALLPFLPDLEELD
ISWNGFVGGTLLSITQQMHLVSKLKILRLGSCRLTTDDVQALGEAFEMIPELEELNLSWN
SKVGGNLPLILQKFQKGSKIQMIELVDCSLTSEDGTFLGQLLPMLQSLEVLDLSINRDIV
GSLNSIAQGLKSTSNLKVLKLHSCGLSQKSVKILDAAFRYLGELRKLDLSCNKDLGGGFE
DSPAQLVMLKHLQVLDLHQCSLTADDVMSLTQVIPLLSNLQELDLSANKKMGSSSENLLS
RLRFLPALKSLVINNCALESETFTALAEASVHLSALEVFNLSWNKCVGGNLKLLLETLKL
SMSLQVLRLSSCSLVTEDVALLASVIQTGHLAKLQKLDLSYNDSICDAGWTMFCQNVRFL
KELIELDISLRPSNFRDCGQWFRHLLYAVTKLPQITEIGMKRWILPASQEEELECFDQDK
KRSIHFDHGGFQ
Sequence length 552
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
URINARY BLADDER CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
UTERINE FIBROID 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
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 28413214 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 37487414 Associate
★☆☆☆☆
Found in Text Mining only
Central Nervous System Neoplasms Central Nervous System Neoplasms GWASCAT_DG 24908248
★☆☆☆☆
Found in Text Mining only
Central Nervous System Neoplasms Central Nervous System Neoplasms GWASDB_DG 24908248
★☆☆☆☆
Found in Text Mining only
Coronary Disease Coronary artery disease Pubtator 24349443 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Diabetes mellitus, type 2 Pubtator 24349443, 26720590, 32296102 Associate
★☆☆☆☆
Found in Text Mining only
Eosinophilia Eosinophilia BEFREE 26462420
★☆☆☆☆
Found in Text Mining only
Eosinophilia Eosinophilia Pubtator 26462420 Associate
★☆☆☆☆
Found in Text Mining only
Eosinophilic esophagitis Eosinophilia BEFREE 26462420
★☆☆☆☆
Found in Text Mining only
Eosinophilic Esophagitis Eosinophilia Pubtator 26462420 Stimulate
★☆☆☆☆
Found in Text Mining only