Gene Gene information from NCBI Gene database.
Entrez ID 55222
Gene name Leucine rich repeat containing 20
Gene symbol LRRC20
Synonyms (NCBI Gene)
-
Chromosome 10
Chromosome location 10q22.1
miRNA miRNA information provided by mirtarbase database.
248
miRTarBase ID miRNA Experiments Reference
MIRT030080 hsa-miR-26b-5p Microarray 19088304
MIRT042109 hsa-miR-484 CLASH 23622248
MIRT722901 hsa-miR-6768-3p HITS-CLIP 19536157
MIRT722900 hsa-miR-22-3p HITS-CLIP 19536157
MIRT722899 hsa-miR-3127-3p HITS-CLIP 19536157
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:0005515 Function Protein binding IPI 25416956, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TCA0
Protein name Leucine-rich repeat-containing protein 20
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 51 109 Leucine rich repeat Repeat
PF13855 LRR_8 97 156 Leucine rich repeat Repeat
Sequence
MLKKMGEAVARVARKVNETVESGSDTLDLAECKLVSFPIGIYKVLRNVSGQIHLITLANN
ELKSLTSKFMTTFSQLRELHLEGNFLHRLPSEVSAL
QHLKAIDLSRNQFQDFPEQLTALP
ALETINLEENEIVDVPVEKLAAMPALRSINLRFNPL
NAEVRVIAPPLIKFDMLMSPEGAR
APLP
Sequence length 184
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBSESSIVE-COMPULSIVE DISORDER 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
Lupus Erythematosus Systemic Systemic lupus erythematosus Pubtator 20659327 Associate
★☆☆☆☆
Found in Text Mining only