Gene Gene information from NCBI Gene database.
Entrez ID 376132
Gene name Leucine rich repeat containing 10
Gene symbol LRRC10
Synonyms (NCBI Gene)
HRLRRPLRRC10A
Chromosome 12
Chromosome location 12q15
miRNA miRNA information provided by mirtarbase database.
120
miRTarBase ID miRNA Experiments Reference
MIRT710257 hsa-miR-214-5p HITS-CLIP 19536157
MIRT710256 hsa-miR-6811-3p HITS-CLIP 19536157
MIRT710255 hsa-miR-6847-3p HITS-CLIP 19536157
MIRT710254 hsa-miR-4284 HITS-CLIP 19536157
MIRT710253 hsa-miR-24-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IBA
GO:0003779 Function Actin binding IEA
GO:0005634 Component Nucleus IEA
GO:0005739 Component Mitochondrion IEA
GO:0005856 Component Cytoskeleton IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610846 20264 ENSG00000198812
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5BKY1
Protein name Leucine-rich repeat-containing protein 10
Protein function May play important roles in cardiac development and/or cardiac function.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 52 110 Leucine rich repeat Repeat
PF13855 LRR_8 75 131 Leucine rich repeat Repeat
Sequence
MGNTIRALVAFIPADRCQNYVVRDLREMPLDKMVDLSGSQLRRFPLHVCSFRELVKLYLS
DNHLNSLPPELGQL
QNLQILALDFNNFKALPQVVCTLKQLCILYLGNNKLCDLPSELSLL
QNLRTLWIEAN
CLTQLPDVVCELSLLKTLHAGSNALRLLPGQLRRLQELRTIWLSGNRLT
DFPTVLLHMPFLEVIDVDWNSIRYFPSLAHLSSLKLVIYDHNPCRNAPKVAKGVRRVGRW
AEETPEPDPRKARRYALVREESQELQAPVPLLPPTNS
Sequence length 277
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
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
ATRIAL FIBRILLATION CTD, Disgenet, GWAS catalog
CTD, Disgenet, GWAS catalog
CTD, Disgenet, GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FLUTTER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, DILATED Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGESTIVE HEART FAILURE Disgenet
★★☆☆☆
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
Atrial Fibrillation Atrial Fibrillation CTD_human_DG 30061737
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Brugada Syndrome Brugada syndrome Pubtator 28032242 Associate
★☆☆☆☆
Found in Text Mining only
Brugada Syndrome (disorder) Brugada Syndrome BEFREE 28032242
★☆☆☆☆
Found in Text Mining only
Cardiomyopathies Cardiomyopathy BEFREE 28032242
★☆☆☆☆
Found in Text Mining only
Cardiomyopathies Cardiomyopathy Pubtator 28032242 Associate
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy Dilated Dilated cardiomyopathy Pubtator 28032242 Associate
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy, Dilated Cardiomyopathy BEFREE 28032242, 29431102
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cardiomyopathy, Familial Idiopathic Cardiomyopathy BEFREE 26017719, 29431102
★☆☆☆☆
Found in Text Mining only
Paroxysmal atrial fibrillation Paroxysmal atrial fibrillation CTD_human_DG 30061737
★☆☆☆☆
Found in Text Mining only