Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
376132
Gene name Gene Name - the full gene name approved by the HGNC.
Leucine rich repeat containing 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LRRC10
Synonyms (NCBI Gene) Gene synonyms aliases
HRLRRP, LRRC10A
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q15
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610846 20264 ENSG00000198812
Protein
UniProt ID 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 categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Atrial Fibrillation Atrial fibrillation N/A N/A GWAS
Dilated Cardiomyopathy Dilated Cardiomyopathy, Dominant N/A N/A ClinVar
Myopathy dilated cardiomyopathy N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Brugada Syndrome Associate 28032242
Cardiomyopathies Associate 28032242
Cardiomyopathy Dilated Associate 28032242
Death Sudden Cardiac Associate 28032242