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Gene Gene information from NCBI Gene database.
Entrez ID 84859
Gene name Leucine rich repeats and calponin homology domain containing 3
Gene symbol LRCH3
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3q29
miRNA miRNA information provided by mirtarbase database.
88 Show/Hide all (88)
miRTarBase ID miRNA Experiments Reference
MIRT044498 hsa-miR-320a CLASH 23622248
MIRT643498 hsa-miR-4639-3p HITS-CLIP 23824327
MIRT661869 hsa-miR-383-3p HITS-CLIP 23824327
MIRT643497 hsa-miR-3917 HITS-CLIP 23824327
MIRT643496 hsa-miR-3615 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6 Show/Hide all (6)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 24255178, 25416956, 29467281, 32296183, 33961781, 35271311
GO:0005737 Component Cytoplasm IC 29467281
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IBA
GO:0005829 Component Cytosol IDA
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.
Q96II8
Protein name DISP complex protein LRCH3 (Leucine-rich repeat and calponin homology domain-containing protein 3)
Protein function As part of the DISP complex, may regulate the association of septins with actin and thereby regulate the actin cytoskeleton.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00307 CH 652 → 766 Calponin homology (CH) domain Domain
PF13855 LRR_8 151 → 208 Leucine rich repeat Repeat
PF13855 LRR_8 84 → 140 Leucine rich repeat Repeat
Sequence
MAAAGLVAVAAAAEYSGTVASGGNLPGVHCGPSSGAGPGFGPGSWSRSLDRALEEAAVTG
VLSLSGRKLREFPRGAANHDLTDTTRADLSRNRLSEIPIEACHFVSLENLNLYQNCIRYI
PEAILNLQALTFLNISRNQL
STLPVHLCNLPLKVLIASNNKLVSLPEEIGHLRHLMELDV
SCNEIQTIPSQIGNLEALRDLNVRRNHL
VHLPEELAELPLIRLDFSCNKITTIPVCYRNL
RHLQTITLDNNPLQSPPAQICIKGKVHIFKYLNIQACKIAPDLPDYDRRPLGFGSCHEEL
YSSRPYGALDSGFNSVDSGDKRWSGNEPTDEFSDLPLRVAEITKEQRLRRESQYQENRGS
LVVTNGGVEHDLDQIDYIDSCTAEEEEAEVRQPKGPDPDSLSSQFMAYIEQRRISHEGSP
VKPVAIREFQKTEDMRRYLHQNRVPAEPSSLLSLSASHNQLSHTDLELHQRREQLVERTR
REAQLAALQYEEEKIRTKQIQRDAVLDFVKQKASQSPQKQHPLLDGVDGECPFPSRRSQH
TDDSALCMSLSGLNQVGCAATLPHSSAFTPLKSDDRPNALLSSPATETVHHSPAYSFPAA
IQRNQPQRPESFLFRAGVRAETNKGHASPLPPSAAPTTDSTDSITGQNSRQREEELELID
QLRKHIEYRLKVSLPCDLGAALTDGVVLCHLANHVRPRSVPSIHVPSPAVPKLTMAKCRR
NVENFLEACRKIGVPQEQLCLPLHILEEKGLSQVAVTVQALLELAP
PKQQQHQLSAV
Sequence length 777
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
LRCH3-related disorder Uncertain significance; Likely benign; Benign ClinVar —
★★★★★
★★☆☆☆
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
Head and Neck Neoplasms Head and neck neoplasm Pubtator 35725478 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Melanoma Melanoma Pubtator 35871080 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only