Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
347731
Gene name Gene Name - the full gene name approved by the HGNC.
Leucine rich repeat transmembrane neuronal 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LRRTM3
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q21.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1121097 hsa-miR-1265 CLIP-seq
MIRT1121098 hsa-miR-1298 CLIP-seq
MIRT1121099 hsa-miR-186 CLIP-seq
MIRT1121100 hsa-miR-3163 CLIP-seq
MIRT1121101 hsa-miR-3622b-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005615 Component Extracellular space IBA 21873635
GO:0031012 Component Extracellular matrix IBA 21873635
GO:0051965 Process Positive regulation of synapse assembly IEA
GO:0098978 Component Glutamatergic synapse IDA 26776509
GO:0098978 Component Glutamatergic synapse IMP 26776509
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610869 19410 ENSG00000198739
Protein
UniProt ID Q86VH5
Protein name Leucine-rich repeat transmembrane neuronal protein 3
Protein function Exhibits a limited synaptogenic activity in vitro, restricted to excitatory presynaptic differentiation (By similarity). May play a role in the development and maintenance of the vertebrate nervous system.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 87 145 Leucine rich repeat Repeat
PF13855 LRR_8 133 193 Leucine rich repeat Repeat
PF13855 LRR_8 157 217 Leucine rich repeat Repeat
PF13855 LRR_8 181 241 Leucine rich repeat Repeat
PF13855 LRR_8 229 290 Leucine rich repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed in neuronal tissues. {ECO:0000269|PubMed:12676565}.
Sequence
MGFNVIRLLSGSAVALVIAPTVLLTMLSSAERGCPKGCRCEGKMVYCESQKLQEIPSSIS
AGCLGLSLRYNSLQKLKYNQFKGLNQLTWLYLDHNHISNIDENAFNGIRRLKELILSSNR
ISYFLNNTFRPV
TNLRNLDLSYNQLHSLGSEQFRGLRKLLSLHLRSNSLRTIPVRIFQDC
RNLELLDLGYNRIRSLARNVFAGMIRLKELHLEHNQFSKLNLALFPRLVSLQNLYLQWNK
I
SVIGQTMSWTWSSLQRLDLSGNEIEAFSGPSVFQCVPNLQRLNLDSNKL
TFIGQEILDS
WISLNDISLAGNIWECSRNICSLVNWLKSFKGLRENTIICASPKELQGVNVIDAVKNYSI
CGKSTTERFDLARALPKPTFKPKLPRPKHESKPPLPPTVGATEPGPETDADAEHISFHKI
IAGSVALFLSVLVILLVIYVSWKRYPASMKQLQQRSLMRRHRKKKRQSLKQMTPSTQEFY
VDYKPTNTETSEMLLNGTGPCTYNKSGSRECEIPLSMNVSTFLAYDQPTISYCGVHHELL
SHKSFETNAQEDTMETHLETELDLSTITTAGRISDHKQQLA
Sequence length 581
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Neurexins and neuroligins
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism spectrum disorder Autism Spectrum Disorders rs724159978, rs75184679, rs119103221, rs9332964, rs121912562, rs1594344233, rs727504317, rs111033204, rs1801086, rs587784464, rs724159948, rs764659822, rs794727977, rs796052733, rs796052728
View all (51 more)
20678249
Tremor Essential Tremor rs387907274, rs763485258, rs551348450 27797806
Unknown
Disease term Disease name Evidence References Source
Ulcerative colitis Ulcerative colitis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 18076107, 19105203, 22393166