Gene Gene information from NCBI Gene database.
Entrez ID 80059
Gene name Leucine rich repeat transmembrane neuronal 4
Gene symbol LRRTM4
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2p12
miRNA miRNA information provided by mirtarbase database.
46
miRTarBase ID miRNA Experiments Reference
MIRT527180 hsa-miR-205-5p PAR-CLIP 22012620
MIRT527179 hsa-miR-1297 PAR-CLIP 22012620
MIRT527178 hsa-miR-26a-5p PAR-CLIP 22012620
MIRT527177 hsa-miR-26b-5p PAR-CLIP 22012620
MIRT527176 hsa-miR-4465 PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0038023 Function Signaling receptor activity IBA
GO:0045202 Component Synapse IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610870 19411 ENSG00000176204
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86VH4
Protein name Leucine-rich repeat transmembrane neuronal protein 4
Protein function May play a role in the development and maintenance of the vertebrate nervous system. Exhibits strong synaptogenic activity, restricted to excitatory presynaptic differentiation (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 64 121 Leucine rich repeat Repeat
PF13855 LRR_8 109 169 Leucine rich repeat Repeat
PF13855 LRR_8 157 217 Leucine rich repeat Repeat
PF13855 LRR_8 229 289 Leucine rich repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed in neuronal tissues. {ECO:0000269|PubMed:12676565}.
Sequence
MGFHLITQLKGMSVVLVLLPTLLLVMLTGAQRACPKNCRCDGKIVYCESHAFADIPENIS
GGSQGLSLRFNSIQKLKSNQFAGLNQLIWLYLDHNYISSVDEDAFQGIRRLKELILSSNK
I
TYLHNKTFHPVPNLRNLDLSYNKLQTLQSEQFKGLRKLIILHLRSNSLKTVPIRVFQDC
RNLDFLDLGYNRLRSLSRNAFAGLLKLKELHLEHNQF
SKINFAHFPRLFNLRSIYLQWNR
IRSISQGLTWTWSSLHNLDLSGNDIQGIEPGTFKCLPNLQKLNLDSNKL
TNISQETVNAW
ISLISITLSGNMWECSRSICPLFYWLKNFKGNKESTMICAGPKHIQGEKVSDAVETYNIC
SEVQVVNTERSHLVPQTPQKPLIIPRPTIFKPDVTQSTFETPSPSPGFQIPGAEQEYEHV
SFHKIIAGSVALFLSVAMILLVIYVSWKRYPASMKQLQQHSLMKRRRKKARESERQMNSP
LQEYYVDYKPTNSETMDISVNGSGPCTYTISGSRECEMPHHMKPLPYYSYDQPVIGYCQA
HQPLHVTKGYETVSPEQDESPGLELGRDHSFIATIARSAAPAIYLERIAN
Sequence length 590
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Neurexins and neuroligins
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
LRRTM4-related disorder Likely benign rs76327576, rs757583021 RCV003897339
RCV003944489
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Anxiety Associate 34684344
Attention Deficit Disorder with Hyperactivity Associate 35052406
Autism Spectrum Disorder Associate 35052406
Autistic Disorder Associate 35052406
Bipolar Disorder Associate 31854516
Cerebrovascular Disorders Associate 35994481
Depressive Disorder Associate 34684344
Tourette Syndrome Associate 35052406