Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10446
Gene name Gene Name - the full gene name approved by the HGNC.
Leucine rich repeat neuronal 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LRRN2
Synonyms (NCBI Gene) Gene synonyms aliases
FIGLER7, GAC1, LRANK1, LRRN5
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q32.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the leucine-rich repeat superfamily. This gene was found to be amplified and overexpressed in malignant gliomas. The encoded protein has homology with other proteins that function as cell-adhesion molecules or a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT039294 hsa-miR-671-5p CLASH 23622248
MIRT1120942 hsa-miR-1273f CLIP-seq
MIRT1120943 hsa-miR-1285 CLIP-seq
MIRT1120944 hsa-miR-1343 CLIP-seq
MIRT1120945 hsa-miR-143 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0007155 Process Cell adhesion TAS 9662332
GO:0007165 Process Signal transduction TAS 9662332
GO:0016020 Component Membrane IEA
GO:0038023 Function Signaling receptor activity IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605492 16914 ENSG00000170382
Protein
UniProt ID O75325
Protein name Leucine-rich repeat neuronal protein 2 (Glioma amplified on chromosome 1 protein) (Leucine-rich repeat neuronal protein 5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 69 129 Leucine rich repeat Repeat
PF13855 LRR_8 93 153 Leucine rich repeat Repeat
PF13855 LRR_8 117 177 Leucine rich repeat Repeat
PF13855 LRR_8 213 273 Leucine rich repeat Repeat
PF13855 LRR_8 310 371 Leucine rich repeat Repeat
PF07679 I-set 427 514 Immunoglobulin I-set domain Domain
Tissue specificity TISSUE SPECIFICITY: Overamplified in malignant gliomas.
Sequence
MRLLVAPLLLAWVAGATAAVPVVPWHVPCPPQCACQIRPWYTPRSSYREATTVDCNDLFL
TAVPPALPAGTQTLLLQSNSIVRVDQSELGYLANLTELDLSQNSFSDARDCDFHALPQLL
SLHLEENQL
TRLEDHSFAGLASLQELYLNHNQL
YRIAPRAFSGLSNLLRLHLNSNLL
RAI
DSRWFEMLPNLEILMIGGNKVDAILDMNFRPLANLRSLVLAGMNLREISDYALEGLQSLE
SLSFYDNQLARVPRRALEQVPGLKFLDLNKNPL
QRVGPGDFANMLHLKELGLNNMEELVS
IDKFALVNLPELTKLDITNNPRLSFIHPRAFHHLPQMETLMLNNNALSALHQQTVESLPN
LQEVGLHGNPI
RCDCVIRWANATGTRVRFIEPQSTLCAEPPDLQRLPVREVPFREMTDHC
LPLISPRSFPPSLQVASGESMVLHCRALAEPEPEIYWVTPAGLRLTPAHAGRRYRVYPEG
TLELRRVTAEEAGLYTCVAQNLVGADTKTVSVVV
GRALLQPGRDEGQGLELRVQETHPYH
ILLSWVTPPNTVSTNLTWSSASSLRGQGATALARLPRGTHSYNITRLLQATEYWACLQVA
FADAHTQLACVWARTKEATSCHRALGDRPGLIAILALAVLLLAAGLAAHLGTGQPRKGVG
GRRPLPPAWAFWGWSAPSVRVVSAPLVLPWNPGRKLPRSSEGETLLPPLSQNS
Sequence length 713
Interactions View interactions
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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
Breast Cancer Breast cancer subtype (triple negative vs luminal A-like) N/A N/A GWAS
Diabetes Type 2 diabetes or prostate cancer (pleiotropy), Type 2 diabetes N/A N/A GWAS
Prostate cancer Prostate cancer (late onset), Prostate cancer N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 34941039