Gene Gene information from NCBI Gene database.
Entrez ID 145581
Gene name Leucine rich repeat and fibronectin type III domain containing 5
Gene symbol LRFN5
Synonyms (NCBI Gene)
C14orf146FIGLER8SALM5
Chromosome 14
Chromosome location 14q21.1
Summary This gene encodes a protein that belongs to the leucine-rich repeat and fibronectin type III domain-containing family of proteins. A similar protein in mouse, a glycosylated transmembrane protein, is thought to function in presynaptic differentiation. [pr
miRNA miRNA information provided by mirtarbase database.
33
miRTarBase ID miRNA Experiments Reference
MIRT1117556 hsa-miR-4282 CLIP-seq
MIRT1117557 hsa-miR-4717-5p CLIP-seq
MIRT2033201 hsa-miR-106a CLIP-seq
MIRT2033202 hsa-miR-106b CLIP-seq
MIRT2033203 hsa-miR-1193 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 27152329
GO:0009986 Component Cell surface IBA
GO:0009986 Component Cell surface IEA
GO:0016020 Component Membrane IEA
GO:0043031 Process Negative regulation of macrophage activation IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612811 20360 ENSG00000165379
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96NI6
Protein name Leucine-rich repeat and fibronectin type-III domain-containing protein 5
Protein function Cell adhesion molecule that mediates homophilic cell-cell adhesion in a Ca(2+)-independent manner. Promotes neurite outgrowth in hippocampal neurons.
PDB 5XNP , 5XNQ , 5XWS , 5XWT
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13306 LRR_5 56 213 BspA type Leucine rich repeat region (6 copies) Repeat
PF07679 I-set 287 374 Immunoglobulin I-set domain Domain
Sequence
MEKILFYLFLIGIAVKAQICPKRCVCQILSPNLATLCAKKGLLFVPPNIDRRTVELRLAD
NFVTNIKRKDFANMTSLVDLTLSRNTISFITPHAFADLRNLRALHLNSNRLTKITNDMFS
GLSNLHHLILNNNQLTLISSTAFDDVFALEELDLSYNNLETIPWDAVEKMVSLHTLSLDH
NMIDNIPKGTFSHLHKMTRLDVTSNKLQKLPPD
PLFQRAQVLATSGIISPSTFALSFGGN
PLHCNCELLWLRRLSREDDLETCASPPLLTGRYFWSIPEEEFLCEPPLITRHTHEMRVLE
GQRATLRCKARGDPEPAIHWISPEGKLISNATRSLVYDNGTLDILITTVKDTGAFTCIAS
NPAGEATQIVDLHI
IKLPHLLNSTNHIHEPDPGSSDISTSTKSGSNTSSSNGDTKLSQDK
IVVAEATSSTALLKFNFQRNIPGIRMFQIQYNGTYDDTLVYRMIPPTSKTFLVNNLAAGT
MYDLCVLAIYDDGITSLTATRVVGCIQFTTEQDYVRCHFMQSQFLGGTMIIIIGGIIVAS
VLVFIIILMIRYKVCNNNGQHKVTKVSNVYSQTNGAQIQGCSVTLPQSVSKQAVGHEENA
QCCKATSDNVIQSSETCSSQDSSTTTSALPPSWTSSTSVSQKQKRKTGTKPSTEPQNEAV
TNVESQNTNRNNSTALQLASRPPDSVTEGPTSKRAHIKPNALLTNVDQIVQETQRLELI
Sequence length 719
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
13
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
EBV-positive nodal T- and NK-cell lymphoma Likely benign rs2502391007 RCV004557780
LRFN5-related disorder Benign; Likely benign rs1886164, rs6572117, rs150248310, rs376202754, rs117966123, rs112647558, rs34676437, rs372315722, rs142220815, rs116217484, rs151006633, rs1448844632 RCV003929733
RCV003984611
RCV003943904
RCV003947410
RCV003932322
RCV003949314
RCV003956882
RCV003946959
RCV003954536
RCV003976565
RCV003950377
RCV003962940
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 31152157
Mental Disorders Associate 31152157
Stomach Neoplasms Associate 35578189