Gene Gene information from NCBI Gene database.
Entrez ID 57863
Gene name Cell adhesion molecule 3
Gene symbol CADM3
Synonyms (NCBI Gene)
BIgRCMT2FFIGSF4BNECL1Necl-1TSLL1synCAM3
Chromosome 1
Chromosome location 1q23.2
Summary The protein encoded by this gene is a calcium-independent cell-cell adhesion protein that can form homodimers or heterodimers with other nectin proteins. The encoded protein has both homophilic and heterophilic cell-cell adhesion activity. This gene is re
miRNA miRNA information provided by mirtarbase database.
155
miRTarBase ID miRNA Experiments Reference
MIRT610632 hsa-miR-8485 HITS-CLIP 23313552
MIRT610631 hsa-miR-4643 HITS-CLIP 23313552
MIRT610629 hsa-miR-8064 HITS-CLIP 23313552
MIRT705023 hsa-miR-377-3p HITS-CLIP 23313552
MIRT610632 hsa-miR-8485 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
GO:0005911 Component Cell-cell junction ISS 12826663
GO:0007155 Process Cell adhesion IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609743 17601 ENSG00000162706
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N126
Protein name Cell adhesion molecule 3 (Brain immunoglobulin receptor) (Immunoglobulin superfamily member 4B) (IgSF4B) (Nectin-like protein 1) (NECL-1) (Synaptic cell adhesion molecule 3) (SynCAM3) (TSLC1-like protein 1) (TSLL1)
Protein function Involved in cell-cell adhesion. Has both calcium-independent homophilic cell-cell adhesion activity and calcium-independent heterophilic cell-cell adhesion activity with IGSF4, NECTIN1 and NECTIN3. Interaction with EPB41L1 may regulate structure
PDB 1Z9M
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set 35 127 Immunoglobulin V-set domain Domain
PF08205 C2-set_2 133 220 CD80-like C2-set immunoglobulin domain Domain
PF13927 Ig_3 232 303 Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1 is expressed mainly in adult and fetal brain. Isoform 2 is highly expressed in adult brain and weakly expressed in placenta. In brain, Isoform 2 is highly expressed in cerebellum. {ECO:0000269|PubMed:11536053, ECO:0000269|Pub
Sequence
Sequence length 398
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Cell adhesion molecules   Adherens junctions interactions
Nectin/Necl trans heterodimerization
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Charcot-Marie-Tooth disease, axonal, type 2FF Likely pathogenic rs2102125471 RCV001678582
★★★★☆
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 Evidence Score
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHARCOT-MARIE-TOOTH DISEASE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EATING DISORDER GWAS catalog
★★☆☆☆
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
Amyotrophic Lateral Sclerosis Amyotrophic lateral sclerosis Pubtator 26401960 Associate
★☆☆☆☆
Found in Text Mining only
Arthritis Arthritis BEFREE 30770760
★☆☆☆☆
Found in Text Mining only
Arthritis Arthritis Pubtator 30770760 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 34497681, 37446311 Associate
★☆☆☆☆
Found in Text Mining only
Craniocerebral Trauma Craniocerebral trauma Pubtator 34969957 Stimulate
★☆☆☆☆
Found in Text Mining only
Glioma Glioma BEFREE 11536053, 19062177
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 19062177
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Prostatic neoplasm Pubtator 21062931 Associate
★☆☆☆☆
Found in Text Mining only
Retinoblastoma Retinoblastoma BEFREE 29808799
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia LHGDN 19165527
★★☆☆☆
Found in Text Mining + Unknown/Other Associations