Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1010
Gene name Gene Name - the full gene name approved by the HGNC.
Cadherin 12
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CDH12
Synonyms (NCBI Gene) Gene synonyms aliases
CDHB
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5p14.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a type II classical cadherin of the cadherin superfamily. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023018 hsa-miR-124-3p Microarray 18668037
MIRT608795 hsa-miR-759 HITS-CLIP 24906430
MIRT608794 hsa-miR-574-5p HITS-CLIP 24906430
MIRT608793 hsa-miR-6867-5p HITS-CLIP 24906430
MIRT608792 hsa-miR-8068 HITS-CLIP 24906430
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000902 Process Cell morphogenesis IBA 21873635
GO:0005509 Function Calcium ion binding IBA 21873635
GO:0005886 Component Plasma membrane TAS
GO:0005912 Component Adherens junction IBA 21873635
GO:0007043 Process Cell-cell junction assembly IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600562 1751 ENSG00000154162
Protein
UniProt ID P55289
Protein name Cadherin-12 (Brain cadherin) (BR-cadherin) (Neural type cadherin 2) (N-cadherin 2)
Protein function Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00028 Cadherin 59 151 Cadherin domain Domain
PF00028 Cadherin 165 260 Cadherin domain Domain
PF00028 Cadherin 274 376 Cadherin domain Domain
PF00028 Cadherin 389 480 Cadherin domain Domain
PF00028 Cadherin 493 590 Cadherin domain Domain
PF01049 Cadherin_C 638 785 Cadherin cytoplasmic region Family
Tissue specificity TISSUE SPECIFICITY: Brain.
Sequence
Sequence length 794
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Adherens junctions interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Multiple myeloma Multiple Myeloma rs11540652, rs78311289, rs121913482, rs397507340, rs121913343, rs121913240, rs121913529, rs730882018, rs1057517992, rs121913527, rs756183569, rs746646631, rs1574706907, rs372078034, rs745380962
View all (38 more)
23502783
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 29662167
Unknown
Disease term Disease name Evidence References Source
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Schizophrenia Schizophrenia GWAS
Hypertension Hypertension GWAS
Associations from Text Mining
Disease Name Relationship Type References
Bipolar Disorder Associate 19567891, 21876473
Breast Neoplasms Stimulate 36315446
Carcinoma Adenoid Cystic Associate 24237488
Colorectal Neoplasms Associate 24237488
Erythrokeratodermia Variabilis Associate 31911611
Heart Defects Congenital Associate 30342662
Hyperkeratosis Epidermolytic Inhibit 35421402
Keratoderma Palmoplantar Associate 31911611
Keratoderma palmoplantaris transgrediens Associate 31911611
Muscular Atrophy Spinal Associate 7731968