Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23109
Gene name Gene Name - the full gene name approved by the HGNC.
Dendrin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DDN
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q13.12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018142 hsa-miR-335-5p Microarray 18185580
MIRT051128 hsa-miR-16-5p CLASH 23622248
MIRT478339 hsa-miR-24-3p PAR-CLIP 23592263
MIRT478338 hsa-miR-6884-5p PAR-CLIP 23592263
MIRT478337 hsa-miR-485-5p PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IEA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IEA
GO:0005515 Function Protein binding IPI 16464232, 16751601
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IDA 16464232
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610588 24458 ENSG00000181418
Protein
UniProt ID O94850
Protein name Dendrin
Protein function Promotes apoptosis of kidney glomerular podocytes. Podocytes are highly specialized cells essential to the ultrafiltration of blood, resulting in the extraction of urine and the retention of protein (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15498 Dendrin 55 709 Nephrin and CD2AP-binding protein, Dendrin Family
Tissue specificity TISSUE SPECIFICITY: Specifically expressed in brain and kidney. Expressed in kidney glomerular capillary loops (at protein level). {ECO:0000269|PubMed:17251388, ECO:0000269|PubMed:18356187}.
Sequence
Sequence length 711
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
Bipolar Disorder Bipolar disorder N/A N/A GWAS
Osteoporosis Osteoporosis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Atrophy Inhibit 30458823
Fibrosis Inhibit 30458823
Kidney Diseases Associate 23667252, 30458823
Renal Insufficiency Associate 30458823