Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5134
Gene name Gene Name - the full gene name approved by the HGNC.
Programmed cell death 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PDCD2
Synonyms (NCBI Gene) Gene synonyms aliases
RP8, ZMYND7
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q27
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a nuclear protein expressed in a variety of tissues. Expression of this gene has been shown to be repressed by B-cell CLL/lymphoma 6 (BCL6), a transcriptional repressor required for lymph node germinal center development, suggesting that
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT054135 hsa-miR-129-1-3p Luciferase reporter assay, qRT-PCR, Western blot 25111461
MIRT054135 hsa-miR-129-1-3p Luciferase reporter assay, qRT-PCR, Western blot 25111461
MIRT054135 hsa-miR-129-1-3p Luciferase reporter assay, qRT-PCR, Western blot 25111461
MIRT054135 hsa-miR-129-1-3p Luciferase reporter assay, qRT-PCR, Western blot 25111461
MIRT1219276 hsa-miR-1197 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
BCL6 Repression 20605493
BCL6 Unknown 11854457;17468402
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 19146857, 32296183, 32814053
GO:0005634 Component Nucleus IBA 21873635
GO:0005737 Component Cytoplasm IEA
GO:0006915 Process Apoptotic process IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600866 8762 ENSG00000071994
Protein
UniProt ID Q16342
Protein name Programmed cell death protein 2 (Zinc finger MYND domain-containing protein 7) (Zinc finger protein Rp-8)
Protein function May be a DNA-binding protein with a regulatory function. May play an important role in cell death and/or in regulation of cell proliferation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01753 zf-MYND 135 172 MYND finger Domain
PF04194 PDCD2_C 189 339 Programmed cell death protein 2, C-terminal putative domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous.
Sequence
MAAAGARPVELGFAESAPAWRLRSEQFPSKVGGRPAWLGAAGLPGPQALACELCGRPLSF
LLQVYAPLPGRPDAFHRCIFLFCCREQPCCAGLRVFRNQLPRKNDFYSYEPPSENPPPET
GESVCLQLKSGAHLCRVCGCLGPKTCSRCHKAYYCSKEHQTLDWRLGHKQACAQPDHLDH
IIPDHNFLFPEFEIVIETEDEIMPEVVEKEDYSEIIGSMGEALEEELDSMAKHESREDKI
FQKFKTQIALEPEQILRYGRGIAPIWISGENIPQEKDIPDCPCGAKRILEFQVMPQLLNY
LKADRLGKSIDWGILAVFTCAESCSLGTGYTEEFVWKQD
VTDTP
Sequence length 344
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Mental depression Endogenous depression 19955554 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 37338518
Carcinoma Hepatocellular Associate 30664177
Depressive Disorder Stimulate 19955554
Drug Related Side Effects and Adverse Reactions Associate 26191203
Fatigue Syndrome Chronic Associate 16049284
Leukemia Associate 22922207, 23760497
Leukemia Myeloid Acute Associate 23760497
Neoplasm Metastasis Inhibit 30664177
Neoplasms Associate 23760497, 30664177