Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1611
Gene name Gene Name - the full gene name approved by the HGNC.
Death associated protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DAP
Synonyms (NCBI Gene) Gene synonyms aliases
DAP1
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5p15.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a basic, proline-rich, 15-kD protein. The protein acts as a positive mediator of programmed cell death that is induced by interferon-gamma. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gen
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005726 hsa-miR-183-5p qRT-PCR 20602797
MIRT018510 hsa-miR-335-5p Microarray 18185580
MIRT923065 hsa-miR-105 CLIP-seq
MIRT923066 hsa-miR-1178 CLIP-seq
MIRT923067 hsa-miR-1207-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0006417 Process Regulation of translation IEA
GO:0006914 Process Autophagy IEA
GO:0006915 Process Apoptotic process IEA
GO:0006915 Process Apoptotic process IGI 7828849
GO:0010507 Process Negative regulation of autophagy IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600954 2672 ENSG00000112977
Protein
UniProt ID P51397
Protein name Death-associated protein 1 (DAP-1)
Protein function Ribosome-binding protein involved in ribosome hibernation, a process during which ribosomes are stabilized in an inactive state and preserved from proteasomal degradation (By similarity). Acts via its association with eiF5a (EIF5A and EIF5A2) at
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15228 DAP 12 102 Death-associated protein Family
Sequence
Sequence length 102
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
Crohn Disease Crohn's disease N/A N/A GWAS
Inflammatory Bowel Disease Inflammatory bowel disease N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Mental Depression Major depressive disorder N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 33213505
Carcinogenesis Associate 22412903
GATA2 Deficiency Associate 12708480
Lupus Erythematosus Systemic Associate 33213505
Lymphoma B Cell Associate 12708480
Melanoma Associate 2299192
Neoplasms Associate 2299192