Gene Gene information from NCBI Gene database.
Entrez ID 92196
Gene name Death associated protein like 1
Gene symbol DAPL1
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2q24.1
miRNA miRNA information provided by mirtarbase database.
11
miRTarBase ID miRNA Experiments Reference
MIRT923191 hsa-miR-1207-3p CLIP-seq
MIRT923192 hsa-miR-1827 CLIP-seq
MIRT923193 hsa-miR-320a CLIP-seq
MIRT923194 hsa-miR-320b CLIP-seq
MIRT923195 hsa-miR-320c CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0006915 Process Apoptotic process IEA
GO:0008283 Process Cell population proliferation IEA
GO:0010467 Process Gene expression IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A0PJW8
Protein name Death-associated protein-like 1 (Early epithelial differentiation-associated protein)
Protein function May play a role in the early stages of epithelial differentiation or in apoptosis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15228 DAP 13 106 Death-associated protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in hair follicle (at protein level). {ECO:0000269|PubMed:15920738}.
Sequence
Sequence length 107
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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)
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANGIOEDEMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBESITY 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
Age related macular degeneration Age-related macular degeneration BEFREE 25680934, 28334846
★☆☆☆☆
Found in Text Mining only
Cataract Cataract Pubtator 34946854 Associate
★☆☆☆☆
Found in Text Mining only
Macular Degeneration Macular degeneration Pubtator 25680934 Associate
★☆☆☆☆
Found in Text Mining only
Vitiligo Vitiligo Pubtator 33463119 Associate
★☆☆☆☆
Found in Text Mining only