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Gene Gene information from NCBI Gene database.
Entrez ID 164284
Gene name APC down-regulated 1 like
Gene symbol APCDD1L
Synonyms (NCBI Gene)
-
Chromosome 20
Chromosome location 20q13.32
miRNA miRNA information provided by mirtarbase database.
37 Show/Hide all (37)
miRTarBase ID miRNA Experiments Reference
MIRT018396 hsa-miR-335-5p Microarray 18185580
MIRT789056 hsa-miR-1183 CLIP-seq
MIRT789057 hsa-miR-1245b-5p CLIP-seq
MIRT789058 hsa-miR-1266 CLIP-seq
MIRT789059 hsa-miR-1321 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0017147 Function Wnt-protein binding IEA
GO:0030178 Process Negative regulation of Wnt signaling pathway 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.
Q8NCL9
Protein name Protein APCDD1-like (Adenomatosis polyposis coli down-regulated 1 protein-like)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14921 APCDDC 36 → 271 Adenomatosis polyposis coli down-regulated 1 Domain
PF14921 APCDDC 274 → 461 Adenomatosis polyposis coli down-regulated 1 Domain
Sequence
Sequence length 501
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway
Wnt signaling pathway
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
Malignant tumor of esophagus Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (6)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinogenesis Carcinogenesis Pubtator 34546854 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Renal cell carcinoma Pubtator 35414787 Inhibit
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 29568882 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Intervertebral Disc Degeneration Intervertebral disc disease Pubtator 38492610 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Lung neoplasms Pubtator 35414787 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Squamous cell carcinoma Pubtator 34546854, 35414787 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only