Gene Gene information from NCBI Gene database.
Entrez ID 115265
Gene name DNA damage inducible transcript 4 like
Gene symbol DDIT4L
Synonyms (NCBI Gene)
REDD2Rtp801L
Chromosome 4
Chromosome location 4q24
miRNA miRNA information provided by mirtarbase database.
22
miRTarBase ID miRNA Experiments Reference
MIRT929358 hsa-miR-105 CLIP-seq
MIRT929359 hsa-miR-141 CLIP-seq
MIRT929360 hsa-miR-200a CLIP-seq
MIRT929361 hsa-miR-3190 CLIP-seq
MIRT929362 hsa-miR-33a CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 25416956, 27107012, 31515488, 32296183, 32814053
GO:0005737 Component Cytoplasm IEA
GO:0005737 Component Cytoplasm ISS
GO:0009968 Process Negative regulation of signal transduction IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607730 30555 ENSG00000145358
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96D03
Protein name DNA damage-inducible transcript 4-like protein (HIF-1 responsive protein RTP801-like) (Protein regulated in development and DNA damage response 2) (REDD-2)
Protein function Inhibits cell growth by regulating the TOR signaling pathway upstream of the TSC1-TSC2 complex and downstream of AKT1.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07809 RTP801_C 65 183 RTP801 C-terminal region Family
Tissue specificity TISSUE SPECIFICITY: Up-regulated in atherosclerotic plaques relative to healthy segments of the same artery. {ECO:0000269|PubMed:15308555}.
Sequence
Sequence length 193
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
CHRONIC OBSTRUCTIVE PULMONARY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MELANOMA CTD
★★☆☆☆
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
Atrial Fibrillation Atrial fibrillation Pubtator 33062700 Associate
★☆☆☆☆
Found in Text Mining only
Heart Diseases Heart disease Pubtator 38003044 Associate
★☆☆☆☆
Found in Text Mining only
melanoma Melanoma CTD_human_DG 16778180
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Multiple Sclerosis Multiple sclerosis Pubtator 38218802 Associate
★☆☆☆☆
Found in Text Mining only
Periodontitis Periodontitis Pubtator 38218802 Associate
★☆☆☆☆
Found in Text Mining only