Gene Gene information from NCBI Gene database.
Entrez ID 28955
Gene name Dexi homolog
Gene symbol DEXI
Synonyms (NCBI Gene)
MYLE
Chromosome 16
Chromosome location 16p13.13
miRNA miRNA information provided by mirtarbase database.
169
miRTarBase ID miRNA Experiments Reference
MIRT040575 hsa-miR-92b-3p CLASH 23622248
MIRT933344 hsa-miR-1285 CLIP-seq
MIRT933345 hsa-miR-3180-5p CLIP-seq
MIRT933346 hsa-miR-3187-5p CLIP-seq
MIRT933347 hsa-miR-378g CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617901 13267 ENSG00000182108
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95424
Protein name Dexamethasone-induced protein (Protein MYLE)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15198 Dexa_ind 1 95 Dexamethasone-induced Family
Tissue specificity TISSUE SPECIFICITY: Highest levels in heart. Also expressed in brain, liver, pancreas, placenta and lung. Up-regulated in emphysematous lung compared to normal lung. {ECO:0000269|PubMed:11472984}.
Sequence
Sequence length 95
Interactions View interactions
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 Evidence Score
ATOPIC ECZEMA 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
Alzheimer Disease Alzheimer disease Pubtator 40382655 Associate
★☆☆☆☆
Found in Text Mining only
Asthma Asthma BEFREE 24388013
★☆☆☆☆
Found in Text Mining only
Asthma Asthma Pubtator 24388013 Associate
★☆☆☆☆
Found in Text Mining only
Autoimmune Diseases Autoimmune Diseases BEFREE 21989056, 23151489, 26616563
★☆☆☆☆
Found in Text Mining only
Autoimmune Diseases Autoimmune disease Pubtator 21989056, 26616563 Associate
★☆☆☆☆
Found in Text Mining only
B-Cell Lymphomas B-Cell Lymphoma BEFREE 23251452
★☆☆☆☆
Found in Text Mining only
Dermatitis Atopic Atopic dermatitis Pubtator 33901562 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Diabetes BEFREE 31570815
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes Mellitus BEFREE 31570815
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 1 Diabetes mellitus, type 1 Pubtator 21989056, 22403184, 25008175 Associate
★☆☆☆☆
Found in Text Mining only