Gene Gene information from NCBI Gene database.
Entrez ID 149685
Gene name Adipogenin
Gene symbol ADIG
Synonyms (NCBI Gene)
SMAF1
Chromosome 20
Chromosome location 20q11.23
Summary ADIG/SMAF1 is an adipocyte-specific protein that plays a role in adipocyte differentiation (Kim et al., 2005 [PubMed 15567149]; Hong et al., 2005 [PubMed 16132694]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
30
miRTarBase ID miRNA Experiments Reference
MIRT017353 hsa-miR-335-5p Microarray 18185580
MIRT768784 hsa-miR-1178 CLIP-seq
MIRT768785 hsa-miR-1275 CLIP-seq
MIRT768786 hsa-miR-1321 CLIP-seq
MIRT768787 hsa-miR-219-1-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus ISS 15567149
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611396 28606 ENSG00000182035
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q0VDE8
Protein name Adipogenin
Protein function Plays a role in stimulating adipocyte differentiation and development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15202 Adipogenin 1 78 Adipogenin Family
Sequence
Sequence length 80
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
SCOLIOSIS 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
Metabolic Diseases Metabolic Diseases BEFREE 23197810
★☆☆☆☆
Found in Text Mining only