Gene Gene information from NCBI Gene database.
Entrez ID 81577
Gene name Gfo/Idh/MocA-like oxidoreductase domain containing 2
Gene symbol GFOD2
Synonyms (NCBI Gene)
-
Chromosome 16
Chromosome location 16q22.1
miRNA miRNA information provided by mirtarbase database.
45
miRTarBase ID miRNA Experiments Reference
MIRT029015 hsa-miR-26b-5p Microarray 19088304
MIRT039383 hsa-miR-421 CLASH 23622248
MIRT1016852 hsa-miR-10a CLIP-seq
MIRT1016853 hsa-miR-10b CLIP-seq
MIRT1016854 hsa-miR-1229 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0005576 Component Extracellular region IEA
GO:0016491 Function Oxidoreductase activity IEA
GO:0030198 Process Extracellular matrix organization IBA
GO:0030198 Process Extracellular matrix organization IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619933 28159 ENSG00000141098
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3B7J2
Protein name Glucose-fructose oxidoreductase domain-containing protein 2 (EC 1.-.-.-)
Protein function Promotes matrix assembly.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01408 GFO_IDH_MocA 6 119 Oxidoreductase family, NAD-binding Rossmann fold Family
PF02894 GFO_IDH_MocA_C 134 284 Oxidoreductase family, C-terminal alpha/beta domain Domain
Sequence
Sequence length 385
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
ANDROGENETIC ALOPECIA 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
Hypercholesterolemia Hypercholesterolemia BEFREE 24064143
★☆☆☆☆
Found in Text Mining only
Panic Disorder Panic disorder Pubtator 35477560 Associate
★☆☆☆☆
Found in Text Mining only