Gene Gene information from NCBI Gene database.
Entrez ID 497661
Gene name Chromosome 18 open reading frame 32
Gene symbol C18orf32
Synonyms (NCBI Gene)
GPIBD25
Chromosome 18
Chromosome location 18q21.1
miRNA miRNA information provided by mirtarbase database.
450
miRTarBase ID miRNA Experiments Reference
MIRT021166 hsa-miR-186-5p Sequencing 20371350
MIRT028171 hsa-miR-93-5p Sequencing 20371350
MIRT708170 hsa-miR-4789-3p HITS-CLIP 21572407
MIRT708169 hsa-miR-4643 HITS-CLIP 21572407
MIRT708168 hsa-miR-466 HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 29275994
GO:0005783 Component Endoplasmic reticulum IDA 29275994
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005811 Component Lipid droplet IDA 29275994
GO:0005811 Component Lipid droplet IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619979 31690 ENSG00000177576
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TCD1
Protein name UPF0729 protein C18orf32 (Putative NF-kappa-B-activating protein 200)
Protein function May activate the NF-kappa-B signaling pathway.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14975 DUF4512 2 75 Domain of unknown function (DUF4512) Family
Sequence
Sequence length 76
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
Glycosylphosphatidylinositol biosynthesis defect 25 Uncertain significance ClinVar
ClinVar, Disgenet, GenCC, HPO
ClinVar, Disgenet, GenCC, HPO
ClinVar, Disgenet, GenCC, HPO
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
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 37438770 Associate
★☆☆☆☆
Found in Text Mining only