Gene Gene information from NCBI Gene database.
Entrez ID 347
Gene name Apolipoprotein D
Gene symbol APOD
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3q29
Summary This gene encodes a component of high density lipoprotein that has no marked similarity to other apolipoprotein sequences. It has a high degree of homology to plasma retinol-binding protein and other members of the alpha 2 microglobulin protein superfamil
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT790044 hsa-miR-214 CLIP-seq
MIRT790045 hsa-miR-3619-5p CLIP-seq
MIRT790046 hsa-miR-3622b-5p CLIP-seq
MIRT790047 hsa-miR-409-5p CLIP-seq
MIRT790048 hsa-miR-4253 CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
NOTCH3 Repression 21705670
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
42
GO ID Ontology Definition Evidence Reference
GO:0000302 Process Response to reactive oxygen species IBA
GO:0000302 Process Response to reactive oxygen species IDA 18419796
GO:0000302 Process Response to reactive oxygen species IEA
GO:0001525 Process Angiogenesis NAS 21705670
GO:0005319 Function Lipid transporter activity NAS 3453108
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
107740 612 ENSG00000189058
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P05090
Protein name Apolipoprotein D (Apo-D) (ApoD)
Protein function APOD occurs in the macromolecular complex with lecithin-cholesterol acyltransferase. It is probably involved in the transport and binding of bilin. Appears to be able to transport a variety of ligands in a number of different contexts.
PDB 2HZQ , 2HZR
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00061 Lipocalin 43 184 Lipocalin / cytosolic fatty-acid binding protein family Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in liver, intestine, pancreas, kidney, placenta, adrenal, spleen, fetal brain tissue and tears.
Sequence
Sequence length 189
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Transport of fatty acids
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
APOD-related disorder Likely benign; Benign rs150664052, rs144811342, rs5952 RCV003921882
RCV003941998
RCV003895753
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Stimulate 30467822, 9751198
Alzheimer Disease Associate 37264161
Androgen Insensitivity Syndrome Associate 19330472, 27583472
Bipolar Disorder Stimulate 11274430
Brain Damage Chronic Associate 25261976
Breast Neoplasms Associate 11167212, 33550915, 34224831, 36243728, 7929425, 8311115, 8883401, 8943263
Carcinoma Hepatocellular Associate 17589901
Carcinoma Squamous Cell Associate 33671013
Carotid Stenosis Associate 30335165
Cerebral Infarction Associate 25261976