Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80832
Gene name Gene Name - the full gene name approved by the HGNC.
Apolipoprotein L4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
APOL4
Synonyms (NCBI Gene) Gene synonyms aliases
APOL-IV, APOLIV
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the apolipoprotein L family. The encoded protein may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver. Alternative splicing result
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT706820 hsa-miR-548n HITS-CLIP 21572407
MIRT706819 hsa-miR-548az-5p HITS-CLIP 21572407
MIRT706818 hsa-miR-548t-5p HITS-CLIP 21572407
MIRT706817 hsa-miR-548l HITS-CLIP 21572407
MIRT706816 hsa-miR-3129-3p HITS-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005615 Component Extracellular space ISS 22261194
GO:0006629 Process Lipid metabolic process NAS 11944986
GO:0006869 Process Lipid transport IEA
GO:0008289 Function Lipid binding IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607254 14867 ENSG00000100336
Protein
UniProt ID Q9BPW4
Protein name Apolipoprotein L4 (Apolipoprotein L-IV) (ApoL-IV)
Protein function May play a role in lipid exchange and transport throughout the body. May participate in reverse cholesterol transport from peripheral cells to the liver (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05461 ApoL 46 348 Apolipoprotein L Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed; the highest levels are in spinal cord, placenta, adrenal gland; also detected in spleen, bone marrow, uterus, trachea, mammary gland and testis; levels are low in brain, heart and pancreas.
Sequence
Sequence length 351
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 35919504
Schizophrenia Associate 18632255