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APOL4 (apolipoprotein L4)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80832
Gene nameGene Name - the full gene name approved by the HGNC.
Apolipoprotein L4
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
APOL4
SynonymsGene synonyms aliases
APOL-IV, APOLIV
ChromosomeChromosome number
22
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q12.3
SummarySummary 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
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Sequence
Sequence length 351
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313
Unknown
Disease name Disease term dbSNP ID References
Delusions Delusions
Hallucinations Hallucinations

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