APOL4 (apolipoprotein L4)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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80832 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Apolipoprotein L4 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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APOL4 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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APOL-IV, APOLIV |
Chromosome
Chromosome number
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22 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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22q12.3 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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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.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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
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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.
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