Reviewed,
UniProtKB/Swiss-Prot Q9BPW4 (APOL4_HUMAN)
Last modified
November 24, 2009.
Version 61.
History...
Clusters with 100%,
90%,
50% identity |
Documents (5) |
Third-party data |
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Names and origin
| Protein names | Recommended name: Apolipoprotein L4 Alternative name(s): Apolipoprotein L-IV Short name=ApoL-IV | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Complete proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 351 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| 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. |
| Subcellular location | Secreted Potential. |
| 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 similarities | Belongs to the apolipoprotein L family. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Lipid transport Transport |
| Cellular component | Secreted |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Signal |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Biological process | lipid metabolic process Non-traceable author statement. Source: UniProtKB lipid transportInferred from electronic annotation. Source: UniProtKB-KW lipoprotein metabolic processInferred from electronic annotation. Source: InterPro |
| Cellular component | extracellular region Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular function | lipid binding Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 3 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9BPW4-1) Also known as: B; This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q9BPW4-2) Also known as: A; The sequence of this isoform differs from the canonical sequence as follows: 1-15: MEGAALLKIFVVCIW → MGSWVQLITSVG | ||||||
| Isoform 3 (identifier: Q9BPW4-3) The sequence of this isoform differs from the canonical sequence as follows: 1-15: MEGAALLKIFVVCIW → MGSWVQLITSVG 111-111: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 21 | 21 | Potential | ||||||
| Chain | 22 – 351 | 330 | Apolipoprotein L4 | PRO_0000002041 | |||||
Natural variations | |||||||||
| Alternative sequence | 1 – 15 | 15 | MEGAA…VVCIW → MGSWVQLITSVG in isoform 2 and isoform 3. | VSP_000295 | |||||
| Alternative sequence | 111 | 1 | Missing in isoform 3. | VSP_024380 | |||||
| Natural variant | 9 | 1 | I → V: dbSNP rs132736. | VAR_053008 | |||||
| Natural variant | 12 | 1 | V → L: dbSNP rs80587. | VAR_053009 | |||||
| Natural variant | 159 | 1 | M → V: dbSNP rs132700. | VAR_053010 | |||||
| Natural variant | 223 | 1 | R → H: dbSNP rs2227168. | VAR_059966 | |||||
| Natural variant | 319 | 1 | A → E: dbSNP rs6000173. | VAR_059967 | |||||
| Natural variant | 326 | 1 | S → L: dbSNP rs6000172. | VAR_059968 | |||||
Sequences
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References
| [1] | "Apolipoprotein L gene family: tissue-specific expression, splicing, promoter regions; discovery of a new gene." Duchateau P.N., Pullinger C.R., Cho M.H., Eng C., Kane J.P. J. Lipid Res. 42:620-630(2001) [PubMed: 11290834] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA] (ISOFORMS 1 AND 2). Tissue: Pancreas. |
| [2] | "The human apolipoprotein L gene cluster: identification, classification, and sites of distribution." Page N.M., Butlin D.J., Lomthaisong K., Lowry P.J. Genomics 74:71-78(2001) [PubMed: 11374903] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 3). Tissue: Placenta. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| AY014915 mRNA. Translation: AAG50353.1. AY014913 AY014912 Genomic DNA. Translation: AAG50350.1. AY014914 mRNA. Translation: AAG50352.1. AY014913 AY014912 Genomic DNA. Translation: AAG50351.1. AF305226 mRNA. Translation: AAK20212.1. | |
| IPI | IPI00028171. IPI00218384. IPI00843938. |
| RefSeq | NP_085146.2. NP_663693.1. |
| UniGene | Hs.115099 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q9BPW4. |
Genome annotation databases | |
| Ensembl | ENST00000352371; ENSP00000338260; ENSG00000100336; Homo sapiens. [Genome view] |
| GeneID | 80832. |
| KEGG | hsa:80832. |
Organism-specific databases | |
| CTD | 80832. |
| GeneCards | GC22M034909. |
| HGNC | HGNC:14867. APOL4. |
| MIM | 607254. gene. |
| PharmGKB | PA24907. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | Q9BPW4. |
| HOVERGEN | Q9BPW4. |
Gene expression databases | |
| ArrayExpress | Q9BPW4. |
| Bgee | Q9BPW4. |
| CleanEx | HS_APOL4. |
| Genevestigator | Q9BPW4. |
| GermOnline | ENSG00000100336. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR008405. ApoL. [Graphical view] |
| PANTHER | PTHR14096. ApoL. 1 hit. |
| Pfam | PF05461. ApoL. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 71250. |
| SOURCE | Search... |
Entry information
| Entry name | APOL4_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9BPW4 Secondary accession number(s): Q9BQ37, Q9BXQ8 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 22 Human chromosome 22: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with


