Human Gene APOC1 (ENST00000592535.6_10) from GENCODE V47lift37
Description: apolipoprotein C1, transcript variant 1 (from RefSeq NM_001645.5)
Gencode Transcript: ENST00000592535.6_10
Gencode Gene: ENSG00000130208.10_12
Transcript (Including UTRs)
Position: hg19 chr19:45,417,865-45,422,603 Size: 4,739 Total Exon Count: 4 Strand: +
Coding Region
Position: hg19 chr19:45,418,149-45,422,487 Size: 4,339 Coding Exon Count: 3
Data last updated at UCSC: 2024-08-22 23:36:26
Sequence and Links to Tools and Databases
Comments and Description Text from UniProtKB
ID: APOC1_HUMAN
DESCRIPTION: RecName: Full=Apolipoprotein C-I; Short=Apo-CIB; Short=ApoC-IB; AltName: Full=Apolipoprotein C1; Contains: RecName: Full=Truncated apolipoprotein C-I; Short=Apo-CIB'; Short=ApoC-IB'; Flags: Precursor;
FUNCTION: Appears to modulate the interaction of APOE with beta- migrating VLDL and inhibit binding of beta-VLDL to the LDL receptor-related protein. Binds free fatty acids and reduces their intracellular esterification.SUBCELLULAR LOCATION: Secreted.TISSUE SPECIFICITY: Synthesized mainly in liver and to a minor degree in intestine. Secreted in plasma.MISCELLANEOUS: Apolipoprotein C-I is present in acidic (APOC1A) and basic (APOC1B) forms in P.paniscus, P.abelii and P.troglodytes and perhaps also in baboons and macaques. In human, the acidic form has become a pseudogene. Apo-CI makes up about 10% of the protein of the VLDL (very low density lipoprotein) and 2% of that of HDL (high density lipoprotein).SIMILARITY: Belongs to the apolipoprotein C1 family.WEB RESOURCE: Name=Wikipedia; Note=Apolipoprotein C1 entry; URL="http://en.wikipedia.org/wiki/Apolipoprotein_C1";
Primer design for this transcript
MalaCards Disease Associations
Comparative Toxicogenomics Database (CTD)
The following chemicals interact with this gene
D016604
Aflatoxin B1
D001564
Benzo(a)pyrene
D004997
Ethinyl Estradiol
C009618
O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphate
D013749
Tetrachlorodibenzodioxin
C111118
2',3,3',4',5-pentachloro-4-hydroxybiphenyl
D015084
2,4-Dichlorophenoxyacetic Acid
D015127
9,10-Dimethyl-1,2-benzanthracene
D000643
Ammonium Chloride
D016718
Arachidonic Acid
D001241
Aspirin
D019256
Cadmium Chloride
D002110
Caffeine
D002211
Capsaicin
D002251
Carbon Tetrachloride
D020111
Chlorodiphenyl (54% Chlorine)
D002994
Clofibrate
D003300
Copper
D019327
Copper Sulfate
D016572
Cyclosporine
D004041
Dietary Fats
D004809
Ephedrine
D005472
Fluorouracil
D019833
Genistein
D018684
Glycine Agents
D006540
Herbicides
D015474
Isotretinoin
D008095
Lithocholic Acid
D008701
Methapyrilene
D008748
Methylcholanthrene
D015735
Mifepristone
D011794
Quercetin
D013629
Tamoxifen
D013752
Tetracycline
D014280
Triglycerides
C043377
acetochlor
C040534
alpha-hexachlorocyclohexane
C470047
aminomethylphosphonic acid
C095105
bexarotene
C006780
bisphenol A
C121718
dicyclanil
C039281
furan
C029424
hydrazine
C008340
mecoprop
C025589
ochratoxin A
C041786
palm oil
C076994
perfluorooctane sulfonic acid
C023036
perfluorooctanoic acid
C060836
pioglitazone
C006253
pirinixic acid
C021751
tanshinone
Common Gene Haplotype Alleles
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
Microarray Expression Data
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mRNA Secondary Structure of 3' and 5' UTRs
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
Protein Domain and Structure Information
InterPro Domains: Graphical view of domain structure IPR006781 - ApoC-I
Pfam Domains: PF04691 - Apolipoprotein C-I (ApoC-1)
Protein Data Bank (PDB) 3-D Structure
ModBase Predicted Comparative 3D Structure on P02654
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Gene Ontology (GO) Annotations with Structured Vocabulary
Molecular Function: GO:0004859 phospholipase inhibitor activity
GO:0005504 fatty acid binding
GO:0031210 phosphatidylcholine binding
GO:0055102 lipase inhibitor activity
GO:0060228 phosphatidylcholine-sterol O-acyltransferase activator activity
Biological Process: GO:0006629 lipid metabolic process
GO:0006641 triglyceride metabolic process
GO:0006869 lipid transport
GO:0008203 cholesterol metabolic process
GO:0010873 positive regulation of cholesterol esterification
GO:0010900 negative regulation of phosphatidylcholine catabolic process
GO:0010916 negative regulation of very-low-density lipoprotein particle clearance
GO:0032374 regulation of cholesterol transport
GO:0032375 negative regulation of cholesterol transport
GO:0033344 cholesterol efflux
GO:0033700 phospholipid efflux
GO:0034369 plasma lipoprotein particle remodeling
GO:0034375 high-density lipoprotein particle remodeling
GO:0034379 very-low-density lipoprotein particle assembly
GO:0034382 chylomicron remnant clearance
GO:0034447 very-low-density lipoprotein particle clearance
GO:0042157 lipoprotein metabolic process
GO:0043085 positive regulation of catalytic activity
GO:0045717 negative regulation of fatty acid biosynthetic process
GO:0045833 negative regulation of lipid metabolic process
GO:0048261 negative regulation of receptor-mediated endocytosis
GO:0050995 negative regulation of lipid catabolic process
GO:0051005 negative regulation of lipoprotein lipase activity
Cellular Component: GO:0005576 extracellular region
GO:0005783 endoplasmic reticulum
GO:0034361 very-low-density lipoprotein particle
GO:0034364 high-density lipoprotein particle
GO:0042627 chylomicron
Descriptions from all associated GenBank mRNAs
AJ249921 - Homo sapiens intergenic region between apoE and apoCI genes.AF308154 - Homo sapiens HERV-E long terminal repeat, complete sequence; and apolipoprotein C-I variant I mRNA, partial cds.AF308155 - Homo sapiens HERV-E long terminal repeat, complete sequence; and apolipoprotein C-I variant II mRNA, partial cds.BC055093 - Homo sapiens apolipoprotein C-I, mRNA (cDNA clone MGC:62029 IMAGE:6567705), complete cds.AK225971 - Homo sapiens mRNA for apolipoprotein C-I precursor variant, clone: FCC113A12.AK312036 - Homo sapiens cDNA, FLJ92313, Homo sapiens apolipoprotein C-I (APOC1), mRNA.JD380117 - Sequence 361141 from Patent EP1572962.BC009698 - Homo sapiens apolipoprotein C-I, mRNA (cDNA clone MGC:9245 IMAGE:3889900), complete cds.X00570 - Human mRNA for precursor of apolipoprotein CI (apo CI).JD477065 - Sequence 458089 from Patent EP1572962.AB528369 - Synthetic construct DNA, clone: pF1KE0201, Homo sapiens APOC1 gene for apolipoprotein C-I, without stop codon, in Flexi system.AM392727 - Synthetic construct Homo sapiens clone IMAGE:100002513 for hypothetical protein (APOC1 gene).GQ129385 - Synthetic construct Homo sapiens clone HAIB:100068650; DKFZo004A1136 apolipoprotein C-I protein (APOC1) gene, partial cds.GQ129384 - Synthetic construct Homo sapiens clone HAIB:100068554; DKFZo008A1135 apolipoprotein C-I protein (APOC1) gene, complete cds.KJ896443 - Synthetic construct Homo sapiens clone ccsbBroadEn_05837 APOC1-like gene, encodes complete protein.CR456907 - Homo sapiens full open reading frame cDNA clone RZPDo834A067D for gene APOC1, apolipoprotein C-I; complete cds, incl. stopcodon.BT007142 - Homo sapiens apolipoprotein C-I mRNA, complete cds.M27359 - Human apolipoprotein CI (apoCI) mRNA, partial cdn.JD309238 - Sequence 290262 from Patent EP1572962.JD456218 - Sequence 437242 from Patent EP1572962.
Biochemical and Signaling Pathways
Other Names for This Gene
Alternate Gene Symbols: APOC1_HUMAN, B2R526, ENST00000592535.1, ENST00000592535.2, ENST00000592535.3, ENST00000592535.4, ENST00000592535.5, NM_001645, P02654, Q6IB97, uc326xsz.1, uc326xsz.2UCSC ID: ENST00000592535.6_10RefSeq Accession: NM_001645.5
Protein: P02654
(aka APOC1_HUMAN or APC1_HUMAN)
Gene Model Information
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Methods, Credits, and Use Restrictions
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for details on how this gene model was made and data restrictions if any.