APOB

GENERAL INFORMATION

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Gene name

APOB

Gene description

Apolipoprotein B

Protein class

Candidate cardiovascular disease genes
Disease related genes
Plasma proteins
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (duodenum, liver, small intestine)
GTEx:Group enriched (liver, small intestine)

Protein evidence

Evidence at protein level

Protein localization

Distinct positivity in plasma.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Secreted protein, tissue location of RNA and protein might differ and correlation is complex.

Data reliability

Supportive based on 2 antibodies.
HPA049793 , CAB016070
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Duodenum

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (duodenum, liver, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (liver, small intestine)

Organ

Expression



GENE INFORMATION

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Gene name

APOB

Synonyms

Description

Apolipoprotein B (HGNC Symbol)

Entrez gene summary

This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels. [provided by RefSeq, Jul 2008]

Chromosome

2

Cytoband

p24.1

Chromosome location (bp)

21001429 - 21044073

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000084674 (version 78.38)

Entrez gene

338

UniProt

P04114 (UniProt - Evidence at protein level)

neXtProt

NX_P04114

Antibodypedia

APOB antibodies


PROTEIN BROWSER

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ENST00000233242
 
ENST00000399256
 
ENST00000616098
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

APOB-001 ENSP00000233242
ENST00000233242
P04114
Show all »
Show » Show » 4563 515.5 Yes 0
APOB-002 ENSP00000382200
ENST00000399256
A8MUN2
Show all »
Show » Show » 828 92.6 Yes 0
APOB-201 ENSP00000477990
ENST00000616098
S5FVK9
Show all »
Show » Show » 4344 489.8 Yes 0