APOA1

GENERAL INFORMATION

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Gene name

APOA1

Gene description

Apolipoprotein A-I

Protein class

Cancer-related genes
Candidate cardiovascular disease genes
Disease related genes
Plasma proteins
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (liver, small intestine)
GTEx:Tissue enriched (liver)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in kidney and liver and positivity in plasma in many tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA046715 , CAB016778
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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:  Tissue enhanced (liver, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression



GENE INFORMATION

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Gene name

APOA1

Synonyms

Description

Apolipoprotein A-I (HGNC Symbol)

Entrez gene summary

This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion, and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. [provided by RefSeq, Jul 2008]

Chromosome

11

Cytoband

q23.3

Chromosome location (bp)

116835751 - 116837950

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000118137 (version 78.38)

Entrez gene

335

UniProt

P02647 (UniProt - Evidence at protein level)

neXtProt

NX_P02647

Antibodypedia

APOA1 antibodies


PROTEIN BROWSER

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ENST00000236850
 
ENST00000359492
 
ENST00000375320
 
ENST00000375323
 
ENST00000375329
 
 
 
 


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)

APOA1-001 ENSP00000236850
ENST00000236850
P02647
Show all »
Show » Show » 267 30.8 Yes 0
APOA1-002 ENSP00000364469
ENST00000375320
P02647
Show all »
Show » Show » 267 30.8 Yes 0
APOA1-003 ENSP00000364472
ENST00000375323
P02647
Show all »
Show » Show » 267 30.8 Yes 0
APOA1-004 ENSP00000352471
ENST00000359492
P02647
Show all »
Show » Show » 267 30.8 Yes 0
APOA1-005 ENSP00000364478
ENST00000375329
F8W696
Show all »
Show » Show » 245 27.9 No 0