ABCG1
ATP-binding cassette sub-family G member 1
Also known as: ABC8, ABCG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P45844
- Gene
- ABCG1
- Ensembl
- ENSG00000160179
- Chromosome
- 21
- Canonical length
- 678 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Golgi apparatus,Vesicles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. It is involved in macrophage cholesterol and phospholipids transport, and may regulate cellular lipid homeostasis in other cell types. Six alternative splice variants have been identified. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
678 residues, UniProt reviewed canonical sequence.
>P45844|ABCG1
1 MACLMAAFSV GTAMNASSYS AEMTEPKSVC VSVDEVVSSN MEATETDLLN GHLKKVDNNL
61 TEAQRFSSLP RRAAVNIEFR DLSYSVPEGP WWRKKGYKTL LKGISGKFNS GELVAIMGPS
121 GAGKSTLMNI LAGYRETGMK GAVLINGLPR DLRCFRKVSC YIMQDDMLLP HLTVQEAMMV
181 SAHLKLQEKD EGRREMVKEI LTALGLLSCA NTRTGSLSGG QRKRLAIALE LVNNPPVMFF
241 DEPTSGLDSA SCFQVVSLMK GLAQGGRSII CTIHQPSAKL FELFDQLYVL SQGQCVYRGK
301 VCNLVPYLRD LGLNCPTYHN PADFVMEVAS GEYGDQNSRL VRAVREGMCD SDHKRDLGGD
361 AEVNPFLWHR PSEEVKQTKR LKGLRKDSSS MEGCHSFSAS CLTQFCILFK RTFLSIMRDS
421 VLTHLRITSH IGIGLLIGLL YLGIGNEAKK VLSNSGFLFF SMLFLMFAAL MPTVLTFPLE
481 MGVFLREHLN YWYSLKAYYL AKTMADVPFQ IMFPVAYCSI VYWMTSQPSD AVRFVLFAAL
541 GTMTSLVAQS LGLLIGAAST SLQVATFVGP VTAIPVLLFS GFFVSFDTIP TYLQWMSYIS
601 YVRYGFEGVI LSIYGLDRED LHCDIDETCH FQKSEAILRE LDVENAKLYL DFIVLGIFFI
661 SLRLIAYFVL RYKIRAERLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ABCG1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 6
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 36 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 36 nTPM
- spleen: 29 nTPM
- lung: 28 nTPM
- retina: 27 nTPM
- parathyroid gland: 23 nTPM
- choroid plexus: 21 nTPM
Single-cell type
- neutrophils: 269 nCPM
- kupffer cells: 266 nCPM
- rod photoreceptor cells: 223 nCPM
- respiratory basal cells: 146 nCPM
- foveolar cells: 136 nCPM
- lymphatic endothelial cells: 135 nCPM
Immune cell
- neutrophil: 37 nTPM
- eosinophil: 36 nTPM
- NK-cell: 7.4 nTPM
- T-reg: 7.4 nTPM
- naive B-cell: 7 nTPM
- memory CD4 T-cell: 6.1 nTPM
Brain region
- basal ganglia: 54 nTPM
- white matter: 52 nTPM
- midbrain: 45 nTPM
- thalamus: 44 nTPM
- choroid plexus: 44 nTPM
- cerebral cortex: 43 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.46
- gnomAD pLI
- 0.11
- gnomAD missense Z
- 2.13
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- amyloid precursor protein catabolic process
- cellular response to high density lipoprotein particle stimulus
- cholesterol efflux
- cholesterol homeostasis
- cholesterol metabolic process
- glycoprotein transport
- high-density lipoprotein particle remodeling
- intracellular cholesterol transport
- low-density lipoprotein particle remodeling
- negative regulation of cholesterol storage
- negative regulation of macrophage derived foam cell differentiation
- phospholipid efflux
- phospholipid homeostasis
- positive regulation of amyloid-beta formation
- positive regulation of cholesterol biosynthetic process
- positive regulation of cholesterol efflux
- positive regulation of protein secretion
- regulation of cholesterol metabolic process
- response to lipid
- reverse cholesterol transport
- transmembrane transport
- xenobiotic detoxification by transmembrane export across the plasma membrane
Molecular functions
- ABC-type sterol transporter activity
- ADP binding
- ATP binding
- ATP hydrolysis activity
- cholesterol binding
- cholesterol transfer activity
- floppase activity
- phosphatidylcholine floppase activity
- phospholipid binding
- protein heterodimerization activity
- protein homodimerization activity
- toxin transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- ABC transporter-like, ATP-binding domain
- AAA+ ATPase domain
- ABC-2 type transporter, transmembrane domain
- ABC transporter-like, conserved site
- P-loop containing nucleoside triphosphate hydrolase
- ABC transporter family G domain
- ATP-binding cassette subfamily G transporters
- ABC transporter
- ABC-2 type transporter
- ABC-2 type transporter
- Pigment precursor permease/Protein ATP-binding cassette sub-family G
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ABCG1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ABCG1 as an antibody target. Whether an autoantibody or antibody against ABCG1 could matter depends on whether native ABCG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ABCG1 is annotated at the cell surface, where native ABCG1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ABCG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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