ABCG4 (ATP binding cassette subfamily G member 4)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 64137 |
| Gene name | ATP binding cassette subfamily G member 4 |
| Gene symbol | ABCG4 |
| Synonyms (NCBI Gene) |
WHITE2
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| Chromosome | 11 |
| Chromosome location | 11q23.3 |
| Summary | The protein encoded by this gene is a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/T |
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miRNA
miRNA information provided by mirtarbase database.
100
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Transcription factors
Transcription factors information provided by TRRUST V2 database.
2
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
39
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9H172 | ||||||||||||||||||||
| Protein name | ATP-binding cassette sub-family G member 4 (EC 7.6.2.-) | ||||||||||||||||||||
| Protein function | ATP-dependent transporter of the ATP-binding cassette (ABC) family that may be involved in the cellular efflux of sterols, in particular cholesterol and desmosterol (a cholesterol precursor), to high-density lipoprotein (HDL) (PubMed:15240127, P | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed specifically in the brain and the eye. {ECO:0000269|PubMed:11856881, ECO:0000269|PubMed:12183068}. | ||||||||||||||||||||
| Sequence |
MAEKALEAVGCGLGPGAVAMAVTLEDGAEPPVLTTHLKKVENHITEAQRFSHLPKRSAVD |
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| Sequence length | 646 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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Related Genes
Genes most often co-reported with ABCG4 across shared curated disease and pathway associations.
5
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to ABCG4 (see Related Genes above), that are NOT already directly curated for ABCG4 itself -- a lead worth checking, not a confirmed association.
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