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Giving unique and meaningful names to every human gene
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Symbol Report: ABCA4 | |
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Giving unique and meaningful names to every human gene
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| Core Data | Database Links | |||||||||||||||||||
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| Approved Symbol + | ABCA4 | RefSeq IDs + | ||||||||||||||||||
| Approved Name + | ATP-binding cassette, sub-family A (ABC1), member 4 | NM_000350 | GenBank | EMBL | DDBJ | UCSC | ||||||||||||||
| HGNC ID + | HGNC:34 | Accession Numbers + | ||||||||||||||||||
| Status + | Approved | U88667 | GenBank | EMBL | DDBJ | UCSC | ||||||||||||||
| Chromosome + | 1p22 | Mouse Genome Database ID + | ||||||||||||||||||
| Previous Symbols + | STGD1, ABCR, RP19, STGD | MGI:109424 | MGD ID | |||||||||||||||||
| Previous Names + | Rat Genome Database ID (mapped data supplied by RGD) + | |||||||||||||||||||
| Aliases + | FFM, ARMD2 | RGD:1309445 | RGD ID | |||||||||||||||||
| Name Aliases + | "Stargardt disease" | Entrez Gene ID + | ||||||||||||||||||
| Locus Type + | gene with protein product | 24 | Gene | Map Viewer | ||||||||||||||||
| CCDS IDs + | ||||||||||||||||||||
| Gene Symbol Links | CCDS747.1 | CCDS ID | ||||||||||||||||||
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Pubmed IDs + | |||||||||||||||||||
| 9490294 | PMID | CiteXplore | ||||||||||||||||||
| VEGA IDs + | ||||||||||||||||||||
| OTTHUMG00000010622 | VEGA GeneView | |||||||||||||||||||
| Specialist Database Links | Ensembl ID (mapped data supplied by Ensembl) + | |||||||||||||||||||
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ENSG00000198691 | Ensembl GeneView | UCSC | |||||||||||||||||
| OMIM ID (mapped data supplied by NCBI) + | ||||||||||||||||||||
| Locus Specific Database Links | 601691 | OMIM | ||||||||||||||||||
| Mutations of the ATP-binding Cassette Transporter Retina | UCSC ID (mapped data supplied by UCSC) + | |||||||||||||||||||
| uc001dqh.2 | UCSC Index | |||||||||||||||||||
| UniProt ID (mapped data supplied by UniProt) + | ||||||||||||||||||||
| P78363 | UniProt | UCSC | ||||||||||||||||||
See Column definitions
for descriptions of the various data fields. Also see our custom downloads page for bulk access to our data
NHGRI |
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