Human (GRCh38.p14) ▼ 
Summary
SequenceProtein InformationGenetic VariationVariant tableVariant imageHaplotypesPopulation comparisonComparison imageExternal ReferencesSupporting evidenceID History.
solute carrier family 22 member 9 [Source:HGNC Symbol;Acc:HGNC:16261]
FLJ23666, OAT4, OAT7, UST3
Chromosome 11: 63,369,785-63,410,294 forward strand.
This transcript has 10 exons, is annotated with 23 domains and features, is associated with 18856 variant alleles and maps to 424 oligo probes.
This transcript is a product of gene ENSG00000149742.10 Show transcript tableHide transcript table
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Exons: 10, Coding exons: 10, Transcript length: 2,366 bps, Translation length: 553 residues
This MANE Select transcript contains ENSP00000279178 and matches to NM_080866.3 and NP_543142.2
This transcript corresponds to the following Uniprot identifiers: Q8IVM8
This transcript is a member of the Human CCDS set: CCDS8043
TSL:1
ENST00000279178.4
Protein coding
Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.
This transcript is a member of the Gencode basic gene set.
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Ensembl release 111 - January 2024 ©
EMBL-EBI
EMBL-EBI
http://useast.ensembl.org
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