Human (GRCh37.p13)
Description

solute carrier family 17 (organic anion transporter), member 3 [Source:HGNC Symbol;Acc:10931]

Gene Synonyms

NPT4

Location

Chromosome 6: 25,833,294-25,882,514 reverse strand.

GRCh37:CM000668.1

About this gene

This gene has 10 transcripts (splice variants), 8 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000397060.4SLC17A3-0022052498aaENSP00000380250.4
 
Protein coding
CCDS47385H0Y9F7 O00476 NM_001098486.1Ensembl CanonicalGENCODE Basic
ENST00000360657.3SLC17A3-0011750420aaENSP00000353873.3
 
Protein coding
CCDS4566H0Y9F7 O00476 -GENCODE Basic
ENST00000361703.6SLC17A3-0031543420aaENSP00000355307.6
 
Protein coding
CCDS4566H0Y9F7 O00476 NM_006632.3GENCODE Basic
ENST00000505420.1SLC17A3-00966151aaENSP00000424027.1
 
Protein coding
H0Y9F7 -CDS 5' incomplete
ENST00000481949.2SLC17A3-00459999aaENSP00000421855.1
 
Protein coding
H0Y9F7 -CDS 5' incomplete
ENST00000506105.1SLC17A3-0061362112aaENSP00000424729.1
 
Nonsense mediated decay
E9PBQ8 --
ENST00000449356.2SLC17A3-010563112aaENSP00000415622.2
 
Nonsense mediated decay
E9PBQ8 --
ENST00000509714.1SLC17A3-0081549No protein-
 
Retained intron
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ENST00000503922.1SLC17A3-0051145No protein-
 
Retained intron
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ENST00000308453.5SLC17A3-0071138No protein-
 
Retained intron
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