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Human (GRCh38.p14)
Description

solute carrier family 25 member 13 [Source:HGNC Symbol;Acc:HGNC:10983]

Gene Synonyms

ARALAR2, CITRIN, CTLN2

Location

Chromosome 7: 96,120,220-96,322,147 reverse strand.

GRCh38:CM000669.2

About this gene

This gene has 8 transcripts (splice variants), 185 orthologues, 49 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000265631.10SLC25A13-2013141675aaENSP00000265631.6
 
Protein coding
CCDS5645Q9UJS0-1 NM_014251.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS ALT1TSL:1
ENST00000416240.6SLC25A13-2023192676aaENSP00000400101.2
 
Protein coding
CCDS55130Q9UJS0-2 -GENCODE PrimaryGENCODE BasicAPPRIS P4TSL:1
ENST00000472162.2SLC25A13-20356873aaENSP00000473505.1
 
Nonsense mediated decay
R4GN64 -TSL:4
ENST00000494085.1SLC25A13-208766No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000490072.5SLC25A13-206578No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000484495.5SLC25A13-204540No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000492869.1SLC25A13-207433No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000487710.1SLC25A13-205201No protein-
 
Protein coding CDS not defined
--TSL:5