Human (GRCh38.p14)
Description

solute carrier family 2 member 13 [Source:HGNC Symbol;Acc:HGNC:15956]

Gene Synonyms

HMIT

Location

Chromosome 12: 39,755,025-40,106,089 reverse strand.

GRCh38:CM000674.2

About this gene

This gene has 4 transcripts (splice variants), 309 orthologues and 13 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000280871.9SLC2A13-2017221648aaENSP00000280871.4
 
Protein coding
CCDS8736Q96QE2 NM_052885.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000380858.1SLC2A13-2023082357aaENSP00000370239.1
 
Protein coding
E9PE47 -GENCODE basicTSL:1
ENST00000465517.1SLC2A13-2031026No protein-
 
Retained intron
--TSL:2
ENST00000505338.1SLC2A13-204436No protein-
 
Retained intron
--TSL:3