Human (GRCh38.p14)
Description

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

Gene Synonyms

HMIT

Location
About this transcript

This transcript has 4 exons, is annotated with 36 domains and features, is associated with 66447 variant alleles and maps to 212 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000280871.9SLC2A13-2017221648aaENSP00000280871.4
 
Protein coding
CCDS8736Q96QE2 NM_052885.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000957640.1SLC2A13-2084181705aaENSP00000627699.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000858172.1SLC2A13-2063866606aaENSP00000528231.1
 
Protein coding
--GENCODE Basic
ENST00000858171.1SLC2A13-2053634525aaENSP00000528230.1
 
Protein coding
--GENCODE Basic
ENST00000858173.1SLC2A13-2073493666aaENSP00000528232.1
 
Protein coding
--GENCODE Basic
ENST00000380858.1SLC2A13-2023082357aaENSP00000370239.1
 
Protein coding
E9PE47 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000465517.1SLC2A13-2031026No protein-
 
Retained intron
--TSL:2
ENST00000505338.1SLC2A13-204436No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 4, Coding exons: 4, Transcript length: 3,082 bps, Translation length: 357 residues

Transcript Support Level (TSL)

TSL:1

Version

ENST00000380858.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.