Advanced notice of Ensembl Tools maintenance
Please note that due to planned maintenance, Ensembl Tools will be unavailable from Tuesday, September 9, at 08:30 AM BST until Wednesday, September 10, at 08:30 AM BST.
Jobs submitted during the maintenance window will be queued and processed once maintenance is complete. We apologise for the inconvenience.

Human (GRCh38.p14)
Description

ATP binding cassette subfamily G member 5 [Source:HGNC Symbol;Acc:HGNC:13886]

Gene Synonyms

STSL

Location

Chromosome 2: 43,812,472-43,838,865 reverse strand.

GRCh38:CM000664.2

About this gene

This gene has 8 transcripts (splice variants), 198 orthologues, 4 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000405322.8ABCG5-2012760651aaENSP00000384513.2
 
Protein coding
CCDS1814Q9H222-1 NM_022436.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000882115.1ABCG5-2062259606aaENSP00000552174.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000882114.1ABCG5-2052147561aaENSP00000552173.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000882116.1ABCG5-2071983516aaENSP00000552175.1
 
Protein coding
--GENCODE Basic
ENST00000882117.1ABCG5-2081044211aaENSP00000552176.1
 
Protein coding
--GENCODE Basic
ENST00000486512.5ABCG5-2033033No protein-
 
Retained intron
--TSL:1
ENST00000644754.1ABCG5-2042896No protein-
 
Retained intron
---
ENST00000409962.1ABCG5-2022512No protein-
 
Retained intron
--TSL:2