Human (GRCh38.p14)
Description

retinol saturase [Source:HGNC Symbol;Acc:HGNC:25991]

Gene Synonyms

FLJ20296

Location

Scaffold HSCHR2_6_CTG1: 268,195-280,769 reverse strand.

GRCh38:MU273340.1

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000709863.1RETSAT-2083141610aaENSP00000517901.1
 
Protein coding
-Ensembl CanonicalGENCODE basic
ENST00000709865.1RETSAT-2101759399aaENSP00000517903.1
 
Protein coding
-CDS 5' incomplete
ENST00000709867.1RETSAT-212765255aaENSP00000517905.1
 
Protein coding
-CDS 5' and 3' incomplete
ENST00000709864.1RETSAT-2092335320aaENSP00000517902.1
 
Nonsense mediated decay
-CDS 5' incomplete
ENST00000709866.1RETSAT-2111500140aaENSP00000517904.1
 
Nonsense mediated decay
-CDS 5' incomplete
ENST00000709868.1RETSAT-213601No protein-
 
Protein coding CDS not defined
--
ENST00000709869.1RETSAT-214660No protein-
 
Retained intron
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