RETSAT
All-trans-retinol 13,14-reductase
Also known as: FLJ20296, RETST_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NUM9
- Gene
- RETSAT
- Ensembl
- ENSG00000042445
- Chromosome
- 2
- Canonical length
- 610 aa
- Protein class
- Enzymes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable all-trans-retinol 13,14-reductase activity. Predicted to be involved in retinol metabolic process. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
610 residues, UniProt reviewed canonical sequence.
>Q6NUM9|RETSAT
1 MWLPLVLLLA VLLLAVLCKV YLGLFSGSSP NPFSEDVKRP PAPLVTDKEA RKKVLKQAFS
61 ANQVPEKLDV VVIGSGFGGL AAAAILAKAG KRVLVLEQHT KAGGCCHTFG KNGLEFDTGI
121 HYIGRMEEGS IGRFILDQIT EGQLDWAPLS SPFDIMVLEG PNGRKEYPMY SGEKAYIQGL
181 KEKFPQEEAI IDKYIKLVKV VSSGAPHAIL LKFLPLPVVQ LLDRCGLLTR FSPFLQASTQ
241 SLAEVLQQLG ASSELQAVLS YIFPTYGVTP NHSAFSMHAL LVNHYMKGGF YPRGGSSEIA
301 FHTIPVIQRA GGAVLTKATV QSVLLDSAGK ACGVSVKKGH ELVNIYCPIV VSNAGLFNTY
361 EHLLPGNARC LPGVKQQLGT VRPGLGMTSV FICLRGTKED LHLPSTNYYV YYDTDMDQAM
421 ERYVSMPREE AAEHIPLLFF AFPSAKDPTW EDRFPGRSTM IMLIPTAYEW FEEWQAELKG
481 KRGSDYETFK NSFVEASMSV VLKLFPQLEG KVESVTAGSP LTNQFYLAAP RGACYGADHD
541 LGRLHPCVMA SLRAQSPIPN LYLTGQDIFT CGLVGALQGA LLCSSAILKR NLYSDLKNLD
601 SRIRAQKKKNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RETSAT can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.22
- Highest tissue expression
- 232 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 232 nTPM
- duodenum: 157 nTPM
- small intestine: 134 nTPM
- liver: 108 nTPM
- colon: 84 nTPM
- rectum: 69 nTPM
Single-cell type
- enterocytes: 271 nCPM
- adipocytes: 218 nCPM
- colonocytes: 206 nCPM
- melanocytes: 105 nCPM
- myonuclei: 94 nCPM
- foveolar cells: 86 nCPM
Immune cell
- non-classical monocyte: 8.8 nTPM
- MAIT T-cell: 6.3 nTPM
- memory CD8 T-cell: 6 nTPM
- NK-cell: 5.2 nTPM
- gdT-cell: 4.8 nTPM
- T-reg: 4.2 nTPM
Brain region
- choroid plexus: 53 nTPM
- white matter: 44 nTPM
- medulla oblongata: 39 nTPM
- basal ganglia: 39 nTPM
- thalamus: 38 nTPM
- hypothalamus: 37 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.11
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.11
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- all-trans-retinol 13
- 14-reductase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- FAD/NAD(P)-binding domain superfamily
- NAD(P)-binding Rossmann-like domain
- All-trans-retinol saturase
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RETSAT as an antibody target. Whether an autoantibody or antibody against RETSAT could matter depends on whether native RETSAT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RETSAT is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label RETSAT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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