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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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RDH10
retinol dehydrogenase 10
Chromosome 8 · 8q21.11
NCBI Gene: 157506Ensembl: ENSG00000121039.11HGNC: HGNC:19975UniProt: Q8IZV5
41PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
nucleusvisual perceptionall-trans-retinol dehydrogenase (NAD+) activityprotein bindingatrial fibrillationhearing lossSensorineural hearing impairmentcervical carcinoma
✦AI Summary

RDH10 (retinol dehydrogenase 10) is a key enzyme in vitamin A metabolism that catalyzes the conversion of all-trans-retinol to all-trans-retinal using NADP as cofactor 1. The enzyme functions as a critical regulatory component in retinoic acid biosynthesis, forming part of a codependent complex with DHRS3 that maintains retinoic acid levels within physiological ranges through negative feedback mechanisms 2. RDH10 is essential for embryonic development, particularly craniofacial morphogenesis, as mutations cause fully penetrant choanal atresia in mice through perturbed retinoid signaling 3. The enzyme operates in dendritic cells as part of a PPARγ-regulated pathway alongside RALDH2 and CRABP2 to produce ATRA for immune function 1. RDH10 also exhibits 11-cis-retinol dehydrogenase activity and physically interacts with visual cycle proteins including CRALBP and RPE65, potentially contributing to retinal chr8 regeneration 4. In pathological contexts, RDH10 overexpression demonstrates antiproliferative effects in hepatocellular carcinoma cells through upregulation of RARβ/p21 pathways 5, while paradoxically promoting epithelial-mesenchymal transition in spinal cord gliomas via PI3K/AKT signaling 6. The gene produces multiple mRNA isoforms through alternative polyadenylation 7.

Sources cited
1
RDH10 converts all-trans-retinol to all-trans-retinal using NADP and functions in dendritic cells with RALDH2 and CRABP2 in PPARγ-regulated ATRA synthesis
PMID: 23833249
2
RDH10 forms a codependent complex with DHRS3 that regulates retinoic acid levels through negative feedback mechanisms
PMID: 28207193
3
RDH10 mutations cause fully penetrant choanal atresia in mice and are essential for craniofacial morphogenesis
PMID: 28169399
4
RDH10 exhibits 11-cis-retinol dehydrogenase activity and physically interacts with visual cycle proteins CRALBP and RPE65
PMID: 19458327
5
RDH10 overexpression produces antiproliferative effects in hepatocellular carcinoma cells through RARβ/p21 pathway upregulation
PMID: 17218779
6
RDH10 promotes epithelial-mesenchymal transition in spinal cord gliomas via PI3K/AKT pathway
PMID: 39180753
7
RDH10 gene produces multiple mRNA isoforms through alternative polyadenylation
PMID: 14596915
Disease Associationsⓘ20
atrial fibrillationOpen Targets
0.45Moderate
hearing lossOpen Targets
0.43Moderate
Sensorineural hearing impairmentOpen Targets
0.35Weak
cervical carcinomaOpen Targets
0.16Weak
benign chondrogenic neoplasmOpen Targets
0.13Weak
Abnormality of refractionOpen Targets
0.13Weak
nerve plexus diseaseOpen Targets
0.13Weak
post term pregnancyOpen Targets
0.12Weak
gliomaOpen Targets
0.10Suggestive
type 2 diabetes mellitusOpen Targets
0.09Suggestive
Epidermal Inclusion CystOpen Targets
0.08Suggestive
diabetes mellitusOpen Targets
0.08Suggestive
schizophreniaOpen Targets
0.06Suggestive
alcohol drinkingOpen Targets
0.06Suggestive
Branchio-otic syndromeOpen Targets
0.05Suggestive
branchiogenic deafness syndromeOpen Targets
0.05Suggestive
cat-eye syndromeOpen Targets
0.04Suggestive
neoplasmOpen Targets
0.04Suggestive
congenital absence of upper arm and forearm with hand presentOpen Targets
0.04Suggestive
branchiootic syndrome 1Open Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
PNPLA4Protein interaction98%STRA6Protein interaction98%RGRProtein interaction97%AOX1Protein interaction92%RDH11Protein interaction91%SORDProtein interaction91%
Tissue Expression6 tissues
Liver
100%
Lung
28%
Heart
20%
Brain
20%
Bone Marrow
15%
Ovary
13%
Gene Interaction Network
Click a node to explore
RDH10PNPLA4STRA6RGRAOX1RDH11SORD
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q8IZV5
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.96LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.60 [0.38–0.96]
RankingsWhere RDH10 stands among ~20K protein-coding genes
  • #10,064of 20,598
    Most Researched41
  • #9,136of 17,882
    Most Constrained (LOEUF)0.96
Genes detectedRDH10
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene.
PMID: 14596915
FEBS Lett · 2003
1.00
2
RDH10, RALDH2, and CRABP2 are required components of PPARγ-directed ATRA synthesis and signaling in human dendritic cells.
PMID: 23833249
J Lipid Res · 2013
0.90
3
Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresia.
PMID: 28169399
Hum Mol Genet · 2017
0.80
4
[[Gene expression of key enzymes for all-trans- retinoic acid biosynthesis - ALDHJAI and RDH10: relationship with co-expression of nuclear receptors RARα and PPARβ/δ genes and some clinical characteristics in multiple myeloma].
PMID: 30695588
Vopr Onkol · 2016
0.70
5
New insights and changing paradigms in the regulation of vitamin A metabolism in development.
PMID: 28207193
Wiley Interdiscip Rev Dev Biol · 2017
0.60