DHRS7C
Dehydrogenase/reductase SDR family member 7C
Also known as: DRS7C_HUMAN, SDR32C2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NNS2
- Gene
- DHRS7C
- Ensembl
- ENSG00000184544
- Chromosome
- 17
- Canonical length
- 312 aa
- Protein class
- Enzymes, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Predicted to enable all-trans-retinol dehydrogenase (NAD+) activity. Predicted to be involved in D-glucose import; intracellular calcium ion homeostasis; and regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum. Predicted to be located in longitudinal sarcoplasmic reticulum and sarcoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
312 residues, UniProt reviewed canonical sequence.
>A6NNS2|DHRS7C
1 MGVMAMLMLP LLLLGISGLL FIYQEVSRLW SKSAVQNKVV VITDAISGLG KECARVFHTG
61 GARLVLCGKN WERLENLYDA LISVADPSKQ TFTPKLVLLD LSDISCVPDV AKEVLDCYGC
121 VDILINNASV KVKGPAHKIS LELDKKIMDA NYFGPITLTK ALLPNMISRR TGQIVLVNNI
181 QGKFGIPFRT TYAASKHAAL GFFDCLRAEV EEYDVVISTV SPTFIRSYHV YPEQGNWEAS
241 IWKFFFRKLT YGVHPVEVAE EVMRTVRRKK QEVFMANPIP KAAVYVRTFF PEFFFAVVAC
301 GVKEKLNVPE EGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DHRS7C 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)
- 0.29
- Highest tissue expression
- 343 nTPM
Expression across tissuesHPA
Tissue
- tongue: 343 nTPM
- skeletal muscle: 289 nTPM
- heart muscle: 102 nTPM
- esophagus: 3.7 nTPM
- salivary gland: 2.3 nTPM
- rectum: 1 nTPM
Single-cell type
- late spermatids: 28 nCPM
- myonuclei: 22 nCPM
- early spermatids: 7.9 nCPM
- corticotrophs: 5 nCPM
- cardiomyocytes: 4.2 nCPM
- thymic myoid cells: 4.1 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 0.9 nTPM
- white matter: 0.9 nTPM
- basal ganglia: 0.4 nTPM
- hippocampal formation: 0.3 nTPM
- amygdala: 0.2 nTPM
- spinal cord: 0.2 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)
- 1.5
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- D-glucose import
- intracellular calcium ion homeostasis
- regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
Molecular functions
- all-trans-retinol dehydrogenase (NAD+) activity
- oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Short-chain dehydrogenase/reductase SDR
- Short-chain dehydrogenase/reductase, conserved site
- NAD(P)-binding domain superfamily
- short chain dehydrogenase
- Dehydrogenase/reductase SDR family member 7C
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DHRS7C as an antibody target. Whether an autoantibody or antibody against DHRS7C could matter depends on whether native DHRS7C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DHRS7C 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 DHRS7C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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