HSDL1
Inactive hydroxysteroid dehydrogenase-like protein 1
Also known as: HSDL1_HUMAN, SDR12C3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q3SXM5
- Gene
- HSDL1
- Ensembl
- ENSG00000103160
- Chromosome
- 16
- Canonical length
- 330 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Vesicles,Intermediate filaments,Mitochondria
OverviewNCBI Gene
Located in intermediate filament cytoskeleton and mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
330 residues, UniProt reviewed canonical sequence.
>Q3SXM5|HSDL1
1 MAAVDSFYLL YREIARSCNC YMEALALVGA WYTARKSITV ICDFYSLIRL HFIPRLGSRA
61 DLIKQYGRWA VVSGATDGIG KAYAEELASR GLNIILISRN EEKLQVVAKD IADTYKVETD
121 IIVADFSSGR EIYLPIREAL KDKDVGILVN NVGVFYPYPQ YFTQLSEDKL WDIINVNIAA
181 ASLMVHVVLP GMVERKKGAI VTISSGSCCK PTPQLAAFSA SKAYLDHFSR ALQYEYASKG
241 IFVQSLIPFY VATSMTAPSN FLHRCSWLVP SPKVYAHHAV STLGISKRTT GYWSHSIQFL
301 FAQYMPEWLW VWGANILNRS LRKEALSCTALocalizationUniProt · AlphaFold · HPA
Whether an antibody against HSDL1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- retina: 32 nTPM
- tongue: 29 nTPM
- thyroid gland: 25 nTPM
- skeletal muscle: 19 nTPM
- cerebral cortex: 19 nTPM
- ovary: 18 nTPM
Single-cell type
- platelets: 61 nCPM
- late primary spermatocytes: 59 nCPM
- rod photoreceptor cells: 46 nCPM
- somatotrophs: 41 nCPM
- differentiating spermatogonia: 37 nCPM
- respiratory ciliated cells: 36 nCPM
Immune cell
- basophil: 21 nTPM
- eosinophil: 11 nTPM
- naive B-cell: 7.6 nTPM
- non-classical monocyte: 6.4 nTPM
- naive CD8 T-cell: 5.6 nTPM
- neutrophil: 5.5 nTPM
Brain region
- pons: 41 nTPM
- hypothalamus: 40 nTPM
- midbrain: 33 nTPM
- basal ganglia: 31 nTPM
- medulla oblongata: 31 nTPM
- cerebral cortex: 30 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about HSDL1.
Disease | ImmuneIEDB
Conditions an epitope on HSDL1 was assayed in.
- ovarian cancer T cell
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)
- 0.92
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.08
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Short-chain dehydrogenase/reductase SDR
- NAD(P)-binding domain superfamily
- short chain dehydrogenase
- 17-beta-hydroxysteroid dehydrogenase type 3-like
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HSDL1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HSDL1 as an antibody target. Whether an autoantibody or antibody against HSDL1 could matter depends on whether native HSDL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HSDL1 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 HSDL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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