Seroatlas · Human Serome Atlas

HSDL2

Hydroxysteroid dehydrogenase-like protein 2

Also known as: C9orf99, HSDL2_HUMAN, SDR13C1

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q6YN16
Gene
HSDL2
Ensembl
ENSG00000119471
Chromosome
9
Canonical length
418 aa
Protein class
Plasma proteins, Predicted intracellular proteins
Subcellular location
Mitochondria

OverviewNCBI Gene

Predicted to enable oxidoreductase activity. Involved in cholesterol homeostasis. Located in mitochondrion and peroxisome. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

418 residues, UniProt reviewed canonical sequence.

>Q6YN16|HSDL2
     1  MLPNTGRLAG CTVFITGASR GIGKAIALKA AKDGANIVIA AKTAQPHPKL LGTIYTAAEE
    61  IEAVGGKALP CIVDVRDEQQ ISAAVEKAIK KFGGIDILVN NASAISLTNT LDTPTKRLDL
   121  MMNVNTRGTY LASKACIPYL KKSKVAHILN ISPPLNLNPV WFKQHCAYTI AKYGMSMYVL
   181  GMAEEFKGEI AVNALWPKTA IHTAAMDMLG GPGIESQCRK VDIIADAAYS IFQKPKSFTG
   241  NFVIDENILK EEGIENFDVY AIKPGHPLQP DFFLDEYPEA VSKKVESTGA VPEFKEEKLQ
   301  LQPKPRSGAV EETFRIVKDS LSDDVVKATQ AIYLFELSGE DGGTWFLDLK SKGGNVGYGE
   361  PSDQADVVMS MTTDDFVKMF SGKLKPTMAF MSGKLKIKGN MALAIKLEKL MNQMNARL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against HSDL2 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)
0.26
Highest tissue expression
169 nTPM

Expression across tissuesHPA

Tissue

  • tongue: 169 nTPM
  • skeletal muscle: 142 nTPM
  • liver: 139 nTPM
  • heart muscle: 86 nTPM
  • adipose tissue: 72 nTPM
  • kidney: 64 nTPM

Single-cell type

  • neutrophils: 470 nCPM
  • myonuclei: 435 nCPM
  • adipocytes: 296 nCPM
  • late spermatids: 233 nCPM
  • hepatocytes: 232 nCPM
  • adrenal cortex cells: 231 nCPM

Immune cell

  • basophil: 55 nTPM
  • neutrophil: 48 nTPM
  • eosinophil: 33 nTPM
  • non-classical monocyte: 12 nTPM
  • myeloid DC: 9.5 nTPM
  • plasmacytoid DC: 9.4 nTPM

Brain region

  • hypothalamus: 51 nTPM
  • midbrain: 50 nTPM
  • thalamus: 48 nTPM
  • basal ganglia: 43 nTPM
  • amygdala: 39 nTPM
  • white matter: 39 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)
0.88
gnomAD pLI
0
gnomAD missense Z
0.9
DepMap mean gene effect
-0.05
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

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads HSDL2 as an antibody target. Whether an autoantibody or antibody against HSDL2 could matter depends on whether native HSDL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

HSDL2 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 HSDL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/HSDL2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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