C20orf173
Uncharacterized protein C20orf173
Also known as: CT173_HUMAN, dJ477O4.4
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96LM9
- Gene
- C20orf173
- Ensembl
- ENSG00000125975
- Chromosome
- 20
- Canonical length
- 149 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Plasma membrane
OverviewNCBI Gene
Predicted to enable beta-galactoside (CMP) alpha-2,3-sialyltransferase activity. Predicted to be involved in ganglioside biosynthetic process via lactosylceramide; protein glycosylation; and sialylation. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
149 residues, UniProt reviewed canonical sequence.
>Q96LM9|C20orf173
1 MLSGPHPSPT FRPNPCPWPC LHSLWMEISP TQLCFLSPGP SPQSPSCCFQ GMNSGSELGK
61 LWRKLFKGIP RLSVSHFDFY CGTCVLLGRP QIPQGSSLGN DIDQYPVVFR NASDQGSWMQ
121 LEMLLRKLSD LVWTSDALSD KILEDGLVPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against C20orf173 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.56
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- testis: 34 nTPM
- retina: 0.1 nTPM
- skin: 0.1 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
Single-cell type
- early spermatids: 504 nCPM
- late spermatids: 149 nCPM
- late primary spermatocytes: 39 nCPM
- leydig cells: 0.9 nCPM
- peritubular myoid cells: 0.3 nCPM
- undifferentiated spermatogonia: 0.3 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
- cerebellum: 3.2 nTPM
- cerebral cortex: 2.8 nTPM
- basal ganglia: 1.9 nTPM
- white matter: 1.4 nTPM
- amygdala: 1.2 nTPM
- hippocampal formation: 1.1 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)
- 1.44
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.28
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- 3-sialyltransferase activity
- beta-galactoside (CMP) alpha-2
Cellular components
Protein domainsUniProt · Pfam · InterPro
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads C20orf173 as an antibody target. Whether an autoantibody or antibody against C20orf173 could matter depends on whether native C20orf173 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
C20orf173 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 C20orf173 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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