HABP4
Intracellular hyaluronan-binding protein 4
Also known as: HABP4_HUMAN, IHABP4, SERBP1L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5JVS0
- Gene
- HABP4
- Ensembl
- ENSG00000130956
- Chromosome
- 9
- Canonical length
- 413 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear membrane,Cytosol
OverviewNCBI Gene
Enables SUMO binding activity. Involved in PML body organization; positive regulation of RNA splicing; and positive regulation of translational initiation. Located in several cellular components, including cytoplasmic stress granule; nuclear lumen; and nuclear membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
413 residues, UniProt reviewed canonical sequence.
>Q5JVS0|HABP4
1 MKGALGSPVA AAGAAMQESF GCVVANRFHQ LLDDESDPFD ILREAERRRQ QQLQRKRRDE
61 AAAAAGAGPR GGRSPAGASG HRAGAGGRRE SQKERKSLPA PVAQRPDSPG GGLQAPGQKR
121 TPRRGEQQGW NDSRGPEGML ERAERRSYRE YRPYETERQA DFTAEKFPDE KPGDRFDRDR
181 PLRGRGGPRG GMRGRGRGGP GNRVFDAFDQ RGKREFERYG GNDKIAVRTE DNMGGCGVRT
241 WGSGKDTSDV EPTAPMEEPT VVEESQGTPE EESPAKVPEL EVEEETQVQE MTLDEWKNLQ
301 EQTRPKPEFN IRKPESTVPS KAVVIHKSKY RDDMVKDDYE DDSHVFRKPA NDITSQLEIN
361 FGNLPRPGRG ARGGTRGGRG RIRRAENYGP RAEVVMQDVA PNPDDPEDFP ALSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HABP4 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)
- 0.71
- Highest tissue expression
- 110 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 110 nTPM
- cerebral cortex: 102 nTPM
- amygdala: 90 nTPM
- midbrain: 78 nTPM
- hippocampal formation: 75 nTPM
- hypothalamus: 72 nTPM
Single-cell type
- late spermatids: 1,345 nCPM
- early spermatids: 310 nCPM
- retinal ganglion cells: 104 nCPM
- vascular smooth muscle cells: 76 nCPM
- retinal amacrine cells: 75 nCPM
- late primary spermatocytes: 73 nCPM
Immune cell
- memory B-cell: 1.9 nTPM
- memory CD4 T-cell: 1.6 nTPM
- memory CD8 T-cell: 1.3 nTPM
- T-reg: 1.3 nTPM
- naive B-cell: 1.1 nTPM
- naive CD4 T-cell: 1.1 nTPM
Brain region
- cerebral cortex: 84 nTPM
- basal ganglia: 81 nTPM
- white matter: 77 nTPM
- medulla oblongata: 74 nTPM
- midbrain: 73 nTPM
- pons: 73 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)
- 0.7
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.13
- DepMap mean gene effect
- 0.01
- 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
- cellular response to mechanical stimulus
- mRNA processing
- PML body organization
- positive regulation of RNA splicing
- positive regulation of translational initiation
- ribosome hibernation
- RNA splicing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HABP4 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 HABP4 as an antibody target. Whether an autoantibody or antibody against HABP4 could matter depends on whether native HABP4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HABP4 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 HABP4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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