HTATIP2
Protein HTATIP2
Also known as: CC3, FLJ26963, HTAI2_HUMAN, SDR44U1, TIP30
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BUP3
- Gene
- HTATIP2
- Ensembl
- ENSG00000109854
- Chromosome
- 11
- Canonical length
- 242 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables protein serine/threonine kinase activity. Involved in import into nucleus and regulation of angiogenesis. Acts upstream of or within positive regulation of programmed cell death; positive regulation of transcription by RNA polymerase II; and protein autophosphorylation. Located in cytosol and nuclear envelope. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
242 residues, UniProt reviewed canonical sequence.
>Q9BUP3|HTATIP2
1 MAETEALSKL REDFRMQNKS VFILGASGET GRVLLKEILE QGLFSKVTLI GRRKLTFDEE
61 AYKNVNQEVV DFEKLDDYAS AFQGHDVGFC CLGTTRGKAG AEGFVRVDRD YVLKSAELAK
121 AGGCKHFNLL SSKGADKSSN FLYLQVKGEV EAKVEELKFD RYSVFRPGVL LCDRQESRPG
181 EWLVRKFFGS LPDSWASGHS VPVVTVVRAM LNNVVRPRDK QMELLENKAI HDLGKAHGSL
241 KPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HTATIP2 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)
- 0.28
- Highest tissue expression
- 128 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 128 nTPM
- small intestine: 114 nTPM
- liver: 91 nTPM
- colon: 83 nTPM
- rectum: 76 nTPM
- stomach: 71 nTPM
Single-cell type
- platelets: 296 nCPM
- enterocytes: 258 nCPM
- esophageal suprabasal cells: 179 nCPM
- extravillous trophoblasts: 161 nCPM
- colonocytes: 160 nCPM
- salivary duct cells: 136 nCPM
Immune cell
- neutrophil: 306 nTPM
- basophil: 235 nTPM
- eosinophil: 172 nTPM
- T-reg: 141 nTPM
- non-classical monocyte: 136 nTPM
- classical monocyte: 134 nTPM
Brain region
- white matter: 52 nTPM
- basal ganglia: 33 nTPM
- choroid plexus: 31 nTPM
- medulla oblongata: 30 nTPM
- cerebral cortex: 30 nTPM
- pons: 28 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)
- 1.9
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.55
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of programmed cell death
- positive regulation of transcription by RNA polymerase II
- protein autophosphorylation
- regulation of translation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HTATIP2 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 HTATIP2 as an antibody target. Whether an autoantibody or antibody against HTATIP2 could matter depends on whether native HTATIP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HTATIP2 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 HTATIP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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