ZNHIT1
Zinc finger HIT domain-containing protein 1
Also known as: CG1I, H_DJ0747G18.14, ZNFN4A1, ZNHI1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43257
- Gene
- ZNHIT1
- Ensembl
- ENSG00000106400
- Chromosome
- 7
- Canonical length
- 154 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables histone binding activity. Involved in muscle cell differentiation and positive regulation of DNA damage response, signal transduction by p53 class mediator. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
154 residues, UniProt reviewed canonical sequence.
>O43257|ZNHIT1
1 MVEKKTSVRS QDPGQRRVLD RAARQRRINR QLEALENDNF QDDPHAGLPQ LGKRLPQFDD
61 DADTGKKKKK TRGDHFKLRF RKNFQALLEE QNLSVAEGPN YLTACAGPPS RPQRPFCAVC
121 GFPSPYTCVS CGARYCTVRC LGTHQETRCL KWTVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNHIT1 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)
- 0.51
- Highest tissue expression
- 337 nTPM
Expression across tissuesHPA
Tissue
- liver: 337 nTPM
- choroid plexus: 183 nTPM
- kidney: 166 nTPM
- spinal cord: 161 nTPM
- midbrain: 149 nTPM
- amygdala: 149 nTPM
Single-cell type
- hepatocytes: 988 nCPM
- esophageal apical cells: 426 nCPM
- esophageal suprabasal cells: 393 nCPM
- enterocytes: 368 nCPM
- gastric progenitor cells: 346 nCPM
- decidual stromal cells: 329 nCPM
Immune cell
- total PBMC: 235 nTPM
- basophil: 232 nTPM
- eosinophil: 221 nTPM
- classical monocyte: 215 nTPM
- non-classical monocyte: 207 nTPM
- intermediate monocyte: 203 nTPM
Brain region
- white matter: 96 nTPM
- cerebellum: 88 nTPM
- medulla oblongata: 87 nTPM
- choroid plexus: 82 nTPM
- thalamus: 80 nTPM
- spinal cord: 80 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)
- 1.58
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.12
- DepMap mean gene effect
- -0.29
- 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
- calcium ion homeostasis
- chromatin remodeling
- heart process
- hematopoietic stem cell homeostasis
- intestinal stem cell homeostasis
- muscle cell differentiation
- negative regulation of G0 to G1 transition
- negative regulation of transcription by RNA polymerase II
- positive regulation of DNA damage response, signal transduction by p53 class mediator
- positive regulation of transcription initiation by RNA polymerase II
- regulation of DNA-templated transcription
- regulation of T cell proliferation
- transcription initiation-coupled chromatin remodeling
- positive regulation of lymphoid progenitor cell differentiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, HIT-type
- HIT zinc finger
- Vps71/ZNHIT1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZNHIT1 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 ZNHIT1 as an antibody target. Whether an autoantibody or antibody against ZNHIT1 could matter depends on whether native ZNHIT1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNHIT1 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 ZNHIT1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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