CXXC5
CXXC-type zinc finger protein 5
Also known as: CXXC5_HUMAN, HSPC195, RINF, WID
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7LFL8
- Gene
- CXXC5
- Ensembl
- ENSG00000171604
- Chromosome
- 5
- Canonical length
- 322 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a retinoid-inducible nuclear protein containing a CXXC-type zinc finger motif. The encoded protein is involved in myelopoiesis, is required for DNA damage-induced p53 activation, regulates the differentiation of C2C12 myoblasts into myocytes, and negatively regulates cutaneous wound healing. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2015]
Canonical amino-acid sequenceUniProt
322 residues, UniProt reviewed canonical sequence.
>Q7LFL8|CXXC5
1 MSSLGGGSQD AGGSSSSSTN GSGGSGSSGP KAGAADKSAV VAAAAPASVA DDTPPPERRN
61 KSGIISEPLN KSLRRSRPLS HYSSFGSSGG SGGGSMMGGE SADKATAAAA AASLLANGHD
121 LAAAMAVDKS NPTSKHKSGA VASLLSKAER ATELAAEGQL TLQQFAQSTE MLKRVVQEHL
181 PLMSEAGAGL PDMEAVAGAE ALNGQSDFPY LGAFPINPGL FIMTPAGVFL AESALHMAGL
241 AEYPMQGELA SAISSGKKKR KRCGMCAPCR RRINCEQCSS CRNRKTGHQI CKFRKCEELK
301 KKPSAALEKV MLPTGAAFRW FQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CXXC5 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)
- 0.64
- Highest tissue expression
- 147 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 147 nTPM
- spinal cord: 88 nTPM
- liver: 85 nTPM
- skeletal muscle: 75 nTPM
- kidney: 74 nTPM
- pancreas: 59 nTPM
Single-cell type
- early spermatids: 770 nCPM
- late primary spermatocytes: 312 nCPM
- esophageal apical cells: 296 nCPM
- retinal horizontal cells: 289 nCPM
- late spermatids: 251 nCPM
- müller glia: 209 nCPM
Immune cell
- naive B-cell: 97 nTPM
- memory B-cell: 85 nTPM
- NK-cell: 72 nTPM
- plasmacytoid DC: 59 nTPM
- MAIT T-cell: 30 nTPM
- total PBMC: 11 nTPM
Brain region
- cerebellum: 232 nTPM
- white matter: 231 nTPM
- medulla oblongata: 213 nTPM
- pons: 165 nTPM
- spinal cord: 161 nTPM
- midbrain: 154 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)
- 0.42
- gnomAD pLI
- 0.89
- gnomAD missense Z
- 1.58
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
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
- negative regulation of transcription by RNA polymerase II
- positive regulation of canonical NF-kappaB signal transduction
- regulation of generation of precursor metabolites and energy
Molecular functions
- DNA-binding transcription factor binding
- methyl-CpG binding
- sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CXXC5 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 CXXC5 as an antibody target. Whether an autoantibody or antibody against CXXC5 could matter depends on whether native CXXC5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CXXC5 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 CXXC5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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