CLIC2
Chloride intracellular channel protein 2
Also known as: CLCNL2, CLIC2_HUMAN, XAP121
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15247
- Gene
- CLIC2
- Ensembl
- ENSG00000155962
- Chromosome
- X
- Canonical length
- 247 aa
- Protein class
- Disease related genes, Human disease related genes, Potential drug targets, Predicted intracellular proteins, Transporters
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
OverviewNCBI Gene
This gene encodes a chloride intracellular channel protein. Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. This protein plays a role in inhibiting the function of ryanodine receptor 2. A mutation in this gene is the cause of an X-linked form of cognitive disability. [provided by RefSeq, Jul 2017]
Canonical amino-acid sequenceUniProt
247 residues, UniProt reviewed canonical sequence.
>O15247|CLIC2
1 MSGLRPGTQV DPEIELFVKA GSDGESIGNC PFCQRLFMIL WLKGVKFNVT TVDMTRKPEE
61 LKDLAPGTNP PFLVYNKELK TDFIKIEEFL EQTLAPPRYP HLSPKYKESF DVGCNLFAKF
121 SAYIKNTQKE ANKNFEKSLL KEFKRLDDYL NTPLLDEIDP DSAEEPPVSR RLFLDGDQLT
181 LADCSLLPKL NIIKVAAKKY RDFDIPAEFS GVWRYLHNAY AREEFTHTCP EDKEIENTYA
241 NVAKQKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLIC2 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
- 1
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- spleen: 47 nTPM
- thyroid gland: 30 nTPM
- lung: 29 nTPM
- lymph node: 28 nTPM
- tonsil: 24 nTPM
- adipose tissue: 22 nTPM
Single-cell type
- kupffer cells: 210 nCPM
- cdc: 197 nCPM
- alveolar cells type 2: 143 nCPM
- alveolar cells type 1: 114 nCPM
- lymphatic endothelial cells: 111 nCPM
- vascular endothelial cells: 110 nCPM
Immune cell
- myeloid DC: 48 nTPM
- intermediate monocyte: 19 nTPM
- non-classical monocyte: 14 nTPM
- plasmacytoid DC: 5.2 nTPM
- classical monocyte: 3.6 nTPM
- total PBMC: 2.1 nTPM
Brain region
- thalamus: 9.6 nTPM
- white matter: 8.4 nTPM
- spinal cord: 8.3 nTPM
- cerebral cortex: 8.1 nTPM
- basal ganglia: 7.9 nTPM
- choroid plexus: 7.8 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)
- 1.09
- gnomAD pLI
- 0.05
- gnomAD missense Z
- 1.27
- DepMap mean gene effect
- 0.16
- 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
- chloride transport
- regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion
- regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Intracellular chloride channel
- Glutathione S-transferase, C-terminal-like
- Thioredoxin-like superfamily
- Glutathione S-transferase, C-terminal domain superfamily
- Glutathione transferase family
- CLIC, N-terminal domain
- Glutathione S-transferase, C-terminal domain
- CLIC-like N-terminal domain
- Chloride intracellular channel protein 2, C-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CLIC2 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 CLIC2 as an antibody target. Whether an autoantibody or antibody against CLIC2 could matter depends on whether native CLIC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLIC2 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 CLIC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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