CIBAR1
CBY1-interacting BAR domain-containing protein 1
Also known as: BARMR1, CBAR1_HUMAN, FAM92A, FAM92A1, FLJ38979
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A1XBS5
- Gene
- CIBAR1
- Ensembl
- ENSG00000188343
- Chromosome
- 8
- Canonical length
- 289 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Mitochondria
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables phospholipid binding activity. Involved in several processes, including inner mitochondrial membrane organization; limb morphogenesis; and membrane tubulation. Located in several cellular components, including centriole; ciliary base; and mitochondrial crista. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
289 residues, UniProt reviewed canonical sequence.
>A1XBS5|CIBAR1
1 MMRRTLENRN AQTKQLQTAV SNVEKHFGEL CQIFAAYVRK TARLRDKADL LVNEINAYAA
61 TETPHLKLGL MNFADEFAKL QDYRQAEVER LEAKVVEPLK TYGTIVKMKR DDLKATLTAR
121 NREAKQLTQL ERTRQRNPSD RHVISQAETE LQRAAMDASR TSRHLEETIN NFERQKMKDI
181 KTIFSEFITI EMLFHGKALE VYTAAYQNIQ NIDEDEDLEV FRNSLYAPDY SSRLDIVRAN
241 SKSPLQRSLS AKCVSGTGQV STCRLRKDQQ AEDDEDDELD VTEEENFLKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CIBAR1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.41
- Highest tissue expression
- 102 nTPM
Expression across tissuesHPA
Tissue
- testis: 102 nTPM
- cerebral cortex: 30 nTPM
- epididymis: 25 nTPM
- choroid plexus: 23 nTPM
- adrenal gland: 22 nTPM
- heart muscle: 22 nTPM
Single-cell type
- early spermatids: 1,493 nCPM
- late primary spermatocytes: 1000 nCPM
- late spermatids: 952 nCPM
- cardiomyocytes: 253 nCPM
- undifferentiated spermatogonia: 108 nCPM
- oocytes: 97 nCPM
Immune cell
- myeloid DC: 3.3 nTPM
- classical monocyte: 2 nTPM
- intermediate monocyte: 1.3 nTPM
- NK-cell: 1.2 nTPM
- T-reg: 0.7 nTPM
- total PBMC: 0.6 nTPM
Brain region
- choroid plexus: 50 nTPM
- cerebral cortex: 41 nTPM
- hippocampal formation: 38 nTPM
- basal ganglia: 38 nTPM
- cerebellum: 37 nTPM
- hypothalamus: 37 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CIBAR1.
Disease | AllUniProt
Conditions CIBAR1 is implicated in, by any mechanism.
- Polydactyly, postaxial, A9 (PAPA9) MIM:618219
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 48 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Polydactyly, postaxial, type A9
- Postaxial polydactyly type A
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)
- 1.11
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- cilium assembly
- inner mitochondrial membrane organization
- limb morphogenesis
- membrane organization
- membrane tubulation
- positive regulation of smoothened signaling pathway
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CIBAR1 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 CIBAR1 as an antibody target. Whether an autoantibody or antibody against CIBAR1 could matter depends on whether native CIBAR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CIBAR1 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 CIBAR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...