CIROP
Ciliated left-right organizer metallopeptidase
Also known as: CIROP_HUMAN, LMLN2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A0A1B0GTW7
- Gene
- CIROP
- Ensembl
- ENSG00000283654
- Chromosome
- 14
- Canonical length
- 788 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted membrane proteins
OverviewNCBI Gene
Predicted to enable peptidase activity. Predicted to be involved in establishment of left/right asymmetry. Predicted to be located in membrane. Predicted to be active in cytoplasm. Implicated in visceral heterotaxy 12. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
788 residues, UniProt reviewed canonical sequence.
>A0A1B0GTW7|CIROP
1 MLLLLLLLLL LPPLVLRVAA SRCLHDETQK SVSLLRPPFS QLPSKSRSSS LTLPSSRDPQ
61 PLRIQSCYLG DHISDGAWDP EGEGMRGGSR ALAAVREATQ RIQAVLAVQG PLLLSRDPAQ
121 YCHAVWGDPD SPNYHRCSLL NPGYKGESCL GAKIPDTHLR GYALWPEQGP PQLVQPDGPG
181 VQNTDFLLYV RVAHTSKCHQ ETVSLCCPGW STAAQSQLTA ALTSWAQRRG FVMLPRLCLK
241 LLGSSNLPTL ASQSIRITGP SVIAYAACCQ LDSEDRPLAG TIVYCAQHLT SPSLSHSDIV
301 MATLHELLHA LGFSGQLFKK WRDCPSGFSV RENCSTRQLV TRQDEWGQLL LTTPAVSLSL
361 AKHLGVSGAS LGVPLEEEEG LLSSHWEARL LQGSLMTATF DGAQRTRLDP ITLAAFKDSG
421 WYQVNHSAAE ELLWGQGSGP EFGLVTTCGT GSSDFFCTGS GLGCHYLHLD KGSCSSDPML
481 EGCRMYKPLA NGSECWKKEN GFPAGVDNPH GEIYHPQSRC FFANLTSQLL PGDKPRHPSL
541 TPHLKEAELM GRCYLHQCTG RGAYKVQVEG SPWVPCLPGK VIQIPGYYGL LFCPRGRLCQ
601 TNEDINAVTS PPVSLSTPDP LFQLSLELAG PPGHSLGKEQ QEGLAEAVLE ALASKGGTGR
661 CYFHGPSITT SLVFTVHMWK SPGCQGPSVA TLHKALTLTL QKKPLEVYHG GANFTTQPSK
721 LLVTSDHNPS MTHLRLSMGL CLMLLILVGV MGTTAYQKRA TLPVRPSASY HSPELHSTRV
781 PVRGIREVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CIROP 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)
- 0.35
- Highest tissue expression
- 0.4 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 0.4 nTPM
- bone marrow: 0.2 nTPM
- epididymis: 0.2 nTPM
- midbrain: 0.2 nTPM
- pituitary gland: 0.2 nTPM
- skin: 0.2 nTPM
Single-cell type
- retinal amacrine cells: 3.5 nCPM
- platelets: 2.8 nCPM
- epicardial cells: 2.3 nCPM
- oligodendrocytes: 1.3 nCPM
- enteric stem cells: 0.6 nCPM
- fibro-adipogenic progenitors: 0.6 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 1.4 nTPM
- basal ganglia: 1.3 nTPM
- white matter: 1.3 nTPM
- midbrain: 1.1 nTPM
- pons: 1.1 nTPM
- cerebral cortex: 1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CIROP.
Disease | AllUniProt
Conditions CIROP is implicated in, by any mechanism.
- Heterotaxy, visceral, 12, autosomal (HTX12) MIM:619702
Disease | GeneticClinVar
10 pathogenic / likely-pathogenic of 21 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Heterotaxy, visceral, 12, autosomal
- Trichothiodystrophy 1, photosensitive
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CIROP as an antibody target. Whether an autoantibody or antibody against CIROP could matter depends on whether native CIROP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CIROP 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 CIROP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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