CATIP
Ciliogenesis-associated TTC17-interacting protein
Also known as: C2orf62, CATIP_HUMAN, MGC50811
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z7H3
- Gene
- CATIP
- Ensembl
- ENSG00000158428
- Chromosome
- 2
- Canonical length
- 387 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Connecting piece,Mid piece
OverviewNCBI Gene
Involved in actin filament polymerization and cilium organization. Located in several cellular components, including actin cytoskeleton; nucleus; and plasma membrane. Implicated in spermatogenic failure 54. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
387 residues, UniProt reviewed canonical sequence.
>Q7Z7H3|CATIP
1 MSSKVYSTGS RAKDHQPSGP ECLPLPEANA EAIDFLSSLH KEELQMLFFS ETLAMVSDTG
61 EPQGELTIEV QRGKYQEKLG MLTYCLFVHA SSRGFLDKML CGNSLLGYLS EKLELMEQHS
121 QDFIKFLILP MERKMSLLKQ DDQLAVTRSI KEGEEVKTGV TSFPWSSIKG FISEAANLVL
181 LRVMAWRRMV PSNARFLTLD TEGKLCYLTY QNLGFQTIQV DHQQAEVFIV EQTVHAEEGI
241 PMSCQYYLLS DGHLAKRIQV GSPGCCIITK MPILREEDEI EPRPVFEKKP LVWEEDMELY
301 SKFLDRKEEL RLGHASYLRQ HPEAHALISD FLLFLLLRQP EDVVTFAAEF FGPFDPWRPS
361 SPALGSSHRP NPFRSLEPEG DARSGAALocalizationUniProt · AlphaFold · HPA
Whether an antibody against CATIP 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- fallopian tube: 19 nTPM
- choroid plexus: 15 nTPM
- testis: 7 nTPM
- epididymis: 4.6 nTPM
- kidney: 4.1 nTPM
- thyroid gland: 3.4 nTPM
Single-cell type
- respiratory ciliated cells: 113 nCPM
- fallopian tube ciliated cells: 111 nCPM
- epididymal efferent duct ciliated cells: 78 nCPM
- ependymal cells: 75 nCPM
- endometrial ciliated cells: 42 nCPM
- late primary spermatocytes: 37 nCPM
Immune cell
- intermediate monocyte: 0.2 nTPM
- neutrophil: 0.2 nTPM
- non-classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- choroid plexus: 12 nTPM
- midbrain: 6.4 nTPM
- medulla oblongata: 5 nTPM
- spinal cord: 4.7 nTPM
- hypothalamus: 2.5 nTPM
- white matter: 2.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CATIP.
Disease | AllUniProt
Conditions CATIP is implicated in, by any mechanism.
- Spermatogenic failure 54 (SPGF54) MIM:619379
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 55 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Spermatogenic failure 54
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)
- 1.16
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ciliogenesis-associated TTC17-interacting protein, dimerization/docking domain
- Ciliogenesis-associated TTC17-interacting protein, N-terminal domain
- Ciliogenesis-associated TTC17-interacting protein, N-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CATIP 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 CATIP as an antibody target. Whether an autoantibody or antibody against CATIP could matter depends on whether native CATIP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CATIP is annotated at the cell surface, where native CATIP is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CATIP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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