TTLL9
Probable tubulin polyglutamylase TTLL9
Also known as: C20orf125, dJ310O13.1, TTLL9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q3SXZ7
- Gene
- TTLL9
- Ensembl
- ENSG00000131044
- Chromosome
- 20
- Canonical length
- 439 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Microtubules,Mitotic spindle,Primary cilium,Basal body,Mid piece,Principal piece,End piece
OverviewNCBI Gene
Predicted to enable tubulin binding activity and tubulin-glutamic acid ligase activity. Predicted to be involved in flagellated sperm motility and microtubule cytoskeleton organization. Predicted to act upstream of or within protein polyglutamylation. Predicted to be located in cytoplasm; microtubule; and motile cilium. Predicted to be active in ciliary basal body. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
439 residues, UniProt reviewed canonical sequence.
>Q3SXZ7|TTLL9
1 MVPSREALLG PGTTAIRCPK KLQNQNYKGH GLSKGKEREQ RASIRFKTTL MNTLMDVLRH
61 RPGWVEVKDE GEWDFYWCDV SWLRENFDHT YMDEHVRISH FRNHYELTRK NYMVKNLKRF
121 RKQLEREAGK LEAAKCDFFP KTFEMPCEYH LFVEEFRKNP GITWIMKPVA RSQGKGIFLF
181 RRLKDIVDWR KDTRSSDDQK DDIPVENYVA QRYIENPYLI GGRKFDLRVY VLVMSVFAEC
241 LLWSGHRRQD VHLTNVAVQK TSPDYHPKKG CKWTLQRFRQ YLASKHGPEA VETLFRDIDN
301 IFVKSLQSVQ KVIISDKHCF ELYGYDILID QDLKPWLLEV NASPSLTASS QEDYELKTCL
361 LEDTLHVVDM EARLTGREKR VGGFDLMWND GPVSREEGAP DLSGMGNFVT NTHLGCVNDR
421 KKQLRQLFCS LQVQKKASSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TTLL9 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)
- 0.32
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 15 nTPM
- testis: 3.1 nTPM
- fallopian tube: 2.5 nTPM
- epididymis: 2.4 nTPM
- basal ganglia: 1.9 nTPM
- hippocampal formation: 1.7 nTPM
Single-cell type
- ependymal cells: 319 nCPM
- choroid plexus epithelial cells: 316 nCPM
- respiratory ciliated cells: 211 nCPM
- late spermatids: 147 nCPM
- fallopian tube ciliated cells: 106 nCPM
- endometrial ciliated cells: 87 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: 22 nTPM
- midbrain: 7 nTPM
- medulla oblongata: 6.2 nTPM
- pons: 4.1 nTPM
- spinal cord: 4.1 nTPM
- hippocampal formation: 3.1 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)
- 1.29
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.44
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- ATP binding
- metal ion binding
- protein-glutamic acid ligase activity, elongating
- tubulin binding
- tubulin-glutamic acid ligase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TTLL9 as an antibody target. Whether an autoantibody or antibody against TTLL9 could matter depends on whether native TTLL9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TTLL9 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 TTLL9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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