TTLL13
Tubulin polyglutamylase TTLL13
Also known as: FLJ46079, MGC33417, TTL13_HUMAN, TTLL13P
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NNM8
- Gene
- TTLL13
- Ensembl
- ENSG00000213471
- Chromosome
- 15
- Canonical length
- 815 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Basal body,Cytosol
OverviewNCBI Gene
Predicted to enable tubulin binding activity and tubulin-glutamic acid ligase activity. Predicted to be involved in microtubule bundle formation. Predicted to be located in cytosol. Predicted to be active in ciliary basal body. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
815 residues, UniProt reviewed canonical sequence.
>A6NNM8|TTLL13
1 MEPSTCRTME SEEDYVEEKE SEKCVKEGVT NPSNSSQQAL LKADYKALKN GVPSPIMATK
61 IPKKVIAPVD TGDLEAGRRK RRRKRRSLAI NLTNCKYESV RRAAQMCGLK EVGEDEEWTL
121 YWTDCAVSLE RVMDMKRFQK INHFPGMTEI CRKDLLARNL NRMYKLYPSE YNIFPRTWCL
181 PADYGDFQSY GRQRKARTYI CKPDSGCQGR GIFITRNPRE IKPGEHMICQ QYISKPLLID
241 GFKFDMRVYV LITSCDPLRI FTYEEGLARF ATTPYMEPSH NNLDNVCMHL TNYAINKHNE
301 NFVRDGAVGS KRKLSTLNIW LQEHSYNPGE LWGDIEDIII KTIISAHSVL RHNYRTCFPQ
361 YLNGGTCACF EILGFDILLD HKLKPWLLEV NHSPSFTTDS CLDQEVKDAL LCDAMTLVNL
421 RGCDKRKVME EDKRRVKERL FQCYRQPRES RKEKTESSHV AMLDQERYED SHLGKYRRIY
481 PGPDTEKYAR FFKHNGSLFQ ETAASKAREE CARQQLEEIR LKQEQQETSG TKRQKARDQN
541 QGESAGEKSR PRAGLQSLST HLAYRNRNWE KELLPGQLDT MRPQEIVEEE ELERMKALLQ
601 RETLIRSLGI VEQLTRLQHP GPQGQKKLHE SRDRLGSQEL KSMSLVLLVL LRGAATEQGA
661 PHFLHPVLPH ESIPRILGAL PSMNAAIPHV PRYHLQPKNF NWTGEPAAIN SCSLSMKKAG
721 RCYFSSARIR LTSQGQASRR LEAINRVLAG SVPPTLTPKQ GYFLQPERVA SDSWTECTLP
781 SMVNSEHRAA KVPLCPASAP MLQRSRALLN INQFRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TTLL13 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)
- 0.46
- Highest tissue expression
- 7.6 nTPM
Expression across tissuesHPA
Tissue
- testis: 7.6 nTPM
- duodenum: 0.1 nTPM
- epididymis: 0.1 nTPM
- rectum: 0.1 nTPM
- retina: 0.1 nTPM
- adipose tissue: 0 nTPM
Single-cell type
- late spermatids: 5.2 nCPM
- early spermatids: 1.7 nCPM
- astrocytes: 0.7 nCPM
- late primary spermatocytes: 0.7 nCPM
- ependymal cells: 0.6 nCPM
- brain excitatory neurons: 0.4 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
- hippocampal formation: 0.3 nTPM
- cerebral cortex: 0.2 nTPM
- pons: 0.2 nTPM
- thalamus: 0.2 nTPM
- white matter: 0.2 nTPM
- amygdala: 0.1 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)
- 1.18
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.71
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
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 TTLL13 as an antibody target. Whether an autoantibody or antibody against TTLL13 could matter depends on whether native TTLL13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TTLL13 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 TTLL13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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