TXLNG
Gamma-taxilin
Also known as: CXorf15, FIAT, FLJ11209, LSR5, MGC126621, MGC126625, TXLNG_HUMAN, TXLNGX
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NUQ3
- Gene
- TXLNG
- Ensembl
- ENSG00000086712
- Chromosome
- X
- Canonical length
- 528 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a member of the taxilin family. The encoded protein binds to the C-terminal coiled-coil region of syntaxin family members 1A, 3A and 4A, and may play a role in intracellular vesicle trafficking. This gene is up-regulated by lipopolysaccharide and the gene product may be involved in cell cycle regulation. The related mouse protein was also shown to inhibit activating transcription factor 4-mediated transcription and thus regulate bone mass accrual. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
Canonical amino-acid sequenceUniProt
528 residues, UniProt reviewed canonical sequence.
>Q9NUQ3|TXLNG
1 MATRVEEAAR GRGGGAEEAT EAGRGGRRRS PRQKFEIGTM EEAGICGLGV KADMLCNSQS
61 NDILQHQGSN CGGTSNKHSL EEDEGSDFIT ENRNLVSPAY CTQESREEIP GGEARTDPPD
121 GQQDSECNRN KEKTLGKEVL LLMQALNTLS TPEEKLAALC KKYADLLEES RSVQKQMKIL
181 QKKQAQIVKE KVHLQSEHSK AILARSKLES LCRELQRHNK TLKEENMQQA REEEERRKEA
241 TAHFQITLNE IQAQLEQHDI HNAKLRQENI ELGEKLKKLI EQYALREEHI DKVFKHKELQ
301 QQLVDAKLQQ TTQLIKEADE KHQREREFLL KEATESRHKY EQMKQQEVQL KQQLSLYMDK
361 FEEFQTTMAK SNELFTTFRQ EMEKMTKKIK KLEKETIIWR TKWENNNKAL LQMAEEKTVR
421 DKEYKALQIK LERLEKLCRA LQTERNELNE KVEVLKEQVS IKAAIKAANR DLATPVMQPC
481 TALDSHKELN TSSKRALGAH LEAEPKSQRS AVQKPPSTGS APAIESVDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TXLNG 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)
- 0.57
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 15 nTPM
- retina: 14 nTPM
- adipose tissue: 14 nTPM
- bone marrow: 14 nTPM
- ovary: 12 nTPM
- lymph node: 12 nTPM
Single-cell type
- somatotrophs: 139 nCPM
- pituicytes/fscs: 111 nCPM
- salivary myoepithelial cells: 100 nCPM
- oocytes: 97 nCPM
- adrenal cortex cells: 95 nCPM
- t-cells: 92 nCPM
Immune cell
- naive CD8 T-cell: 4.4 nTPM
- naive B-cell: 4.1 nTPM
- MAIT T-cell: 4 nTPM
- naive CD4 T-cell: 4 nTPM
- T-reg: 3.8 nTPM
- memory B-cell: 3.7 nTPM
Brain region
- cerebellum: 20 nTPM
- choroid plexus: 18 nTPM
- white matter: 16 nTPM
- hypothalamus: 16 nTPM
- basal ganglia: 15 nTPM
- cerebral cortex: 15 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)
- 0.16
- gnomAD pLI
- 1
- gnomAD missense Z
- 0.09
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TXLNG 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 TXLNG as an antibody target. Whether an autoantibody or antibody against TXLNG could matter depends on whether native TXLNG is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TXLNG 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 TXLNG as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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