TXLNB
Beta-taxilin
Also known as: C6orf198, dJ522B19.2, DKFZp451A175, MDP77, TXLNB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N3L3
- Gene
- TXLNB
- Ensembl
- ENSG00000164440
- Chromosome
- 6
- Canonical length
- 684 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable syntaxin binding activity. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
684 residues, UniProt reviewed canonical sequence.
>Q8N3L3|TXLNB
1 MEANHSEQLS AERQSTPPGD SSSLPSHNGL EKEDGQDSPT PVQPPEKEAS VHPDISEELN
61 RQLEDIINTY GSAASTAGKE GSARASEQPE NAESPDNEDG DCEETTEEAG REPVASGEPP
121 TVKEPVSNKE QKLEKKILKG LGKEANLLMQ NLNKLQTPEE KFDFLFKKYA ELLDEHRTEQ
181 KKLKLLQKKQ VQIQKEKDQL QGEHSRAILA RSKLESLCRE LQRHNKTLKE EALQRAREEE
241 EKRKEITSHF QSTLTDIQGQ IEQQSERNMK LCQENTELAE KLKSIIDQYE LREEHLDKIF
301 KHRELQQKLV DAKLEQAQEM MKEAEERHKR EKEYLLNQAA EWKLQAKVLK EQETVLQAQL
361 TLYSGRFEEF QSTLTKSNEV FATFKQEMDK TTKKMKKLEK DTATWKARFE NCNKALLDMI
421 EEKALRAKEY ECFVMKIGRL ENLCRALQEE RNELHKKIRD AEISEKDDQS QHNSDEEPES
481 NVSVDQEIDA EEVNSVQTAV KNLATAFMII HHPESTPHQS KETQPEIGSS QESADAALKE
541 PEQPPLIPSR DSESPLPPLT PQAEAEGGSD AEPPSKASNS PAGLGAETQC EGLPVGAQAD
601 QASWKPEAEA SGQAPQAPTE ASLQKMEADV PAPACAAEEH VAAMVPACEP SRQPPRAAAE
661 ELPVGASAGP QPRNVADTNL EGVDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TXLNB 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)
- 0.59
- Highest tissue expression
- 281 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 281 nTPM
- tongue: 177 nTPM
- heart muscle: 77 nTPM
- ovary: 8.2 nTPM
- thymus: 7.2 nTPM
- esophagus: 4.1 nTPM
Single-cell type
- myonuclei: 195 nCPM
- thymic myoid cells: 132 nCPM
- late spermatids: 57 nCPM
- cardiomyocytes: 54 nCPM
- early spermatids: 19 nCPM
- late primary spermatocytes: 11 nCPM
Immune cell
- memory B-cell: 1.9 nTPM
- naive B-cell: 0.8 nTPM
- neutrophil: 0.7 nTPM
- memory CD8 T-cell: 0.3 nTPM
- MAIT T-cell: 0.2 nTPM
- gdT-cell: 0.1 nTPM
Brain region
- spinal cord: 4.8 nTPM
- medulla oblongata: 4.4 nTPM
- white matter: 4.4 nTPM
- hypothalamus: 3.8 nTPM
- hippocampal formation: 3.1 nTPM
- midbrain: 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)
- 1.11
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.64
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TXLNB 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 TXLNB as an antibody target. Whether an autoantibody or antibody against TXLNB could matter depends on whether native TXLNB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TXLNB 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 TXLNB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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