DRAXIN
Draxin
Also known as: C1orf187, DRAXI_HUMAN, FLJ34999, Neucrin
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NBI3
- Gene
- DRAXIN
- Ensembl
- ENSG00000162490
- Chromosome
- 1
- Canonical length
- 349 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted in brain
OverviewNCBI Gene
Enables molecular adaptor activity. Predicted to be involved in negative regulation of canonical Wnt signaling pathway and nervous system development. Predicted to act upstream of or within negative regulation of axon extension and negative regulation of hippocampal neuron apoptotic process. Predicted to be active in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
349 residues, UniProt reviewed canonical sequence.
>Q8NBI3|DRAXIN
1 MAGPAIHTAP MLFLVLLLPL ELSLAGALAP GTPARNLPEN HIDLPGPALW TPQASHHRRR
61 GPGKKEWGPG LPSQAQDGAV VTATRQASRL PEAEGLLPEQ SPAGLLQDKD LLLGLALPYP
121 EKENRPPGWE RTRKRSREHK RRRDRLRLHQ GRALVRGPSS LMKKAELSEA QVLDAAMEES
181 STSLAPTMFF LTTFEAAPAT EESLILPVTS LRPQQAQPRS DGEVMPTLDM ALFDWTDYED
241 LKPDGWPSAK KKEKHRGKLS SDGNETSPAE GEPCDHHQDC LPGTCCDLRE HLCTPHNRGL
301 NNKCFDDCMC VEGLRCYAKF HRNRRVTRRK GRCVEPETAN GDQGSFINVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DRAXIN 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.65
- Highest tissue expression
- 1 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 1 nTPM
- cerebellum: 1 nTPM
- amygdala: 0.9 nTPM
- cerebral cortex: 0.8 nTPM
- salivary gland: 0.6 nTPM
- bone marrow: 0.5 nTPM
Single-cell type
- nk-cells: 16 nCPM
- t-cells: 4.3 nCPM
- undifferentiated spermatogonia: 3.5 nCPM
- brain inhibitory neurons: 3.4 nCPM
- late spermatids: 3.1 nCPM
- neutrophil progenitors: 2.6 nCPM
Immune cell
- basophil: 2.4 nTPM
- neutrophil: 0.8 nTPM
- gdT-cell: 0.5 nTPM
- classical monocyte: 0.3 nTPM
- memory CD8 T-cell: 0.3 nTPM
- MAIT T-cell: 0.2 nTPM
Brain region
- thalamus: 11 nTPM
- medulla oblongata: 7.6 nTPM
- amygdala: 5.3 nTPM
- basal ganglia: 4.9 nTPM
- cerebral cortex: 4.7 nTPM
- white matter: 4.7 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)
- 1.53
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.32
- DepMap mean gene effect
- 0.03
- 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
- anterior commissure morphogenesis
- axon guidance
- dorsal spinal cord development
- forebrain development
- hippocampal neuron apoptotic process
- negative regulation of axon extension
- negative regulation of canonical Wnt signaling pathway
- negative regulation of hippocampal neuron apoptotic process
- Wnt signaling pathway
- commissural neuron differentiation in spinal cord
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Draxin
- Draxin
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DRAXIN 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 DRAXIN as an antibody target. Whether an autoantibody or antibody against DRAXIN could matter depends on whether native DRAXIN is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DRAXIN is annotated as secreted, so native DRAXIN circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label DRAXIN as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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