gene

WNT10B

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about WNT10B: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

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Summary

Page for WNT10B Gene

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🧬 Gene Info

Gene Symbol	WNT10B
Chromosome	12q13.12
Function	is a protein-coding gene encoding a secreted signaling molecule critical for embryonic development, tissue homeostasis, and cellular differentiation.
Molecular Weight	42 kDa
Amino Acids	30 aa
Pathways	WNT, Wnt, Wnt signaling, Wnt pathway
UniProt ID	Q9Y5Q1
NCBI Gene ID	7480
Ensembl ID	ENSG00000169884
OMIM	605397
GeneCards	WNT10B
Human Protein Atlas	WNT10B
Signal peptide	N-terminal 25-30 amino acids for secretion
Wnt domain	Conserved ~350 amino acid signaling domain
12 conserved cysteine residues	Form disulfide bonds
Associated Diseases	neurodegeneration
Databases	GeneCards HPA STRING

🔮 Predicted Structure: WNT10B — AlphaFold Q9Y5Q1 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

WNT10B Gene

gene · 583 words

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Pathway Diagram

graph TD
    WNT10B["WNT10B"]
    neurodegeneration["neurodegeneration"]
    WNT10B -->|"implicated_in"| neurodegeneration
    style WNT10B fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Incoming (0)

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Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

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No targeting hypotheses

Mentioning Analyses (0)

Scientific analyses that reference this entity

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Experiments (0)

Experimental studies targeting or related to this entity

Experiment	Type	Disease	Score	Feasibility	Model	Status	Est. Cost
No experiments found

Related Papers (0)

Scientific publications cited in analyses involving this entity

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Debates (0)

Multi-agent debates referencing this entity

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Related Research

Hypotheses and analyses mentioning WNT10B in their description or question text

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