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Gene : Pcdh9 R. norvegicus
Primary Identifier  ? RGD:1306348 Name  ? protocadherin 9
Secondary Identifier  ? 1306348 Pharm GKB Identifier  PA33008
NCBI Gene Number  306091 Gene Type  protein-coding
description  ENCODES a protein that exhibits calcium ion binding (inferred) AND INVOLVED IN forebrain development AND ASSOCIATED WITH autism spectrum disorder (ortholog) AND Chromosome 13q Deletion Syndrome (ortholog) AND chromosome 13q14 deletion syndrome (ortholog) AND FOUND IN cell-cell contact zone (ortholog) AND growth cone (ortholog) AND INTERACTS WITH 1 2-dimethylhydrazine AND 17alpha-ethynylestradiol AND 2 2' 4 4'-Tetrabromodiphenyl ether
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Sequence Feature Displayer

Homologue Displayer

Genomics

104 Overlapping Features

Proteomics

Uni Prot Comments Displayer

0 Proteins

Function

Gene Ontology Displayer

Cytoscape Network Displayer

3 Do Annotation

0 Mp Annotation

0 Pw Annotation

Gene --> Homologue Disease Annotations

Gene --> Homologue Mammalian Phenotype

Gene --> Homologue RGD Pathway Annotation

Literature

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Other

0 Cross References

3 Data Sets

1 Organism

1 Synonyms





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