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Summary Expression Phenotypes Gene Literature (0) GO Terms (0) Nucleotides (7) Proteins (2) Interactants (1) Wiki
XB-GENEPAGE-876680
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 cyp21a2.2

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cytochrome P450 family 21 subfamily A member 2, gene 2

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( Nomenclature history )

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electron transport

Protein Function :


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Diseases: 


Disease Ontology:
congenital adrenal hyperplasia

MIM:
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

External Links:
 
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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