congenital stationary night blindness 2A Disease Ontology Browser

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congenital stationary night blindness 2A (DOID:0110871)
Alliance: disease page
Synonyms: congenital stationary night blindness 2A X-linked
Alt IDs: OMIM:300071
Definition: A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23.

Disease References using Mouse Models (6)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Allelic Composition	Genetic Background	Reference	Phenotypes
Cacna1ftm1Ntbh/Cacna1ftm1Ntbh	B6.129-Cacna1f^tm1Ntbh	J:102753	View
Cacna1fnob2/Cacna1fnob2	AXB6/PgnJ	J:123811	View
Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie	B6.Cg-Cacna1f^tm1.1Sdie/J	J:212726	View
Cacna1ftm1.2Sdie/Cacna1ftm1.2Sdie	B6.Cg-Cacna1f^tm1.2Sdie/J	J:212726	View
Cacna1fnob9/Cacna1fnob9	B6(PWD)-Cacna1f^nob9/BocJ	J:267160	View
Cacna1ftm1Ntbh/Y	B6.129-Cacna1f^tm1Ntbh	J:102753	View
Cacna1fnob2/Y	AXB6/PgnJ	J:123811	View
Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie	involves: C57BL/6	J:206214	View
Cacna1ftm1.1Sdie/Cacna1f+	involves: C57BL/6	J:206214	View
Cacna1ftm1.2Sdie/Y	B6.Cg-Cacna1f^tm1.2Sdie/J	J:212726	View
Cacna1ftm1.1Sdie/Y	B6.Cg-Cacna1f^tm1.1Sdie/J	J:212726	View
Cacna1ftm1.1Sdie/Y	involves: C57BL/6	J:206214	View