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Nyxnob
Spontaneous Allele Detail
Nomenclature
Symbol: Nyxnob
Name: nyctalopin; no b wave
MGI ID: MGI:2177945
Synonyms: nob
Gene: Nyx  Location: ChrX:13466110-13489313 bp, + strand  Genetic Position: ChrX, 8.37 cM
Mutation
origin
Strain of Origin:  BALB/cGr-nr
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Nyx Mutation:  0 strains or lines available
Notes
Arose spontaneously on BALB/cGr-nr/nr (nervous) and then transferred to BALB/cByJ inbred strain (J:50824).

References
Original:  J:50824 Pardue MT, et al., A naturally occurring mouse model of X-linked congenital stationary night blindness. Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2443-9
All:  13 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory