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Nnc1C3H/HeJ
QTL Variant Detail
Summary
QTL variant: Nnc1C3H/HeJ
Name: neuron number control 1; C3H/HeJ
MGI ID: MGI:3036086
QTL: Nnc1  Location: unknown  Genetic Position: Chr11, Syntenic
Variant
origin
Strain of Specimen:  C3H/HeJ
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers increased retinal ganglion cell numbers compared to C57BL/6J. (J:45194)
Inheritance:    Other (see notes)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Notes
Nnc1 exhibits additive inheritance.

Mapping and Phenotype information for this QTL, its variants and associated markers

J:45194

Using BXH and BXD RI lines, a quantitative locus, Nnc1 , was mapped to mouse Chromosome 11 between Hoxb and Krt1 in the region of the Tstap91a locus. Nnc1 is involved with determining retinal ganglion numbers in mice.

References
Original:  J:45194 Williams RW, et al., Natural variation in neuron number in mice is linked to a major quantitative trait locus on Chr 11. J Neurosci. 1998 Jan 1;18(1):138-46
All:  1 reference(s)

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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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory