Symbol
Name
ID
|
|
|
STS
|
D7Mit19,D7Mit31
|
|
Synonyms
|
skc35
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian
homology
|
|
|
Sequences
|
All sequences(32)
|
Alleles
and
phenotypes
|
All alleles(105) :
Spontaneous(26)
Chemically induced(8)
Radiation induced(71)
Other(1)
| Numerous mutations at this locus result in albinism or hypopigmentation. Albinism is associated with reduced number of optic nerve fibers and mutants can have impaired vision. Some alleles are lethal. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
Phenotype Images (6)
|
|
Polymorphisms
|
All PCR and RFLP(28) :
PCR(2)
RFLP(26)
SNPs within 2kb(456 from dbSNP Build 128)
|
Gene Ontology
(GO)
classifications
|
|
|
Expression
|
Literature Summary: (11 records)
Data Summary:
Assays (3)
Results (8)
Tissues (4)
Images (8)
Theiler Stages: 19,20,22,25
| |
Assay Type |
Assays |
|
Results |
| |
RNA in situ |
3 |
|
8 |
cDNA source data(48)
External Resources:
Allen Brain Atlas
GENSAT
GEO
|
Molecular
reagents
|
All nucleic(168)
Genomic(82)
cDNA(53)
Primer pair(2)
Other(31)
Microarray probesets(3)
|
Other database
links
|
|
Protein
domains
|
Graphical View
of Protein Domain Structure
|
|
References
|
(Earliest)
J:100
Haldane JBS et al.,
"Reduplication in mice"
J Genet 1915;5():133-135
(Latest)
J:149703
Whitney IE et al.,
"Multiple genes on chromosome 7 regulate dopaminergic amacrine cell number in the mouse retina."
Invest Ophthalmol Vis Sci 2009 May;50(5):1996-2003
|
All references(450)
|
Other
accession IDs
|
MGD-MRK-15315, MGD-MRK-1695, MGI:2671628
|
