Symbol
Name
ID
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Synonyms
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3322401A10Rik, BNIP-H, ji
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Genetic Map
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Sequence Map
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Mammalian
homology
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Sequences
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All sequences(23)
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Alleles
and
phenotypes
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All alleles(6) :
Gene trapped(1)
Spontaneous(4)
Chemically induced(1)
| Mutants homozygous for a severe allele show progressive impaired coordination and seizures beginning by 10-16 days of age and die by 4 weeks of age. Homozygotes for milder alleles have abnormal gait, slightly diminished body size and reduced male fertility. |
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Polymorphisms
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SNPs within 2kb(65 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (1 records)
Data Summary:
Assays (2)
Results (18)
Tissues (9)
Images (3)
Theiler Stages: 24,28
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Assay Type |
Assays |
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Results |
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RNA in situ |
1 |
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9 |
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Northern blot |
1 |
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9 |
cDNA source data(47)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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Molecular
reagents
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All nucleic(48)
cDNA(48)
Microarray probesets(4)
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Other database
links
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Protein
domains
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| InterPro ID |
Description |
| IPR001251 |
Cellular retinaldehyde-binding/triple function, C-terminal |
Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:300
Snell GD,
"Linkage of jittery and waltzing in the mouse"
J Hered 1945;36():279-80
(Latest)
J:149430
Concepcion D et al.,
"Multipotent genetic suppression of retrotransposon-induced mutations by Nxf1 through fine-tuning of alternative splicing."
PLoS Genet 2009 May;5(5):e1000484
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All references(15)
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Other
accession IDs
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MGD-MRK-10693, MGD-MRK-11529, MGI:2143893, MGI:2442176, MGI:96640
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