Symbol
Name
ID
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Synonyms
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1810018P12Rik, Atpsk2, Sk2
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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(37)
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Alleles and phenotypes
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All alleles(3) :
Gene trapped(2)
Spontaneous(1)
| Mice homozygous for mutation s in this gene display delayed growth and shorter limbs and other abnormalities in bone formation. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
Phenotype Images (1)
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Polymorphisms
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PCR(1)
SNPs within 2kb(396 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (5 records)
Data Summary:
Assays (5)
Results (71)
Tissues (56)
Images (28)
Theiler Stages: 19,20,21,22,24,28
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Assay Type |
Assays |
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Results |
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RT-PCR |
3 |
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17 |
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RNA in situ |
2 |
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54 |
cDNA source data(58)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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Molecular reagents
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All nucleic(67)
Genomic(2)
cDNA(58)
Primer pair(6)
Other(1)
Microarray probesets(5)
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Pathways
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Other database links
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Protein domains
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| InterPro ID |
Description |
| IPR002650 |
Sulphate adenylyltransferase |
| IPR002891 |
Adenylylsulphate kinase, C-terminal |
| IPR014729 |
Rossmann-like alpha/beta/alpha sandwich fold |
| IPR015947 |
Pseudouridine synthase/archaeosine transglycosylase-like |
Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:5109
Lane PW et al.,
"Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia, brachymorphic, and stubby."
J Hered 1968 Sep-Oct;59(5):300-8
(Latest)
J:152865
Georgas K et al.,
"Analysis of early nephron patterning reveals a role for distal RV proliferation in fusion to the ureteric tip via a cap mesenchyme-derived connecting segment."
Dev Biol 2009 Aug 15;332(2):273-86
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All references(44)
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Other accession IDs
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MGD-MRK-1582, MGI:1921420, MGI:2147481, MGI:88171
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