Symbol
Name
ID
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Synonyms
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Pkca
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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(31)
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Alleles and phenotypes
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All alleles(8) :
Targeted, knock-out(3)
Gene trapped(5)
| Homozygous null mice show no overt macroscopic abnormalities, however examination of one line revealed increased cardiac muscle contractility and protection against heart failure. |
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Polymorphisms
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RFLP(5)
SNPs within 2kb(1964 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (47 records)
Data Summary:
Assays (7)
Results (221)
Tissues (160)
Images (18)
Theiler Stages: 21,22,23,24,25,26,28
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Assay Type |
Assays |
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Results |
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Western blot |
2 |
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17 |
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RT-PCR |
2 |
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92 |
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RNA in situ |
2 |
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109 |
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Immunohistochemistry |
1 |
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3 |
cDNA source data(72)
External Resources:
Allen Brain Atlas
GENSAT
GEO
ArrayExpress
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Molecular reagents
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All nucleic(85)
Genomic(3)
cDNA(74)
Primer pair(7)
Other(1)
Antibodies(3)
Microarray probesets(2)
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Other database links
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Protein domains
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| InterPro ID |
Description |
| IPR000008 |
C2 calcium-dependent membrane targeting |
| IPR000719 |
Protein kinase, catalytic domain |
| IPR000961 |
AGC-kinase, C-terminal |
| IPR002219 |
Protein kinase C-like, phorbol ester/diacylglycerol binding |
| IPR002290 |
Serine/threonine-protein kinase domain |
| IPR008271 |
Serine/threonine-protein kinase, active site |
| IPR008973 |
C2 calcium/lipid-binding domain, CaLB |
| IPR011009 |
Protein kinase-like domain |
| IPR014375 |
Protein kinase C, alpha/beta/gamma types |
| IPR015745 |
Protein kinase C |
| IPR017441 |
Protein kinase, ATP binding site |
| IPR017442 |
Serine/threonine-protein kinase-like domain |
| IPR017892 |
Protein kinase, C-terminal |
| IPR018029 |
C2 membrane targeting protein |
| IPR020454 |
Diacylglycerol/phorbol-ester binding |
| IPR020477 |
C2 region |
Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:12309
Yang-Feng TL et al.,
"Protein kinase C genes in the mouse: Pkca maps to MMU 11 and Pkcc to MMU7."
Cytogenet Cell Genet 1987;46():723
(Latest)
J:152506
Jin ZB et al.,
"Targeted deletion of miR-182, an abundant retinal microRNA."
Mol Vis 2009;15():523-33
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All references(145)
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Other accession IDs
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MGD-MRK-13327, MGI:2144325
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