Symbol
Name
ID
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Synonyms
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Cnx31, connexin 31, Cx31, D4Wsu144e, Gjb-3
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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(26)
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Alleles
and
phenotypes
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All alleles(73) :
Targeted, other(3)
Gene trapped(70)
| Homozygous null mice exhibit partial lethality and transient placental dysmorphogenesis but no impairment in hearing or skin differentiation. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
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Polymorphisms
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SNPs within 2kb(41 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
|
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Expression
|
Literature Summary: (16 records)
Data Summary:
Assays (4)
Results (13)
Tissues (7)
Images (2)
Theiler Stages: 13,20,25,28
| |
Assay Type |
Assays |
|
Results |
| |
RT-PCR |
4 |
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13 |
cDNA source data(63)
External Resources:
Allen Brain Atlas
GEO
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Molecular
reagents
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All nucleic(67)
cDNA(63)
Primer pair(4)
Antibodies(1)
Microarray probesets(2)
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Other database
links
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Protein
domains
|
Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:858
Willecke K et al.,
"The diversity of connexin genes encoding gap junctional proteins."
Eur J Cell Biol 1991 Oct;56(1):1-7
(Latest)
J:152946
Sferruzzi-Perri AN et al.,
"Csf2 null mutation alters placental gene expression and trophoblast glycogen cell and giant cell abundance in mice."
Biol Reprod 2009 Jul;81(1):207-21
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All references(34)
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Other
accession IDs
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MGD-MRK-10093, MGD-MRK-10098, MGD-MRK-35792, MGI:107326
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