Symbol
Name
ID
|
|
|
Synonyms
|
A830038F04Rik, mKIAA0735
|
|
Genetic Map
|
|
Chromosome 7
|
cytoband D1
|
|
|
|
Mapping data(
3)
|
|
|
|
Sequence Map
|
|
Mammalian
homology
|
|
|
Sequences
|
All sequences(34)
|
Alleles
and
phenotypes
|
All alleles(2) :
Targeted, knock-out(2)
| Homozygotes for a targeted null mutation are phenotypically normal, and Sv2a/Sv2b double knockouts are no more affected than Sv2a single knockouts. |
|
|
Polymorphisms
|
SNPs within 2kb(288 from dbSNP Build 128)
|
Gene Ontology
(GO)
classifications
|
|
|
Expression
|
Literature Summary: (18 records)
Data Summary:
Assays (3)
Results (113)
Tissues (106)
Images (23)
Theiler Stages: 21,22,23,24,25,26,28
| |
Assay Type |
Assays |
|
Results |
| |
Western blot |
1 |
|
7 |
| |
RNA in situ |
2 |
|
106 |
cDNA source data(35)
External Resources:
Allen Brain Atlas
GENSAT
GEO
ArrayExpress
|
Molecular
reagents
|
All nucleic(36)
cDNA(36)
Antibodies(1)
Microarray probesets(1)
|
Other database
links
|
|
Protein
domains
|
| InterPro ID |
Description |
| IPR005828 |
General substrate transporter |
| IPR005829 |
Sugar transporter, conserved site |
| IPR005988 |
Synaptic vesicle protein SV2 |
| IPR011701 |
Major facilitator superfamily MFS-1 |
| IPR016196 |
Major facilitator superfamily, general substrate transporter |
Graphical View
of Protein Domain Structure
|
|
References
|
(Earliest)
J:33098
Gautam M et al.,
"Defective neuromuscular synaptogenesis in agrin-deficient mutant mice."
Cell 1996 May 17;85(4):525-35
(Latest)
J:148272
Morgans CW et al.,
"Loss of the Synaptic Vesicle Protein SV2B results in reduced neurotransmission and altered synaptic vesicle protein expression in the retina."
PLoS ONE 2009;4(4):e5230
|
All references(28)
|
Other
accession IDs
|
MGI:2142055, MGI:2443605
|
Analysis Tools
MGI BioMart