|Institutional Source||Beutler Lab|
|Synonyms||presynaptic cytomatrix protein|
|Is this an essential gene?||Possibly non essential (E-score: 0.341)|
|Stock #||R2293 (G1)|
|Chromosomal Location||108096022-108190384 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to T at 108113067 bp|
|Amino Acid Change||Alanine to Threonine at position 1829 (A1829T)|
|Ref Sequence||ENSEMBL: ENSMUSP00000035208 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000035208]|
|Predicted Effect||possibly damaging
AA Change: A1829T
PolyPhen 2 Score 0.466 (Sensitivity: 0.89; Specificity: 0.90)
AA Change: A1829T
|Predicted Effect||probably benign
|Meta Mutation Damage Score||0.018|
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Neurotransmitters are released from a specific site in the axon terminal called the active zone, which is composed of synaptic vesicles and a meshwork of cytoskeleton underlying the plasma membrane. The protein encoded by this gene is thought to be a scaffolding protein involved in organizing the presynaptic cytoskeleton. The gene is expressed primarily in neurons in the brain. A similar gene product in rodents is concentrated in the active zone of axon terminals and tightly associated with cytoskeletal structures, and is essential for regulating neurotransmitter release from a subset of synapses. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mutants lacking functional protein exhibit impaired hippocampal and photoreceptor synaptic transmission, aberrant photoreceptor ribbon synapse formation, and spontaneous epileptic seizures. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Bsn||
(F):5'- ACCATGTCACAGCATGCCAG -3'
(R):5'- ATACGGAGATCCTTTCCAGAGCC -3'
(F):5'- TCATTCCGGTGAGGTCCAG -3'
(R):5'- CTCGACTTTGGCCAGGGTTC -3'