|Institutional Source||Beutler Lab|
|Gene Name||dihydropyrimidinase-like 2|
|Synonyms||DRP2, Crmp2, Ulip2, TOAD-64|
|Is this an essential gene?||Possibly essential (E-score: 0.505)|
|Stock #||R5640 (G1)|
|Chromosomal Location||66802864-66868688 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to T at 66834368 bp|
|Amino Acid Change||Valine to Isoleucine at position 108 (V108I)|
|Ref Sequence||ENSEMBL: ENSMUSP00000022629 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000022629]|
|Predicted Effect||probably benign
AA Change: V108I
PolyPhen 2 Score 0.428 (Sensitivity: 0.89; Specificity: 0.90)
AA Change: V108I
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the collapsin response mediator protein family. Collapsin response mediator proteins form homo- and hetero-tetramers and facilitate neuron guidance, growth and polarity. The encoded protein promotes microtubule assembly and is required for Sema3A-mediated growth cone collapse, and also plays a role in synaptic signaling through interactions with calcium channels. This gene has been implicated in multiple neurological disorders, and hyperphosphorylation of the encoded protein may play a key role in the development of Alzheimer's disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]
PHENOTYPE: Mice homozygous for a knock-in allele exhibit abnormal dendritic patterning. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Dpysl2||
(F):5'- GAACAAAGCGAGACCTACCGTG -3'
(R):5'- GGATCTGAGTCGTTCATGCG -3'
(F):5'- GGTCCTTCACCAGAGCTTC -3'
(R):5'- GGCTAGTCCAGTGCCAAGTTTC -3'