|List |< first << previous [record 12 of 51] next >> last >||
|Institutional Source||Beutler Lab|
|Gene Name||contactin associated protein-like 3|
|Is this an essential gene?||Probably non essential (E-score: 0.061)|
|Stock #||R0840 (G1)|
|Chromosomal Location||64736182-64903955 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 64787910 bp|
|Amino Acid Change||Serine to Glycine at position 380 (S380G)|
|Ref Sequence||ENSEMBL: ENSMUSP00000089140 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000091554]|
|Predicted Effect||possibly damaging
AA Change: S380G
PolyPhen 2 Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)
AA Change: S380G
|Meta Mutation Damage Score||0.0929|
|Coding Region Coverage||
|Validation Efficiency||100% (51/51)|
|MGI Phenotype||FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the NCP family of cell-recognition molecules. This family represents a distinct subgroup of the neurexins. NCP proteins mediate neuron-glial interactions in vertebrates and glial-glial contact in invertebrates. The protein encoded by this gene may play a role in cell recognition within the nervous system. Alternatively spliced transcript variants encoding different isoforms have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Cntnap3||
(F):5'- AGAGGAGAGATCAAACCCATGTCTTCAA -3'
(R):5'- catctcaccatcccACAACAGGATTAAA -3'
(F):5'- ACAGAACGACTCTGAGTTCTCTTG -3'
(R):5'- ccatcccACAACAGGATTAAAAATAC -3'