|Institutional Source||Beutler Lab|
|Gene Name||WD repeat containing, antisense to Trp73|
|Synonyms||DD57, Wdr8, 5330425N03Rik, 2610044M17Rik|
|Is this an essential gene?||Possibly essential (E-score: 0.664)|
|Stock #||R0633 (G1)|
|Chromosomal Location||154142372-154167420 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to A at 154142491 bp|
|Amino Acid Change||Phenylalanine to Tyrosine at position 16 (F16Y)|
|Ref Sequence||ENSEMBL: ENSMUSP00000030895 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000030895] [ENSMUST00000105644]|
|Predicted Effect||probably damaging
AA Change: F16Y
PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
AA Change: F16Y
|Predicted Effect||probably benign
|Predicted Effect||noncoding transcript
|Coding Region Coverage||
|MGI Phenotype||FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Studies of the related mouse protein suggest that the encoded protein may play a role in the process of ossification. [provided by RefSeq, Mar 2009]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Wrap73||
(F):5'- GCCCCTTTAAGACTCAAACTCGGAC -3'
(R):5'- GTGCCCTCAAATGTGTGAAAGCAG -3'
(F):5'- TTTAAGACTCAAACTCGGACTTCCC -3'
(R):5'- GTGTGAAAGCAGAGTCATCTTATCC -3'