|Institutional Source||Beutler Lab|
|Gene Name||ubiquitin associated and SH3 domain containing, A|
|Synonyms||5830413C03Rik, Sts-2, TULA|
|Is this an essential gene?||Non essential (E-score: 0.000)|
|Stock #||R7041 (G1)|
|Chromosomal Location||31207873-31242202 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to G at 31228210 bp|
|Amino Acid Change||Serine to Glycine at position 347 (S347G)|
|Ref Sequence||ENSEMBL: ENSMUSP00000045890 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000048656]|
|Predicted Effect||probably benign
AA Change: S347G
PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
AA Change: S347G
|Coding Region Coverage||
|Validation Efficiency||96% (53/55)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of two family members belonging to the T-cell ubiquitin ligand (TULA) family. Both family members can negatively regulate T-cell signaling. This family member can facilitate growth factor withdrawal-induced apoptosis in T cells, which may occur via its interaction with AIF, an apoptosis-inducing factor. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]
PHENOTYPE: Homozygous null mice are viable and healthy with no abnormalities detected in any of the hematopoietic lineages. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Ubash3a||
(F):5'- ACCAGAAACCATGATGAGGC -3'
(R):5'- AGTAGAAATGCAACAACCTTCAGGA -3'
(F):5'- ATGATGAGGCCATGTCATGCCTC -3'
(R):5'- CACAGCAGGTTTTAACTCAGG -3'