|Institutional Source||Beutler Lab|
|Is this an essential gene?||Non essential (E-score: 0.000)|
|Stock #||R0517 (G1)|
|Chromosomal Location||29124181-29182471 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to G at 29157133 bp|
|Amino Acid Change||Serine to Arginine at position 1874 (S1874R)|
|Ref Sequence||ENSEMBL: ENSMUSP00000051492 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000061578]|
|Predicted Effect||probably benign
AA Change: S1874R
PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
AA Change: S1874R
|Predicted Effect||noncoding transcript
|Meta Mutation Damage Score||0.1051|
|Coding Region Coverage||
|Validation Efficiency||100% (62/62)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein named for its homology to the Sen1p protein of fungi which has RNA helicase activity encoded by a domain at the C-terminal end of the protein. The protein encoded by this gene contains a DNA/RNA helicase domain at its C-terminal end which suggests that it may be involved in both DNA and RNA processing. Mutations in this gene have been associated with ataxia-ocular apraxia-2 (AOA2) and an autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS4). [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit male infertility due to arrested male meiosis and reduced female fertility. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Setx||
(F):5'- TGCAACAGTTCCACGTAGTGCTC -3'
(R):5'- AGGACCAGCAGCAGCTAAAATGTC -3'
(F):5'- CACGTAGTGCTCCACCAG -3'
(R):5'- TGTCCTAACACAAACTTGTCTTAC -3'