|Institutional Source||Beutler Lab|
|Gene Name||glycerol-3-phosphate acyltransferase, mitochondrial|
|Is this an essential gene?||Possibly non essential (E-score: 0.254)|
|Stock #||R1556 (G1)|
|Chromosomal Location||55069734-55099451 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to G at 55076331 bp|
|Amino Acid Change||Valine to Alanine at position 647 (V647A)|
|Ref Sequence||ENSEMBL: ENSMUSP00000057635 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000061856]|
|Predicted Effect||possibly damaging
AA Change: V647A
PolyPhen 2 Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)
AA Change: V647A
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a mitochondrial enzyme which prefers saturated fatty acids as its substrate for the synthesis of glycerolipids. This metabolic pathway's first step is catalyzed by the encoded enzyme. Two forms for this enzyme exist, one in the mitochondria and one in the endoplasmic reticulum. Two alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]
PHENOTYPE: Homozygous mutant mice weighed less than controls and showed reduced triacylglycerol levels in the liver and plasma. The glycerolipid fatty acid composition is also disrupted in mutant mice. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Gpam||
(F):5'- TCTTCTGAGTAGAGAGCGGCTTTCC -3'
(R):5'- GGCATTAAGCTCAGTAGCACTCCC -3'
(F):5'- TCAATGTCCGTATGCCAGAG -3'
(R):5'- TAGCACTCCCTATAGTTGGGGAC -3'