Incidental Mutation 'R7375:Mogat2'
ID 572334
Institutional Source Beutler Lab
Gene Symbol Mogat2
Ensembl Gene ENSMUSG00000052396
Gene Name monoacylglycerol O-acyltransferase 2
Synonyms DGAT2L5, Mgat2
MMRRC Submission 045458-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.104) question?
Stock # R7375 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 98868291-98887818 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 98872905 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 93 (K93R)
Ref Sequence ENSEMBL: ENSMUSP00000064041 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000064231]
AlphaFold Q80W94
Predicted Effect probably damaging
Transcript: ENSMUST00000064231
AA Change: K93R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000064041
Gene: ENSMUSG00000052396
AA Change: K93R

DomainStartEndE-ValueType
Pfam:DAGAT 39 334 9.1e-120 PFAM
Meta Mutation Damage Score 0.6673 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (59/59)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is an enzyme that catalyzes the synthesis of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA. The encoded protein is important in the uptake of dietary fat by the small intestine. This protein forms a complex with diacylglycerol O-acyltransferase 2 in the endoplasmic reticulum, and this complex catalyzes the synthesis of triacylglycerol. [provided by RefSeq, Dec 2015]
PHENOTYPE: Mice homozygous for a null allele exhibit resistance to diet induced obesity, hyperinsulinemia, hyperlipidemia, and steatosis with decreased lipid absorption and increased oxygen consumption when fed a high fat diet. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 A G 5: 8,968,671 (GRCm39) I337V probably benign Het
Abl2 A G 1: 156,450,184 (GRCm39) D117G probably damaging Het
Arhgap5 T A 12: 52,563,365 (GRCm39) L112* probably null Het
Brinp3 C G 1: 146,777,748 (GRCm39) L732V possibly damaging Het
Ccdc168 A T 1: 44,099,694 (GRCm39) I468N possibly damaging Het
Cfap91 T A 16: 38,155,980 (GRCm39) H81L probably damaging Het
Cmya5 T G 13: 93,228,169 (GRCm39) K2306N probably damaging Het
Col16a1 A C 4: 129,959,294 (GRCm39) K680T unknown Het
Col28a1 T A 6: 7,998,499 (GRCm39) T1137S possibly damaging Het
Crnn A T 3: 93,056,452 (GRCm39) T413S possibly damaging Het
Csf1 A G 3: 107,655,495 (GRCm39) L512P possibly damaging Het
Dlx3 C A 11: 95,011,461 (GRCm39) A105D possibly damaging Het
Dnah3 T G 7: 119,550,900 (GRCm39) T161P probably damaging Het
Dnah7b A G 1: 46,342,794 (GRCm39) D3435G probably damaging Het
Dpp10 A G 1: 123,295,524 (GRCm39) I541T probably benign Het
Efcc1 T C 6: 87,728,838 (GRCm39) V431A possibly damaging Het
Enpp5 T C 17: 44,391,868 (GRCm39) I99T probably benign Het
Gm11232 C T 4: 71,675,583 (GRCm39) W59* probably null Het
Gxylt2 A T 6: 100,727,383 (GRCm39) T166S probably benign Het
Herc6 A T 6: 57,628,791 (GRCm39) probably null Het
Itga2 T C 13: 115,005,753 (GRCm39) I476V probably benign Het
Kcnq5 T C 1: 21,539,710 (GRCm39) T403A possibly damaging Het
Klhl42 A G 6: 146,993,538 (GRCm39) K170R probably benign Het
Klk13 T C 7: 43,370,582 (GRCm39) probably null Het
Krt32 G T 11: 99,972,050 (GRCm39) R433S probably benign Het
Lrp1 G T 10: 127,375,217 (GRCm39) T4461N probably damaging Het
Mapk10 A T 5: 103,124,256 (GRCm39) M256K probably null Het
Myh1 G T 11: 67,101,254 (GRCm39) V677L probably damaging Het
Naip5 T C 13: 100,356,204 (GRCm39) Q1137R probably benign Het
Naip5 G T 13: 100,356,205 (GRCm39) Q1137K not run Het
Oog4 G A 4: 143,165,544 (GRCm39) T201M possibly damaging Het
Or4a70 C T 2: 89,324,036 (GRCm39) G207R possibly damaging Het
Pik3c2a T C 7: 115,975,621 (GRCm39) T649A probably damaging Het
Plec T A 15: 76,061,555 (GRCm39) H2794L possibly damaging Het
Pros1 T A 16: 62,744,913 (GRCm39) N509K probably damaging Het
Psme3ip1 G A 8: 95,309,636 (GRCm39) L119F probably benign Het
Psme4 T A 11: 30,722,700 (GRCm39) probably null Het
Ptprf A G 4: 118,070,011 (GRCm39) V1457A probably benign Het
Rad50 A G 11: 53,543,055 (GRCm39) probably null Het
Rfx5 C T 3: 94,866,053 (GRCm39) P451S unknown Het
Scpppq1 G T 5: 104,219,123 (GRCm39) probably null Het
Sdk1 G T 5: 141,984,598 (GRCm39) V728L probably benign Het
Sfxn4 T C 19: 60,847,112 (GRCm39) D57G probably benign Het
Slc10a4 A G 5: 73,169,650 (GRCm39) D425G probably benign Het
Slc17a5 C T 9: 78,495,174 (GRCm39) A26T probably benign Het
Slc22a26 A T 19: 7,760,509 (GRCm39) probably null Het
Slc22a30 A G 19: 8,382,055 (GRCm39) L72P probably damaging Het
Slco6c1 T C 1: 97,009,146 (GRCm39) T447A possibly damaging Het
Slco6d1 A G 1: 98,349,172 (GRCm39) N81S probably damaging Het
Stard9 T C 2: 120,495,483 (GRCm39) probably null Het
Tecpr1 T C 5: 144,145,417 (GRCm39) E610G possibly damaging Het
Tmem81 G T 1: 132,435,301 (GRCm39) V36L possibly damaging Het
Trabd2b G T 4: 114,467,194 (GRCm39) K474N probably benign Het
Tspan33 T C 6: 29,713,519 (GRCm39) F149L probably benign Het
Ttn A G 2: 76,606,683 (GRCm39) Y18076H probably damaging Het
Utrn G A 10: 12,516,764 (GRCm39) R2277C probably damaging Het
Vmn2r101 T A 17: 19,831,652 (GRCm39) D549E probably damaging Het
Vmn2r107 T A 17: 20,576,138 (GRCm39) I156K probably benign Het
Wwc2 T G 8: 48,316,955 (GRCm39) S713R unknown Het
Xndc1 C A 7: 101,730,687 (GRCm39) probably null Het
Zfp810 A G 9: 22,201,833 (GRCm39) probably null Het
Other mutations in Mogat2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01343:Mogat2 APN 7 98,881,775 (GRCm39) missense possibly damaging 0.60
IGL02052:Mogat2 APN 7 98,887,771 (GRCm39) start codon destroyed probably null 0.99
IGL02153:Mogat2 APN 7 98,872,761 (GRCm39) missense possibly damaging 0.94
R0227:Mogat2 UTSW 7 98,872,339 (GRCm39) missense probably benign 0.02
R0490:Mogat2 UTSW 7 98,872,351 (GRCm39) missense probably benign 0.11
R1331:Mogat2 UTSW 7 98,872,722 (GRCm39) missense possibly damaging 0.66
R1546:Mogat2 UTSW 7 98,881,766 (GRCm39) missense probably damaging 1.00
R2879:Mogat2 UTSW 7 98,871,573 (GRCm39) missense possibly damaging 0.46
R4954:Mogat2 UTSW 7 98,887,724 (GRCm39) missense possibly damaging 0.95
R5040:Mogat2 UTSW 7 98,887,724 (GRCm39) missense possibly damaging 0.95
R5184:Mogat2 UTSW 7 98,872,842 (GRCm39) missense possibly damaging 0.90
R5822:Mogat2 UTSW 7 98,869,112 (GRCm39) missense possibly damaging 0.82
R6056:Mogat2 UTSW 7 98,872,720 (GRCm39) missense possibly damaging 0.95
R6256:Mogat2 UTSW 7 98,869,102 (GRCm39) missense probably damaging 1.00
R6500:Mogat2 UTSW 7 98,871,553 (GRCm39) missense probably benign 0.04
R7358:Mogat2 UTSW 7 98,881,673 (GRCm39) missense possibly damaging 0.93
Y5408:Mogat2 UTSW 7 98,872,837 (GRCm39) missense probably damaging 1.00
Z1177:Mogat2 UTSW 7 98,872,836 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCCAGACATGATGTAATCTCGGAAG -3'
(R):5'- GAACAATTTGCCCAGAGCCAG -3'

Sequencing Primer
(F):5'- TAATCTCGGAAGAAGGGGGCC -3'
(R):5'- AGAGCCAGCACCCAGTCTG -3'
Posted On 2019-09-13