Incidental Mutation 'R0105:Mogat1'
ID 33230
Institutional Source Beutler Lab
Gene Symbol Mogat1
Ensembl Gene ENSMUSG00000012187
Gene Name monoacylglycerol O-acyltransferase 1
Synonyms mDC2, 0610030A14Rik, Dgat2l1, MGAT1, 1110064N14Rik
MMRRC Submission 038391-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R0105 (G1)
Quality Score 225
Status Validated (trace)
Chromosome 1
Chromosomal Location 78487628-78514810 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 78500307 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 124 (T124A)
Ref Sequence ENSEMBL: ENSMUSP00000109152 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000012331] [ENSMUST00000113524] [ENSMUST00000134947] [ENSMUST00000149732] [ENSMUST00000152111]
AlphaFold Q91ZV4
Predicted Effect probably benign
Transcript: ENSMUST00000012331
AA Change: T124A

PolyPhen 2 Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000012331
Gene: ENSMUSG00000012187
AA Change: T124A

DomainStartEndE-ValueType
Pfam:DAGAT 40 335 3.2e-117 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000113524
AA Change: T124A

PolyPhen 2 Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000109152
Gene: ENSMUSG00000012187
AA Change: T124A

DomainStartEndE-ValueType
Pfam:DAGAT 40 335 3.2e-117 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000134947
AA Change: T124A

PolyPhen 2 Score 0.114 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000116178
Gene: ENSMUSG00000012187
AA Change: T124A

DomainStartEndE-ValueType
Pfam:DAGAT 40 201 2.9e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000149732
AA Change: T93A

PolyPhen 2 Score 0.101 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000117903
Gene: ENSMUSG00000012187
AA Change: T93A

DomainStartEndE-ValueType
Pfam:DAGAT 9 247 3.4e-91 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000152111
SMART Domains Protein: ENSMUSP00000123427
Gene: ENSMUSG00000012187

DomainStartEndE-ValueType
Pfam:DAGAT 40 82 1.9e-9 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 94.9%
Validation Efficiency 100% (70/70)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Acyl-CoA:monoacylglycerol acyltransferase (MOGAT; EC 2.3.1.22) catalyzes the synthesis of diacylglycerols, the precursor of physiologically important lipids such as triacylglycerol and phospholipids (Yen et al., 2002 [PubMed 12077311]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased body weight in female, but not, male mice and does not ameliorate hepatic steatosis in lipodystrophic or obese mice. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5530400C23Rik G A 6: 133,271,277 (GRCm39) R107K probably benign Het
A530053G22Rik T C 6: 60,379,137 (GRCm39) noncoding transcript Het
Adcy9 A G 16: 4,106,252 (GRCm39) V954A probably damaging Het
Aldh8a1 T A 10: 21,271,438 (GRCm39) M388K probably damaging Het
Ankhd1 A G 18: 36,779,819 (GRCm39) I1720M probably damaging Het
Atp6v0a4 T C 6: 38,030,064 (GRCm39) probably benign Het
C1qtnf4 T A 2: 90,720,707 (GRCm39) *327R probably null Het
C1s1 T C 6: 124,518,277 (GRCm39) probably benign Het
Cdsn A C 17: 35,867,035 (GRCm39) R521S possibly damaging Het
Cgnl1 T C 9: 71,563,384 (GRCm39) M848V probably benign Het
Cog3 A G 14: 75,959,580 (GRCm39) S591P probably damaging Het
Col6a3 A G 1: 90,725,883 (GRCm39) V1375A possibly damaging Het
Cplane1 T A 15: 8,216,876 (GRCm39) V698D probably benign Het
Cr1l A G 1: 194,794,720 (GRCm39) probably benign Het
Crmp1 T A 5: 37,441,479 (GRCm39) D520E probably damaging Het
Ctdspl2 T A 2: 121,807,801 (GRCm39) probably benign Het
Dnah6 C T 6: 73,132,262 (GRCm39) A1147T probably damaging Het
Dsg2 T C 18: 20,735,111 (GRCm39) S1030P probably benign Het
Elavl3 C A 9: 21,948,129 (GRCm39) V12F possibly damaging Het
Fam20b T C 1: 156,518,140 (GRCm39) E218G probably damaging Het
Fam227a T C 15: 79,505,033 (GRCm39) D466G possibly damaging Het
Fto G A 8: 92,249,430 (GRCm39) E421K probably damaging Het
Gab2 T C 7: 96,948,279 (GRCm39) Y290H probably damaging Het
Gm973 A G 1: 59,621,633 (GRCm39) Q591R probably null Het
Gsdmc2 T C 15: 63,700,026 (GRCm39) T249A probably benign Het
Il15ra T A 2: 11,735,459 (GRCm39) probably null Het
Il1rl1 CTTGTTGTTGTTGTTGTTG CTTGTTGTTGTTGTTGTTGTTG 1: 40,481,734 (GRCm39) probably benign Het
Il6ra A G 3: 89,784,125 (GRCm39) I382T probably damaging Het
Isy1 G A 6: 87,796,167 (GRCm39) R257W probably damaging Het
Krt76 T C 15: 101,793,347 (GRCm39) T564A unknown Het
Lhpp T C 7: 132,232,254 (GRCm39) S57P probably damaging Het
Lrrk1 G T 7: 65,942,089 (GRCm39) D716E probably damaging Het
Mcm3ap T A 10: 76,335,368 (GRCm39) D1263E probably damaging Het
Mroh7 T C 4: 106,568,467 (GRCm39) T48A possibly damaging Het
Nccrp1 T C 7: 28,246,463 (GRCm39) D33G probably benign Het
Neurog1 G T 13: 56,399,050 (GRCm39) D232E probably benign Het
Or4a71 T C 2: 89,358,707 (GRCm39) T16A probably benign Het
Or4c105 T A 2: 88,648,253 (GRCm39) V246D probably damaging Het
Otog C A 7: 45,937,790 (GRCm39) T1833K possibly damaging Het
Perm1 C A 4: 156,302,682 (GRCm39) H409N probably benign Het
Pik3r5 A T 11: 68,381,337 (GRCm39) E174D probably damaging Het
Pkhd1 G A 1: 20,593,956 (GRCm39) Q1386* probably null Het
Pla2r1 T C 2: 60,345,325 (GRCm39) R344G possibly damaging Het
Plekha5 G A 6: 140,537,473 (GRCm39) R646K possibly damaging Het
Plekhg4 G A 8: 106,108,644 (GRCm39) V1202M possibly damaging Het
Ppil4 A G 10: 7,674,210 (GRCm39) Y118C probably damaging Het
Prrc2b G T 2: 32,103,323 (GRCm39) E934* probably null Het
Psmb9 A G 17: 34,406,249 (GRCm39) F12S probably benign Het
Ptdss2 T C 7: 140,732,793 (GRCm39) W183R probably damaging Het
Ptpn4 C T 1: 119,615,335 (GRCm39) probably null Het
Reln G A 5: 22,253,813 (GRCm39) R600W probably damaging Het
Scml4 T A 10: 42,806,595 (GRCm39) V161E probably damaging Het
Sdcbp2 A T 2: 151,431,478 (GRCm39) T284S probably benign Het
Slc22a29 T C 19: 8,137,991 (GRCm39) probably benign Het
Slc35e1 T C 8: 73,246,415 (GRCm39) probably benign Het
Spen T C 4: 141,197,121 (GRCm39) probably benign Het
Sumf2 T A 5: 129,878,735 (GRCm39) probably benign Het
Tbx10 A G 19: 4,043,121 (GRCm39) probably benign Het
Tex10 C A 4: 48,468,957 (GRCm39) V73F probably damaging Het
Tgm5 C A 2: 120,907,493 (GRCm39) G77W probably damaging Het
Tnfrsf21 T A 17: 43,351,082 (GRCm39) probably null Het
Treml2 C T 17: 48,609,856 (GRCm39) T96I probably damaging Het
Trim65 T C 11: 116,016,892 (GRCm39) *523W probably null Het
Zcchc17 T A 4: 130,243,099 (GRCm39) D28V probably benign Het
Zhx2 T C 15: 57,686,091 (GRCm39) F487L probably damaging Het
Zkscan6 T A 11: 65,712,811 (GRCm39) L248Q probably damaging Het
Other mutations in Mogat1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0056:Mogat1 UTSW 1 78,500,407 (GRCm39) missense probably damaging 0.99
R0056:Mogat1 UTSW 1 78,500,407 (GRCm39) missense probably damaging 0.99
R0105:Mogat1 UTSW 1 78,500,307 (GRCm39) missense probably benign 0.17
R0357:Mogat1 UTSW 1 78,488,677 (GRCm39) missense probably benign 0.01
R1146:Mogat1 UTSW 1 78,500,250 (GRCm39) missense probably benign 0.09
R1146:Mogat1 UTSW 1 78,500,250 (GRCm39) missense probably benign 0.09
R1716:Mogat1 UTSW 1 78,514,681 (GRCm39) missense probably benign 0.01
R3799:Mogat1 UTSW 1 78,505,775 (GRCm39) missense probably benign 0.00
R4168:Mogat1 UTSW 1 78,488,672 (GRCm39) missense possibly damaging 0.77
R5485:Mogat1 UTSW 1 78,500,307 (GRCm39) missense probably benign 0.17
R5929:Mogat1 UTSW 1 78,500,370 (GRCm39) missense probably benign 0.00
R6640:Mogat1 UTSW 1 78,500,411 (GRCm39) missense probably damaging 0.99
R6841:Mogat1 UTSW 1 78,499,496 (GRCm39) missense probably damaging 1.00
R7842:Mogat1 UTSW 1 78,499,502 (GRCm39) critical splice donor site probably null
R8179:Mogat1 UTSW 1 78,504,255 (GRCm39) missense possibly damaging 0.58
R9708:Mogat1 UTSW 1 78,488,633 (GRCm39) missense probably damaging 0.99
R9788:Mogat1 UTSW 1 78,499,342 (GRCm39) missense probably benign 0.00
Z1177:Mogat1 UTSW 1 78,505,890 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- AGATGGGAACCCTTCCACTTCTCAC -3'
(R):5'- ACATCAAGCAACTGCTGCTGCC -3'

Sequencing Primer
(F):5'- CCACTTCTCACTGACCCG -3'
(R):5'- AGTGGCTGTATCACCAAGC -3'
Posted On 2013-05-09