Incidental Mutation 'R1127:Ces2g'
ID 96310
Institutional Source Beutler Lab
Gene Symbol Ces2g
Ensembl Gene ENSMUSG00000031877
Gene Name carboxylesterase 2G
Synonyms 2210023G05Rik
MMRRC Submission 039200-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.047) question?
Stock # R1127 (G1)
Quality Score 225
Status Not validated
Chromosome 8
Chromosomal Location 105688350-105696169 bp(+) (GRCm39)
Type of Mutation splice site (6 bp from exon)
DNA Base Change (assembly) T to C at 105694094 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000049315 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043183]
AlphaFold E9PV38
Predicted Effect probably null
Transcript: ENSMUST00000043183
SMART Domains Protein: ENSMUSP00000049315
Gene: ENSMUSG00000031877

DomainStartEndE-ValueType
Pfam:COesterase 11 539 1.4e-176 PFAM
Pfam:Abhydrolase_3 144 245 4.9e-11 PFAM
Pfam:Peptidase_S9 159 331 8.1e-7 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212330
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 98.7%
  • 3x: 97.5%
  • 10x: 93.1%
  • 20x: 80.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700088E04Rik T C 15: 79,019,403 (GRCm39) D179G probably benign Het
Aadacl2fm2 G A 3: 59,659,314 (GRCm39) E256K probably benign Het
Adh7 C T 3: 137,927,490 (GRCm39) A12V probably benign Het
Ankhd1 T A 18: 36,767,399 (GRCm39) N1179K probably damaging Het
Ankrd50 T C 3: 38,511,336 (GRCm39) T344A probably benign Het
Aplf T C 6: 87,623,273 (GRCm39) T269A probably benign Het
Cavin4 T C 4: 48,663,637 (GRCm39) S6P probably damaging Het
Cyp2c66 A T 19: 39,151,812 (GRCm39) N176Y probably damaging Het
Dnah3 T A 7: 119,522,253 (GRCm39) D3980V probably damaging Het
Drc7 G T 8: 95,799,416 (GRCm39) E530D probably damaging Het
Dst A G 1: 34,314,358 (GRCm39) T6434A probably damaging Het
Dtx3l A G 16: 35,759,127 (GRCm39) S41P possibly damaging Het
Eef1b2 G A 1: 63,218,616 (GRCm39) probably null Het
Eml3 C T 19: 8,913,672 (GRCm39) T43I probably damaging Het
Fam110b T A 4: 5,799,434 (GRCm39) L284Q probably damaging Het
Gpr33 A C 12: 52,070,252 (GRCm39) H262Q probably damaging Het
Igfals T G 17: 25,099,455 (GRCm39) L182R probably damaging Het
Lamc1 A G 1: 153,126,205 (GRCm39) F496L possibly damaging Het
Muc4 T A 16: 32,569,343 (GRCm39) H134Q possibly damaging Het
Nckap1 C T 2: 80,348,286 (GRCm39) S889N probably benign Het
Nxn A T 11: 76,164,895 (GRCm39) C205* probably null Het
Oga G A 19: 45,740,594 (GRCm39) R914* probably null Het
Or11l3 T C 11: 58,516,284 (GRCm39) E196G probably damaging Het
Or52h9 C A 7: 104,202,293 (GRCm39) H56N possibly damaging Het
Pamr1 A T 2: 102,469,698 (GRCm39) I415F possibly damaging Het
Ppp4r4 G A 12: 103,545,327 (GRCm39) G200E probably damaging Het
Pramel29 G A 4: 143,933,694 (GRCm39) T471I probably damaging Het
Prdm16 C A 4: 154,613,256 (GRCm39) S57I probably damaging Het
Psmd11 A G 11: 80,362,410 (GRCm39) K157R possibly damaging Het
Ptprn2 G A 12: 117,175,628 (GRCm39) probably null Het
Pus7 G A 5: 23,973,793 (GRCm39) H234Y probably benign Het
Rd3l A G 12: 111,946,717 (GRCm39) Y20H probably benign Het
Stk31 A G 6: 49,386,141 (GRCm39) D160G probably damaging Het
Sycp2 C T 2: 178,016,159 (GRCm39) E768K possibly damaging Het
Tango6 T C 8: 107,415,527 (GRCm39) V116A probably benign Het
Ttn C T 2: 76,697,574 (GRCm39) probably benign Het
Vmn2r114 ATTT ATT 17: 23,509,906 (GRCm39) probably null Het
Xylb T C 9: 119,212,443 (GRCm39) I427T probably damaging Het
Zc3h7a T G 16: 10,956,939 (GRCm39) D890A probably damaging Het
Other mutations in Ces2g
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00832:Ces2g APN 8 105,694,471 (GRCm39) splice site probably benign
IGL00901:Ces2g APN 8 105,691,761 (GRCm39) missense probably benign 0.01
IGL02101:Ces2g APN 8 105,691,769 (GRCm39) splice site probably null
IGL02146:Ces2g APN 8 105,693,576 (GRCm39) missense possibly damaging 0.94
IGL02624:Ces2g APN 8 105,691,380 (GRCm39) missense probably damaging 1.00
IGL03091:Ces2g APN 8 105,691,386 (GRCm39) missense probably damaging 1.00
PIT4810001:Ces2g UTSW 8 105,691,521 (GRCm39) missense possibly damaging 0.52
R0025:Ces2g UTSW 8 105,692,628 (GRCm39) splice site probably benign
R0025:Ces2g UTSW 8 105,692,628 (GRCm39) splice site probably benign
R0122:Ces2g UTSW 8 105,694,932 (GRCm39) missense probably damaging 0.96
R0494:Ces2g UTSW 8 105,693,199 (GRCm39) missense probably benign
R1337:Ces2g UTSW 8 105,690,597 (GRCm39) missense possibly damaging 0.63
R1619:Ces2g UTSW 8 105,693,984 (GRCm39) missense probably damaging 1.00
R1813:Ces2g UTSW 8 105,693,569 (GRCm39) missense probably benign 0.32
R2240:Ces2g UTSW 8 105,689,134 (GRCm39) missense probably benign 0.11
R2255:Ces2g UTSW 8 105,694,046 (GRCm39) missense probably damaging 1.00
R2307:Ces2g UTSW 8 105,695,044 (GRCm39) missense probably benign 0.01
R2566:Ces2g UTSW 8 105,692,621 (GRCm39) critical splice donor site probably null
R4026:Ces2g UTSW 8 105,691,377 (GRCm39) missense probably damaging 0.99
R4469:Ces2g UTSW 8 105,692,602 (GRCm39) missense probably benign 0.14
R4631:Ces2g UTSW 8 105,694,094 (GRCm39) splice site probably null
R4859:Ces2g UTSW 8 105,694,094 (GRCm39) splice site probably null
R4900:Ces2g UTSW 8 105,693,989 (GRCm39) nonsense probably null
R4925:Ces2g UTSW 8 105,691,526 (GRCm39) missense probably benign 0.27
R5524:Ces2g UTSW 8 105,693,527 (GRCm39) missense probably benign 0.00
R5556:Ces2g UTSW 8 105,694,074 (GRCm39) missense probably benign 0.14
R6795:Ces2g UTSW 8 105,694,449 (GRCm39) missense probably damaging 0.96
R6988:Ces2g UTSW 8 105,690,540 (GRCm39) missense probably benign
R7653:Ces2g UTSW 8 105,689,285 (GRCm39) missense probably damaging 1.00
R7724:Ces2g UTSW 8 105,693,484 (GRCm39) missense probably benign 0.02
R7740:Ces2g UTSW 8 105,692,962 (GRCm39) missense probably damaging 0.98
R7856:Ces2g UTSW 8 105,693,014 (GRCm39) missense not run
R8123:Ces2g UTSW 8 105,693,555 (GRCm39) missense probably benign 0.06
R8690:Ces2g UTSW 8 105,693,605 (GRCm39) missense probably benign 0.01
R8724:Ces2g UTSW 8 105,692,955 (GRCm39) missense probably benign 0.01
R8732:Ces2g UTSW 8 105,689,195 (GRCm39) missense possibly damaging 0.78
R8825:Ces2g UTSW 8 105,693,954 (GRCm39) missense probably benign 0.13
R9441:Ces2g UTSW 8 105,690,623 (GRCm39) missense possibly damaging 0.52
R9688:Ces2g UTSW 8 105,691,304 (GRCm39) missense probably benign 0.42
Z1177:Ces2g UTSW 8 105,690,593 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTTCAGCGTGAGTACCACTGTGAC -3'
(R):5'- GTTGTCTGGCCTCAAATTATTGGCG -3'

Sequencing Primer
(F):5'- CACTGTGACAACGCTTAGTGG -3'
(R):5'- GGCCTCAAATTATTGGCGTTACTAC -3'
Posted On 2014-01-05