Incidental Mutation 'R6199:Ces1e'
ID503104
Institutional Source Beutler Lab
Gene Symbol Ces1e
Ensembl Gene ENSMUSG00000061959
Gene Namecarboxylesterase 1E
SynonymsEs22, Eg, egasyn, Es-22
MMRRC Submission 044339-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R6199 (G1)
Quality Score225.009
Status Validated
Chromosome8
Chromosomal Location93201218-93229619 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 93217535 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Leucine at position 218 (F218L)
Ref Sequence ENSEMBL: ENSMUSP00000135636 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034173] [ENSMUST00000176282]
Predicted Effect probably damaging
Transcript: ENSMUST00000034173
AA Change: F219L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000034173
Gene: ENSMUSG00000061959
AA Change: F219L

DomainStartEndE-ValueType
Pfam:COesterase 1 546 1.7e-174 PFAM
Pfam:Abhydrolase_3 137 282 5.2e-12 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000175983
Predicted Effect probably damaging
Transcript: ENSMUST00000176282
AA Change: F218L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000135636
Gene: ENSMUSG00000061959
AA Change: F218L

DomainStartEndE-ValueType
Pfam:COesterase 1 545 8.9e-166 PFAM
Pfam:Abhydrolase_3 136 292 2.7e-10 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.4%
Validation Efficiency 100% (53/53)
MGI Phenotype PHENOTYPE: Mice homozygous for a spontaneous mutation lack stable microsomal beta-glucuronidase and display altered processing of lysosomal beta-glucuronidase in liver. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adck1 A T 12: 88,441,117 D206V possibly damaging Het
Ank2 T A 3: 127,004,006 D685V probably damaging Het
Baz2b A G 2: 59,978,675 S77P probably benign Het
C430049E01Rik T C 8: 71,525,465 N83D probably benign Het
Ceacam5 A T 7: 17,714,885 T59S probably benign Het
Cps1 TGTCCATTGGTC TGTC 1: 67,162,615 probably null Het
Dab1 C T 4: 104,731,751 A524V probably benign Het
Eftud2 A T 11: 102,840,057 V843E probably damaging Het
Fuca2 G T 10: 13,506,039 W232L probably damaging Het
Gdf7 T C 12: 8,298,832 D155G unknown Het
Ggcx G T 6: 72,430,139 V753F possibly damaging Het
Ghrhr A T 6: 55,379,188 T89S probably benign Het
Gpr151 T C 18: 42,578,554 K353R probably benign Het
Gpr75 T C 11: 30,891,527 L144P probably damaging Het
Gsdmc2 A G 15: 63,825,113 I403T probably benign Het
H2-M1 A G 17: 36,671,167 S181P probably benign Het
Ick T C 9: 78,164,639 V531A probably benign Het
Igsf5 C T 16: 96,421,739 S61L possibly damaging Het
Insc A T 7: 114,791,166 probably null Het
Izumo4 G A 10: 80,702,873 G53D probably damaging Het
Ksr1 G A 11: 79,020,441 P693S possibly damaging Het
Lgals4 G A 7: 28,835,892 R27H probably damaging Het
Lpcat2b A G 5: 107,433,305 R167G probably benign Het
Man1a C T 10: 54,014,456 V288I possibly damaging Het
Map2 T G 1: 66,425,478 S1676A probably damaging Het
Mbl1 G T 14: 41,153,615 V9F unknown Het
Mrgprb8 T A 7: 48,389,303 C241S probably benign Het
Mrpl2 T C 17: 46,649,086 L227P probably damaging Het
Mthfd1 T A 12: 76,288,911 V253E probably damaging Het
Mthfd1 A G 12: 76,303,680 H464R probably damaging Het
Mug2 T A 6: 122,047,439 M490K probably benign Het
Naip6 C T 13: 100,300,600 A472T probably benign Het
Notch1 A G 2: 26,469,899 V1268A probably damaging Het
Olfr1415 A T 1: 92,491,542 I71N possibly damaging Het
Olfr876 C A 9: 37,804,881 probably null Het
Pgm2 A T 4: 99,978,954 I412F probably damaging Het
Plaur A T 7: 24,465,203 Q44L possibly damaging Het
Ppara T C 15: 85,787,233 Y112H probably damaging Het
Ppm1h G A 10: 122,920,739 V430M probably damaging Het
Prpf40a T C 2: 53,157,915 M197V probably benign Het
Prph A G 15: 99,056,832 T35A probably benign Het
Prrc2c C T 1: 162,682,516 G780S probably damaging Het
Ptchd3 T A 11: 121,831,082 N260K probably benign Het
Ptprz1 A G 6: 23,002,471 D1520G probably benign Het
Samd9l T A 6: 3,376,686 I192L probably benign Het
Slc39a10 T C 1: 46,835,833 D103G probably damaging Het
Smndc1 G A 19: 53,383,632 T117M probably benign Het
Tesk2 A G 4: 116,792,170 D159G probably damaging Het
Tmem2 G A 19: 21,844,822 G1194S probably benign Het
Tns2 C T 15: 102,108,934 R281C probably damaging Het
Vmn2r108 A T 17: 20,462,382 N853K probably benign Het
Wdfy3 C T 5: 101,872,965 R2491Q possibly damaging Het
Other mutations in Ces1e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00900:Ces1e APN 8 93217617 missense probably damaging 0.98
IGL01358:Ces1e APN 8 93214150 missense probably damaging 0.99
IGL01597:Ces1e APN 8 93210373 missense probably benign 0.01
IGL01875:Ces1e APN 8 93223896 missense probably benign 0.03
IGL02244:Ces1e APN 8 93212349 splice site probably null
IGL03260:Ces1e APN 8 93223917 missense probably benign 0.00
IGL03302:Ces1e APN 8 93223893 critical splice donor site probably null
chaingun UTSW 8 93223958 missense probably damaging 1.00
Chomper UTSW 8 93201839 critical splice donor site probably null
PIT4651001:Ces1e UTSW 8 93215083 missense probably benign 0.00
R0158:Ces1e UTSW 8 93219429 missense probably benign 0.09
R0317:Ces1e UTSW 8 93224039 missense probably benign 0.03
R0530:Ces1e UTSW 8 93219521 splice site probably benign
R0626:Ces1e UTSW 8 93224043 missense probably benign 0.01
R3013:Ces1e UTSW 8 93203287 missense probably benign 0.26
R3815:Ces1e UTSW 8 93201839 critical splice donor site probably null
R4810:Ces1e UTSW 8 93208631 missense probably benign 0.00
R4883:Ces1e UTSW 8 93224088 missense probably benign 0.07
R5155:Ces1e UTSW 8 93201406 makesense probably null
R5262:Ces1e UTSW 8 93223958 missense probably damaging 1.00
R5287:Ces1e UTSW 8 93208612 missense probably benign 0.00
R5403:Ces1e UTSW 8 93208612 missense probably benign 0.00
R5410:Ces1e UTSW 8 93210442 missense possibly damaging 0.94
R5813:Ces1e UTSW 8 93221677 nonsense probably null
R5891:Ces1e UTSW 8 93203266 missense possibly damaging 0.93
R5966:Ces1e UTSW 8 93219373 critical splice donor site probably null
R6381:Ces1e UTSW 8 93217578 missense probably damaging 1.00
R6620:Ces1e UTSW 8 93223918 missense probably damaging 1.00
R6753:Ces1e UTSW 8 93215128 missense probably damaging 0.96
R7180:Ces1e UTSW 8 93215144 missense probably damaging 1.00
R7393:Ces1e UTSW 8 93210417 missense probably benign 0.31
R7421:Ces1e UTSW 8 93215075 missense probably benign 0.00
X0014:Ces1e UTSW 8 93203275 missense probably damaging 1.00
Z1088:Ces1e UTSW 8 93210418 missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- TTTCCGTTGTCTAATGCTGAGC -3'
(R):5'- AGACATGTATTAGGCCTGCAGAG -3'

Sequencing Primer
(F):5'- CCGTTGTCTAATGCTGAGCAATAAAC -3'
(R):5'- GGCCTGCAGAGCACAACTTATTTC -3'
Posted On2018-02-27