Mutagenetix > Incidental Mutation

Incidental Mutation 'R6988:Ces2g'

543085

Institutional Source

Beutler Lab

Gene Symbol

Ces2g

Ensembl Gene

ENSMUSG00000031877

Gene Name

carboxylesterase 2G

Synonyms

2210023G05Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

R6988 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

104961718-104969537 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to C at 104963908 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Alanine at position 107 (G107A)

Ref Sequence

ENSEMBL: ENSMUSP00000049315 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000043183] [ENSMUST00000212820]

AlphaFold

E9PV38

Predicted Effect

probably benign
Transcript: ENSMUST00000043183
AA Change: G107A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000049315
Gene: ENSMUSG00000031877
AA Change: G107A

Domain	Start	End	E-Value	Type
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

probably benign
Transcript: ENSMUST00000212820

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.2%
20x: 97.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700013G24Rik	T	G	4: 137,454,579 (GRCm38)	L15W	probably damaging	Het
4930550C14Rik	G	A	9: 53,411,756 (GRCm38)	V31I	possibly damaging	Het
4932415D10Rik	T	C	10: 82,291,899 (GRCm38)	D1759G	possibly damaging	Het
Adgre1	C	T	17: 57,408,445 (GRCm38)	S255F	probably benign	Het
Aff4	T	G	11: 53,398,237 (GRCm38)	S404R	probably damaging	Het
Akr1c19	A	T	13: 4,233,758 (GRCm38)		probably benign	Het
Ankrd31	T	A	13: 96,878,249 (GRCm38)	I1342K	probably damaging	Het
Arhgap5	T	A	12: 52,518,125 (GRCm38)	D626E	possibly damaging	Het
Arhgef1	G	A	7: 24,916,923 (GRCm38)	V332I	probably benign	Het
AY358078	A	G	14: 51,826,187 (GRCm38)	E430G	probably damaging	Het
B4gat1	T	A	19: 5,040,434 (GRCm38)	I395N	probably benign	Het
Bub1b	T	A	2: 118,636,830 (GRCm38)	I878N	probably damaging	Het
Ccdc150	C	T	1: 54,355,709 (GRCm38)	Q745*	probably null	Het
Ccl19	A	T	4: 42,754,885 (GRCm38)	I87N	probably damaging	Het
Chpt1	A	G	10: 88,488,406 (GRCm38)	V180A	probably damaging	Het
Col2a1	T	C	15: 98,004,454 (GRCm38)	T14A	unknown	Het
Dnah7a	T	C	1: 53,582,625 (GRCm38)	I1114V	possibly damaging	Het
Dnah7c	T	C	1: 46,666,213 (GRCm38)	I2462T	possibly damaging	Het
Dnah8	T	C	17: 30,643,275 (GRCm38)	F208S	probably damaging	Het
Dnhd1	A	G	7: 105,714,210 (GRCm38)	E3993G	probably damaging	Het
Erv3	C	T	2: 131,855,966 (GRCm38)	D158N	possibly damaging	Het
Exoc6	T	A	19: 37,609,091 (GRCm38)	F647I	probably damaging	Het
Fbrs	G	A	7: 127,479,508 (GRCm38)		probably benign	Het
Fgfr1op2	T	C	6: 146,589,965 (GRCm38)	F109L	probably damaging	Het
Fv1	T	C	4: 147,869,271 (GRCm38)	F98S	possibly damaging	Het
Gm436	A	G	4: 144,686,325 (GRCm38)	F15S	probably benign	Het
H2-M10.1	T	C	17: 36,325,592 (GRCm38)	K107E	probably benign	Het
Hspg2	A	T	4: 137,528,890 (GRCm38)	Q1436L	probably damaging	Het
Ighv1-74	T	C	12: 115,802,763 (GRCm38)	Y79C	probably damaging	Het
Kcnj1	G	A	9: 32,396,585 (GRCm38)	V102I	probably benign	Het
Mnt	C	A	11: 74,842,809 (GRCm38)		probably benign	Het
Mrpl15	T	C	1: 4,782,660 (GRCm38)	T112A	probably benign	Het
Ncdn	T	C	4: 126,747,189 (GRCm38)	D506G	probably benign	Het
Ogdh	C	T	11: 6,313,806 (GRCm38)	R81*	probably null	Het
Olfr791	T	A	10: 129,526,673 (GRCm38)	S149T	probably benign	Het
Olfr815	G	C	10: 129,902,409 (GRCm38)	F100L	probably damaging	Het
Pole	G	T	5: 110,329,583 (GRCm38)	V1863F	probably damaging	Het
Pramel5	T	C	4: 144,274,007 (GRCm38)		probably benign	Het
Rabep1	A	G	11: 70,934,537 (GRCm38)	K636E	probably damaging	Het
Rasgrf2	T	A	13: 91,885,635 (GRCm38)	Y1151F	probably benign	Het
Rrad	A	G	8: 104,630,636 (GRCm38)	V93A	probably damaging	Het
Sesn3	A	T	9: 14,310,257 (GRCm38)	R118*	probably null	Het
Slc27a3	T	C	3: 90,386,290 (GRCm38)	N596S	probably benign	Het
Snx19	C	A	9: 30,428,935 (GRCm38)	D456E	probably damaging	Het
Supt20	T	C	3: 54,698,597 (GRCm38)	S35P	probably damaging	Het
Syde2	G	T	3: 146,019,809 (GRCm38)	R885L	probably benign	Het
Synm	G	A	7: 67,733,658 (GRCm38)	L1419F	probably damaging	Het
Tcrg-V6	G	T	13: 19,190,644 (GRCm38)	G40W	possibly damaging	Het
Tekt2	A	G	4: 126,323,443 (GRCm38)	F221L	probably benign	Het
Ticam1	C	T	17: 56,269,900 (GRCm38)	E732K	probably benign	Het
Tmem39b	A	G	4: 129,693,148 (GRCm38)	I90T	possibly damaging	Het
Trib2	A	G	12: 15,815,338 (GRCm38)	S79P	probably damaging	Het
Usp32	T	C	11: 85,010,143 (GRCm38)	M1084V	probably benign	Het
Vmn1r181	T	C	7: 23,984,847 (GRCm38)	F246L	probably damaging	Het
Wnt16	A	G	6: 22,288,511 (GRCm38)	D2G	probably damaging	Het
Zfp462	A	G	4: 55,080,716 (GRCm38)	E1357G	probably benign	Het
Zhx3	A	G	2: 160,779,868 (GRCm38)	M793T	probably benign	Het

Other mutations in Ces2g

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00832:Ces2g	APN	8	104,967,839 (GRCm38)	splice site	probably benign
IGL00901:Ces2g	APN	8	104,965,129 (GRCm38)	missense	probably benign	0.01
IGL02101:Ces2g	APN	8	104,965,137 (GRCm38)	splice site	probably null
IGL02146:Ces2g	APN	8	104,966,944 (GRCm38)	missense	possibly damaging	0.94
IGL02624:Ces2g	APN	8	104,964,748 (GRCm38)	missense	probably damaging	1.00
IGL03091:Ces2g	APN	8	104,964,754 (GRCm38)	missense	probably damaging	1.00
PIT4810001:Ces2g	UTSW	8	104,964,889 (GRCm38)	missense	possibly damaging	0.52
R0025:Ces2g	UTSW	8	104,965,996 (GRCm38)	splice site	probably benign
R0025:Ces2g	UTSW	8	104,965,996 (GRCm38)	splice site	probably benign
R0122:Ces2g	UTSW	8	104,968,300 (GRCm38)	missense	probably damaging	0.96
R0494:Ces2g	UTSW	8	104,966,567 (GRCm38)	missense	probably benign
R1127:Ces2g	UTSW	8	104,967,462 (GRCm38)	splice site	probably null
R1337:Ces2g	UTSW	8	104,963,965 (GRCm38)	missense	possibly damaging	0.63
R1619:Ces2g	UTSW	8	104,967,352 (GRCm38)	missense	probably damaging	1.00
R1813:Ces2g	UTSW	8	104,966,937 (GRCm38)	missense	probably benign	0.32
R2240:Ces2g	UTSW	8	104,962,502 (GRCm38)	missense	probably benign	0.11
R2255:Ces2g	UTSW	8	104,967,414 (GRCm38)	missense	probably damaging	1.00
R2307:Ces2g	UTSW	8	104,968,412 (GRCm38)	missense	probably benign	0.01
R2566:Ces2g	UTSW	8	104,965,989 (GRCm38)	critical splice donor site	probably null
R4026:Ces2g	UTSW	8	104,964,745 (GRCm38)	missense	probably damaging	0.99
R4469:Ces2g	UTSW	8	104,965,970 (GRCm38)	missense	probably benign	0.14
R4631:Ces2g	UTSW	8	104,967,462 (GRCm38)	splice site	probably null
R4859:Ces2g	UTSW	8	104,967,462 (GRCm38)	splice site	probably null
R4900:Ces2g	UTSW	8	104,967,357 (GRCm38)	nonsense	probably null
R4925:Ces2g	UTSW	8	104,964,894 (GRCm38)	missense	probably benign	0.27
R5524:Ces2g	UTSW	8	104,966,895 (GRCm38)	missense	probably benign	0.00
R5556:Ces2g	UTSW	8	104,967,442 (GRCm38)	missense	probably benign	0.14
R6795:Ces2g	UTSW	8	104,967,817 (GRCm38)	missense	probably damaging	0.96
R7653:Ces2g	UTSW	8	104,962,653 (GRCm38)	missense	probably damaging	1.00
R7724:Ces2g	UTSW	8	104,966,852 (GRCm38)	missense	probably benign	0.02
R7740:Ces2g	UTSW	8	104,966,330 (GRCm38)	missense	probably damaging	0.98
R7856:Ces2g	UTSW	8	104,966,382 (GRCm38)	missense	not run
R8123:Ces2g	UTSW	8	104,966,923 (GRCm38)	missense	probably benign	0.06
R8690:Ces2g	UTSW	8	104,966,973 (GRCm38)	missense	probably benign	0.01
R8724:Ces2g	UTSW	8	104,966,323 (GRCm38)	missense	probably benign	0.01
R8732:Ces2g	UTSW	8	104,962,563 (GRCm38)	missense	possibly damaging	0.78
R8825:Ces2g	UTSW	8	104,967,322 (GRCm38)	missense	probably benign	0.13
R9441:Ces2g	UTSW	8	104,963,991 (GRCm38)	missense	possibly damaging	0.52
R9688:Ces2g	UTSW	8	104,964,672 (GRCm38)	missense	probably benign	0.42
Z1177:Ces2g	UTSW	8	104,963,961 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTGGCTGCCCTAGAAATCTG -3'
(R):5'- AAACTCAGGTTGCTTTTGTCCC -3'

Sequencing Primer
(F):5'- AGCTTTCACTGAGCCTATGG -3'
(R):5'- AGGTTGCTTTTGTCCCTTCTAAC -3'

Posted On

2018-11-28