Mutagenetix > Incidental Mutation

Incidental Mutation 'R4656:Ces1b'

352441

Institutional Source

Beutler Lab

Gene Symbol

Ces1b

Ensembl Gene

ENSMUSG00000078964

Gene Name

carboxylesterase 1B

Synonyms

Gm5158

MMRRC Submission

041916-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R4656 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

93783356-93806645 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 93784042 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glutamine at position 488 (E488Q)

Ref Sequence

ENSEMBL: ENSMUSP00000105210 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109582]

AlphaFold

D3Z5G7

Predicted Effect

probably damaging
Transcript: ENSMUST00000109582
AA Change: E488Q

PolyPhen 2 Score 0.965 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000105210
Gene: ENSMUSG00000078964
AA Change: E488Q

Domain	Start	End	E-Value	Type
Pfam:COesterase	1	547	7.6e-168	PFAM
Pfam:Abhydrolase_3	136	245	8.5e-11	PFAM

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.8%

Validation Efficiency

96% (80/83)

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310003L06Rik	G	A	5: 88,112,534 (GRCm39)		probably benign	Het
4931406B18Rik	T	A	7: 43,150,565 (GRCm39)	H69L	probably benign	Het
Ace2	T	C	X: 162,936,110 (GRCm39)	S84P	probably benign	Het
Adgb	A	C	10: 10,281,050 (GRCm39)	N656K	probably damaging	Het
Ago3	G	T	4: 126,257,545 (GRCm39)	Y495*	probably null	Het
Ahnak	G	A	19: 8,982,219 (GRCm39)	V1168M	possibly damaging	Het
Armc10	A	G	5: 21,866,548 (GRCm39)	R271G	probably benign	Het
Atp4a	T	G	7: 30,419,373 (GRCm39)		probably benign	Het
Casp1	C	T	9: 5,304,324 (GRCm39)	P333S	probably damaging	Het
Ceacam9	C	T	7: 16,457,574 (GRCm39)	A34V	probably benign	Het
Ces2h	A	T	8: 105,741,271 (GRCm39)	T88S	possibly damaging	Het
Cfap410	G	A	10: 77,817,450 (GRCm39)	R59H	probably benign	Het
Col2a1	C	T	15: 97,874,057 (GRCm39)	G1375D	unknown	Het
Cyp1a1	T	C	9: 57,609,893 (GRCm39)	F436L	probably damaging	Het
Dcaf7	T	C	11: 105,944,624 (GRCm39)	V269A	probably damaging	Het
Disp2	T	C	2: 118,621,044 (GRCm39)	L592P	probably damaging	Het
Eda2r	T	A	X: 96,385,239 (GRCm39)	Q171L	probably damaging	Het
Egln2	A	G	7: 26,858,618 (GRCm39)	V408A	probably benign	Het
Gabpb2	A	G	3: 95,096,252 (GRCm39)	L325P	probably damaging	Het
Gigyf1	C	A	5: 137,523,477 (GRCm39)	Y936*	probably null	Het
Gm14149	A	T	2: 151,072,684 (GRCm39)		noncoding transcript	Het
Gnl2	C	T	4: 124,934,790 (GRCm39)	Q149*	probably null	Het
Gpr107	C	T	2: 31,104,261 (GRCm39)	T522M	probably damaging	Het
Grpr	T	A	X: 162,297,992 (GRCm39)	S351C	probably damaging	Het
Gsdma	T	C	11: 98,563,907 (GRCm39)	L287P	probably damaging	Het
Herc1	A	G	9: 66,301,993 (GRCm39)	T652A	probably damaging	Het
Ifi204	C	A	1: 173,587,927 (GRCm39)		probably benign	Het
Irx2	T	C	13: 72,779,417 (GRCm39)	S234P	probably damaging	Het
Itgal	T	A	7: 126,921,725 (GRCm39)	D808E	probably damaging	Het
Krt13	C	A	11: 100,010,189 (GRCm39)	R264L	probably damaging	Het
Marchf1	T	A	8: 66,839,071 (GRCm39)	L38I	probably benign	Het
Megf9	T	C	4: 70,367,004 (GRCm39)	H326R	probably damaging	Het
Mif4gd	G	T	11: 115,499,163 (GRCm39)		probably benign	Het
Mroh9	A	T	1: 162,893,593 (GRCm39)	M194K	probably damaging	Het
Nhlrc3	A	G	3: 53,370,501 (GRCm39)	S22P	probably damaging	Het
Nipal2	A	T	15: 34,577,714 (GRCm39)		probably null	Het
Nr1h4	A	G	10: 89,334,115 (GRCm39)	S78P	probably benign	Het
Ofcc1	G	A	13: 40,168,864 (GRCm39)	T841I	probably damaging	Het
Olfr908	A	T	9: 38,427,852 (GRCm39)	N175Y	probably damaging	Het
Or1e30	A	T	11: 73,678,337 (GRCm39)	D191V	probably damaging	Het
Or52d13	C	T	7: 103,109,695 (GRCm39)	R235Q	probably benign	Het
Pdzd2	A	G	15: 12,385,797 (GRCm39)	V991A	probably benign	Het
Pex1	G	A	5: 3,654,880 (GRCm39)		probably null	Het
Plch1	G	T	3: 63,611,598 (GRCm39)	A859E	probably damaging	Het
Pramel32	T	C	4: 88,548,202 (GRCm39)	T68A	probably benign	Het
Ranbp2	A	G	10: 58,289,244 (GRCm39)	K84R	possibly damaging	Het
Rbm14	T	C	19: 4,861,463 (GRCm39)	Y25C	probably damaging	Het
Rmi2	A	G	16: 10,653,186 (GRCm39)	D78G	probably damaging	Het
Serpina3k	C	A	12: 104,311,532 (GRCm39)	T370K	probably damaging	Het
Shc2	A	T	10: 79,457,003 (GRCm39)	L538M	probably damaging	Het
Skint1	A	G	4: 111,878,674 (GRCm39)	K202R	probably damaging	Het
Slc22a29	C	A	19: 8,195,664 (GRCm39)	S125I	possibly damaging	Het
Slc5a9	C	A	4: 111,748,941 (GRCm39)		probably null	Het
Slco4c1	A	T	1: 96,768,970 (GRCm39)	D297E	probably benign	Het
Slco6d1	T	C	1: 98,350,928 (GRCm39)	F136S	probably benign	Het
Smg1	A	T	7: 117,812,174 (GRCm39)	V39E	probably benign	Het
Spns1	G	T	7: 125,973,474 (GRCm39)		probably benign	Het
Spsb1	A	G	4: 149,990,867 (GRCm39)		probably null	Het
Sspo	T	G	6: 48,431,010 (GRCm39)	I631S	possibly damaging	Het
Syne2	T	C	12: 76,078,147 (GRCm39)	L4694P	probably damaging	Het
Taf5l	T	C	8: 124,724,844 (GRCm39)	E325G	probably benign	Het
Tars1	A	T	15: 11,394,350 (GRCm39)	S96T	probably damaging	Het
Tdrd12	T	C	7: 35,184,679 (GRCm39)	K745E	probably damaging	Het
Tenm3	A	G	8: 48,746,761 (GRCm39)	Y1015H	probably damaging	Het
Trpv3	T	A	11: 73,186,240 (GRCm39)	M677K	probably damaging	Het
Txlnb	A	T	10: 17,691,024 (GRCm39)	K191N	probably damaging	Het
Ubr1	A	G	2: 120,756,494 (GRCm39)	V711A	probably benign	Het
Uqcrb	T	C	13: 67,049,603 (GRCm39)	T41A	probably benign	Het
Usp6nl	A	G	2: 6,445,973 (GRCm39)	Y627C	probably damaging	Het
Vezf1	A	G	11: 87,965,493 (GRCm39)	D245G	probably damaging	Het
Vmn2r66	A	G	7: 84,661,204 (GRCm39)	W9R	possibly damaging	Het
Wdr17	C	T	8: 55,134,434 (GRCm39)	G349R	probably damaging	Het
Wdr35	T	A	12: 9,066,619 (GRCm39)	M749K	probably benign	Het
Wrn	A	T	8: 33,826,019 (GRCm39)		probably null	Het
Zfy1	T	G	Y: 729,626 (GRCm39)	T339P	unknown	Het

Other mutations in Ces1b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01406:Ces1b	APN	8	93,798,622 (GRCm39)	missense	probably damaging	0.98
IGL01939:Ces1b	APN	8	93,806,059 (GRCm39)	missense	probably damaging	1.00
IGL02314:Ces1b	APN	8	93,791,524 (GRCm39)	missense	possibly damaging	0.95
IGL02338:Ces1b	APN	8	93,783,675 (GRCm39)	missense	possibly damaging	0.77
IGL02647:Ces1b	APN	8	93,783,672 (GRCm39)	missense	probably benign	0.00
IGL02833:Ces1b	APN	8	93,806,038 (GRCm39)	missense	probably damaging	1.00
IGL03038:Ces1b	APN	8	93,793,680 (GRCm39)	missense	probably benign
IGL03149:Ces1b	APN	8	93,791,502 (GRCm39)	splice site	probably benign
FR4548:Ces1b	UTSW	8	93,794,720 (GRCm39)	missense	probably null
IGL02802:Ces1b	UTSW	8	93,783,594 (GRCm39)	missense	possibly damaging	0.64
R0382:Ces1b	UTSW	8	93,802,680 (GRCm39)	splice site	probably benign
R0893:Ces1b	UTSW	8	93,806,056 (GRCm39)	missense	probably benign	0.11
R0959:Ces1b	UTSW	8	93,794,775 (GRCm39)	missense	probably damaging	1.00
R1386:Ces1b	UTSW	8	93,794,705 (GRCm39)	missense	probably benign	0.02
R1440:Ces1b	UTSW	8	93,794,736 (GRCm39)	missense	probably damaging	0.97
R1667:Ces1b	UTSW	8	93,783,532 (GRCm39)	missense	possibly damaging	0.75
R2113:Ces1b	UTSW	8	93,794,783 (GRCm39)	missense	probably benign
R2193:Ces1b	UTSW	8	93,806,505 (GRCm39)	missense	probably benign	0.00
R2508:Ces1b	UTSW	8	93,799,969 (GRCm39)	missense	possibly damaging	0.75
R4776:Ces1b	UTSW	8	93,789,658 (GRCm39)	missense	possibly damaging	0.92
R5108:Ces1b	UTSW	8	93,798,541 (GRCm39)	missense	probably damaging	1.00
R5117:Ces1b	UTSW	8	93,799,837 (GRCm39)	critical splice donor site	probably null
R5308:Ces1b	UTSW	8	93,793,645 (GRCm39)	missense	probably benign	0.00
R5381:Ces1b	UTSW	8	93,791,647 (GRCm39)	missense	probably benign	0.02
R5392:Ces1b	UTSW	8	93,798,590 (GRCm39)	missense	probably damaging	0.98
R5614:Ces1b	UTSW	8	93,794,836 (GRCm39)	missense	probably benign	0.00
R5816:Ces1b	UTSW	8	93,799,890 (GRCm39)	missense	probably benign	0.05
R6554:Ces1b	UTSW	8	93,791,619 (GRCm39)	missense	probably benign	0.03
R6576:Ces1b	UTSW	8	93,783,547 (GRCm39)	missense	probably benign	0.06
R6601:Ces1b	UTSW	8	93,806,109 (GRCm39)	missense	probably benign
R6662:Ces1b	UTSW	8	93,790,697 (GRCm39)	missense	probably benign	0.33
R6753:Ces1b	UTSW	8	93,793,648 (GRCm39)	nonsense	probably null
R6904:Ces1b	UTSW	8	93,787,038 (GRCm39)	missense	probably damaging	0.96
R7267:Ces1b	UTSW	8	93,806,132 (GRCm39)	missense	possibly damaging	0.58
R7371:Ces1b	UTSW	8	93,783,982 (GRCm39)	critical splice donor site	probably null
R7396:Ces1b	UTSW	8	93,789,757 (GRCm39)	missense	probably benign	0.00
R7992:Ces1b	UTSW	8	93,786,987 (GRCm39)	missense	probably benign	0.34
R8022:Ces1b	UTSW	8	93,795,943 (GRCm39)	critical splice donor site	probably null
R8728:Ces1b	UTSW	8	93,798,576 (GRCm39)	missense	probably benign
R8809:Ces1b	UTSW	8	93,786,949 (GRCm39)	missense	probably damaging	1.00
R8809:Ces1b	UTSW	8	93,786,948 (GRCm39)	missense	probably damaging	1.00
R9268:Ces1b	UTSW	8	93,798,583 (GRCm39)	missense	probably damaging	1.00
R9476:Ces1b	UTSW	8	93,799,890 (GRCm39)	missense	probably damaging	0.97
R9638:Ces1b	UTSW	8	93,806,534 (GRCm39)	missense	probably benign
R9667:Ces1b	UTSW	8	93,791,637 (GRCm39)	missense	probably benign	0.02
R9745:Ces1b	UTSW	8	93,790,625 (GRCm39)	missense	probably benign
R9757:Ces1b	UTSW	8	93,806,501 (GRCm39)	missense	probably benign	0.02
X0024:Ces1b	UTSW	8	93,789,645 (GRCm39)	missense	probably benign
Z1088:Ces1b	UTSW	8	93,791,594 (GRCm39)	missense	probably damaging	0.96
Z1177:Ces1b	UTSW	8	93,802,782 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TTAGGAATGGCCCATCTGACTC -3'
(R):5'- TTGACCCCTGAACATGCAC -3'

Sequencing Primer
(F):5'- GAATGGCCCATCTGACTCTAGAG -3'
(R):5'- CACAGTGATTAGCCAGGGTCTTC -3'

Posted On

2015-10-08